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Sample records for sarcocystis neurona sporocysts

  1. Early migration of Sarcocystis neurona in ponies fed sporocysts.

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    Elitsur, E; Marsh, A E; Reed, S M; Dubey, J P; Oglesbee, M J; Murphy, J E; Saville, W J A

    2007-10-01

    Sarcocystis neurona is the most important cause of equine protozoal myeloencephalitis (EPM), a neurologic disease of the horse. In the present work, the kinetics of S. neurona invasion is determined in the equine model. Six ponies were orally inoculated with 250 x 10(6) S. neurona sporocysts via nasogastric intubation and killed on days 1, 2, 3, 5, 7, and 9 postinoculation (PI). At necropsy, tissue samples were examined for S. neurona infection. The parasite was isolated from the mesenteric lymph nodes at 1, 2, and 7 days PI; the liver at 2, 5, and 7 days PI; and the lungs at 5, 7, and 9 days PI by bioassays in interferon gamma gene knock out mice (KO) and from cell culture. Microscopic lesions consistent with an EPM infection were observed in brain and spinal cord of ponies killed 7 and 9 days PI. Results suggest that S. neurona disseminates quickly in tissue of naive ponies.

  2. Antibody index and specific antibody quotient in horses after intragastric administration of Sarcocystis neurona sporocysts.

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    Heskett, Katherine A; Mackay, Robert J

    2008-03-01

    To investigate the use of a specific antibody index (AI) that relates Sarcocystis neurona-specific IgG quotient (Q(SN)) to total IgG quotient (Q(IgG)) for the detection of the anti-S neurona antibody fraction of CNS origin in CSF samples obtained from horses after intragastric administration of S neurona sporocysts. 18 adult horses. 14 horses underwent intragastric inoculation (day 0) with S neurona sporocysts, and 4 horses remained unchallenged; blood and CSF samples were collected on days - 1 and 84. For purposes of another study, some challenged horses received intermittent administration of ponazuril (20 mg/kg, PO). Sarcocystis neurona-specific IgG concentrations in CSF (SN(CSF)) and plasma (SN(plasma)) were measured via a direct ELISA involving merozoite lysate antigen and reported as ELISA units (EUs; arbitrary units based on a nominal titer for undiluted immune plasma of 100,000 EUs/mL). Total IgG concentrations in CSF (IgG(CSF)) and plasma (IgG(plasma)) were quantified via a sandwich ELISA and a radial immunodiffusion assay, respectively; Q(SN), Q(IgG), and AI were calculated. Following sporocyst challenge, mean +/- SEM SN(CSF) and SN(plasma) increased significantly (from 8.8 +/- 1.0 EUs/mL to 270.0 +/- 112.7 EUs/mL and from 1,737 +/- 245 EUs/mL to 43,169 +/- 13,770 EUs/mL, respectively). Challenge did not affect total IgG concentration, Q(SN), Q(IgG), or AI. S neurona-specific IgG detected in CSF samples from sporocyst-challenged horses appeared to be extraneural in origin; thus, this experimental challenge may not reliably result in CNS infection. Calculation of a specific AI may have application to the diagnosis of S neurona-associated myeloencephalitis in horses.

  3. The gamma interferon knockout mouse model for sarcocystis neurona: comparison of infectivity of sporocysts and merozoites and routes of inoculation.

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    Dubey, J P; Lindsay, D S; Kwok, O C; Shen, S K

    2001-10-01

    The dose-related infectivity of Sarcocystis neurona sporocysts and merozoites of 2 recent isolates of S. neurona was compared in gamma interferon knockout (KO) mice. Tenfold dilutions of sporocysts or merozoites were bioassayed in mice, cell culture, or both. All 8 mice, fed 1,000 sporocysts, developed neurological signs with demonstrable S. neurona in their tissues. Of 24 mice fed low numbers of sporocysts (100, 10, 1), 18 became ill by 4 wk postinoculation, and S. neurona was demonstrated in their brains; antibodies (S. neurona agglutination test) to S. neurona and S. neurona parasites were not found in tissues of the 6 mice that were fed sporocysts and survived for >39 days. One thousand culture-derived merozoites of these 2 isolates were pathogenic to all 8 mice inoculated subcutaneously (s.c.). Of the 24 mice inoculated s.c. with merozoites numbering 100, 10, or 1, only 3 mice had demonstrable S. neurona infection; antibodies to S. neurona were not found in the 21 mice that had no demonstrable organisms. As few as 10 merozoites were infective for cell cultures. These results demonstrate that at least 1,000 merozoites are needed to cause disease in KO mice. Sarcocystis neurona sporocysts were infective to mice by the s.c. route.

  4. Parasitemia in an immunocompetent horse experimentally challenged with Sarcocystis neurona sporocysts.

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    Rossano, M G; Schott, H C; Murphy, A J; Kaneene, J B; Sellon, D C; Hines, M T; Hochstatter, T; Bell, J A; Mansfield, L S

    2005-01-04

    Equine protozoal myeloencephalitis (EPM) is a serious neurological disease of horses in Americans. Most cases are attributed to infection of the central nervous system with Sarcocystis neurona. Parasitemia has not been demonstrated in immunocompetent horses, but has been documented in one immunocompromised foal. The objective of this study was to isolate viable S. neurona from the blood of immunocompetent horses. Horses used in this study received orally administered S. neurona sporocysts (strain SN 37-R) daily for 112 days at the following doses: 100/day for 28 days, followed by 500/day for 28 days, followed by 1000/day for 56 days. On day 98 of the study, six yearling colts were selected for attempted culture of S. neurona from blood, two testing positive, two testing suspect and two testing negative for antibodies against S. neurona on day 84 of the study. Two 10 ml tubes with EDTA were filled from each horse by jugular venipuncture and the plasma fraction rich in mononuclear cells was pipetted onto confluent equine dermal cell cultures. The cultures were monitored weekly for parasite growth for 12 weeks. Merozoites grown from cultures were harvested and tested using S. neurona-specific PCR with RFLP to confirm species identity. PCR products were sequenced and compared to known strains of S. neurona. After 38 days of in vitro incubation, one cell culture from a horse testing positive for antibodies against S. neurona was positive for parasite growth while the five remaining cultures remained negative for parasite growth for all 12 weeks. The Sarcocystis isolate recovered from cell culture was confirmed to be S. neurona by PCR with RFLP. Gene sequence analysis revealed that the isolate was identical to the challenge strain SN-37R and differed from two known strains UCD1 and MIH1. To our knowledge this is the first report of parasitemia with S. neurona in an immunocompetent horse.

  5. Sarcocystis neurona manipulation using culture-derived merozoites for bradyzoite and sporocyst production.

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    Chaney, Sarah B; Marsh, Antoinette E; Lewis, Stephanie; Carman, Michelle; Howe, Daniel K; Saville, William J; Reed, Stephen M

    2017-04-30

    Equine protozoal myeloencephalitis (EPM) remains a significant central nervous system disease of horses in the American continents. Sarcocystis neurona is considered the primary causative agent and its intermediate life stages are carried by a wide host-range including raccoons (Procyon lotor) in North America. S. neurona sarcocysts mature in raccoon skeletal muscle and can produce central nervous system disease in raccoons, mirroring the clinical presentation in horses. The study aimed to develop laboratory tools whereby the life cycle and various life stages of S. neurona could be better studied and manipulated using in vitro and in vivo systems and compare the biology of two independent isolates. This study utilized culture-derived parasites from S. neurona strains derived from a raccoon or from a horse to initiate raccoon infections. Raccoon tissues, including fresh and cryopreserved tissues, were used to establish opossum (Didelphis virginiana) infections, which then shed sporocyts with retained biological activity to cause encephalitis in mice. These results demonstrate that sarcocysts can be generated using in vitro-derived S. neurona merozoites, including an isolate originally derived from a naturally infected horse with clinical EPM. This study indicates the life cycle can be significantly manipulated in the laboratory without affecting subsequent stage development, allowing further purification of strains and artificial maintenance of the life cycle. Published by Elsevier B.V.

  6. Prevalence of and risk factors associated with the presence of Sarcocystis neurona sporocysts in opossum (Didelphis virginiana) from Michigan: a retrospective study.

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    Elsheikha, Hany M; Murphy, Alice J; Mansfield, Linda S

    2004-11-10

    From April 1996 to December 2002 the prevalence of Sarcocystis neurona sporocysts in North American opossum (Didelphis virginiana) in Southern Michigan was estimated. Sporocysts of S. neurona were found in intestinal scrapings from 31 (15%) of 206 examined opossum. The frequency of infection was higher in adult animals (26/206; 12.6%) and females (19/206; 9.2%) than in juveniles (5/206; 2.4%) and males (12/206; 5.8%). Also, prevalence of S. neurona sporocysts in opossums in relation to factors such as age, sex, season, body condition, presence of concomitant infection, and presence of young in the pouch of females was studied in detail over the course of the year, 2002. Univariate analyses identified the following factors as being associated with the presence of S. neurona sporocysts in opossums: (i) for age, adult (odd ratio [OR] = 2.074, P = 0.0005); (ii) for sex, female (OR = 7.016, P = 0.0119); (iii) for season, summer (OR = 7.917, P = 0.0032) and spring (OR = 4.071, P = 0.1063); (iv) for body condition, poor (OR = 3.50, P = 0.1200) and good (OR = 1.167, P = 0.8637); (v) for the presence of concomitant infection (OR = 23.056, P = 0001), and (vi) for the presence of young in the pouch of females (OR = 40.083, P = 0.0001). Multivariate logistic-regression analyses selected the following factors as being significantly associated with presence of S. neurona sporocysts in opossums: (i) for the presence of concomitant infection (OR = 8.722, P = 0.0160) and (ii) for the presence of young in the pouch of females (OR = 31.915, P = 0.0065). The prevalence of S. neurona sporocysts in D. virginiana suggests that this opossum may constitute an ample reservoir of infection to other animals in the northern United States.

  7. Sarcocystis neurona infection in gamma interferon gene knockout (KO) mice: comparative infectivity of sporocysts in two strains of KO mice, effect of trypsin digestion on merozoite viability, and infectivity of bradyzoites to KO mice and cell culture.

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    Dubey, J P; Sundar, N; Kwok, O C H; Saville, W J A

    2013-09-01

    The protozoan Sarcocystis neurona is the primary cause of Equine Protozoal Myeloencephalitis (EPM). EPM or EPM-like illness has been reported in horses, sea otters, and several other mammals. The gamma interferon gene knockout (KO) mouse is often used as a model to study biology and discovery of new therapies against S. neurona because it is difficult to induce clinical EPM in other hosts, including horses. In the present study, infectivity of three life cycle stages (merozoites, bradyzoites, sporozoites) to KO mice and cell culture was studied. Two strains of KO mice (C57-black, and BALB/c-derived, referred here as black or white) were inoculated orally graded doses of S. neurona sporocysts; 12 sporocysts were infective to both strains of mice and all infected mice died or became ill within 70 days post-inoculation. Although there was no difference in infectivity of sporocysts to the two strains of KO mice, the disease was more severe in black mice. S. neurona bradyzoites were not infectious to KO mice and cell culture. S. neurona merozoites survived 120 min incubation in 0.25% trypsin, indicating that trypsin digestion can be used to recover S. neurona from tissues of acutely infected animals. Published by Elsevier B.V.

  8. Serologic responses of cats against experimental Sarcocystis neurona infections.

    Science.gov (United States)

    Dubey, J P; Lindsay, D S; Saville, W J A

    2002-08-02

    Sarcocystis neurona is the most important cause of a neurologic disease of horses, equine protozoal myeloencephalitis (EPM). Cats and other carnivores can act as its intermediate hosts and horses are aberrant hosts. Little is known of the sero-epidemiology of S. neurona infections in cats. In the present study, antibodies to S. neurona were evaluated by the S. neurona agglutination test (SAT). Cats fed sporocysts from the feces of naturally infected opossums or inoculated intramuscularly with S. neurona merozoites developed high levels (> or =1:4000) of SAT antibodies. Antibodies to S. neurona were not found in a cat inoculated with merozoites of the closely related parasite, Sarcocystis falcatula. These results should be useful in studying sero-epidemiology of S. neurona infections in cats.

  9. Lack of Sarcocystis neurona antibody response in Virginia opossums (Didelphis virginiana) fed Sarcocystis neurona-infected muscle tissue.

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    Cheadle, M A; Lindsay, D S; Greiner, E C

    2006-06-01

    Serum was collected from laboratory-reared Virginia opossums (Didelphis virginiana) to determine whether experimentally infected opossums shedding Sarcocystis neurona sporocysts develop serum antibodies to S. neurona merozoite antigens. Three opossums were fed muscles from nine-banded armadillos (Dasypus novemcinctus), and 5 were fed muscles from striped skunks (Mephitis mephitis). Serum was also collected from 26 automobile-killed opossums to determine whether antibodies to S. neurona were present in these opossums. Serum was analyzed using the S. neurona direct agglutination test (SAT). The SAT was modified for use with a filter paper collection system. Antibodies to S. neurona were not detected in any of the serum samples from opossums, indicating that infection in the opossum is localized in the small intestine. Antibodies to S. neurona were detected in filter-paper-processed serum samples from 2 armadillos naturally infected with S. neurona.

  10. Experimental inoculation of domestic cats (Felis domesticus) with Sarcocystis neurona or S. neurona-like merozoites.

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    Butcher, M; Lakritz, J; Halaney, A; Branson, K; Gupta, G D; Kreeger, J; Marsh, A E

    2002-07-29

    Sarcocystis neurona is the parasite most commonly associated with equine protozoal myeloencephalitis (EPM). Recently, cats (Felis domesticus) have been demonstrated to be an experimental intermediate host in the life cycle of S. neurona. This study was performed to determine if cats experimentally inoculated with culture-derived S. neurona merozoites develop tissue sarcocysts infectious to opossums (Didelphis virginiana), the definitive host of S. neurona. Four cats were inoculated with S. neurona or S. neurona-like merozoites and all developed antibodies reacting to S. neurona merozoite antigens, but tissue sarcocysts were detected in only two cats. Muscle tissues from the experimentally inoculated cats with and without detectable sarcocysts were fed to laboratory-reared opossums. Sporocysts were detected in gastrointestinal (GI) scrapings of one opossum fed experimentally infected feline tissues. The study results suggest that cats can develop tissue cysts following inoculation with culture-derived Sarcocystis sp. merozoites in which the particular isolate was originally derived from a naturally infected cat with tissue sarcocysts. This is in contrast to cats which did not develop tissue cysts when inoculated with S. neurona merozoites originally derived from a horse with EPM. These results indicate present biological differences between the culture-derived merozoites of two Sarcocystis isolates, Sn-UCD 1 and Sn-Mucat 2.

  11. Experimental infection of ponies with Sarcocystis fayeri and differentiation from Sarcocystis neurona infections in horses.

    Science.gov (United States)

    Saville, W J A; Dubey, J P; Oglesbee, M J; Sofaly, C D; Marsh, A E; Elitsur, E; Vianna, M C; Lindsay, D S; Reed, S M

    2004-12-01

    Sarcocystis neurona and Sarcocystis fayeri infections are common in horses in the Americas. Their antemortem diagnosis is important because the former causes a neurological disorder in horses, whereas the latter is considered nonpathogenic. There is a concern that equine antibodies to S. fayeri might react with S. neurona antigens in diagnostic tests. In this study, 4 ponies without demonstrable serum antibodies to S. neurona by Western immunoblot were used. Three ponies were fed 1 x 10(5) to 1 x 10(7) sporocysts of S. fayeri obtained from dogs that were fed naturally infected horse muscles. All ponies remained asymptomatic until the termination of the experiment, day 79 postinoculation (PI). All serum samples collected were negative for antibodies to S. neurona using the Western blot at the initial screening, just before inoculation with S. fayeri (day 2) and weekly until day 79 PI. Cerebrospinal fluid samples from each pony were negative for S. neurona antibodies. Using the S. neurona agglutination test, antibodies to S. neurona were not detected in 1:25 dilution of sera from any samples, except that from pony no. 4 on day 28; this pony had received 1 X 10(7) sporocysts. Using indirect immunofluorescence antibody tests (IFATs), 7 serum samples were found to be positive for S. neurona antibodies from 1:25 to 1:400 dilutions. Sarcocystis fayeri sarcocysts were found in striated muscles of all inoculated ponies, with heaviest infections in the tongue. All sarcocysts examined histologically appeared to contain only microcytes. Ultrastructurally, S. fayeri sarcocysts could be differentiated from S. neurona sarcocysts by the microtubules (mt) in villar protrusions on sarcocyst walls; in S. fayeri the mt extended from the villar tips to the pellicle of zoites, whereas in S. neurona the mt were restricted to the middle of the cyst wall. Results indicate that horses with S. fayeri infections may be misdiagnosed as being S. neurona infected using IFAT, and further research

  12. Sarcocystis neurona encephalitis in a dog.

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    Cooley, A J; Barr, B; Rejmanek, D

    2007-11-01

    A 1.5-year-old male Feist dog was presented to a veterinarian for reluctance to stand on the hind legs. Treatment included dexamethasone and resulted in a favorable initial response, but posterior paresis returned and progressed to recumbency, hyperesthesia, and attempts to bite the owner. The dog was euthanized. The brain was negative for rabies by fluorescent antibody analysis. Multiple foci of encephalitis were found in the cerebrum and particularly in the cerebellum. Protozoa morphologically consistent with Sarcocystis sp. were identified at sites of intense inflammation and malacia. Additionally, multiple schizonts were identified in areas without inflammation. Immunohistochemistry using both polyclonal and monoclonal antibodies specific for Sarcocystis neurona was strongly positive. No reaction to polyclonal antisera for Toxoplasma gondii or Neospora caninum was found. Polymerase chain reaction confirmed that the protozoa were S. neurona. Additional aberrant hosts for S. neurona other than horses have been identified, but S. neurona encephalitis has not been documented previously in the dog.

  13. Effect of intermittent oral administration of ponazuril on experimental Sarcocystis neurona infection of horses.

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    Mackay, Robert J; Tanhauser, Susan T; Gillis, Karen D; Mayhew, Ian G; Kennedy, Tom J

    2008-03-01

    To evaluate the effect of intermittent oral administration of ponazuril on immunoconversion against Sarcocystis neurona in horses inoculated intragastrically with S neurona sporocysts. 20 healthy horses that were seronegative for S neurona-specific IgG. 5 control horses were neither inoculated with sporocysts nor treated. Other horses (5 horses/group) each received 612,500 S neurona sporocysts via nasogastric tube (day 0) and were not treated or were administered ponazuril (20 mg/kg, PO) every 7 days (beginning on day 5) or every 14 days (beginning on day 12) for 12 weeks. Blood and CSF samples were collected on day - 1 and then every 14 days after challenge for western blot assessment of immunoconversion. Clinical signs of equine protozoal myeloencephalitis (EPM) were monitored, and tissues were examined histologically after euthanasia. Sera from all challenged horses yielded positive western blot results within 56 days. Immunoconversion in CSF was detected in only 2 of 5 horses that were treated weekly; all other challenged horses immunoconverted within 84 days. Weekly administration of ponazuril significantly reduced the antibody response against the S neurona 17-kd antigen in CSF. Neurologic signs consistent with EPM did not develop in any group; likewise, histologic examination of CNS tissue did not reveal protozoa or consistent degenerative or inflammatory changes. Administration of ponazuril every 7 days, but not every 14 days, significantly decreased intrathecal anti-S neurona antibody responses in horses inoculated with S neurona sporocysts. Protocols involving intermittent administration of ponazuril may have application in prevention of EPM.

  14. California mussels (Mytilus californianus) as sentinels for marine contamination with Sarcocystis neurona.

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    Michaels, Lauren; Rejmanek, Daniel; Aguilar, Beatriz; Conrad, Patricia; Shapiro, Karen

    2016-05-01

    Sarcocystis neurona is a terrestrial parasite that can cause fatal encephalitis in the endangered Southern sea otter (Enhydra lutris nereis). To date, neither risk factors associated with marine contamination nor the route of S. neurona infection to marine mammals has been described. This study evaluated coastal S. neurona contamination using California mussels (Mytilus californianus) as sentinels for pathogen pollution. A field investigation was designed to test the hypotheses that (1) mussels can serve as sentinels for S. neurona contamination, and (2) S. neurona contamination in mussels would be highest during the rainy season and in mussels collected near freshwater. Initial validation of molecular assays through sporocyst spiking experiments revealed the ITS-1500 assay to be most sensitive for detection of S. neurona, consistently yielding parasite amplification at concentrations ⩾5 sporocysts/1 mL mussel haemolymph. Assays were then applied on 959 wild-caught mussels, with detection of S. neurona confirmed using sequence analysis in three mussels. Validated molecular assays for S. neurona detection in mussels provide a novel toolset for investigating marine contamination with this parasite, while confirmation of S. neurona in wild mussels suggests that uptake by invertebrates may serve as a route of transmission to susceptible marine animals.

  15. Sarcocystis neurona and Neospora caninum in Brazilian opossums (Didelphis spp.): Molecular investigation and in vitro isolation of Sarcocystis spp.

    Science.gov (United States)

    Gondim, Leane S Q; Jesus, Rogério F; Ribeiro-Andrade, Müller; Silva, Jean C R; Siqueira, Daniel B; Marvulo, Maria F V; Aléssio, Felipe M; Mauffrey, Jean-François; Julião, Fred S; Savani, Elisa San Martin Mouriz; Soares, Rodrigo M; Gondim, Luís F P

    2017-08-30

    Sarcocystis neurona and Neospora spp. are protozoan parasites that induce neurological diseases in horses and other animal species. Opossums (Didelphis albiventris and Didelphis virginiana) are definitive hosts of S. neurona, which is the major cause of equine protozoal myeloencephalitis (EPM). Neospora caninum causes abortion in cattle and infects a wide range of animal species, while N. hughesi is known to induce neurologic disease in equids. The aims of this study were to investigate S. neurona and N. caninum in tissues from opossums in the northeastern Brazil, and to isolate Brazilian strains of Sarcocystis spp. from wild opossums for comparison with previously isolated strains. Carcasses of 39 opossums from Bahia state were available for molecular identification of Sarcocystis spp. and N. caninum in their tissues, and for sporocyst detection by intestinal scraping. In addition, Sarcocystis-like sporocysts from nine additional opossums, obtained in São Paulo state, were tested. Sarcocystis DNA was found in 16 (41%) of the 39 opossums' carcasses; N. caninum DNA was detected in tissues from three opossums. The sporocysts from the nine additional opossums from São Paulo state were tested by bioassay and induced infection in nine budgerigars, but in none of the gamma-interferon knockout mice. In vitro isolation was successful using tissues from all nine budgerigars. The isolated strains were maintained in CV-1 and Vero cells. Three of nine isolates presented contamination in cell culture and were discarded. Analysis of six isolates based on five loci showed that these parasites were genetically different from each other and also distinct from S. neurona, S. falcatula, S. lindsayi, and S. speeri. In conclusion, opossums in the studied regions were infected with N. caninum and Sarcocystis spp. and represent a potential source of infection to other animals. This is the first report of N. caninum infection in tissues from black-eared opossum (D. aurita or D

  16. Molecular characterization of Sarcocystis neurona strains from opossums (Didelphis virginiana) and intermediate hosts from Central California.

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    Rejmanek, Daniel; Miller, Melissa A; Grigg, Michael E; Crosbie, Paul R; Conrad, Patricia A

    2010-05-28

    Sarcocystis neurona is a significant cause of neurological disease in horses and other animals, including the threatened Southern sea otter (Enhydra lutris nereis). Opossums (Didelphis virginiana), the only known definitive hosts for S. neurona in North America, are an introduced species in California. S. neurona DNA isolated from sporocysts and/or infected tissues of 10 opossums, 6 horses, 1 cat, 23 Southern sea otters, and 1 harbor porpoise (Phocoena phocoena) with natural infections was analyzed based on 15 genetic markers, including the first internal transcribed spacer (ITS-1) region; the 25/396 marker; S. neurona surface antigen genes (snSAGs) 2, 3, and 4; and 10 different microsatellites. Based on phylogenetic analysis, most of the S. neurona strains segregated into three genetically distinct groups. Additionally, fifteen S. neurona samples from opossums and several intermediate hosts, including sea otters and horses, were found to be genetically identical across all 15 genetic markers, indicating that fatal encephalitis in Southern sea otters and equine protozoal myeloencephalitis (EPM) in horses is strongly linked to S. neurona sporocysts shed by opossums. (c) 2010 Elsevier B.V. All rights reserved.

  17. Sarcocystis neurona infections in raccoons (Procyon lotor): evidence for natural infection with sarcocysts, transmission of infection to opossums (Didelphis virginiana), and experimental induction of neurologic disease in raccoons.

    Science.gov (United States)

    Dubey, J P; Saville, W J; Stanek, J F; Lindsay, D S; Rosenthal, B M; Oglesbee, M J; Rosypal, A C; Njoku, C J; Stich, R W; Kwok, O C; Shen, S K; Hamir, A N; Reed, S M

    2001-10-24

    Equine protozoal myeloencephalitis (EPM) is a serious neurologic disease of horses in the Americas and Sarcocystis neurona is the most common etiologic agent. The distribution of S. neurona infections follows the geographical distributions of its definitive hosts, opossums (Didelphis virginiana, Didelphis albiventris). Recently, cats and skunks were reported as experimental and armadillos as natural intermediate hosts of S. neurona. In the present report, raccoons (Procyon lotor) were identified as a natural intermediate host of S. neurona. Two laboratory-raised opossums were found to shed S. neurona-like sporocysts after ingesting tongues of naturally-infected raccoons. Interferon-gamma gene knockout (KO) mice fed raccoon-opossum-derived sporocysts developed neurologic signs. S. neurona was identified immunohistochemically in tissues of KO mice fed sporocysts and the parasite was isolated in cell cultures inoculated with infected KO mouse tissues. The DNA obtained from the tongue of a naturally-infected raccoon, brains of KO mice that had neurological signs, and from the organisms recovered in cell cultures inoculated with brains of neurologic KO mice, corresponded to that of S. neurona. Two raccoons fed mature S. neurona sarcocysts did not shed sporocysts in their feces, indicating raccoons are not likely to be its definitive host. Two raccoons fed sporocysts from opossum feces developed clinical illness and S. neurona-associated encephalomyelitis was found in raccoons killed 14 and 22 days after feeding sporocysts; schizonts and merozoites were seen in encephalitic lesions.

  18. Life cycle of Sarcocystis neurona in its natural intermediate host, the raccoon, Procyon lotor.

    Science.gov (United States)

    Stanek, J F; Dubey, J P; Oglesbee, M J; Reed, S M; Lindsay, D S; Capitini, L A; Njoku, C J; Vittitow, K L; Saville, W J A

    2002-12-01

    Sarcocystis neurona causes encephalomyelitis in many species of mammals and is the most important cause of neurologic disease in the horse. Its complete life cycle is unknown, particularly its development and localization in the intermediate host. Recently, the raccoon (Procyon lotor) was recognized as a natural intermediate host of S. neurona. In the present study, migration and development of S. neurona was studied in 10 raccoons that were fed S. neurona sporocysts from experimentally infected opossums; 4 raccoons served as controls. Raccoons were examined at necropsy 1, 3, 5, 7, 10, 14, 15, 22, 37, and 77 days after feeding on sporocysts (DAFS). Tissue sections of most of the organs were studied histologically and reacted with anti-S. neurona-specific polyclonal rabbit serum in an immunohistochemical test. Parasitemia was demonstrated in peripheral blood of raccoons 3 and 5 DAFS. Individual zoites were seen in histologic sections of intestines of raccoons euthanized 1, 3, and 5 DAFS. Schizonts and merozoites were seen in many tissues 7 to 22 DAFS, particularly in the brain. Sarcocysts were seen in raccoons killed 22 DAFS. Sarcocysts at 22 DAFS were immature and seen only in skeletal muscle. Mature sarcocysts were seen in all skeletal samples, particularly in the tongue of the raccoon 77 DAFS; these sarcocysts were infective to laboratory-raised opossums. This is the first report of the complete development of S. neurona schizonts and sarcocysts in a natural intermediate host.

  19. Evidence to support horses as natural intermediate hosts for Sarcocystis neurona.

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    Mullaney, Thomas; Murphy, Alice J; Kiupel, Matti; Bell, Julia A; Rossano, Mary G; Mansfield, Linda S

    2005-10-10

    Opossums (Didelphis spp.) are the definitive host for the protozoan parasite Sarcocystis neurona, the causative agent of equine protozoal myeloencephalitis (EPM). Opossums shed sporocysts in feces that can be ingested by true intermediate hosts (cats, raccoons, skunks, armadillos and sea otters). Horses acquire the parasite by ingestion of feed or water contaminated by opossum feces. However, horses have been classified as aberrant intermediate hosts because the terminal asexual sarcocyst stage that is required for transmission to the definitive host has not been found in their tissues despite extensive efforts to search for them [Dubey, J.P., Lindsay, D.S., Saville, W.J., Reed, S.M., Granstrom, D.E., Speer, C.A., 2001b. A review of Sarcocystis neurona and equine protozoal myeloencephalitis (EPM). Vet. Parasitol. 95, 89-131]. In a 4-month-old filly with neurological disease consistent with EPM, we demonstrate schizonts in the brain and spinal cord and mature sarcocysts in the tongue and skeletal muscle, both with genetic and morphological characteristics of S. neurona. The histological and electron microscopic morphology of the schizonts and sarcocysts were identical to published features of S. neurona [Stanek, J.F., Dubey, J.P., Oglesbee, M.J., Reed, S.M., Lindsay, D.S., Capitini, L.A., Njoku, C.J., Vittitow, K.L., Saville, W.J., 2002. Life cycle of Sarcocystis neurona in its natural intermediate host, the raccoon, Procyon lotor. J. Parasitol. 88, 1151-1158]. DNA from schizonts and sarcocysts from this horse produced Sarcocystis specific 334bp PCR products [Tanhauser, S.M., Yowell, C.A., Cutler, T.J., Greiner, E.C., MacKay, R.J., Dame, J.B., 1999. Multiple DNA markers differentiate Sarcocystis neurona and Sarcocystis falcatula. J. Parasitol. 85, 221-228]. Restriction fragment length polymorphism (RFLP) analysis of these PCR products showed banding patterns characteristic of S. neurona. Sequencing, alignment and comparison of both schizont and sarcocyst DNA

  20. Effect of daily administration of pyrantel tartrate in preventing infection in horses experimentally challenged with Sarcocystis neurona.

    Science.gov (United States)

    Rossano, Mary G; Schott, Harold C; Kaneene, John B; Murphy, Alice J; Kruttlin, Elizabeth A; Hines, Melissa T; Sellon, Debra C; Patterson, Jon S; Elsheikha, Hany M; Dubey, J P; Mansfield, Linda S

    2005-05-01

    To determine whether daily administration of pyrantel tartrate can prevent infection in horses experimentally challenged with Sarcocystis neurona. 24 mixed-breed specific-pathogen-free weanling horses, 10 adult horses, 1 opossum, and 6 mice. Sarcocystis neurona-naïve weanling horses were randomly allocated to 2 groups. Group A received pyrantel tartrate at the labeled dose, and group B received a nonmedicated pellet. Both groups were orally inoculated with 100 sporocysts/d for 28 days, 500 sporocysts/d for 28 days, and 1000 sporocysts/d for 56 days. Blood samples were collected weekly, and CSF was collected monthly. Ten seronegative adult horses were monitored as untreated, uninfected control animals. All serum and CSF samples were tested by use of western blot tests to detect antibodies against S. neurona. At the end of the study, the number of seropositive and CSF-positive horses in groups A and B were compared by use of the Fisher exact test. Time to seroconversion on the basis of treatment groups and sex of horses was compared in 2 univariable Cox proportional hazards models. After 134 days of sporocyst inoculation, no significant differences were found between groups A and B for results of western blot tests of serum or CSF There were no significant differences in number of days to seroconversion on the basis of treatment groups or sex of horses. The control horses remained seronegative. Daily administration of pyrantel tartrate at the current labeled dose does not prevent S. neurona infection in horses.

  1. Development and evaluation of a Sarcocystis neurona-specific IgM capture enzyme-linked immunosorbent assay.

    Science.gov (United States)

    Murphy, J E; Marsh, A E; Reed, S M; Meadows, C; Bolten, K; Saville, W J A

    2006-01-01

    Equine protozoal myeloencephalitis (EPM) is a serious neurologic disease of horses caused primarily by the protozoal parasite Sarcocystis neurona. Currently available antemortem diagnostic testing has low specificity. The hypothesis of this study was that serum and cerebrospinal fluid (CSF) of horses experimentally challenged with S neurona would have an increased S neurona-specific IgM (Sn-IgM) concentration after infection, as determined by an IgM capture enzyme linked immunoassay (ELISA). The ELISA was based on the S neurona low molecular weight protein SNUCD-1 antigen and the monoclonal antibody 2G5 labeled with horseradish peroxidase. The test was evaluated using serum and CSF from 12 horses experimentally infected with 1.5 million S neurona sporocysts and 16 horses experimentally infected with varying doses (100 to 100,000) of S neurona sporocysts, for which results of histopathologic examination of the central nervous system were available. For horses challenged with 1.5 million sporocysts, there was a significant increase in serum Sn-IgM concentrations compared with values before infection at weeks 2-6 after inoculation (P neurona, there were significant increases in serum Sn-IgM concentration at various points in time after inoculation, depending on the challenge dose (P < .01). In addition, there was a significant increase between the CSF Sn-IgM concentrations before and after inoculation (P < .0001). These results support further evaluation of the assay as a diagnostic test during the acute phase of EPM.

  2. Infection of immunodeficient horses with Sarcocystis neurona does not result in neurologic disease.

    Science.gov (United States)

    Sellon, Debra C; Knowles, Donald P; Greiner, Ellis C; Long, Maureen T; Hines, Melissa T; Hochstatter, Tressa; Tibary, Ahmed; Dame, John B

    2004-11-01

    Equine protozoal myeloencephalitis is a progressive neurologic disease of horses most commonly caused by infection with the apicomplexan parasite Sarcocystis neurona. Factors affecting neuroinvasion and neurovirulence have not been determined. We investigated the pathogenesis of infection with S. neurona in horses with severe combined immune deficiency (SCID). Two immunocompetent (IC) Arabian horses and two Arabian horses with SCID were infected orally with 5 x 10(5) sporocysts of S. neurona. Four IC horses and one SCID horse were infected intravenously (i.v.) with 5 x 10(8) merozoites of the WSU-1 isolate of S. neurona. Despite prolonged parasitemia and persistent infection of visceral tissues (skeletal muscle, cardiac muscle, lung, liver, and spleen) as demonstrated by PCR and culture, SCID horses did not develop neurologic signs after oral or i.v. infection. S. neurona was undetectable in the neuronal tissues of SCID horses by either PCR, immunohistochemistry, or culture. In contrast, although parasitemia was undetectable in orally infected IC horses and of only short duration in i.v. infected IC horses, four of six IC horses developed neurologic signs. S. neurona was detectable by PCR and/or culture of neural tissue but not visceral tissue of IC horses with neurologic disease. Infected SCID horses are unable to clear S. neurona from visceral tissues, but the infection does not result in neurologic signs; in contrast, IC horses rapidly control parasitemia and infection of visceral tissues but frequently experience neuroinvasion and exhibit clinical signs of neurologic disease.

  3. Prevalence and risk factors associated with Sarcocystis neurona infections in opossums (Didelphis virginiana) from central California.

    Science.gov (United States)

    Rejmanek, Daniel; Vanwormer, Elizabeth; Miller, Melissa A; Mazet, Jonna A K; Nichelason, Amy E; Melli, Ann C; Packham, Andrea E; Jessup, David A; Conrad, Patricia A

    2009-12-03

    Sarcocystis neurona, a protozoal parasite shed by opossums (Didelphis virginiana), has been shown to cause significant morbidity and mortality in horses, sea otters, and other marine mammals. Over the course of 3 years (fall 2005-summer 2008), opossums from central California were tested for infection with S. neurona. Of 288 opossums sampled, 17 (5.9%) were infected with S. neurona based on the molecular characterization of sporocysts from intestinal scrapings or feces. Risk factors evaluated for association with S. neurona infection in opossums included: age, sex, location, season, presence of pouch young in females, concomitant infection, and sampling method (live-trapped or traffic-killed). Multivariate logistic regression analysis identified that opossums in the Central Valley were 9 times more likely to be infected than those near the coast (p=0.009). Similarly, opossum infection was 5 times more likely to be detected during the reproductive season (March-July; p=0.013). This first investigation of S. neurona infection prevalence and associated risk factors in opossums in the western United States can be used to develop management strategies aimed at reducing the incidence of S. neurona infections in susceptible hosts, including horses and threatened California sea otters (Enhydra lutris neries).

  4. High prevalence of Sarcocystis calchasi sporocysts in European Accipiter hawks.

    Science.gov (United States)

    Olias, Philipp; Olias, Lena; Krücken, Jürgen; Lierz, Michael; Gruber, Achim D

    2011-02-10

    The emerging Sarcocystis calchasi induces a severe and lethal central nervous disease in its intermediate host, the domestic pigeon (Columba livia f. domestica). Experimental studies have identified the Northern goshawk (Accipiter g. gentilis) as final host. Phylogenetically closely related European sparrowhawks (Accipiter n. nisus) and wood pigeons (Columba palumbus) have been found to harbor genetically closely related Sarcocystis spp. However, data on the prevalence and potential interspecies occurrence of these parasites are lacking. Here, we report that European Accipiter hawks (Accipitrinae) are highly infected with S. calchasi, S. columbae and Sarcocystis sp. ex A. nisus in their small intestine. Thirty-one of 50 (62%) Northern goshawks necropsied during 1997-2008 were positive for S. calchasi in a newly established species-specific semi-nested PCR assay based on the first internal transcribed spacer region. Unexpectedly, 14 of 20 (71.4%) European sparrowhawks tested also positive. In addition, birds of both species were found to be infested with S. columbae and an, as yet, unnamed Sarcocystis sp. recently isolated from European sparrowhawks. These findings raise new questions about the host specificity of S. calchasi and its high virulence in domestic pigeons, since sparrowhawks only rarely prey on pigeons. Notably, isolated sporocysts from both infected Accipiter spp. measured 8 μm × 11.9 μm, precluding a preliminary identification of S. calchasi in feces of Accipiter hawks based on morphology alone. Importantly, three of four Northern goshawks used in falconry tested positive for S. calchasi. In conclusion, the results indicate that both European Accipter spp. in Germany serve as natural final hosts of S. calchasi and suggest that falconry and pigeon sport may serve as risk factors for the spread of this pathogen in domestic pigeons.

  5. Brown-headed cowbirds (Molothrus ater) harbor Sarcocystis neurona and act as intermediate hosts.

    Science.gov (United States)

    Mansfield, L S; Mehler, S; Nelson, K; Elsheikha, H M; Murphy, A J; Knust, B; Tanhauser, S M; Gearhart, P M; Rossano, M G; Bowman, D D; Schott, H C; Patterson, J S

    2008-05-06

    We tested the hypothesis that brown-headed cowbirds (Molothrus ater) harbor Sarcocystis neurona, the agent of equine protozoal myeloencephalitis (EPM), and act as intermediate hosts for this parasite. In summer 1999, wild caught brown-headed cowbirds were collected and necropsied to determine infection rate with Sarcocystis spp. by macroscopic inspection. Seven of 381 (1.8%) birds had grossly visible sarcocysts in leg muscles with none in breast muscles. Histopathology revealed two classes of sarcocysts in leg muscles, thin-walled and thick-walled suggesting two species. Electron microscopy showed that thick-walled cysts had characteristics of S. falcatula and thin-walled cysts had characteristics of S. neurona. Thereafter, several experiments were conducted to confirm that cowbirds had viable S. neurona that could be transmitted to an intermediate host and cause disease. Specific-pathogen-free opossums fed cowbird leg muscle that was enriched for muscle either with or without visible sarcocysts all shed high numbers of sporocysts by 4 weeks after infection, while the control opossum fed cowbird breast muscle was negative. These sporocysts were apparently of two size classes, 11.4+/-0.7 microm by 7.6+/-0.4 microm (n=25) and 12.6+/-0.6 microm by 8.0+/-0 microm (n=25). When these sporocysts were excysted and introduced into equine dermal cell tissue culture, schizogony occurred, most merozoites survived and replicated long term and merozoites sampled from the cultures with long-term growth were indistinguishable from known S. neurona isolates. A cowbird Sarcocystis isolate, Michigan Cowbird 1 (MICB1), derived from thin-walled sarcocysts from cowbirds that was passaged in SPF opossums and tissue culture went on to produce neurological disease in IFNgamma knockout mice indistinguishable from that of the positive control inoculated with S. neurona. This, together with the knowledge that S. falcatula does not cause lesions in IFNgamma knockout mice, showed that cowbird

  6. Sarcocystis neurona infections in sea otter (Enhydra lutris): evidence for natural infections with sarcocysts and transmission of infection to opossums (Didelphis virginiana)

    Science.gov (United States)

    Dubey, J.P.; Rosypal, A.C.; Rosenthal, B.M.; Thomas, N.J.; Lindsay, D.S.; Stanek, J.F.; Reed, S.M.; Saville, W.J.A.

    2001-01-01

    Although Sarcocystis neurona has been identified in an array of terrestrial vertebrates, recent recognition of its capacity to infect marine mammals was unexpected. Here, sarcocysts from 2 naturally infected sea otters (Enhydra lutris) were characterized biologically, ultrastructurally, and genetically. DNA was extracted from frozen muscle of the first of these sea otters and was characterized as S. neurona by polymerase chain reation (PCR) amplification followed by restriction fragment length polymorphism analysis and sequencing. Sarcocysts from sea otter no. 1 were up to 350 I?m long, and the villar protrusions on the sarcocyst wall were up to 1.3 I?m long and up to 0.25 I?m wide. The villar protrusions were tapered towards the villar tip. Ultrastructurally, sarcocysts were similar to S. neurona sarcocysts from the muscles of cats experimentally infected with S. neurona sporocysts. Skeletal muscles from a second sea otter failed to support PCR amplification of markers considered diagnostic for S. neurona but did induce the shedding of sporocysts when fed to a laboratory-raised opossum (Didelphis virginiana). Such sporocysts were subsequently fed to knockout mice for the interferon-gamma gene, resulting in infections with an agent identified as S. neurona on the basis of immunohistochemistry, serum antibodies, and diagnostic sequence detection. Thus, sea otters exposed to S. neurona may support the development of mature sarcocysts that are infectious to competent definitive hosts.

  7. Penetration of equine leukocytes by merozoites of Sarcocystis neurona.

    Science.gov (United States)

    Lindsay, David S; Mitchell, Sheila M; Yang, Jibing; Dubey, J P; Gogal, Robert M; Witonsky, Sharon G

    2006-06-15

    Horses are considered accidental hosts for Sarcocystis neurona and they often develop severe neurological disease when infected with this parasite. Schizont stages develop in the central nervous system (CNS) and cause the neurological lesions associated with equine protozoal myeloencephalitis. The present study was done to examine the ability of S. neurona merozoites to penetrate and develop in equine peripheral blood leukocytes. These infected host cells might serve as a possible transport mechanism into the CNS. S. neurona merozoites penetrated equine leukocytes within 5 min of co-culture. Infected leukocytes were usually monocytes. Infected leukocytes were present up to the final day of examination at 3 days. Up to three merozoites were present in an infected monocyte. No development to schizont stages was observed. All stages observed were in the host cell cytoplasm. We postulate that S. neurona merozoites may cross the blood brain barrier hidden inside leukocytes. Once inside the CNS these merozoites can egress and invade additional cells and cause encephalitis.

  8. Prevalence of agglutinating antibodies to Sarcocystis neurona in skunks (Mephitis Mephitis), raccoons (Procyon lotor), and opossums (Didelphis Virginiana) from Connecticut.

    Science.gov (United States)

    Mitchell, Sheila M; Richardson, Dennis J; Cheadle, M Andy; Zajac, Anne M; Lindsay, David S

    2002-10-01

    Equine protozoal myeloencephalitis is the most important protozoan disease of horses in North America and is usually caused by Sarcocystis neurona. Natural cases of encephalitis caused by S. neurona have been reported in skunks (Mephitis mephitis) and raccoons (Procyon lotor). Opossums (Didelphis spp.) are the only known definitive host. Sera from 24 striped skunks, 12 raccoons, and 7 opossums (D. virginiana) from Connecticut were examined for agglutinating antibodies to S. neurona using the S. neurona agglutination test (SAT) employing formalin-fixed merozoites as antigen. The SAT was validated for skunk sera using pre- and postinfection serum samples from 2 experimentally infected skunks. Of the 24 (46%) skunks 11 were positive, and all 12 raccoons were positive for S. neurona antibodies. None of the 7 opossums was positive for antibodies to S. neurona. These results suggest that exposure to sporocysts of S. neurona by intermediate hosts is high in Connecticut. The absence of antibodies in opossums collected from the same areas is most likely because of the absence of systemic infection in the definitive host.

  9. Molecular typing of Sarcocystis neurona: current status and future trends.

    Science.gov (United States)

    Elsheikha, Hany M; Mansfield, Linda S

    2007-10-21

    Sarcocystis neurona is an important protozoal pathogen because it causes the serious neurological disease equine protozoal myeloencephalitis (EPM). The capacity of this organism to cause a wide spectrum of neurological signs in horses and the broad geographic distribution of observed cases in the Americas drive the need for sensitive, reliable and rapid typing methods to characterize strains. Various molecular methods have been developed and used to diagnose EPM due to S. neurona, to identify S. neurona isolates and to determine the heterogeneity and evolutionary relatedness within this species and related Sarcocystis spp. These methods included sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), immuno-fluorescent assay (IFA), slide agglutination test (SAT), SnSAG-specific ELISA, random amplified polymorphic DNA (RAPD), PCR-based restriction fragment length polymorphism (RFLP), amplified fragment length polymorphism (AFLP) fingerprinting, and sequence analysis of surface protein genes, ribosomal genes, microsatellite alleles and other molecular markers. Here, the utility of these molecular methods is reviewed and evaluated with respect to the need for molecular approaches that utilize well-characterized polymorphic, simple, independent, and stable genetic markers. These tools have the potential to add to knowledge of the genetic population structure of S. neurona and to provide new insights into the pathogenesis of EPM and S. neurona epidemiology. In particular, these methods provide new tools to address the hypothesis that particular genetic variants are associated with adverse clinical outcomes (severe pathotypes). The ultimate goal is to utilize them in future studies to improve treatment and prevention strategies.

  10. Sarcocyst Development in Raccoons (Procyon lotor) Inoculated with Different Strains of Sarcocystis neurona Culture-Derived Merozoites.

    Science.gov (United States)

    Dryburgh, E L; Marsh, A E; Dubey, J P; Howe, D K; Reed, S M; Bolten, K E; Pei, W; Saville, W J A

    2015-08-01

    Sarcocystis neurona is considered the major etiologic agent of equine protozoal myeloencephalitis (EPM), a neurological disease in horses. Raccoon ( Procyon lotor ) is considered the most important intermediate host in the life cycle of S. neurona in the United States; S. neurona sarcocysts do mature in raccoon muscles, and raccoons also develop clinical signs simulating EPM. The focus of this study was to determine if sarcocysts would develop in raccoons experimentally inoculated with different host-derived strains of in vitro-cultivated S. neurona merozoites. Four raccoons were inoculated with strains derived from a raccoon, a sea otter, a cat, and a horse. Raccoon tissues were fed to laboratory-raised opossums ( Didelphis virginiana ), the definitive host of S. neurona . Intestinal scraping revealed sporocysts in opossums who received muscle tissue from raccoons inoculated with the raccoon-derived or the sea otter-derived isolates. These results demonstrate that sarcocysts can mature in raccoons inoculated with in vitro-derived S. neurona merozoites. In contrast, the horse and cat-derived isolates did not produce microscopically or biologically detected sarcocysts. Immunoblot analysis revealed both antigenic and antibody differences when testing the inoculated raccoons. Immunohistochemical staining indicated differences in staining between the merozoite and sarcocyst stages. The successful infections achieved in this study indicates that the life cycle can be manipulated in the laboratory without affecting subsequent stage development, thereby allowing further purification of strains and artificial maintenance of the life cycle.

  11. Clinical Sarcocystis neurona, Sarcocystis canis, Toxoplasma gondii, and Neospora caninum infections in dogs.

    Science.gov (United States)

    Dubey, J P; Chapman, Jennifer L; Rosenthal, Benjamin M; Mense, M; Schueler, Ronald L

    2006-04-15

    Sarcocystis neurona, Sarcocystis canis, Toxoplasma gondii, and Neospora caninum are related apicomplexans that can cause systemic illness in many species of animals, including dogs. We investigated one breeder's 25 Basset Hounds for these infections. In addition, tissues from dogs and other non-canine hosts previously reported as S. canis infections were studied retrospectively. Schizonts resembling those of S. neurona, and recognized by polyclonal rabbit anti-S. neurona antibodies, were found in six of eight retrospective cases, as well as in two additional dogs (one Basset Hound, one Springer Spaniel) not previously reported. S. neurona schizonts were found in several tissues including the central nervous system, lungs, and kidneys. Fatal toxoplasmosis was diagnosed in an adult dog, and neosporosis was diagnosed in an adult and a pup related to the one diagnosed with S. neurona. No serological reactivity to S. neurona antibodies occurred when S. canis-like liver schizonts were retrospectively assayed from two dogs, a dolphin, a sea lion, a horse, a chinchilla, a black or either of two polar bears. Sequencing conserved (18S) and variable (ITS-1) portions of nuclear ribosomal DNA isolated from the schizont-laden liver of a polar bear distinguished it from all previously characterized species of Sarcocystis. We take this genetic signature as provisionally representative of S. canis, an assumption that should be tested with future sequencing of similar liver infections in other mammalian hosts. These findings further extend the uncharacteristically broad intermediate host range for S. neurona, which also causes a neurologic disease in cats, mink, raccoons, skunks, Pacific harbor seals, ponies, zebras, lynxes, and sea otters. Further work is necessary to delineate the causative agent(s) of other cases of canine sarcocystosis, and in particular to specify the attributes of S. canis, which corresponds morphologically to infections reported from wide range of terrestrial

  12. Sarcocystis neurona retinochoroiditis in a sea otter (Enhydra lutris kenyoni)

    Science.gov (United States)

    Dubey, J.P.; Thomas, N.J.

    2011-01-01

    Sarcocystis neurona is an important cause of fatal disease in sea otters in the USA. Encephalitis is the predominant lesion and parasites are confined to the central nervous system and muscles. Here we report retinochoroiditis in a sea otter (Enhydra lutris kenyoni) found dead on Copalis Beach, WA, USA. Salient lesions were confined to the brain and eye. Multifocal nonsuppurative meningoencephalitis was present in the cerebrum and cerebellum associated with S. neurona schizonts. The retina of one eye had a focus of inflammation that contained numerous S. neurona schizonts and merozoites. The focus extended from the retinal pigment epithelium inward through all layers of the retina, but inflammation was most concentrated at the inner surface of the tapetum and the outer retina. The inner and outer nuclear layers of the retina were disorganized and irregular at the site of inflammation. There was severe congestion and mild hemorrhage in the choroid, and mild hemorrhage into the vitreous body. Immunohistochemistry with S. neurona-specific polyclonal rabbit antibodies stained schizonts and merozoites. To our knowledge this is the first report of S. neurona-associated retinochoroiditis in any naturally infected animal.

  13. Sarcocystis neurona retinochoroiditis in a sea otter (Enhydra lutris kenyoni)

    Science.gov (United States)

    Dubey, J.P.; Thomas, N.J.

    2011-01-01

    Sarcocystis neurona is an important cause of fatal disease in sea otters in the USA. Encephalitis is the predominant lesion and parasites are confined to the central nervous system and muscles. Here we report retinochoroiditis in a sea otter (Enhydra lutris kenyoni) found dead on Copalis Beach, WA, USA. Salient lesions were confined to the brain and eye. Multifocal nonsuppurative meningoencephalitis was present in the cerebrum and cerebellum associated with S. neurona schizonts. The retina of one eye had a focus of inflammation that contained numerous S. neurona schizonts and merozoites. The focus extended from the retinal pigment epithelium inward through all layers of the retina, but inflammation was most concentrated at the inner surface of the tapetum and the outer retina. The inner and outer nuclear layers of the retina were disorganized and irregular at the site of inflammation. There was severe congestion and mild hemorrhage in the choroid, and mild hemorrhage into the vitreous body. Immunohistochemistry with S. neurona-specific polyclonal rabbit antibodies stained schizonts and merozoites. To our knowledge this is the first report of S. neurona-associated retinochoroiditis in any naturally infected animal. ?? 2011 Elsevier B.V.

  14. Efficacy of decoquinate against Sarcocystis neurona in cell cultures.

    Science.gov (United States)

    Lindsay, David S; Nazir, M Mudasser; Maqbool, Azhar; Ellison, Siobhan P; Strobl, Jeannine S

    2013-09-01

    Decoquinate is a quinolone anticoccidial approved for use in the prevention of intestinal coccidiosis in farm animals. This compound has good activity against Toxoplasma gondii and Neospora caninum in cell cultures. The drug acts on the parasites' mitochondria. The activity of decoquinate against developing merozoites of 2 isolates of Sarcocystis neurona was examined in cell culture. Merozoite production at 10 days was completely inhibited when decoquinate was used at 20 or 240 nM. The IC50 of decoquinate was 0.5 ± 0.09nM for the Sn6 isolate of S. neurona from a horse and 1.1 ± 0.6 nM for the SnOP15 isolate of S. neurona from an opossum. Levamisole was toxic at 5 μg/ml and no synergism was observed when decoquinate was combined with levamisole and tested against the Sn3YFP isolate of S. neurona. Decoquinate was cidal for developing schizonts of S. neurona at 240 nM. Copyright © 2013 Elsevier B.V. All rights reserved.

  15. Molecular genetic transfection of the coccidian parasite Sarcocystis neurona.

    Science.gov (United States)

    Gaji, Rajshekhar Y; Zhang, Deqing; Breathnach, Cormac C; Vaishnava, Shipra; Striepen, Boris; Howe, Daniel K

    2006-11-01

    Sarcocystis neurona is an apicomplexan parasite that is the major cause of equine protozoal myeloencephalitis (EPM). The biology of this pathogen remains poorly understood in part due to unavailability of molecular genetic tools. Hence, with an objective to develop DNA transfection capabilities for S. neurona, the 5' flanking region of the SnSAG1 gene was isolated from a genomic library and used to construct expression plasmids. In transient assays, the reporter molecules beta-galactosidase (beta-gal) and yellow fluorescent protein (YFP) could be detected in electroporated S. neurona, thereby confirming the feasibility of transgene expression in this organism. Stable transformation of S. neurona was achieved using a mutant dihydrofolate reductase thymidylate synthase (DHFR-TS) gene of Toxoplasma gondii that confers resistance to pyrimethamine. This selection system was used to create transgenic S. neurona that stably express beta-gal and YFP. As shown in this study, these transgenic clones can be useful for analyzing growth rate of parasites in vitro and for assessing drug sensitivities. More importantly, the DNA transfection methods described herein should greatly facilitate studies examining intracellular parasitism by this important coccidian pathogen.

  16. Sarcocystis neurona retinochoroiditis in a sea otter (Enhydra lutris kenyoni).

    Science.gov (United States)

    Dubey, J P; Thomas, N J

    2011-12-29

    Sarcocystis neurona is an important cause of fatal disease in sea otters in the USA. Encephalitis is the predominant lesion and parasites are confined to the central nervous system and muscles. Here we report retinochoroiditis in a sea otter (Enhydra lutris kenyoni) found dead on Copalis Beach, WA, USA. Salient lesions were confined to the brain and eye. Multifocal nonsuppurative meningoencephalitis was present in the cerebrum and cerebellum associated with S. neurona schizonts. The retina of one eye had a focus of inflammation that contained numerous S. neurona schizonts and merozoites. The focus extended from the retinal pigment epithelium inward through all layers of the retina, but inflammation was most concentrated at the inner surface of the tapetum and the outer retina. The inner and outer nuclear layers of the retina were disorganized and irregular at the site of inflammation. There was severe congestion and mild hemorrhage in the choroid, and mild hemorrhage into the vitreous body. Immunohistochemistry with S. neurona-specific polyclonal rabbit antibodies stained schizonts and merozoites. To our knowledge this is the first report of S. neurona-associated retinochoroiditis in any naturally infected animal. Copyright © 2011 Elsevier B.V. All rights reserved.

  17. Sarcocystis neurona: molecular characterization of enolase domain I region and a comparison to other protozoa.

    Science.gov (United States)

    Bolten, K E; Marsh, A E; Reed, S M; Dubey, J P; Toribio, R E; Saville, W J A

    2008-09-01

    Sarcocystis neurona causes protozoal myeloencephalitis and has the ability to infect a wide host range in contrast to other Sarcocystis species. In the current study, five S. neurona isolates from a variety of sources, three Sarcocystis falcatula, one Sarcocystis dasypi/S. neurona-like isolate, and one Besnoitia darlingi isolate were used to compare the enolase 2 gene segment containing the domain I region to previously sequenced enolase genes from Neospora caninum, Neospora hughesi, Toxoplasma gondii, Plasmodium falciparum, and Trypanosoma cruzi; enolase 2 segment containing domain I region is highly conserved amongst these parasites of veterinary and medical importance. Immunohistochemistry results indicates reactivity of T. gondii enolase 1 and 2 antibodies to S. neurona merozoites and metrocytes, but no reactivity of anti-enolase 1 to the S. neurona bradyzoite stage despite reactivity to T. gondii bradyzoites, suggesting expression differences between organisms.

  18. A review of Sarcocystis spp. shed by opossums (Didelphis spp. in Brazil

    Directory of Open Access Journals (Sweden)

    Samantha Yuri Oshiro Branco Valadas

    2016-08-01

    Full Text Available South American opossums are the definitive hosts of Sarcocystis neurona, Sarcocystis falcatula, Sarcocystis speeri and Sarcocystis lindsayi. The sporocysts of these species of Sarcocystis are morphologically similar and methods like infectivity and pathogenicity for intermediate hosts (immunodeficient mice and psittacine birds and molecular tools are used for identification. Opossums are synanthropic wild animals, and widely distributed in Brazilian territory. Previous studies have shown high environmental contamination with S. neurona sporocysts in several Brazilian regions. This paper reviews information on Sarcocystis spp. shed by various opossum species and its occurrence in Brazil.

  19. Investigação de anticorpos contra Sarcocystis neurona e Sarcocystis cruzi em equinos

    Directory of Open Access Journals (Sweden)

    A. M. Antonello

    2015-10-01

    Full Text Available ABSTRACTSarcocystis neurona is the primary agent for Equine Protozoal Myeloencephalitis (EPM, important neurological disease characterized by behavior or muscular changes, that impairs animal performance and husbandry. Sarcocystis cruzi is a pathogen related to myositis in cattle. Although related the life cycles of the parasites are distinct. S. neurona has opossums (Didelphis spp. and S. cruzi, dogs as definitive hosts. However, S. neurona and S. cruzi may undergo cross-reactivity in serological tests, interfering on results of EPM ante-mortem diagnostic tests. In the present study, serology of 189 mares was performed by indirect immunofluorescence antibody test, using antigens of S. neurona and S. cruzi in order to assess the exposure degree of animals to antigens. Analyzing the results, it was observed that most of the animals (84.13% reacted with at least one protozoal species and the number of animals which showed antibodies against S. cruzi was greater than S. neurona (80.42% and 33.86%, respectively and a third of seropositive animals reacted to antigens of both species.

  20. Biological characterisation of Sarcocystis neurona isolated from a Southern sea otter (Enhydra lutris nereis)

    Science.gov (United States)

    Lindsay, D.S.; Thomas, N.J.; Dubey, J.P.

    2000-01-01

    Sarcocystis neurona was isolated from the brain of a juvenile, male southern sea otter (Enhydra lutris nereis) suffering from CNS disease. Schizonts and merozoites in tissue sections of the otter's brain reacted with anti-S. neurona antiserum immunohistochemically. Development in cell culture was by endopolyogeny and mature schizonts were first observed at 3 days postinoculation. PCR of merozoite DNA using primer pairs JNB33/JNB54 and restriction enzyme digestion of the 1100 bp product with Dra I indicated the organism was S. neurona. Four of four interferon-γ gene knockout mice inoculated with merozoites developed S. neurona-associated encephalitis. Antibodies to S. neurona but not Sarcocystis falcatula, Toxoplasma gondii, or Neospora caninum were present in the serum of inoculated mice. This is the first isolation of S. neurona from the brain of a non-equine host.

  1. Detection of antibodies against Sarcocystis neurona, neospora spp., and Toxoplasma gondii in horses from Costa Rica

    Science.gov (United States)

    Serum samples from 315 horses from Costa Rica, Central America were examined for the presence of antibodies against Sarcocystis neurona, Neospora spp., and Toxoplasma gondii using the SnSAG2 ELISA, the NhSAG1 ELISA, and the modified agglutination test, respectively. Anti-S. neurona antibodies were f...

  2. Exposure to Sarcocystis spp. in horses from Spain determined by Western blot analysis using Sarcocystis neurona merozoites as heterologous antigen.

    Science.gov (United States)

    Arias, M; Yeargan, M; Francisco, I; Dangoudoubiyam, S; Becerra, P; Francisco, R; Sánchez-Andrade, R; Paz-Silva, A; Howe, D K

    2012-04-30

    Horses serve as an intermediate host for several species of Sarcocystis, all of which utilize canids as the definitive host. Sarcocystis spp. infection and formation of latent sarcocysts in horses often appears to be subclinical, but morbidity can occur, especially when the parasite burden is large. A serological survey was conducted to determine the presence of antibodies against Sarcocystis spp. in seemingly healthy horses from the Galicia region of Spain. Western blot analyses using Sarcocystis neurona merozoites as heterologous antigen suggested greater than 80% seroprevalance of Sarcocystis spp. in a sample set of 138 horses. The serum samples were further tested with enzyme-linked immunosorbent assays (ELISAs) based on recombinant S. neurona-specific surface antigens (rSnSAGs). As expected for horses from the Eastern Hemisphere, less than 4% of the serum samples were positive when analyzed with either the rSnSAG2 or the rSnSAG4/3 ELISAs. An additional 246 horses were tested using the rSnSAG2 ELISA, which revealed that less than 3% of the 384 samples were seropositive. Collectively, the results of this serologic study suggested that a large proportion of horses from this region of Spain are exposed to Sarcocystis spp. Furthermore, the anti-Sarcocystis seroreactivity in these European horses could be clearly distinguished from anti-S. neurona antibodies using the rSnSAG2 and rSnSAG4/3 ELISAs. Copyright © 2011 Elsevier B.V. All rights reserved.

  3. Epidemiology of Sarcocystis neurona infections in domestic cats (Felis domesticus) and its association with equine protozoal myeloencephalitis (EPM) case farms and feral cats from a mobile spay and neuter clinic.

    Science.gov (United States)

    Stanek, J F; Stich, R W; Dubey, J P; Reed, S M; Njoku, C J; Lindsay, D S; Schmall, L M; Johnson, G K; LaFave, B M; Saville, W J A

    2003-11-28

    Equine protozoal myeloencephalitis (EPM) is a serious neurologic disease in the horse most commonly caused by Sarcocystis neurona. The domestic cat (Felis domesticus) is an intermediate host for S. neurona. In the present study, nine farms, known to have prior clinically diagnosed cases of EPM and a resident cat population were identified and sampled accordingly. In addition to the farm cats sampled, samples were also collected from a mobile spay and neuter clinic. Overall, serum samples were collected in 2001 from 310 cats, with samples including barn, feral and inside/outside cats. Of these 310 samples, 35 were from nine horse farms. Horse serum samples were also collected and traps were set for opossums at each of the farms. The S. neurona direct agglutination test (SAT) was used for both the horse and cat serum samples (1:25 dilution). Fourteen of 35 (40%) cats sampled from horse farms had circulating S. neurona agglutinating antibodies. Twenty-seven of the 275 (10%) cats from the spay/neuter clinic also had detectable S. neurona antibodies. Overall, 115 of 123 (93%) horses tested positive for anti-S. neurona antibodies, with each farm having greater than a 75% exposure rate among sampled horses. Twenty-one opossums were trapped on seven of the nine farms. Eleven opossums had Sarcocystis sp. sporocysts, six of them were identified as S. neurona sporocysts based on bioassays in gamma-interferon gene knockout mice with each opossum representing a different farm. Demonstration of S. neurona agglutinating antibodies in domestic and feral cats corroborates previous research demonstrating feral cats to be naturally infected, and also suggests that cats can be frequently infected with S. neurona and serve as one of several natural intermediate hosts for S. neurona.

  4. Molecular identification of Sarcocystis rileyi sporocysts in red foxes (Vulpes vulpes) and raccoon dogs (Nyctereutes procyonoides) in Lithuania.

    Science.gov (United States)

    Prakas, Petras; Liaugaudaitė, Simona; Kutkienė, Liuda; Sruoga, Aniolas; Švažas, Saulius

    2015-05-01

    Despite the fact that Sarcocystis rileyi is one of the earliest described species of the genus Sarcocystis forming macrocysts in ducks, the life cycle of this species is still unknown in Europe. Sarcocystis spp. oocysts/sporocysts were observed in faeces of four of 23 (17.4 %) and in small intestine mucosal scrapings of four of 20 (20.0 %) red foxes (Vulpes vulpes) and in small intestine mucosal scrapings of seven of 13 (53.8 %) raccoon dogs (Nyctereutes procyonoides) hunted in Lithuania. A very small number of Sarcocystis sporocysts measuring 11.9 × 8.3 μm (n = 5) was found in faecal samples, whereas considerably more sporulated Sarcocystis oocysts and free sporocysts were detected in the small intestines of red foxes and raccoon dogs. These sporocysts measured 12.9 × 8.1 μm (n = 16) and 12.1 × 8.1 μm (n = 54) in red foxes and raccoon dogs, respectively. Using species-specific PCR and subsequent sequencing, internal transcribed spacer 1 (ITS-1) region partial sequences of oocysts/sporocysts from small intestine mucosal scrapings of six raccoon dogs and three red foxes were identified as belonging to S. rileyi. The present study provides strong evidence showing that the red fox and the raccoon dog can serve as final hosts of S. rileyi in Europe; however, transmission experiments are needed for the ultimate approval.

  5. Prevalence of antibodies to Sarcocystis neurona in cats from Virginia and Pennsylvania.

    Science.gov (United States)

    Hsu, Vasha; Grant, David C; Dubey, J P; Zajac, Anne M; Lindsay, David S

    2010-08-01

    Sarcocystis neurona is best known as the causative agent of equine protozoal myeloencephalitis of horses in the Americas. Domestic cats ( Felis domesticus ) were the first animals described as an intermediate host for S. neurona . However, S. neurona -associated encephalitis has also been reported in naturally infected cats in the United States. Thus, cats can be implicated in the life cycle of S. neurona as natural intermediate hosts. The present study examined the seroprevalence of IgG antibodies to merozoites of S. neurona in populations of domestic cats from Virginia and Pennsylvania. Overall, sera or plasma from 441 cats (Virginia = 232, Pennsylvania = 209) were tested by an indirect immunofluorescent assay at a 1ratio50 dilution. Antibodies to S. neurona were found in 32 (7%) of 441 cats. Of these, 22 (9%) of the 232 cats from Virginia and 10 (5%) of the 209 cats from Pennsylvania were seropositive for S. neurona .

  6. Rhinitis and disseminated disease in a ferret (Mustela putorius furo) naturally infected with Sarcocystis neurona.

    Science.gov (United States)

    Britton, Ann P; Dubey, J P; Rosenthal, Benjamin M

    2010-04-19

    Naturally occurring Sarcocystis neurona infection in a ferret (Mustela putorius furo) with rhinitis and disseminated disease are described for the first time. The ferret exhibited severe rhinitis with intra-lesional S. neurona merozoites and schizonts. Diagnosis was confirmed immunohistochemically by staining with S. neurona-specific antibodies, and by phylogenetic analyses of conserved and variable portions of nuclear ribosomal DNA. On the basis of intense schizogony in the nasal mucosa, we propose the possibility of an olfactory nerve pathway route of infection for S. neurona meningoencephalitis.

  7. Systems based analysis of the Sarcocystis neurona genome identifies pathways that contribute to a heteroxenous life cycle

    Science.gov (United States)

    Sarcocystis neurona is a member of the Coccidia, a clade of single-celled parasites of medical and veterinary importance including Eimeria, Sarcocystis, Neospora and Toxoplasma. Unlike Eimeria, a single host enteric pathogen, Sarcocystis, Neospora and Toxoplasma are two host parasites that infect an...

  8. Has Sarcocystis neurona Dubey et al., 1991 (Sporozoa: Apicomplexa: Sarcocystidae) cospeciated with its intermediate hosts?

    Science.gov (United States)

    Elsheikha, Hany M

    2009-08-26

    The question of how Sarcocystis neurona is able to overcome species barrier and adapt to new hosts is central to the understanding of both the evolutionary origin of S. neurona and the prediction of its field host range. Therefore, it is worth reviewing current knowledge on S. neurona host specificity. The available host range data for S. neurona are discussed in relation to a subject of evolutionary importance-specialist or generalist and its implications to understand the strategies of host adaptation. Current evidences demonstrate that a wide range of hosts exists for S. neurona. This parasite tends to be highly specific for its definitive host but much less so for its intermediate host (I.H.). The unique specificity of S. neurona for its definitive host may be mediated by a probable long coevolutionary relationship of the parasite and carnivores in a restricted ecological niche 'New World'. This might be taken as evidence that carnivores are the 'original' host group for S. neurona. Rather, the capacity of S. neurona to exploit an unusually large number of I.H. species probably indicates that S. neurona maintains non-specificity to its I.H. as an adaptive response to insure the survival of the parasite in areas in which the 'preferred' host is not available. This review concludes with the view that adaptation of S. neurona to a new host is a complex interplay that involves a large number of determinants.

  9. An update on Sarcocystis neurona infections in animals and equine protozoal myeloencephalitis (EPM).

    Science.gov (United States)

    Dubey, J P; Howe, D K; Furr, M; Saville, W J; Marsh, A E; Reed, S M; Grigg, M E

    2015-04-15

    Equine protozoal myeloencephalitis (EPM) is a serious disease of horses, and its management continues to be a challenge for veterinarians. The protozoan Sarcocystis neurona is most commonly associated with EPM. S. neurona has emerged as a common cause of mortality in marine mammals, especially sea otters (Enhydra lutris). EPM-like illness has also been recorded in several other mammals, including domestic dogs and cats. This paper updates S. neurona and EPM information from the last 15 years on the advances regarding life cycle, molecular biology, epidemiology, clinical signs, diagnosis, treatment and control. Published by Elsevier B.V.

  10. Enzyme-Linked Immunosorbent Assays for Detection of Equine Antibodies Specific to Sarcocystis neurona Surface Antigens†

    Science.gov (United States)

    Hoane, Jessica S.; Morrow, Jennifer K.; Saville, William J.; Dubey, J. P.; Granstrom, David E.; Howe, Daniel K.

    2005-01-01

    Sarcocystis neurona is the primary causative agent of equine protozoal myeloencephalitis (EPM), a common neurologic disease of horses in the Americas. We have developed a set of enzyme-linked immunosorbent assays (ELISAs) based on the four major surface antigens of S. neurona (SnSAGs) to analyze the equine antibody response to S. neurona. The SnSAG ELISAs were optimized and standardized with a sample set of 36 equine sera that had been characterized by Western blotting against total S. neurona parasite antigen, the current gold standard for S. neurona serology. The recombinant SnSAG2 (rSnSAG2) ELISA showed the highest sensitivity and specificity at 95.5% and 92.9%, respectively. In contrast, only 68.2% sensitivity and 71.4% specificity were achieved with the rSnSAG1 ELISA, indicating that this antigen may not be a reliable serological marker for analyzing antibodies against S. neurona in horses. Importantly, the ELISA antigens did not show cross-reactivity with antisera to Sarcocystis fayeri or Neospora hughesi, two other equine parasites. The accuracy and reliability exhibited by the SnSAG ELISAs suggest that these assays will be valuable tools for examining the equine immune response against S. neurona infection, which may help in understanding the pathobiology of this accidental parasite-host interaction. Moreover, with modification and further investigation, the SnSAG ELISAs have potential for use as immunodiagnostic tests to aid in the identification of horses affected by EPM. PMID:16148170

  11. Enzyme-linked immunosorbent assays for detection of equine antibodies specific to Sarcocystis neurona surface antigens.

    Science.gov (United States)

    Hoane, Jessica S; Morrow, Jennifer K; Saville, William J; Dubey, J P; Granstrom, David E; Howe, Daniel K

    2005-09-01

    Sarcocystis neurona is the primary causative agent of equine protozoal myeloencephalitis (EPM), a common neurologic disease of horses in the Americas. We have developed a set of enzyme-linked immunosorbent assays (ELISAs) based on the four major surface antigens of S. neurona (SnSAGs) to analyze the equine antibody response to S. neurona. The SnSAG ELISAs were optimized and standardized with a sample set of 36 equine sera that had been characterized by Western blotting against total S. neurona parasite antigen, the current gold standard for S. neurona serology. The recombinant SnSAG2 (rSnSAG2) ELISA showed the highest sensitivity and specificity at 95.5% and 92.9%, respectively. In contrast, only 68.2% sensitivity and 71.4% specificity were achieved with the rSnSAG1 ELISA, indicating that this antigen may not be a reliable serological marker for analyzing antibodies against S. neurona in horses. Importantly, the ELISA antigens did not show cross-reactivity with antisera to Sarcocystis fayeri or Neospora hughesi, two other equine parasites. The accuracy and reliability exhibited by the SnSAG ELISAs suggest that these assays will be valuable tools for examining the equine immune response against S. neurona infection, which may help in understanding the pathobiology of this accidental parasite-host interaction. Moreover, with modification and further investigation, the SnSAG ELISAs have potential for use as immunodiagnostic tests to aid in the identification of horses affected by EPM.

  12. Antigenic evaluation of a recombinant baculovirus-expressed Sarcocystis neurona SAG1 antigen.

    Science.gov (United States)

    Gupta, G D; Lakritz, J; Saville, W J; Livingston, R S; Dubey, J P; Middleton, J R; Marsh, A E

    2004-10-01

    Sarcocystis neurona is the primary parasite associated with equine protozoal myeloencephalitis (EPM). This is a commonly diagnosed neurological disorder in the Americas that infects the central nervous system of horses. Current serologic assays utilize culture-derived parasites as antigen. This method requires large numbers of parasites to be grown in culture, which is labor intensive and time consuming. Also, a culture-derived whole-parasite preparation contains conserved antigens that could cross-react with antibodies against other Sarcocystis species and members of Sarcocystidae such as Neospora spp., Hammondia spp., and Toxoplasma gondii. Therefore, there is a need to develop an improved method for the detection of S. neurona-specific antibodies. The sera of infected horses react strongly to surface antigen 1 (SnSAG1), an approximately 29-kDa protein, in immunoblot analysis, suggesting that it is an immunodominant antigen. The SnSAG1 gene of S. neurona was cloned, and recombinant S. neurona SAG1 protein (rSnSAG1-Bac) was expressed with the use of a baculovirus system. By immunoblot analysis, the rSnSAG1-Bac antigen detected antibodies to S. neurona from naturally infected and experimentally inoculated equids, cats, rabbit, mice, and skunk. This is the first report of a baculovirus-expressed recombinant S. neurona antigen being used to detect anti-S. neurona antibodies in a variety of host species.

  13. Prevalence of antibodies against Neospora spp. and Sarcocystis neurona in donkeys from northeastern Brazil

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    Solange Maria Gennari

    2016-03-01

    Full Text Available Abstract Sarcocystis neurona and Neospora hughesi are coccidian protozoa that can cause neurological illness in horses in America. In this study we report seroprevalence of Neospora spp. andS. neurona in sera of 333 donkeys from the northeastern region of Brazil. Antibodies to Neospora spp. were detected in 2% (7 donkeys of 333 sera tested by the indirect fluorescent antibody test (IFAT with a cut-off dilution of 1:40. Antibodies to S. neurona were found in 3% (10 donkeys of the samples tested by IFAT (cut-off ≥50 and 21% (69 donkeys by the direct agglutination test (SAT ≥50. The SAT and IFAT results for S. neurona showed a poor concordance (value of Kappa=0.051. This is the first report ofNeospora spp. antibodies in Brazilian donkeys and the first detection of antibodies against S. neurona in this animal species.

  14. Daily feeding of diclazuril top dress pellets in foals reduces seroconversion to Sarcocystis neurona.

    Science.gov (United States)

    Pusterla, Nicola; Packham, Andrea; Mackie, Sarah; Kass, Philip H; Hunyadi, Laszlo; Conrad, Patricia A

    2015-11-01

    Thirty-three foals from a farm with a high exposure rate to Sarcocystis neurona were assigned to either an untreated or a diclazuril-treated group. Treated foals received daily 0.5 mg/kg of diclazuril pellets from 1 to 12 months of age. Monthly blood was tested for IgG against S. neurona using the indirect fluorescent antibody test. Following ingestion of colostral antibodies to S. neurona, there was a steady and continuous decline in seroprevalence to S. neurona until foals from both groups reached weaning age. Thereafter, the untreated foal group showed a significant increase in monthly seroprevalence compared to the diclazuril-treated foal group. The difference in temporal seroprevalence could be explained by the successful reduction of S. neurona infection in foals receiving a daily low-dose diclazuril. Copyright © 2015 Elsevier Ltd. All rights reserved.

  15. Prevalence of antibodies against Neospora spp. and Sarcocystis neurona in donkeys from northeastern Brazil.

    Science.gov (United States)

    Gennari, Solange Maria; Pena, Hilda Fátima de Jesus; Lindsay, David Scott; Lopes, Marcos Gomes; Soares, Herbert Sousa; Cabral, Aline Diniz; Vitaliano, Sérgio Netto; Amaku, Marcos

    2016-01-01

    Sarcocystis neurona and Neospora hughesi are coccidian protozoa that can cause neurological illness in horses in America. In this study we report seroprevalence of Neospora spp. andS. neurona in sera of 333 donkeys from the northeastern region of Brazil. Antibodies to Neospora spp. were detected in 2% (7 donkeys) of 333 sera tested by the indirect fluorescent antibody test (IFAT) with a cut-off dilution of 1:40. Antibodies to S. neurona were found in 3% (10 donkeys) of the samples tested by IFAT (cut-off ≥50) and 21% (69 donkeys) by the direct agglutination test (SAT ≥50). The SAT and IFAT results for S. neurona showed a poor concordance (value of Kappa=0.051). This is the first report of Neospora spp. antibodies in Brazilian donkeys and the first detection of antibodies against S. neurona in this animal species.

  16. Prevalence of antibodies to Sarcocystis neurona and Neospora hughesi in horses from Mexico

    Science.gov (United States)

    The risk of equine protozoal myeloencephalitis (EPM) to horses in Mexico has not been established. Serum samples from 495 horses in Durango State, Mexico were examined for the presence of antibodies to Sarcocystis neurona and Neospora hughesi using enzyme-linked immunosorbent assays (ELISAs) based o...

  17. Bobcat (Lynx rufus) as a new natural intermediate host for Sarcocystis neurona

    Science.gov (United States)

    The protozoan Sarcocystis neurona is an important cause of severe clinical disease of horses (called equine protozoal myeloencephalitis, EPM), marine mammals, companion animals, and several species of wildlife animals in the Americas. The Virginia opossum (Didelphis virginiana) is its definitive hos...

  18. Toxoplasma gondii, Neospora caninum, Sarcocystis neurona, and Sarcocystis canis-like infections in marine mammals.

    Science.gov (United States)

    Dubey, J P; Zarnke, R; Thomas, N J; Wong, S K; Van Bonn, W; Briggs, M; Davis, J W; Ewing, R; Mense, M; Kwok, O C H; Romand, S; Thulliez, P

    2003-10-30

    Toxoplasma gondii, Neospora caninum, Sarcocystis neurona, and S. canis are related protozoans that can cause mortality in many species of domestic and wild animals. Recently, T. gondii and S. neurona were recognized to cause encephalitis in marine mammals. As yet, there is no report of natural exposure of N. caninum in marine mammals. In the present study, antibodies to T. gondii and N. caninum were assayed in sera of several species of marine mammals. For T. gondii, sera were diluted 1:25, 1:50, and 1:500 and assayed in the T. gondii modified agglutination test (MAT). Antibodies (MAT > or =1:25) to T. gondii were found in 89 of 115 (77%) dead, and 18 of 30 (60%) apparently healthy sea otters (Enhydra lutris), 51 of 311 (16%) Pacific harbor seals (Phoca vitulina), 19 of 45 (42%) sea lions (Eumetopias jubatus) [corrected] 5 of 32 (16%) ringed seals (Phoca hispida), 4 of 8 (50%) bearded seals (Erignathus barbatus), 1 of 9 (11.1%) spotted seals (Phoca largha), 138 of 141 (98%) Atlantic bottlenose dolphins (Tursiops truncatus), and 3 of 53 (6%) walruses (Odobenus rosmarus). For N. caninum, sera were diluted 1:40, 1:80, 1:160, and 1:320 and examined with the Neospora agglutination test (NAT) using mouse-derived tachyzoites. NAT antibodies were found in 3 of 53 (6%) walruses, 28 of 145 (19%) sea otters, 11 of 311 (3.5%) harbor seals, 1 of 27 (3.7%) sea lions, 4 of 32 (12.5%) ringed seals, 1 of 8 (12.5%) bearded seals, and 43 of 47 (91%) bottlenose dolphins. To our knowledge, this is the first report of N. caninum antibodies in any marine mammal, and the first report of T. gondii antibodies in walruses and in ringed, bearded, spotted, and ribbon seals. Current information on T. gondii-like and Sarcocystis-like infections in marine mammals is reviewed. New cases of clinical S. canis and T. gondii infections are also reported in sea lions, and T. gondii infection in an Antillean manatee (Trichechus manatus manatus).

  19. Toxoplasma gondii, Neospora caninum, Sarcocystis neurona, and Sarcocystis canis-like infections in marine mammals

    Science.gov (United States)

    Dubey, J.P.; Zarnke, R.; Thomas, N.J.; Wong, S.K.; Vanbonn, W.; Briggs, M.; Davis, J.W.; Ewing, R.; Mense, M.; Kwok, O.C.H.; Romand, S.; Thulliez, P.

    2003-01-01

    Toxoplasma gondii, Neospora caninum, Sarcocystis neurona, and S. canis are related protozoans that can cause mortality in many species of domestic and wild animals. Recently, T. gondii and S. neurona were recognized to cause encephalitis in marine mammals. As yet, there is no report of natural exposure of N. caninum in marine mammals. In the present study, antibodies to T. gondii and N. caninum were assayed in sera of several species of marine mammals. For T. gondii, sera were diluted 1:25, 1:50, and 1:500 and assayed in the T. gondii modified agglutination test (MAT). Antibodies (MAT a?Y1:25) to T. gondii were found in 89 of 115 (77%) dead, and 18 of 30 (60%) apparently healthy sea otters (Enhydra lutris), 51 of 311 (16%) Pacific harbor seals (Phoca vitulina), 19 of 45 (42%) sea lions (Zalophus californianus), 5 of 32 (16%) ringed seals (Phoca hispida), 4 of 8 (50%) bearded seals (Erignathus barbatus), 1 of 9 (11.1%) spotted seals (Phoca largha), 138 of 141 (98%) Atlantic bottlenose dolphins (Tursiops truncatus), and 3 of 53 (6%) walruses (Odobenus rosmarus). For N. caninum, sera were diluted 1:40, 1:80, 1:160, and 1:320 and examined with the Neospora agglutination test (NAT) using mouse-derived tachyzoites. NAT antibodies were found in 3 of 53 (6%) walruses, 28 of 145 (19%) sea otters, 11 of 311 (3.5%) harbor seals, 1 of 27 (3.7%) sea lions, 4 of 32 (12.5%) ringed seals, 1 of 8 (12.5%) bearded seals, and 43 of 47 (91%) bottlenose dolphins. To our knowledge, this is the first report of N. caninum antibodies in any marine mammal, and the first report of T. gondii antibodies in walruses and in ringed, bearded, spotted, and ribbon seals. Current information on T. gondii-like and Sarcocystis-like infections in marine mammals is reviewed. New cases of clinical S. canis and T. gondii infections are also reported in sea lions, and T. gondii infection in an Antillean manatee (Trichechus manatus manatus).

  20. Effects of Experimental Sarcocystis neurona-Induced Infection on Immunity in an Equine Model

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    S. Rochelle Lewis

    2014-01-01

    Full Text Available Sarcocystis neurona is the most common cause of Equine Protozoal Myeloencephalitis (EPM, affecting 0.5–1% horses in the United States during their lifetimes. The objective of this study was to evaluate the equine immune responses in an experimentally induced Sarcocystis neurona infection model. Neurologic parameters were recorded prior to and throughout the 70-day study by blinded investigators. Recombinant SnSAG1 ELISA for serum and CSF were used to confirm and track disease progression. All experimentally infected horses displayed neurologic signs after infection. Neutrophils, monocytes, and lymphocytes from infected horses displayed significantly delayed apoptosis at some time points. Cell proliferation was significantly increased in S. neurona-infected horses when stimulated nonspecifically with PMA/I but significantly decreased when stimulated with S. neurona compared to controls. Collectively, our results suggest that horses experimentally infected with S. neurona manifest impaired antigen specific response to S. neurona, which could be a function of altered antigen presentation, lack of antigen recognition, or both.

  1. Effects of Experimental Sarcocystis neurona-Induced Infection on Immunity in an Equine Model.

    Science.gov (United States)

    Lewis, S Rochelle; Ellison, Siobhan P; Dascanio, John J; Lindsay, David S; Gogal, Robert M; Werre, Stephen R; Surendran, Naveen; Breen, Meghan E; Heid, Bettina M; Andrews, Frank M; Buechner-Maxwell, Virginia A; Witonsky, Sharon G

    2014-01-01

    Sarcocystis neurona is the most common cause of Equine Protozoal Myeloencephalitis (EPM), affecting 0.5-1% horses in the United States during their lifetimes. The objective of this study was to evaluate the equine immune responses in an experimentally induced Sarcocystis neurona infection model. Neurologic parameters were recorded prior to and throughout the 70-day study by blinded investigators. Recombinant SnSAG1 ELISA for serum and CSF were used to confirm and track disease progression. All experimentally infected horses displayed neurologic signs after infection. Neutrophils, monocytes, and lymphocytes from infected horses displayed significantly delayed apoptosis at some time points. Cell proliferation was significantly increased in S. neurona-infected horses when stimulated nonspecifically with PMA/I but significantly decreased when stimulated with S. neurona compared to controls. Collectively, our results suggest that horses experimentally infected with S. neurona manifest impaired antigen specific response to S. neurona, which could be a function of altered antigen presentation, lack of antigen recognition, or both.

  2. Use of proteinase K in the excystation of Sarcocystis cruzi sporocysts for in vitro culture and DNA extraction.

    Science.gov (United States)

    Ndiritu, W; Cawthorn, R J; Kibenge, F S

    1994-03-01

    Proteinase K was used for the cleaning of Sarcocystis cruzi (Apicomplexa) sporocysts prior to excystation. Bovine pulmonary endothelial cell cultures inoculated with the excysted sporozoites remained free of bacterial contamination for the duration of the experiment and had high yields of merozoites. The excysted sporozoites also yielded genomic DNA that could be labelled efficiently with 32P dATP by the random priming method.

  3. Seroepidemiology of Sarcocystis neurona and Neospora hughesi infections in domestic donkeys (Equus asinus in Durango, Mexico

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    Alvarado-Esquivel Cosme

    2017-01-01

    Full Text Available There is currently no information regarding Sarcocystis neurona and Neospora hughesi infections in donkeys in Mexico. Here, we determined the presence of antibodies against S. neurona and N. hughesi in donkeys in the northern Mexican state of Durango. Serum samples of 239 domestic donkeys (Equus asinus were assayed for S. neurona and N. hughesi antibodies using home-made enzyme-linked immunoassays; six (2.5% of the 239 donkeys tested seropositive for S. neurona. The seroprevalence of S. neurona infection was comparable among donkeys regardless of their origin, health status, or sex. Multivariate analysis showed that seropositivity to S. neurona was associated with increased age (OR = 2.95; 95% CI: 1.11–7.82; p = 0.02. Antibodies to N. hughesi were found in two (0.8% of the 239 donkeys. Both exposed donkeys were healthy, 3- and 6-year-old females. This is the first evidence of S. neurona and N. hughesi infections in donkeys in Mexico.

  4. Seroepidemiology of Sarcocystis neurona and Neospora hughesi infections in domestic donkeys (Equus asinus) in Durango, Mexico.

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    Alvarado-Esquivel, Cosme; Howe, Daniel K; Yeargan, Michelle R; Alvarado-Esquivel, Domingo; Alfredo Zamarripa-Barboza, José; Dubey, Jitender P

    2017-01-01

    There is currently no information regarding Sarcocystis neurona and Neospora hughesi infections in donkeys in Mexico. Here, we determined the presence of antibodies against S. neurona and N. hughesi in donkeys in the northern Mexican state of Durango. Serum samples of 239 domestic donkeys (Equus asinus) were assayed for S. neurona and N. hughesi antibodies using home-made enzyme-linked immunoassays; six (2.5%) of the 239 donkeys tested seropositive for S. neurona. The seroprevalence of S. neurona infection was comparable among donkeys regardless of their origin, health status, or sex. Multivariate analysis showed that seropositivity to S. neurona was associated with increased age (OR = 2.95; 95% CI: 1.11-7.82; p = 0.02). Antibodies to N. hughesi were found in two (0.8%) of the 239 donkeys. Both exposed donkeys were healthy, 3- and 6-year-old females. This is the first evidence of S. neurona and N. hughesi infections in donkeys in Mexico. © C. Alvarado-Esquivel et al., published by EDP Sciences, 2017.

  5. Sarcocystis neurona-specific immunoglobulin G in the serum and cerebrospinal fluid of horses administered S neurona vaccine.

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    Witonsky, Sharon; Morrow, Jennifer K; Leger, Clare; Dascanio, John; Buechner-Maxwell, Virginia; Palmer, Wally; Kline, Kristen; Cook, Anne

    2004-01-01

    A vaccine against Sarcocystis neurona, which induces equine protozoal myeloencephalitis (EPM), has received conditional licensure in the United States. A major concern is whether the immunoglobulin G (IgG) response elicited by the vaccine will compromise the use of Western blotting (WB) as a diagnostic tool in vaccinated horses with neurologic disease. Our goals were to determine if vaccination (1) causes seroconversion: (2) causes at least a transient increase in S neurona-specific IgG in the cerebrospinal fluid (CSF); and (3) induces an IgG response that can be differentiated from that induced by natural exposure. Horses included in the study (n = 29) were older than 6 months with no evidence of neurologic disease. The presence or absence of anti-S neurona antibodies in the serum of each horse was determined by WB analysis. Seropositive horses had CSF collected and submitted for cytology, CSF index, and WB analysis. The vaccine was administered to all the horses and boostered 3-4 weeks later. On day 14 after the 2nd administration, serum and CSF were collected and analyzed. Eighty-nine percent (8 of 9) of the initial seronegative horses seroconverted after vaccination, of which 57% (4 of 7) had anti-S neurona IgG in their CSE Eighty percent (16 of 20) of the seropositive horses had an increase in serum S neurona IgG after vaccination. Of the 6 of 20 horses that were initially seropositive/CSF negative, 2 were borderline positive for anti-S neurona IgG in the CSF, 2 tested positive, and 2 were excluded because the CSF sample had been contaminated by blood. There were no WB banding patterns that distinguished samples from horses that seroconverted due to vaccination versus natural exposure. Caution must be used in interpreting WB analysis from neurologic horses that have been recently vaccinated for EPM.

  6. Risk of postnatal exposure to Sarcocystis neurona and Neospora hughesi in horses.

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    Duarte, Paulo C; Conrad, Patricia A; Wilson, W David; Ferraro, Gregory L; Packham, Andrea E; Bowers-Lepore, Jeanne; Carpenter, Tim E; Gardner, Ian A

    2004-08-01

    To estimate risk of exposure and age at first exposure to Sarcocystis neurona and Neospora hughesi and time to maternal antibody decay in foals. 484 Thoroughbred and Warmblood foals from 4 farms in California. Serum was collected before and after colostrum ingestion and at 3-month intervals thereafter. Samples were tested by use of the indirect fluorescent antibody test; cutoff titers were > or = 40 and > or = 160 for S neurona and N hughesi, respectively. Risk of exposure to S neurona and N hughesi during the study were 8.2% and 3.1%, respectively. Annual rate of exposure was 3.1% for S neurona and 1.7% for N hughesi. There was a significant difference in the risk of exposure to S neurona among farms but not in the risk of exposure to N hughesi. Median age at first exposure was 1.2 years for S neurona and 0.8 years for N hughesi. Highest prevalence of antibodies against S neurona and N hughesi was 6% and 2.1 %, respectively, at a mean age of 1.7 and 1.4 years, respectively. Median time to maternal antibody decay was 96 days for S neurona and 91 days for N hughesi. There were no clinical cases of equine protozoal myeloenchaphlitis (EPM). Exposure to S neurona and N hughesi was low in foals between birth and 2.5 years of age. Maternally acquired antibodies may cause false-positive results for 3 or 4 months after birth, and EPM was a rare clinical disease in horses < or = 2.5 years of age.

  7. Risk of transplacental transmission of Sarcocystis neurona and Neospora hughesi in California horses.

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    Duarte, Paulo C; Conrad, Patricia A; Barr, Bradd C; Wilson, W David; Ferraro, Gregory L; Packham, Andrea E; Carpenter, Tim E; Gardner, Ian A

    2004-12-01

    The study objective was to assess the risk of transplacental transmission of Sarcocystis neurona and Neospora hughesi in foals from 4 California farms during 3 foaling seasons. Serum of presuckle foals and serum and colostrum of periparturient mares were tested using indirect fluorescent antibody tests for S. neurona and N. hughesi. Serum antibody titers were neurona and N. hughesi in mares increased with age. Mares neurona and N. hughesi, respectively, than mares from California. The strength of association between positivity to either parasite and state of birth decreased as age increased. Mares positive for S. neurona and N. hughesi were 2.2 and 1.7 times more likely, respectively, to have a previous abortion than negative mares, adjusted for age and state of birth. The annual mortality rate for mares was 4%. The annual incidence rate of equine protozoal myeloencephalitis was 0.2%. In conclusion, there was no detectable risk of transplacental transmission of S. neurona and N. hughesi. Prevalence of antibodies against both parasites in mares increased with age.

  8. Horses experimentally infected with Sarcocystis neurona develop altered immune responses in vitro.

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    Witonsky, Sharon G; Ellison, Siobhan; Yang, Jibing; Gogal, Robert M; Lawler, Heather; Suzuki, Yasuhiro; Sriranganathan, Namalwar; Andrews, Frank; Ward, Daniel; Lindsay, David S

    2008-10-01

    Equine protozoal myeloencephalitis (EPM) due to Sarcocystis neurona infection is 1 of the most common neurologic diseases in horses in the United States. The mechanisms by which most horses resist disease, as well as the possible mechanisms by which the immune system may be suppressed in horses that develop EPM, are not known. Therefore, the objectives of this study were to determine whether horses experimentally infected with S. neurona developed suppressed immune responses. Thirteen horses that were negative for S. neurona antibodies in serum and cerebrospinal fluid (CSF) were randomly assigned to control (n = 5) or infected (n = 8) treatment groups. Neurologic exams and cerebrospinal fluid analyses were performed prior to, and following, S. neurona infection. Prior to, and at multiple time points following infection, immune parameters were determined. All 8 S. neurona-infected horses developed clinical signs consistent with EPM, and had S. neurona antibodies in the serum and CSF. Both infected and control horses had increased percentages (P < 0.05) of B cells at 28 days postinfection. Infected horses had significantly decreased (P < 0.05) proliferation responses as measured by thymidine incorporation to nonspecific mitogens phorbol myristate acetate (PMA) and ionomycin (I) as soon as 2 days postinfection.

  9. Self-mating in the definitive host potentiates clonal outbreaks of the apicomplexan parasites Sarcocystis neurona and Toxoplasma gondii.

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    Jered M Wendte

    Full Text Available Tissue-encysting coccidia, including Toxoplasma gondii and Sarcocystis neurona, are heterogamous parasites with sexual and asexual life stages in definitive and intermediate hosts, respectively. During its sexual life stage, T. gondii reproduces either by genetic out-crossing or via clonal amplification of a single strain through self-mating. Out-crossing has been experimentally verified as a potent mechanism capable of producing offspring possessing a range of adaptive and virulence potentials. In contrast, selfing and other life history traits, such as asexual expansion of tissue-cysts by oral transmission among intermediate hosts, have been proposed to explain the genetic basis for the clonal population structure of T. gondii. In this study, we investigated the contributing roles self-mating and sexual recombination play in nature to maintain clonal population structures and produce or expand parasite clones capable of causing disease epidemics for two tissue encysting parasites. We applied high-resolution genotyping against strains isolated from a T. gondii waterborne outbreak that caused symptomatic disease in 155 immune-competent people in Brazil and a S. neurona outbreak that resulted in a mass mortality event in Southern sea otters. In both cases, a single, genetically distinct clone was found infecting outbreak-exposed individuals. Furthermore, the T. gondii outbreak clone was one of several apparently recombinant progeny recovered from the local environment. Since oocysts or sporocysts were the infectious form implicated in each outbreak, the expansion of the epidemic clone can be explained by self-mating. The results also show that out-crossing preceded selfing to produce the virulent T. gondii clone. For the tissue encysting coccidia, self-mating exists as a key adaptation potentiating the epidemic expansion and transmission of newly emerged parasite clones that can profoundly shape parasite population genetic structures or cause

  10. Self-mating in the definitive host potentiates clonal outbreaks of the apicomplexan parasites Sarcocystis neurona and Toxoplasma gondii.

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    Wendte, Jered M; Miller, Melissa A; Lambourn, Dyanna M; Magargal, Spencer L; Jessup, David A; Grigg, Michael E

    2010-12-23

    Tissue-encysting coccidia, including Toxoplasma gondii and Sarcocystis neurona, are heterogamous parasites with sexual and asexual life stages in definitive and intermediate hosts, respectively. During its sexual life stage, T. gondii reproduces either by genetic out-crossing or via clonal amplification of a single strain through self-mating. Out-crossing has been experimentally verified as a potent mechanism capable of producing offspring possessing a range of adaptive and virulence potentials. In contrast, selfing and other life history traits, such as asexual expansion of tissue-cysts by oral transmission among intermediate hosts, have been proposed to explain the genetic basis for the clonal population structure of T. gondii. In this study, we investigated the contributing roles self-mating and sexual recombination play in nature to maintain clonal population structures and produce or expand parasite clones capable of causing disease epidemics for two tissue encysting parasites. We applied high-resolution genotyping against strains isolated from a T. gondii waterborne outbreak that caused symptomatic disease in 155 immune-competent people in Brazil and a S. neurona outbreak that resulted in a mass mortality event in Southern sea otters. In both cases, a single, genetically distinct clone was found infecting outbreak-exposed individuals. Furthermore, the T. gondii outbreak clone was one of several apparently recombinant progeny recovered from the local environment. Since oocysts or sporocysts were the infectious form implicated in each outbreak, the expansion of the epidemic clone can be explained by self-mating. The results also show that out-crossing preceded selfing to produce the virulent T. gondii clone. For the tissue encysting coccidia, self-mating exists as a key adaptation potentiating the epidemic expansion and transmission of newly emerged parasite clones that can profoundly shape parasite population genetic structures or cause devastating disease

  11. Serological investigation of transplacental infection with Neospora hughesi and Sarcocystis neurona in broodmares.

    Science.gov (United States)

    Pusterla, Nicola; Mackie, Sarah; Packham, Andrea; Conrad, Patricia A

    2014-12-01

    The aim of the present study was to investigate the likelihood of transplacental transmission of Neospora hughesi and Sarcocystis neurona in foals, born from seropositive mares. Three broodmares with persistent N. hughesi infection gave birth to eight healthy foals over a period of 7 years. These foals were seropositive to N. hughesi prior to colostrum ingestion, with titers ranging between 640 and 20,480, measured by indirect fluorescence antibody test (IFAT). Of 174 foals born at another farm to mares with a high seroprevalence to S. neurona, only one (with a pre-colostrum antibody titer of 80) tested seropositive. Transplacental transmission of N. hughesi seems to occur from latently infected mares to their foals, while this route of transmission does not seem to occur commonly for S. neurona. Copyright © 2014 Elsevier Ltd. All rights reserved.

  12. Systems-based analysis of the Sarcocystis neurona genome identifies pathways that contribute to a heteroxenous life cycle.

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    Blazejewski, Tomasz; Nursimulu, Nirvana; Pszenny, Viviana; Dangoudoubiyam, Sriveny; Namasivayam, Sivaranjani; Chiasson, Melissa A; Chessman, Kyle; Tonkin, Michelle; Swapna, Lakshmipuram S; Hung, Stacy S; Bridgers, Joshua; Ricklefs, Stacy M; Boulanger, Martin J; Dubey, Jitender P; Porcella, Stephen F; Kissinger, Jessica C; Howe, Daniel K; Grigg, Michael E; Parkinson, John

    2015-02-10

    Sarcocystis neurona is a member of the coccidia, a clade of single-celled parasites of medical and veterinary importance including Eimeria, Sarcocystis, Neospora, and Toxoplasma. Unlike Eimeria, a single-host enteric pathogen, Sarcocystis, Neospora, and Toxoplasma are two-host parasites that infect and produce infectious tissue cysts in a wide range of intermediate hosts. As a genus, Sarcocystis is one of the most successful protozoan parasites; all vertebrates, including birds, reptiles, fish, and mammals are hosts to at least one Sarcocystis species. Here we sequenced Sarcocystis neurona, the causal agent of fatal equine protozoal myeloencephalitis. The S. neurona genome is 127 Mbp, more than twice the size of other sequenced coccidian genomes. Comparative analyses identified conservation of the invasion machinery among the coccidia. However, many dense-granule and rhoptry kinase genes, responsible for altering host effector pathways in Toxoplasma and Neospora, are absent from S. neurona. Further, S. neurona has a divergent repertoire of SRS proteins, previously implicated in tissue cyst formation in Toxoplasma. Systems-based analyses identified a series of metabolic innovations, including the ability to exploit alternative sources of energy. Finally, we present an S. neurona model detailing conserved molecular innovations that promote the transition from a purely enteric lifestyle (Eimeria) to a heteroxenous parasite capable of infecting a wide range of intermediate hosts. Sarcocystis neurona is a member of the coccidia, a clade of single-celled apicomplexan parasites responsible for major economic and health care burdens worldwide. A cousin of Plasmodium, Cryptosporidium, Theileria, and Eimeria, Sarcocystis is one of the most successful parasite genera; it is capable of infecting all vertebrates (fish, reptiles, birds, and mammals-including humans). The past decade has witnessed an increasing number of human outbreaks of clinical significance associated with

  13. In vitro efficacy of nitro- and halogeno-thiazolide/thiadiazolide derivatives against Sarcocystis neurona.

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    Gargala, G; Le Goff, L; Ballet, J J; Favennec, L; Stachulski, A V; Rossignol, J F

    2009-06-10

    Sarcocystis neurona is an obligate intracellular parasite that causes equine protozoal myeloencephalitis (EPM). The aim of this work was to document inhibitory activities of nitazoxanide (NTZ, [2-acetolyloxy-N-(5-nitro 2-thiazolyl) benzamide]) and new thiazolides/thiadiazolides on S. neurona in vitro development, and investigate their structure-activity relationships. S. neurona was grown in bovine turbinate cell cultures. At concentrations varying from 1.0 to 5.0mg/L, nitazoxanide and 21 of 32 second generation thiazolide/thiadiazolide agents exerted a > or =95% maximum inhibition on S. neurona development. Most active agents were either NO(2) or halogen substituted in position 5 of their thiazole moiety. In contrast, other 5-substitutions such as hydrogen, methyl, SO(2)CH(3), and CH(3) negatively impacted activity. Compared with derivatives with an acetylated benzene moiety, deacetylated compounds which most probably represent primary metabolites exhibited similar inhibitory activities. Present data provide the first evidence of in vitro inhibitory activities of nitazoxanide and new thiazolides/thiadiazolides on S. neurona development. Active halogeno-thiazolide/thiadiazolides may provide a valuable nitro-free alternative to nitazoxanide for EPM treatment depending on further evaluation of their in vivo activities.

  14. The identification of a sequence related to apicomplexan enolase from Sarcocystis neurona.

    Science.gov (United States)

    Wilson, A P; Thelen, J J; Lakritz, J; Brown, C R; Marsh, A E

    2004-11-01

    Equine protozoal myeloencephalitis (EPM) is a neurological disease caused by Sarcocystis neurona, an apicomplexan parasite. S. neurona is also associated with EPM-like diseases in marine and small mammals. The mechanisms of transmission and ability to infect a wide host range remain obscure; therefore, characterization of essential proteins may provide evolutionary information allowing the development of novel chemotherapeutics that target non-mammalian biochemical pathways. In the current study, two-dimensional electrophoresis and matrix-assisted laser desorption ionization-time of flight (MALDI-ToF) mass spectrometry were combined to characterize and identify an enolase protein from S. neurona based on peptide homology to the Toxoplasma gondii protein. Enolase is thought to be a vestigial, non-photosynthetic protein resulting from an evolutionary endosymbiosis event of an apicomplexan ancestor with green algae. Enolase has also been suggested to play a role in parasite stage conversion for T. gondii. Characterization of this protein in S. neurona and comparison to other protozoans indicate a biochemical similarity of S. neurona enolase to other tissue-cyst forming coccidians that cause encephalitis.

  15. Dual Sarcocystis neurona and Toxoplasma gondii infection in a northern sea otter from Washington state, USA

    Science.gov (United States)

    Lindsay, D.S.; Thomas, N.J.; Rosypal, A.C.; Dubey, J.P.

    2001-01-01

    Dual Sarcocystis neurona and Toxoplasma gondii infection was observed in a Northern sea otter from Washington, USA. The animal was found stranded, convulsed, and died shortly thereafter. Encephalitis caused by both S. neurona and T. gondii was demonstrated in histological sections of brain. Immunohistochemical examination of sections with S. neurona specific antisera demonstrated developmental stages that divided by endopolygeny and produced numerous merozoites. PCR of brain tissue from the sea otter using primer pairs JNB33/JNB54 resulted in amplification of a 1100 bp product. This PCR product was cut in to 884 and 216 bp products by Dra I but was not cut by Hinf I indicating that it was S. neurona [J. Parasitol. 85 (1999) 221]. No PCR product was detected in the brain of a sea otter which had no lesions of encephalitis. Examination of brain sections using T. gondii specific antisera demonstrated tachyzoites and tissue cysts of T. gondii. The lesions induced by T. gondii suggested that the sea otter was suffering from reactivated toxoplasmosis. T. gondii was isolated in mice inoculated with brain tissue. A cat that was fed infected mouse brain tissue excreted T. gondii oocysts which were infective for mice. This is apparently the first report of dual S. neurona and T. gondii in a marine mammal.

  16. Parasitemia due to Sarcocystis neurona-like infection in a clinically ill domestic cat.

    Science.gov (United States)

    Zitzer, Nina C; Marsh, Antoinette E; Burkhard, Mary Jo; Radin, M Judith; Wellman, Maxey L; Jugan, Maria; Parker, Valerie

    2017-09-11

    An 8-year-old, 6-kg, male neutered Domestic Shorthair cat was presented to The Ohio State University Veterinary Medical Center (OSU-VMC) for difficulty breathing. Physical examination and thoracic radiographs indicated pneumonia, a soft-tissue mass in the left caudal lung lobe, and diffuse pleural effusion. The effusion was classified as modified transudate. Rare extracellular elongated (~5-7 μm × 1-2 μm) zoites with a central round to oval-shaped purple to deep purple vesicular nucleus with coarsely stippled chromatin and light blue cytoplasm were seen on a peripheral blood smear. Serum IgG and IgM were positive for Sarcocystis sp. antibodies and negative for Toxoplasma gondii antibodies, suggesting that the infection was acute rather than a recrudescence of prior infection. This organism was most consistent with either Sarcocystis neurona or Sarcocystis dasypi based on DNA sequence analysis of PCR products using COC ssRNA, ITS-1, snSAG2, and JNB25/JD396 primer sets. This is the first report to visualize by light microscopy circulating Sarcocystis sp. merozoites in the peripheral blood of a domestic cat. Therefore, Sarcocystis should be considered as a differential diagnosis in cats with suspected systemic protozoal infection. © 2017 American Society for Veterinary Clinical Pathology.

  17. Genome-Wide Identification and Evolutionary Analysis of Sarcocystis neurona Protein Kinases

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    Edwin K. Murungi

    2017-03-01

    Full Text Available The apicomplexan parasite Sarcocystis neurona causes equine protozoal myeloencephalitis (EPM, a degenerative neurological disease of horses. Due to its host range expansion, S. neurona is an emerging threat that requires close monitoring. In apicomplexans, protein kinases (PKs have been implicated in a myriad of critical functions, such as host cell invasion, cell cycle progression and host immune response evasion. Here, we used various bioinformatics methods to define the kinome of S. neurona and phylogenetic relatedness of its PKs to other apicomplexans. We identified 97 putative PKs clustering within the various eukaryotic kinase groups. Although containing the universally-conserved PKA (AGC group, S. neurona kinome was devoid of PKB and PKC. Moreover, the kinome contains the six-conserved apicomplexan CDPKs (CAMK group. Several OPK atypical kinases, including ROPKs 19A, 27, 30, 33, 35 and 37 were identified. Notably, S. neurona is devoid of the virulence-associated ROPKs 5, 6, 18 and 38, as well as the Alpha and RIO kinases. Two out of the three S. neurona CK1 enzymes had high sequence similarities to Toxoplasma gondii TgCK1-α and TgCK1-β and the Plasmodium PfCK1. Further experimental studies on the S. neurona putative PKs identified in this study are required to validate the functional roles of the PKs and to understand their involvement in mechanisms that regulate various cellular processes and host-parasite interactions. Given the essentiality of apicomplexan PKs in the survival of apicomplexans, the current study offers a platform for future development of novel therapeutics for EPM, for instance via application of PK inhibitors to block parasite invasion and development in their host.

  18. Genome-Wide Identification and Evolutionary Analysis of Sarcocystis neurona Protein Kinases.

    Science.gov (United States)

    Murungi, Edwin K; Kariithi, Henry M

    2017-03-21

    The apicomplexan parasite Sarcocystis neurona causes equine protozoal myeloencephalitis (EPM), a degenerative neurological disease of horses. Due to its host range expansion, S. neurona is an emerging threat that requires close monitoring. In apicomplexans, protein kinases (PKs) have been implicated in a myriad of critical functions, such as host cell invasion, cell cycle progression and host immune response evasion. Here, we used various bioinformatics methods to define the kinome of S. neurona and phylogenetic relatedness of its PKs to other apicomplexans. We identified 97 putative PKs clustering within the various eukaryotic kinase groups. Although containing the universally-conserved PKA (AGC group), S. neurona kinome was devoid of PKB and PKC. Moreover, the kinome contains the six-conserved apicomplexan CDPKs (CAMK group). Several OPK atypical kinases, including ROPKs 19A, 27, 30, 33, 35 and 37 were identified. Notably, S. neurona is devoid of the virulence-associated ROPKs 5, 6, 18 and 38, as well as the Alpha and RIO kinases. Two out of the three S. neurona CK1 enzymes had high sequence similarities to Toxoplasma gondii TgCK1-α and TgCK1-β and the Plasmodium PfCK1. Further experimental studies on the S. neurona putative PKs identified in this study are required to validate the functional roles of the PKs and to understand their involvement in mechanisms that regulate various cellular processes and host-parasite interactions. Given the essentiality of apicomplexan PKs in the survival of apicomplexans, the current study offers a platform for future development of novel therapeutics for EPM, for instance via application of PK inhibitors to block parasite invasion and development in their host.

  19. Identification of a dithiol-dependent nucleoside triphosphate hydrolase in Sarcocystis neurona.

    Science.gov (United States)

    Zhang, Deqing; Gaji, Rajshekhar Y; Howe, Daniel K

    2006-09-01

    A putative nucleoside triphosphate hydrolase (NTPase) gene was identified in a database of expressed sequence tags (ESTs) from the apicomplexan parasite Sarcocystis neurona. Analysis of culture-derived S. neurona merozoites demonstrated a dithiol-dependent NTPase activity, consistent with the presence of a homologue to the TgNTPases of Toxoplasma gondii. A complete cDNA was obtained for the S. neurona gene and the predicted amino acid sequence shared 38% identity with the two TgNTPase isoforms from T. gondii. Based on the obvious homology, the S. neurona protein was designated SnNTP1. The SnNTP1 cDNA encodes a polypeptide of 714 amino acids with a predicted 22-residue signal peptide and an estimated mature molecular mass of 70kDa. Southern blot analysis of the SnNTP1 locus revealed that the gene exists as a single copy in the S. neurona genome, unlike the multiple gene copies that have been observed in T. gondii and Neospora caninum. Analyses of the SnNTP1 protein demonstrated that it is soluble and secreted into the culture medium by extracellular merozoites. Surprisingly, indirect immunofluorescence analysis of intracellular S. neurona revealed apical localisation of SnNTP1 and temporal expression characteristics that are comparable with the microneme protein SnMIC10. The absence of SnNTP1 during much of endopolygeny implies that this protein does not serve a function during intracellular growth and development of S. neurona schizonts. Instead, SnNTP1 may play a role in events that occur during or proximal to merozoite egress from and/or invasion into cells.

  20. A genetically diverse but distinct North American population of Sarcocystis neurona includes an overrepresented clone described by 12 microsatellite alleles.

    Science.gov (United States)

    Asmundsson, Ingrid M; Dubey, J P; Rosenthal, Benjamin M

    2006-09-01

    The population genetics and systematics of most coccidians remain poorly defined despite their impact on human and veterinary health. Non-recombinant parasite clones characterized by distinct transmission and pathogenesis traits persist in the coccidian Toxoplasma gondii despite opportunities for sexual recombination. In order to determine whether this may be generally true for tissue-cyst forming coccidia, and to address evolutionary and taxonomic problems within the genus Sarcocystis, we characterized polymorphic microsatellite markers in Sarcocystis neurona, the major causative agent of equine protozoal myeloencephalitis (EPM). Bayesian statistical modeling, phylogenetic reconstruction based on genotypic chord distances, and analyses of linkage disequilibrium were employed to examine the population structure within S. neurona and closely related Sarcocystis falcatula isolates from North and South America. North American S. neurona were clearly differentiated from those of South America and also from isolates of S. falcatula. Although S. neurona is characterized by substantial allelic and genotypic diversity typical of interbreeding populations, one genotype occurs with significantly excessive frequency; thus, some degree of asexual propagation of S. neurona clones may naturally occur. Finally, S. neurona isolated from disparate North American localities and diverse hosts (opossums, a Southern sea otter, and horses) comprise a single genetic population. Isolates associated with clinical neurological disease bear no obvious distinction as measured by these presumably neutral genetic markers.

  1. Investigation of SnSPR1, a novel and abundant surface protein of Sarcocystis neurona merozoites.

    Science.gov (United States)

    Zhang, Deqing; Howe, Daniel K

    2008-04-15

    An expressed sequence tag (EST) sequencing project has produced over 15,000 partial cDNA sequences from the equine pathogen Sarcocystis neurona. While many of the sequences are clear homologues of previously characterized genes, a significant number of the S. neurona ESTs do not exhibit similarity to anything in the extensive sequence databases that have been generated. In an effort to characterize parasite proteins that are novel to S. neurona, a seemingly unique gene was selected for further investigation based on its abundant representation in the collection of ESTs and the predicted presence of a signal peptide and glycolipid anchor addition on the encoded protein. The gene was expressed in E. coli, and monospecific polyclonal antiserum against the recombinant protein was produced by immunization of a rabbit. Characterization of the native protein in S. neurona merozoites and schizonts revealed that it is a low molecular weight surface protein that is expressed throughout intracellular development of the parasite. The protein was designated Surface Protein 1 (SPR1) to reflect its display on the outer surface of merozoites and to distinguish it from the ubiquitous SAG/SRS surface antigens of the heteroxenous Coccidia. Interestingly, infection assays in the presence of the polyclonal antiserum suggested that SnSPR1 plays some role in attachment and/or invasion of host cells by S. neurona merozoites. The work described herein represents a general template for selecting and characterizing the various unidentified gene sequences that are plentiful in the EST databases for S. neurona and other apicomplexans. Furthermore, this study illustrates the value of investigating these novel sequences since it can offer new candidates for diagnostic or vaccine development while also providing greater insight into the biology of these parasites.

  2. Prevalence of antibodies to Sarcocystis neurona and Neospora hughesi in horses from Mexico.

    Science.gov (United States)

    Yeargan, Michelle R; Alvarado-Esquivel, Cosme; Dubey, Jitender P; Howe, Daniel K

    2013-01-01

    Equine protozoal myeloencephalitis (EPM) is a debilitating disease of horses caused by Sarcocystis neurona and Neospora hughesi. Sera from 495 horses in Durango State, Mexico were tested for anti-protozoal antibodies using enzyme-linked immunosorbent assays (ELISAs) based on major surface antigens of these two parasites. Antibodies to S. neurona were detected in 240 (48.5%) of the 495 horse sera tested with the rSnSAG2/4/3 trivalent ELISA. Multivariate analysis showed that exposure to S. neurona was associated with age, feeding grains and crops, and small herd size. Antibodies to N. hughesi were found in 15 (3.0%) of the 495 horse sera tested with the rNhSAG1 ELISA and confirmed by Western blot of N. hughesi tachyzoite antigen. This is the first report of S. neurona and N. hughesi exposure in horses in Mexico, and it affirms that EPM should be in the differential diagnosis for horses exhibiting signs of neurologic disease in this country. © M.R. Yeargan et al., published by EDP Sciences, 2013.

  3. Immune response to Sarcocystis neurona infection in naturally infected horses with equine protozoal myeloencephalitis.

    Science.gov (United States)

    Yang, Jibing; Ellison, Siobhan; Gogal, Robert; Norton, Heather; Lindsay, David S; Andrews, Frank; Ward, Daniel; Witonsky, Sharon

    2006-06-15

    Equine protozoal myeloencephalitis (EPM) is one of the most common neurologic diseases of horses in the United States. The primary etiologic agent is Sarcocystis neurona. Currently, there is limited knowledge regarding the protective or pathophysiologic immune response to S. neurona infection or the subsequent development of EPM. The objectives of this study were to determine whether S. neurona infected horses with clinical signs of EPM had altered or suppressed immune responses compared to neurologically normal horses and if blood sample storage would influence these findings. Twenty clinically normal horses and 22 horses with EPM, diagnosed by the presence of S. neurona specific antibodies in the serum and/or cerebrospinal (CSF) and clinical signs, were evaluated for differences in the immune cell subsets and function. Our results demonstrated that naturally infected horses had significantly (Pneurona in horses, as well as to determine the mechanism associated with suppressed in vitro proliferation responses. Finally, overnight storage of blood samples appears to alter T lymphocyte phenotypes and viability among leukocytes.

  4. Prevalence of antibodies to Trypanosoma cruzi, Toxoplasma gondii, Encephalitozonn cuniculi, Sarcocystis neurona, Besnoitia darlingi, and Neospora caninum in North American opossum, Didelphis virginiana, from Southern Louisian

    Science.gov (United States)

    We examined the prevalence of antibodies to zoonotic protozoan parasites (Trypanosoma cruzi, Toxoplasma gondii, and Encephalitozoon cuniculi) and protozoan’s of veterinary importance (Neospora caninum, Sarcocystis neurona and Besnoitia darlingi) in a population of North American opossums (Didelphis...

  5. Cross-sectional study of serum antibodies against Sarcocystis neurona in cats tested for antibodies against Toxoplasma gondii.

    Science.gov (United States)

    Rossano, Mary G; Murphy, Alice J; Vrable, Ruth A; Vanzo, Nicole E; Lewis, Stacy K; Sheline, Katherine D; Kaneene, John B; Mansfield, Linda S

    2002-08-15

    To determine apparent seroprevalence of antibodies against Sarcocystis neurona in a population of domestic cats previously tested for antibodies against Toxoplasma gondii. Cross-sectional study. Serum from 196 domestic cats. Banked serum samples submitted to the Michigan State University Animal Health Diagnostic Laboratory for T. gondii diagnostic testing were tested for antibodies against S. neurona by use of an indirect fluorescent antibody (IFA) test and a western blot test. Submission records were analyzed to determine descriptive statistics and test for associations between positive results of a test for S. neurona and other variables in the data set. 10 of 196 (5%) samples yielded positive results for antibodies against S. neurona by use of western blot analysis, whereas 27 samples yielded positive results by use of the IFA. No association was found between S. neurona western blot test results and T. gondii test results, age, sex, or the reason for T. gondii testing. The S. neurona IFA titer was positively and significantly associated with positive results of western blot analysis. Domestic cats are not likely to play a substantial role as intermediate hosts in the natural life cycle of S. neurona. Results indicate that natural infection of domestic cats may occur, and small animal practitioners should be aware of this fact when evaluating cats with neurologic disease. The S. neurona IFA test had lower specificity than western blot analysis.

  6. Detection of antibodies against Sarcocystis neurona, Neospora spp., and Toxoplasma gondii in horses from Costa Rica.

    Science.gov (United States)

    Dangoudoubiyam, S; Oliveira, J B; Víquez, C; Gómez-García, A; González, O; Romero, J J; Kwok, O C H; Dubey, J P; Howe, D K

    2011-06-01

    Serum samples from 315 horses from Costa Rica, Central America, were examined for the presence of antibodies against Sarcocystis neurona, Neospora spp., and Toxoplasma gondii by using the surface antigen (SAG) SnSAG2 enzyme-linked immunosorbent assay (ELISA), the NhSAG1 ELISA, and the modified agglutination test, respectively. Anti- S. neurona antibodies were found in 42.2% of the horses by using the SnSAG2 ELISA. Anti- Neospora spp. antibodies were found in only 3.5% of the horses by using the NhSAG1 ELISA, and only 1 of these horses was confirmed seropositive by Western blot. Antibodies to T. gondii were found in 34.0% of the horses tested, which is higher than in previous reports from North and South America. The finding of anti- S. neurona antibodies in horses from geographical areas where Didelphis marsupialis has wide distribution suggests that D. marsupialis is a potential definitive host for this parasite and a source of infection for these horses.

  7. Exposure of free-living jaguars to Toxoplasma gondii, Neospora caninum and Sarcocystis neurona in the Brazilian Pantanal

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    Selma Samiko Miyazaki Onuma

    2014-12-01

    Full Text Available Toxoplasma gondii, Neospora caninum and Sarcocystis neurona are related apicomplexan parasites that cause reproductive and neurological disorders in a wide range of domestic and wild animals. In the present study, the immunofluorescence antibody test (IFAT was used to investigate the presence of antibodies against T. gondii, N. caninum and S. neurona in the sera of 11 free-living jaguars (Panthera onca in two protected areas in the Pantanal region of Mato Grosso state, Brazil. Ten jaguars (90.9% showed seropositivity for T. gondii, eight (72.7% for S. neurona, and seven (63.6% for N. caninum antigens. Our findings reveal exposure of jaguars to these related coccidian parasites and circulation of these pathogens in this wild ecosystem. To the best of our knowledge, this is the first serological detection of N. caninum and S. neurona in free-living jaguars.

  8. Modest genetic differentiation among North American populations of Sarcocystis neurona may reflect expansion in its geographic range.

    Science.gov (United States)

    Sundar, N; Asmundsson, I M; Thomas, N J; Samuel, M D; Dubey, J P; Rosenthal, B M

    2008-03-25

    Sarcocystis neurona is an important cause of neurological disease in horses (equine protozoal myeloencephalitis, EPM) and sea otters in the United States. In addition, EPM-like disease has been diagnosed in several other land and marine mammals. Opossums are its only definitive hosts. Little genetic diversity among isolates of S. neurona from different hosts has been reported. Here, we used 11 microsatellites to characterize S. neurona DNA isolated from natural infections in 22 sea otters (Enhydra lutris) from California and Washington and in 11 raccoons (Procyon lotor) and 1 striped skunk (Mephitis mephitis) from Wisconsin. By jointly analyzing these 34 isolates with 26 isolates previously reported, we determined that geographic barriers may limit S. neurona dispersal and that only a limited subset of possible parasite genotypes may have been introduced to recently established opossum populations. Moreover, our study confirms that diverse intermediate hosts share a common infection source, the opossum (Didelphis virginiana).

  9. Exposure of free-living jaguars to Toxoplasma gondii, Neospora caninum and Sarcocystis neurona in the Brazilian Pantanal.

    Science.gov (United States)

    Onuma, Selma Samiko Miyazaki; Melo, Andréia Lima Tomé; Kantek, Daniel Luis Zanella; Crawshaw-Junior, Peter Gransden; Morato, Ronaldo Gonçalves; May-Júnior, Joares Adenílson; Pacheco, Thábata dos Anjos; Aguiar, Daniel Moura de

    2014-01-01

    Toxoplasma gondii, Neospora caninum and Sarcocystis neurona are related apicomplexan parasites that cause reproductive and neurological disorders in a wide range of domestic and wild animals. In the present study, the immunofluorescence antibody test (IFAT) was used to investigate the presence of antibodies against T. gondii, N. caninum and S. neurona in the sera of 11 free-living jaguars (Panthera onca) in two protected areas in the Pantanal region of Mato Grosso state, Brazil. Ten jaguars (90.9%) showed seropositivity for T. gondii, eight (72.7%) for S. neurona, and seven (63.6%) for N. caninum antigens. Our findings reveal exposure of jaguars to these related coccidian parasites and circulation of these pathogens in this wild ecosystem. To the best of our knowledge, this is the first serological detection of N. caninum and S. neurona in free-living jaguars.

  10. Genetic variation among isolates of Sarcocystis neurona, the agent of protozoal myeloencephalitis, as revealed by amplified fragment length polymorphism markers.

    Science.gov (United States)

    Elsheikha, H M; Schott, H C; Mansfield, L S

    2006-06-01

    Sarcocystis neurona causes serious neurological disease in horses and other vertebrates in the Americas. Based on epidemiological data, this parasite has recently emerged. Here, the genetic diversity of Sarcocystis neurona was evaluated using the amplified fragment length polymorphism (AFLP) method. Fifteen S. neurona taxa from different regions collected over the last 10 years were used; six isolates were from clinically diseased horses, eight isolates were from wild-caught opossums (Didelphis virginiana), and one isolate was from a cowbird (Molothrus ater). Additionally, four outgroup taxa were also fingerprinted. Nine primer pairs were used to generate AFLP patterns, with a total number of amplified fragments ranging from 30 to 60, depending on the isolate and primers tested. Based on the presence/absence of amplified AFLP fragments and pairwise similarity values, all the S. neurona isolates tested were clustered in one monophyletic group. No significant correlation could be found between genomic similarity and host origin of the S. neurona isolates. AFLP revealed significant intraspecific genetic variations, and S. neurona appeared as a highly variable species. Furthermore, linkage disequilibrium analysis suggested that S. neurona populations within Michigan have an intermediate type of population structure that includes characteristics of both clonal and panamictic population structures. AFLP is a reliable molecular technique that has provided one of the most informative approaches to ascertain phylogenetic relationships in S. neurona and its closest relatives, allowing them to be clustered by relative similarity using band matching and unweighted pair group method with arithmetic mean analysis, which may be applicable to other related protozoal species.

  11. Selective inhibition of Sarcocystis neurona calcium-dependent protein kinase 1 for equine protozoal myeloencephalitis therapy.

    Science.gov (United States)

    Ojo, Kayode K; Dangoudoubiyam, Sriveny; Verma, Shiv K; Scheele, Suzanne; DeRocher, Amy E; Yeargan, Michelle; Choi, Ryan; Smith, Tess R; Rivas, Kasey L; Hulverson, Matthew A; Barrett, Lynn K; Fan, Erkang; Maly, Dustin J; Parsons, Marilyn; Dubey, Jitender P; Howe, Daniel K; Van Voorhis, Wesley C

    2016-12-01

    Sarcocystis neurona is the most frequent cause of equine protozoal myeloencephalitis, a debilitating neurological disease of horses that can be difficult to treat. We identified SnCDPK1, the S. neurona homologue of calcium-dependent protein kinase 1 (CDPK1), a validated drug target in Toxoplasma gondii. SnCDPK1 shares the glycine "gatekeeper" residue of the well-characterized T. gondii enzyme, which allows the latter to be targeted by bumped kinase inhibitors. This study presents detailed molecular and phenotypic evidence that SnCDPK1 can be targeted for rational drug development. Recombinant SnCDPK1 was tested against four bumped kinase inhibitors shown to potently inhibit both T. gondii (Tg) CDPK1 and T. gondii tachyzoite growth. SnCDPK1 was inhibited by low nanomolar concentrations of these BKIs and S. neurona growth was inhibited at 40-120nM concentrations. Thermal shift assays confirmed these bumped kinase inhibitors bind CDPK1 in S. neurona cell lysates. Treatment with bumped kinase inhibitors before or after invasion suggests that bumped kinase inhibitors interfere with S. neurona mammalian host cell invasion in the 0.5-2.5μM range but interfere with intracellular division at 2.5μM. In vivo proof-of-concept experiments were performed in a murine model of S. neurona infection. The experimental infected groups treated for 30days with compound BKI-1553 (n=10 mice) had no signs of disease, while the infected control group had severe signs and symptoms of infection. Elevated antibody responses were found in 100% of control infected animals, but only 20% of BKI-1553 treated infected animals. Parasites were found in brain tissues of 100% of the control infected animals, but only in 10% of the BKI-1553 treated animals. The bumped kinase inhibitors used in these assays have been chemically optimized for potency, selectivity and pharmacokinetic properties, and hence are good candidates for treatment of equine protozoal myeloencephalitis. Copyright © 2016

  12. Acute onset of encephalomyelitis with atypical lesions associated with dual infection of Sarcocystis neurona and Toxoplasma gondii in a dog.

    Science.gov (United States)

    Gerhold, Richard; Newman, Shelley J; Grunenwald, Caroline M; Crews, Amanda; Hodshon, Amy; Su, Chunlei

    2014-10-15

    A two-year-old male, neutered, basset hound-beagle mix with progressive neurological impairment was examined postmortem. Grossly, the dog had multiple raised masses on the spinal cord between nerve roots. Microscopically, the dog had protozoal myeloencephalitis. Toxoplasma gondii and Sarcocystis neurona were detected in the CNS by immunohistochemistry and polymerase chain reaction (PCR). Sarcocysts in formalin-fixed muscle were negative for Sarcocystis by PCR. Banked serum was negative for T. gondii using the modified agglutination test, suggesting an acute case of T. gondii infection or immunosuppression; however, no predisposing immunosuppressive diseases, including canine distemper, were found. To the authors' knowledge, this is the first report of dual T. gondii and S. neurona infection in a dog. Published by Elsevier B.V.

  13. Prevalence of antibodies to Neospora caninum, Sarcocystis neurona, and Toxoplasma gondii in wild horses from central Wyoming.

    Science.gov (United States)

    Dubey, J P; Mitchell, S M; Morrow, J K; Rhyan, J C; Stewart, L M; Granstrom, D E; Romand, S; Thulliez, P; Saville, W J; Lindsay, D S

    2003-08-01

    Sarcocystis neurona, Neospora caninum, N. hughesi, and Toxoplasma gondii are 4 related coccidians considered to be associated with encephalomyelitis in horses. The source of infection for N. hughesi is unknown, whereas opossums, dogs, and cats are the definitive hosts for S. neurona, N. caninum, and T. gondii, respectively. Seroprevalence of these coccidians in 276 wild horses from central Wyoming outside the known range of the opossum (Didelphis virginiana) was determined. Antibodies to T. gondii were found only in 1 of 276 horses tested with the modified agglutination test using 1:25, 1:50, and 1:500 dilutions. Antibodies to N. caninum were found in 86 (31.1%) of the 276 horses tested with the Neospora agglutination test--the titers were 1:25 in 38 horses, 1:50 in 15, 1:100 in 9, 1:200 in 8, 1:400 in 4, 1:800 in 2, 1:1,600 in 2, 1:3,200 in 2, and 1:12,800 in 1. Antibodies to S. neurona were assessed with the serum immunoblot; of 276 horses tested, 18 had antibodies considered specific for S. neurona. Antibodies to S. neurona also were assessed with the S. neurona direct agglutination test (SAT). Thirty-nine of 265 horses tested had SAT antibodies--in titers of 1:50 in 26 horses and 1:100 in 13. The presence of S. neurona antibodies in horses in central Wyoming suggests that either there is cross-reactivity between S. neurona and some other infection or a definitive host other than opossum is the source of infection. In a retrospective study, S. neurona antibodies were not found by immunoblot in the sera of 243 horses from western Canada outside the range of D. virginiana.

  14. Comparison of prevalence factors in horses with and without seropositivity to Neospora hughesi and/or Sarcocystis neurona.

    Science.gov (United States)

    Pusterla, Nicola; Tamez-Trevino, Eva; White, Alexandria; Vangeem, Joshua; Packham, Andrea; Conrad, Patricia A; Kass, Philip

    2014-05-01

    Equine protozoal myeloencephalitis is a commonly diagnosed neurological disease of horses in North America and is caused by infection with Sarcocystis neurona or Neospora hughesi. The aim of this study was to compare prevalence factors among horses seropositive or seronegative to N. hughesi and/or S. neurona. A total of 3123 submissions were included in the study, with horses originating from 49 States. Thirty-eight animals from 21 States tested seropositive for N. hughesi only, 840 horses from 40 States were seropositive for S. neurona only, 25 horses from 14 States were seropositive for both protozoa, and 2220 horses from 49 States tested seronegative for both parasites. Significant associations were found between geographical location (State), month of submission, breed and serological status. Copyright © 2014 Elsevier Ltd. All rights reserved.

  15. Sarcocystis neurona schizonts-associated encephalitis, chorioretinitis, and myositis in a two-month-old dog simulating toxoplasmosis, and presence of mature sarcocysts in muscles.

    Science.gov (United States)

    Dubey, J P; Black, S S; Verma, S K; Calero-Bernal, R; Morris, E; Hanson, M A; Cooley, A J

    2014-05-28

    Sarcocystis neurona is an unusual species of the genus Sarcocystis. Opossums (Didelphis virginianus, D. albiventris) are the definitive hosts and several other species, including dogs, cats, marine mammals, and horses are intermediate or aberrant hosts. Sarcocysts are not known to form in aberrant hosts. Sarcocystis neurona causes fatal disease in horses (Equine Protozoal Myeloencephalitis, EPM). There are numerous reports of fatal EPM-like infections in other species, usually with central nervous system signs and associated with the schizont stage of S. neurona. Here, we report fatal disseminated S. neurona infection in a nine-week-old golden retriever dog from Mississippi, USA. Protozoal merozoites were identified in smears of the cerebrospinal fluid. Microscopically, lesions and protozoa were identified in eyes, tongue, heart, liver, intestines, nasal turbinates, skeletal muscle and brain, which reacted intensely with S. neurona polyclonal antibodies. Mature sarcocysts were seen in sections of muscles. These sarcocysts were ultrastructurally similar to those of S. neurona from experimentally infected animals. These data suggest that the dog is another intermediate host for S. neurona. Data suggest that the dog was transplacentally infected. Copyright © 2014 Elsevier B.V. All rights reserved.

  16. Frequency of antibodies against Sarcocystis neurona and Neospora caninum in domestic cats in the state of Bahia, Brazil.

    Science.gov (United States)

    Meneses, Iris Daniela Santos de; Andrade, Müller Ribeiro; Uzêda, Rosângela Soares; Bittencourt, Marta Vasconcelos; Lindsay, David Scott; Gondim, Luís Fernando Pita

    2014-01-01

    Sarcocystis neurona is the major agent of equine protozoal myeloencephalitis. It infects several mammalian species in the Americas, where the definitive hosts, marsupials of the genus Didelphis (D. virginiana and D. albiventris) are found. Domestic cats are one of the confirmed intermediate hosts of the parasite; however, antibodies against S. neurona had never before been demonstrated in Brazilian cats. The aim of this study was to determine whether cats in Bahia, Brazil, are exposed to the parasite. A total of 272 feline serum samples (134 from feral and 138 from house cats) were subjected to an indirect fluorescent antibody test using cultured merozoites of S. neurona as antigen. Positivity was detected in 4.0% (11/272) of the tested samples, with titers ranging from 25 to 800. The feline sera were also tested for antibodies against the protozoan Neospora caninum, with an observed antibody frequency of 2.9%. To the author's knowledge, this is the first study to report antibodies against S. neurona in Brazilian cats. We conclude that cats are exposed to the parasite in the region of this study. Further investigations are needed to confirm the role of cats in the transmission cycle of S. neurona in Brazil.

  17. Frequency of antibodies against Sarcocystis neurona and Neospora caninum in domestic cats in the state of Bahia, Brazil

    Directory of Open Access Journals (Sweden)

    Iris Daniela Santos de Meneses

    2014-12-01

    Full Text Available Sarcocystis neurona is the major agent of equine protozoal myeloencephalitis. It infects several mammalian species in the Americas, where the definitive hosts, marsupials of the genus Didelphis (D. virginiana and D. albiventris are found. Domestic cats are one of the confirmed intermediate hosts of the parasite; however, antibodies against S. neurona had never before been demonstrated in Brazilian cats. The aim of this study was to determine whether cats in Bahia, Brazil, are exposed to the parasite. A total of 272 feline serum samples (134 from feral and 138 from house cats were subjected to an indirect fluorescent antibody test using cultured merozoites of S. neurona as antigen. Positivity was detected in 4.0% (11/272 of the tested samples, with titers ranging from 25 to 800. The feline sera were also tested for antibodies against the protozoan Neospora caninum, with an observed antibody frequency of 2.9%. To the author's knowledge, this is the first study to report antibodies against S. neurona in Brazilian cats. We conclude that cats are exposed to the parasite in the region of this study. Further investigations are needed to confirm the role of cats in the transmission cycle of S. neurona in Brazil.

  18. Analysis of the Sarcocystis neurona microneme protein SnMIC10: protein characteristics and expression during intracellular development.

    Science.gov (United States)

    Hoane, Jessica S; Carruthers, Vernon B; Striepen, Boris; Morrison, David P; Entzeroth, Rolf; Howe, Daniel K

    2003-07-01

    Sarcocystis neurona, an apicomplexan parasite, is the primary causative agent of equine protozoal myeloencephalitis. Like other members of the Apicomplexa, S. neurona zoites possess secretory organelles that contain proteins necessary for host cell invasion and intracellular survival. From a collection of S. neurona expressed sequence tags, we identified a sequence encoding a putative microneme protein based on similarity to Toxoplasma gondii MIC10 (TgMIC10). Pairwise sequence alignments of SnMIC10 to TgMIC10 and NcMIC10 from Neospora caninum revealed approximately 33% identity to both orthologues. The open reading frame of the S. neurona gene encodes a 255 amino acid protein with a predicted 39-residue signal peptide. Like TgMIC10 and NcMIC10, SnMIC10 is predicted to be hydrophilic, highly alpha-helical in structure, and devoid of identifiable adhesive domains. Antibodies raised against recombinant SnMIC10 recognised a protein band with an apparent molecular weight of 24 kDa in Western blots of S. neurona merozoites, consistent with the size predicted for SnMIC10. In vitro secretion assays demonstrated that this protein is secreted by extracellular merozoites in a temperature-dependent manner. Indirect immunofluorescence analysis of SnMIC10 showed a polar labelling pattern, which is consistent with the apical position of the micronemes, and immunoelectron microscopy provided definitive localisation of the protein to these secretory organelles. Further analysis of SnMIC10 in intracellular parasites revealed that expression of this protein is temporally regulated during endopolygeny, supporting the view that micronemes are only needed during host cell invasion. Collectively, the data indicate that SnMIC10 is a microneme protein that is part of the excreted/secreted antigen fraction of S. neurona. Identification and characterisation of additional S. neurona microneme antigens and comparisons to orthologues in other Apicomplexa could provide further insight into the

  19. Limited genetic diversity among Sarcocystis neurona strains infecting southern sea otters precludes distinction between marine and terrestrial isolates.

    Science.gov (United States)

    Wendte, J M; Miller, M A; Nandra, A K; Peat, S M; Crosbie, P R; Conrad, P A; Grigg, M E

    2010-04-19

    Sarcocystis neurona is an apicomplexan parasite identified as a cause of fatal neurological disease in the threatened southern sea otter (Enhydra lutris nereis). In an effort to characterize virulent S. neurona strains circulating in the marine ecosystem, this study developed a range of markers relevant for molecular genotyping. Highly conserved sequences within the 18S ribosomal gene array, the plastid-encoded RNA polymerase (RPOb) and the cytochrome c oxidase subunit 1 mitochondrial gene (CO1) were assessed for their ability to distinguish isolates at the genus and species level. For within-species comparisons, five surface antigens (SnSAG1-SnSAG5) and one high resolution microsatellite marker (Sn9) were developed as genotyping markers to evaluate intra-strain diversity. Molecular analysis at multiple loci revealed insufficient genetic diversity to distinguish terrestrial isolates from strains infecting marine mammals. Furthermore, SnSAG specific primers applied against DNA from the closely related species, Sarcocystis falcatula, lead to the discovery of highly similar orthologs to SnSAG2, 3, and 4, calling into question the specificity of diagnostic tests based on these antigens. The results of this study suggest a population genetic structure for S. neurona similar to that reported for the related parasite, Toxoplasma gondii, dominated by a limited number of successful genotypes. Published by Elsevier B.V.

  20. Evidence that Surface Proteins Sn14 and Sn16 of Sarcocystis neurona Merozoites Are Involved in Infection and Immunity†

    Science.gov (United States)

    Liang, Fang Ting; Granstrom, David E.; Zhao, Xiao Min; Timoney, John F.

    1998-01-01

    Sarcocystis neurona is the etiologic agent of equine protozoal myeloencephalitis (EPM). Based on an analysis of 25,000 equine serum and cerebrospinal fluid (CSF) samples, including samples from horses with neurologic signs typical of EPM or with histologically or parasitologically confirmed EPM, four major immunoblot band patterns have been identified. Twenty-three serum and CSF samples representing each of the four immunoblot patterns were selected from 220 samples from horses with neurologic signs resembling EPM and examined for inhibitory effects on the infectivity of S. neurona by an in vitro neutralization assay. A high correlation between immunoblot band pattern and neutralizing activity was detected. Two proteins, Sn14 and Sn16 (14 and 16 kDa, respectively), appeared to be important for in vitro infection. A combination of the results of surface protein labeling, immunoprecipitation, Western blotting, and trypsin digestion suggests that these molecules are surface proteins and may be useful components of a vaccine against S. neurona infection. Although S. neurona is an obligate intracellular parasite, it is potentially a target for specific antibodies which may lyse merozoites via complement or inhibit their attachment and penetration to host cells. PMID:9573058

  1. Seroprevalence of Toxoplasma gondii, Sarcocystis neurona, and Encephalitozoon cuniculi in three species of lemurs from St. Catherines Island, GA, USA.

    Science.gov (United States)

    Yabsley, Michael J; Jordan, Carly N; Mitchell, Sheila M; Norton, Terry M; Lindsay, David S

    2007-03-15

    In the current study, we determined the seroprevalence of Toxoplasma gondii, Sarcocystis neurona, and Encephalitozoon cuniculi in three species of lemurs from St. Catherines Island, Georgia. Serum samples were tested from 52 ring-tailed lemurs (Lemur catta), six blue-eyed black lemurs (Eulemur macaco flavifrons), and four black and white ruffed lemurs (Varecia variegata variegata) using an agglutination assay. Three ring-tailed lemurs (5.8%) were positive for T. gondii (titer of 1:50); one ring-tailed lemur (1.9%) and one black and white ruffed lemur (25%) were positive for S. neurona (titers of 1:1000); and one ring-tailed lemur (1.9%) was positive for E. cuniculi (titer of 1:400). All blue-eyed black lemurs were negative for antibodies to T. gondii, S. neurona, and E. cuniculi. This is the first detection of antibodies to T. gondii in ring-tailed lemurs and antibodies to S. neurona and E. cuniculi in any species of prosimian.

  2. Phylogenetic relationships of Sarcocystis neurona of horses and opossums to other cyst-forming coccidia deduced from SSU rRNA gene sequences.

    Science.gov (United States)

    Elsheikha, Hany M; Lacher, David W; Mansfield, Linda S

    2005-11-01

    Phylogenetic analyses based on sequences of the nuclear-encoded small subunit rRNA (ssurRNA) gene were performed to examine the origin, phylogeny, and biogeographic relationships of Sarcocystis neurona isolates from opossums and horses from the State of Michigan, USA, in relation to other cyst-forming coccidia. A total of 31 taxa representing all recognized subfamilies and genera of Sarcocystidae were included in the analyses with clonal isolates of two opossum and two horse S. neurona. Phylogenies obtained by the four tree-building methods were consistent with the classical taxonomy based on morphological criteria. The "isosporid" coccidia Neospora, Toxoplasma, Besnoitia, Isospora lacking stieda bodies, and Hyaloklossia formed a sister group to the Sarcocystis spp. Sarcocystis species were divided into three main lineages; S. neurona isolates were located in the second lineage and clustered with S. mucosa, S. dispersa, S. lacertae, S. rodentifelis, S. muris, and Frenkelia spp. Alignment of S. neurona SSU rRNA gene sequences of Michigan opossum isolates (MIOP5, MIOP20) and a S. neurona Michigan horse isolate (MIH8) showed 100% identity. These Michigan isolates differed in 2/1085 bp (0.2%) from a Kentucky S. neurona horse isolate (SN5). Additionally, S. neurona isolates from horses and opossums were identical based on the ultrastructural features and PCR-RFLP analyses thus forming a phylogenetically indistinct group in these regions. These findings revealed the concordance between the morphological and molecular data and confirmed that S. neurona from opossums and horses originated from the same phylogenetic origin.

  3. Seroprevalences of anti-Sarcocystis neurona and anti-Neospora hughesi antibodies among healthy equids in the United States.

    Science.gov (United States)

    James, Kaitlyn E; Smith, Woutrina A; Conrad, Patricia A; Packham, Andrea E; Guerrero, Leopoldo; Ng, Mitchell; Pusterla, Nicola

    2017-06-01

    OBJECTIVE To describe the general seroprevalence of anti-Sarcocystis neurona and anti-Neospora hughesi antibodies among healthy equids by use of indirect fluorescent antibody tests and determine potential risk factors for seropositivity. DESIGN Cross-sectional study. SAMPLE Whole blood samples collected from 5,250 equids (1 sample/animal) across 18 states in the United States during October 2013. PROCEDURES Information regarding potential risk factors (geographic region, breed, primary use, sex, and age) was collected along with the blood samples. For each equid, an indirect fluorescent antibody test was used to determine serum titers of antibody against each of the 2 protozoal parasites. Mixed-effects logistic regression models were created to determine ORs for seropositivity. RESULTS The overall seroprevalence of anti-S neurona and anti-N hughesi antibodies in the tested equids was 78% and 34%, respectively. Of the equids, 31% were seropositive and 18% were seronegative for antibodies against both parasites. Factors associated with equids being seropositive for anti-S neurona antibodies were residence in the South, warmblood breed, and age > 5 years. Seroprevalence of anti-N hughesi antibodies did not differ among equids in different states across the country, but warmblood breed and age > 5 years were associated with seropositivity. CONCLUSIONS AND CLINICAL RELEVANCE With regard to risk factors for S neurona and N hughesi exposure and antibody response among tested equids, older age was not unexpected; however, the influences of warmblood breed and geographic location on seropositivity for anti-S neurona antibody but not for anti-N hughesi antibody deserve further investigation.

  4. Phylogenetic congruence of Sarcocystis neurona Dubey et al., 1991 (Apicomplexa: Sarcocystidae) in the United States based on sequence analysis and restriction fragment length polymorphism (RFLP).

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    Elsheikha, Hany M; Murphy, Alice J; Mansfield, Linda S

    2005-07-01

    The objectives of the present study were to assess the genetic diversity, phylogeny and phylogeographical relationships of available Sarcocystis neurona isolates from different localities in the United States. All 13 Sarcocystis isolates from different hosts were subjected to polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) analyses using two published DNA markers (25/396 and 33/54). The 334 bp sequence of the 25/396 marker of these isolates and Besnoitia darlingi, B. bennetti, Toxoplasma gondii and Neospora caninum were sequenced and compared. Phylogenetic analysis was performed using neighbour-joining (NJ), maximum parsimony (MP) and minimum evolution (ME) methods based on the sequences of the 25/396 marker of the 13 Sarcocystis isolates obtained in this study and sequences of 10 related isolates from GenBank. Phylogenetic trees revealed a close relatedness among S. neurona isolates in the US (nucleotide sequence diversity neurona into two separate groups: a northern US group and a Southern US group. These findings suggest a correlation between grouping of the isolates and geographical segregation and were consistent with a genetic bottleneck hypothesis during opossum colonisation of North America. These data do not support either the view of S. neurona as a single super-species or its division into multiple subspecies.

  5. Anti-Sarcocystis neurona immunostaining associated with equine protozoal myeloencephalitis in Brazil Imunomarcação de Sarcocystis neurona associada com um caso de mieloencefalite protozoária eqüina no Brasil

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    Tatiane Alves da Paixão

    2007-12-01

    Full Text Available A retrospective study (1942 to 2005 of histopathological lesions included samples of central nervous system (SNC from 203 animals in the Equidae family. A total of 42.4% of these samples had significant pathological changes, which were classified as inflammatory (62.8%, degenerative (25.6%, circulatory (10.5%, and neoplasic (1.1% lesions. Immunohistochemistry anti-Sarcocystis neurona antigens was performed in all the cases with inflammatory changes (54, of which one of the case of encephalitis resulted positive to immunostaining. Although evidence of EPM (Equine Protozoal Myeloencephalitis has been previously reported in Brazil, to the best of our knowledge, this is the first report in which characteristic EPM lesion was associated with anti-S. neurona immunostaining in Brazil.Em um estudo retrospectivo (de 1942 a 2005, amostras do sistema nervoso central de 203 eqüídeos foram avaliadas para a presença de alterações histológicas. Dessas amostras, 42,4% apresentaram alguma lesão histopatológica significativa, das quais foram classificadas como alterações inflamatórias (62,8%, degenerativas (25,6%, circulatórias (10,5% e neoplásicas (1,1%. Fragmentos de SNC dos 54 animais com alterações inflamatórias foram avaliados para detecção de antígenos de Sarocystis neurona pela técnica de imunoistoquímica, que foi positiva em um caso de encefalite em eqüino. Embora haja registros de MPE no Brasil, este é o primeiro caso confirmado imunoistoquimicamente.

  6. Diagnosis and treatment of Sarcocystis neurona-induced myositis in a free-ranging California sea lion.

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    Carlson-Bremer, Daphne P; Gulland, Frances M D; Johnson, Christine K; Colegrove, Kathleen M; Van Bonn, William G

    2012-02-01

    An underweight, lethargic adult female California sea lion (Zalophus californianus) became stranded along the California shore and was captured and transported to a rehabilitation hospital for assessment and care. Initial physical assessment revealed the sea lion was lethargic and in poor body condition. Active myositis was diagnosed on the basis of concurrent elevations in activities of alanine aminotransferase and creatine kinase detected during serum biochemical analysis. Infection with Sarcocystis neurona was diagnosed after serologic titers increased 4-fold over a 3-week period. Diagnosis was confirmed on the basis of histopathologic findings, positive results on immunohistochemical staining, and results of quantitative PCR assay on biopsy specimens obtained from the diaphragm and muscles of the dorsal cervical region. Anticoccidial treatment was instituted with ponazuril (10 mg/kg [4.5 mg/lb], PO, q 24 h) and continued for 28 days. Prednisone (0.2 mg/kg [0.09 mg/lb], PO, q 12 h) was administered for 2 days and then every 24 hours for 5 days to treat associated inflammation. At the end of treatment, the sea lion was clinically normal, alanine aminotransferase and creatine kinase values were within reference limits, and antibody titers against S neurona had decreased 6-fold. The sea lion was released approximately 3 months after becoming stranded. S neurona-induced myositis was diagnosed in a free-ranging California sea lion. On the basis of the successful treatment and release of this sea lion, anticoccidial treatment should be considered for marine mammals in which protozoal disease is diagnosed.

  7. Purine salvage in the apicomplexan Sarcocystis neurona, and generation of hypoxanthine-xanthine-guanine phosphoribosyltransferase-deficient clones for positive-negative selection of transgenic parasites.

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    Dangoudoubiyam, Sriveny; Zhang, Zijing; Howe, Daniel K

    2014-09-01

    Sarcocystis neurona is an apicomplexan parasite that causes severe neurological disease in horses and marine mammals. The Apicomplexa are all obligate intracellular parasites that lack purine biosynthesis pathways and rely on the host cell for their purine requirements. Hypoxanthine-xanthine-guanine phosphoribosyltransferase (HXGPRT) and adenosine kinase (AK) are key enzymes that function in two complementary purine salvage pathways in apicomplexans. Bioinformatic searches of the S. neurona genome revealed genes encoding HXGPRT, AK and all of the major purine salvage enzymes except purine nucleoside phosphorylase. Wild-type S. neurona were able to grow in the presence of mycophenolic acid (MPA) but were inhibited by 6-thioxanthine (6-TX), suggesting that the pathways involving either HXGPRT or AK are functional in this parasite. Prior work with Toxoplasma gondii demonstrated the utility of HXGPRT as a positive-negative selection marker. To enable the use of HXGPRT in S. neurona, the SnHXGPRT gene sequence was determined and a gene-targeting plasmid was transfected into S. neurona. SnHXGPRT-deficient mutants were selected with 6-TX, and single-cell clones were obtained. These Sn∆HXG parasites were susceptible to MPA and could be complemented using the heterologous T. gondii HXGPRT gene. In summary, S. neurona possesses both purine salvage pathways described in apicomplexans, thus allowing the use of HXGPRT as a positive-negative drug selection marker in this parasite.

  8. A novel Sarcocystis neurona genotype XIII is associated with severe encephalitis in an unexpectedly broad range of marine mammals from the northeastern Pacific Ocean.

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    Barbosa, Lorraine; Johnson, Christine K; Lambourn, Dyanna M; Gibson, Amanda K; Haman, Katherine H; Huggins, Jessica L; Sweeny, Amy R; Sundar, Natarajan; Raverty, Stephen A; Grigg, Michael E

    2015-08-01

    Sarcocystis neurona is an important cause of protozoal encephalitis among marine mammals in the northeastern Pacific Ocean. To characterise the genetic type of S. neurona in this region, samples from 227 stranded marine mammals, most with clinical or pathological evidence of protozoal disease, were tested for the presence of coccidian parasites using a nested PCR assay. The frequency of S. neurona infection was 60% (136/227) among pinnipeds and cetaceans, including seven marine mammal species not previously known to be susceptible to infection by this parasite. Eight S. neurona fetal infections identified this coccidian parasite as capable of being transmitted transplacentally. Thirty-seven S. neurona-positive samples were multilocus sequence genotyped using three genetic markers: SnSAG1-5-6, SnSAG3 and SnSAG4. A novel genotype, referred to as Type XIII within the S. neurona population genetic structure, has emerged recently in the northeastern Pacific Ocean and is significantly associated with an increased severity of protozoal encephalitis and mortality among multiple stranded marine mammal species. Published by Elsevier Ltd.

  9. SnSAG5 is an alternative surface antigen of Sarcocystis neurona strains that is mutually exclusive to SnSAG1.

    Science.gov (United States)

    Crowdus, Carolyn A; Marsh, Antoinette E; Saville, Willliam J; Lindsay, David S; Dubey, J P; Granstrom, David E; Howe, Daniel K

    2008-11-25

    Sarcocystis neurona is an obligate intracellular parasite that causes equine protozoal myeloencephalitis (EPM). Previous work has identified a gene family of paralogous surface antigens in S. neurona called SnSAGs. These surface proteins are immunogenic in their host animals, and are therefore candidate molecules for development of diagnostics and vaccines. However, SnSAG diversity exists in strains of S. neurona, including the absence of the major surface antigen gene SnSAG1. Instead, sequence for an alternative SnSAG has been revealed in two of the SnSAG1-deficient strains. Herein, we present data characterizing this new surface protein, which we have designated SnSAG5. The results indicated that the protein encoded by the SnSAG5 sequence is indeed a surface-associated molecule that has characteristics consistent with the other SAGs identified in S. neurona and related parasites. Importantly, Western blot analyses of a collection of S. neurona strains demonstrated that 6 of 13 parasite isolates express SnSAG5 as a dominant surface protein instead of SnSAG1. Conversely, SnSAG5 was not detected in SnSAG1-positive strains. One strain, which was isolated from the brain of a sea otter, did not express either SnSAG1 or SnSAG5. Genetic analysis with SnSAG5-specific primers confirmed the presence of the SnSAG5 gene in Western blot-positive strains, while also suggesting the presence of a novel SnSAG sequence in the SnSAG1-deficient, SnSAG5-deficient otter isolate. The findings provide further indication of S. neurona strain diversity, which has implications for diagnostic testing and development of vaccines against EPM as well as the population biology of Sarcocystis cycling in the opossum definitive host.

  10. Sarcocystis neurona merozoites express a family of immunogenic surface antigens that are orthologues of the Toxoplasma gondii surface antigens (SAGs) and SAG-related sequences.

    Science.gov (United States)

    Howe, Daniel K; Gaji, Rajshekhar Y; Mroz-Barrett, Meaghan; Gubbels, Marc-Jan; Striepen, Boris; Stamper, Shelby

    2005-02-01

    Sarcocystis neurona is a member of the Apicomplexa that causes myelitis and encephalitis in horses but normally cycles between the opossum and small mammals. Analysis of an S. neurona expressed sequence tag (EST) database revealed four paralogous proteins that exhibit clear homology to the family of surface antigens (SAGs) and SAG-related sequences of Toxoplasma gondii. The primary peptide sequences of the S. neurona proteins are consistent with the two-domain structure that has been described for the T. gondii SAGs, and each was predicted to have an amino-terminal signal peptide and a carboxyl-terminal glycolipid anchor addition site, suggesting surface localization. All four proteins were confirmed to be membrane associated and displayed on the surface of S. neurona merozoites. Due to their surface localization and homology to T. gondii surface antigens, these S. neurona proteins were designated SnSAG1, SnSAG2, SnSAG3, and SnSAG4. Consistent with their homology, the SnSAGs elicited a robust immune response in infected and immunized animals, and their conserved structure further suggests that the SnSAGs similarly serve as adhesins for attachment to host cells. Whether the S. neurona SAG family is as extensive as the T. gondii SAG family remains unresolved, but it is probable that additional SnSAGs will be revealed as more S. neurona ESTs are generated. The existence of an SnSAG family in S. neurona indicates that expression of multiple related surface antigens is not unique to the ubiquitous organism T. gondii. Instead, the SAG gene family is a common trait that presumably has an essential, conserved function(s).

  11. Sarcocystis neurona Merozoites Express a Family of Immunogenic Surface Antigens That Are Orthologues of the Toxoplasma gondii Surface Antigens (SAGs) and SAG-Related Sequences†

    Science.gov (United States)

    Howe, Daniel K.; Gaji, Rajshekhar Y.; Mroz-Barrett, Meaghan; Gubbels, Marc-Jan; Striepen, Boris; Stamper, Shelby

    2005-01-01

    Sarcocystis neurona is a member of the Apicomplexa that causes myelitis and encephalitis in horses but normally cycles between the opossum and small mammals. Analysis of an S. neurona expressed sequence tag (EST) database revealed four paralogous proteins that exhibit clear homology to the family of surface antigens (SAGs) and SAG-related sequences of Toxoplasma gondii. The primary peptide sequences of the S. neurona proteins are consistent with the two-domain structure that has been described for the T. gondii SAGs, and each was predicted to have an amino-terminal signal peptide and a carboxyl-terminal glycolipid anchor addition site, suggesting surface localization. All four proteins were confirmed to be membrane associated and displayed on the surface of S. neurona merozoites. Due to their surface localization and homology to T. gondii surface antigens, these S. neurona proteins were designated SnSAG1, SnSAG2, SnSAG3, and SnSAG4. Consistent with their homology, the SnSAGs elicited a robust immune response in infected and immunized animals, and their conserved structure further suggests that the SnSAGs similarly serve as adhesins for attachment to host cells. Whether the S. neurona SAG family is as extensive as the T. gondii SAG family remains unresolved, but it is probable that additional SnSAGs will be revealed as more S. neurona ESTs are generated. The existence of an SnSAG family in S. neurona indicates that expression of multiple related surface antigens is not unique to the ubiquitous organism T. gondii. Instead, the SAG gene family is a common trait that presumably has an essential, conserved function(s). PMID:15664946

  12. Improved detection of equine antibodies against Sarcocystis neurona using polyvalent ELISAs based on the parasite SnSAG surface antigens.

    Science.gov (United States)

    Yeargan, Michelle R; Howe, Daniel K

    2011-02-28

    Equine protozoal myeloencephalitis (EPM) is a common neurologic disease of horses that is caused by the apicomplexan pathogen Sarcocystis neurona. To help improve serologic diagnosis of S. neurona infection, we have modified existing enzyme-linked immunosorbent assays (ELISAs) based on the immunogenic parasite surface antigens SnSAG2, SnSAG3, and SnSAG4 to make the assays polyvalent, thereby circumventing difficulties associated with parasite antigenic variants and diversity in equine immune responses. Two approaches were utilized to achieve polyvalence: (1) mixtures of the individual recombinant SnSAGs (rSnSAGs) were included in single ELISAs; (2) a collection of unique SnSAG chimeras that fused protein domains from different SnSAG surface antigens into a single recombinant protein were generated for use in the ELISAs. These new assays were assessed using a defined sample set of equine sera and cerebrospinal fluids (CSFs) that had been characterized by Western blot and/or were from confirmed EPM horses. While all of the polyvalent ELISAs performed relatively well, the highest sensitivity and specificity (100%/100%) were achieved with assays containing the rSnSAG4/2 chimera (Domain 1 of SnSAG4 fused to SnSAG2) or using a mixture of rSnSAG3 and rSnSAG4. The rSnSAG4 antigen alone and the rSnSAG4/3 chimera (Domain 1 of SnSAG4 fused to Domain 2 of SnSAG3) exhibited the next best accuracy at 95.2% sensitivity and 100% specificity. Binding ratios and percent positivity (PP) ratios, determined by comparing the mean values for positive versus negative samples, showed that the most advantageous signal to noise ratios were provided by rSnSAG4 and the rSnSAG4/3 chimera. Collectively, our results imply that a polyvalent ELISA based on SnSAG4 and SnSAG3, whether as a cocktail of two proteins or as a single chimeric protein, can give optimal results in serologic testing of serum or CSF for the presence of antibodies against S. neurona. The use of polyvalent SnSAG ELISAs will

  13. Seroepidemiology of Sarcocystis neurona, Toxoplasma gondii and Neospora spp. among horses in the south of the state of Minas Gerais, Brazil

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    Manoel Junqueira Maciel Ribeiro

    2016-01-01

    Full Text Available Abstract The present study used the indirect fluorescent antibody test (IFAT to determine the seroprevalence of Sarcocystis neurona, Toxoplasma gondii and Neospora spp., and evaluated the variables associated with these infections among 506 apparently healthy horses, reared in the south of the state of Minas Gerais, Brazil. This study was conducted between April 2012 and October 2013. Among the horses, the true prevalence of S. neurona was 26% (95% CI: 22.0-30.4%, T. gondii 19.9% (95% CI: 15.5-24.8% and Neospora spp. 23.9% (95% CI: 19.9-28.1%; and among the farms, 88.3% (95% CI: 74.4-91.6%, 71.6% (95% CI: 41-92.8% and 85% (95% CI: 70.7-96.1%, respectively. Regarding mixed infection, 17 horses (3.4% were seropositive for both S. neurona and T. gondii, 16 (3.2% for T. gondii and Neospora spp. and 14 (2.8% for S. neurona and Neospora spp. The associations between seropositivity and variables relating to the structure of the farm, management and health were analyzed using the logistic regression analysis, through the generalized estimating equations (GEE. The results suggest that the south of Minas Gerais is an enzootic area for S. neurona, T. gondii and Neospora spp. among horses, with prevalence of asymptomatic subclinical or chronic infections.

  14. Effects of blood contamination of cerebrospinal fluid on results of indirect fluorescent antibody tests for detection of antibodies against Sarcocystis neurona and Neospora hughesi.

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    Finno, Carrie J; Packham, Andrea E; David Wilson, W; Gardner, Ian A; Conrad, Patricia A; Pusterla, Nicola

    2007-05-01

    The purpose of this study was to determine the effect of blood contamination of cerebrospinal fluid (CSF) on the results of indirect fluorescent antibody tests (IFATs) for Sarcocystis neurona and Neospora hughesi. The in vitro study used antibody-negative CSF collected from non-neurologic horses immediately after euthanasia and blood samples from 40 healthy horses that had a range of IFAT antibody titers against S. neurona and N. hughesi. Serial dilutions of whole blood were made in seronegative CSF to generate blood-contaminated CSF with red blood cell (RBC) concentrations ranging from 10 to 100,000 RBCs/microl. The blood-contaminated CSF samples were then tested for antibodies against both pathogens using IFAT. Blood contamination of CSF had no detectable effect on IFAT results for S. neurona or N. hughesi at any serologic titer when the RBC concentration in CSF was or=5) for S. neurona and N. hughesi were detected only when the corresponding serum titers were >or=160 and >or=80, respectively. The IFAT performed on CSF is reliable for testing horses for equine protozoal myeloencephalitis caused by S. neurona or N. hughesi, even when blood contamination causes the RBC concentration in CSF to be up to 10,000 RBCs/microl.

  15. Seroepidemiology of Sarcocystis neurona, Toxoplasma gondii and Neospora spp. among horses in the south of the state of Minas Gerais, Brazil.

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    Ribeiro, Manoel Junqueira Maciel; Rosa, Marina Helena Figueredo; Bruhn, Fábio Raphael Pascoti; Garcia, Adriana de Mello; Rocha, Christiane Maria Barcellos Magalhães da; Guimarães, Antônio Marcos

    2016-06-07

    The present study used the indirect fluorescent antibody test (IFAT) to determine the seroprevalence of Sarcocystis neurona, Toxoplasma gondii and Neospora spp., and evaluated the variables associated with these infections among 506 apparently healthy horses, reared in the south of the state of Minas Gerais, Brazil. This study was conducted between April 2012 and October 2013. Among the horses, the true prevalence of S. neurona was 26% (95% CI: 22.0-30.4%), T. gondii 19.9% (95% CI: 15.5-24.8%) and Neospora spp. 23.9% (95% CI: 19.9-28.1%); and among the farms, 88.3% (95% CI: 74.4-91.6%), 71.6% (95% CI: 41-92.8%) and 85% (95% CI: 70.7-96.1%), respectively. Regarding mixed infection, 17 horses (3.4%) were seropositive for both S. neurona and T. gondii, 16 (3.2%) for T. gondii and Neospora spp. and 14 (2.8%) for S. neurona and Neospora spp. The associations between seropositivity and variables relating to the structure of the farm, management and health were analyzed using the logistic regression analysis, through the generalized estimating equations (GEE). The results suggest that the south of Minas Gerais is an enzootic area for S. neurona, T. gondii and Neospora spp. among horses, with prevalence of asymptomatic subclinical or chronic infections.

  16. Ultrastructural and molecular confirmation of the development of Sarcocystis neurona tissue cysts in the central nervous system of southern sea otters (Enhydra lutris nereis).

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    Miller, M A; Barr, B C; Nordhausen, R; James, E R; Magargal, S L; Murray, M; Conrad, P A; Toy-Choutka, S; Jessup, D A; Grigg, M E

    2009-10-01

    In 2004, three wild sea otters were diagnosed with putative Sarcocystis neurona-associated meningoencephalitis by histopathology and immunohistochemistry. Schizonts, free merozoites and tissue cysts were observed in the brains of all three infected animals. Tissue cysts walls from sea otter 1 (SO1) stained positively using anti-S. neurona polyclonal antiserum. However, positive staining does not preclude infection by closely related or cross-reactive tissue cyst-forming coccidian parasites. Two immature tissue cysts in the brain of SO1 were examined using transmission electron microscopy. Ultrastructural features included cyst walls with thin villous projections up to 1 microm long with tapered ends and a distinctive, electron-dense outer lining layer composed of linearly-arranged, semi-circular structures with a "hobnailed" surface contour. Small numbers of microtubules extended down through the villi into the underlying granular layer. Metrocytes were short and plump with an anterior apical complex, 22 sub-pellicular microtubules, numerous free ribosomes and no rhoptries. Some metrocytes appeared to be dividing, with two adjacent nuclear profiles. Collectively these ultrastructural features were compatible with developing protozoal cysts and were similar to prior descriptions of S. neurona tissue cysts. Panspecific 18S rDNA primers were utilized to identify protozoa infecting the brains of these otters and DNA amplification and additional sequencing at the ITS1 locus confirmed that all three otters were infected with S. neurona. No other Sarcocystis spp. were detected in the brains or skeletal muscles of these animals by immunohistochemistry or PCR. We believe this is the first ultrastructural and molecular confirmation of the development of S. neurona tissue cysts in the CNS of any animal.

  17. Prevalence of agglutinating antibodies to Toxoplasma gondii and Sarcocystis neurona in beavers (Castor canadensis) from Massachusetts

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    Jordan, C.N.; Kaur, T.; Koenen, K.; DeStefano, S.; Zajac, A.M.; Lindsay, D.S.

    2005-01-01

    The present study examined the seroprevalence of Toxoplasma gondii and Sarcocystls neurona in a population of beavers (Castor canadensis) from Massachusetts. Sixty-two blood samples were collected during the field seasons over 3 consecutive years from different animals. Blood was collected onto filter paper and shipped to the Department of Biomedical Sciences, Virginia Tech, Blacksburg, Virginia, for parasite testing. The samples were tested at dilutions of 1:25, 1:50, and 1:100 against each parasite antigen by modified agglutination tests to determine whether antibodies to either parasite were present in the blood. Six of 62 samples (10%) were positive for T. gondii, with 2 samples having titers of 1:25 and 4 having titers of 1:50. Four of 62 samples (6%) were positive for S. neurona, with 2 samples having titers of 1:25 and 2 having titers of 1:50. ?? American Society of Pathologists 2005.

  18. Evidence that antibodies against recombinant SnSAG1 of Sarcocystis neurona merozoites are involved in infection and immunity in equine protozoal myeloencephalitis.

    Science.gov (United States)

    Ellison, Siobhan; Witonsky, Sharon

    2009-07-01

    Sarcocystis neurona is the principal etiologic agent of equine protozoal myeloencephalitis (EPM). An immunodominant protein of S. neurona, SnSAG-1, is expressed by the majority of S. neurona merozoites isolated from spinal tissues of horses diagnosed with EPM and may be a candidate for diagnostic tests and prophylaxis for EPM. Five horses were vaccinated with adjuvanted recombinant SnSAG1 (rSnSAG1) and 5 control (sham vaccinated) horses were vaccinated with adjuvant only. Serum was evaluated pre- and post-vaccination, prior to challenge, for antibodies against rSnSAG1 and inhibitory effects on the infectivity of S. neurona by an in vitro serum neutralization assay. The effect of vaccination with rSnSAG1 on in vivo infection by S. neurona was evaluated by challenging all the horses with S. neurona merozoites. Blinded daily examinations and 4 blinded neurological examinations were used to evaluate the presence of clinical signs of EPM. The 5 vaccinated horses developed serum and cerebrospinal fluid (CSF) titers of SnSAG1, detected by enzyme-linked immunosorbent assay (ELISA), post-vaccination. Post-vaccination serum from vaccinated horses was found to have an inhibitory effect on merozoites, demonstrated by in vitro bioassay. Following the challenge, the 5 control horses displayed clinical signs of EPM, including ataxia. While 4 of the 5 vaccinated horses did not become ataxic. One rSnSAG-1 vaccinated horse showed paresis in 1 limb with muscle atrophy. All horses showed mild, transient, cranial nerve deficits; however, disease did not progress to ataxia in rSnSAG-1 vaccinated horses. The study showed that vaccination with rSnSAG-1 produced antibodies in horses that neutralized merozoites when tested by in vitro culture and significantly reduced clinical signs demonstrated by in vivo challenge.

  19. Prevalence of antibodies to Trypanosoma cruzi, Leishmania infantum, Encephalitozoon cuniculi, Sarcocystis neurona, and Neospora caninum in Capybara, Hydrochoerus hydrochaeris, from São Paulo State, Brazil.

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    Valadas, Samantha; Gennari, Solange Maria; Yai, Lucia Eiko Oishi; Rosypal, Alexa C; Lindsay, David S

    2010-06-01

    Little is known about the importance of capybara, Hydrochoerus hydrochaeris, as reservoirs for parasites of zoonotic or veterinary importance. Sera from 63 capybaras, from 6 counties in the state of São Paulo, Brazil, were examined for antibodies to Trypanosoma cruzi, Leishmania infantum, Encephalitozoon cuniculi, Sarcocystis neurona, and Neospora caninum using an indirect immunofluorescent antibody test. Five (8%) of the 63 capybaras had antibodies to T. cruzi epimastigotes. None of the samples from capybara reacted positively with L. infantum promastigotes or with spores of E. cuniculi . Two (3%) of the serum samples were positive for antibodies to S. neurona merozoites, and 2 (3%) of the serum samples were positive for antibodies to N. caninum tachyzoites. A serum sample from 1 capybara was positive for antibodies to both T. cruzi and N. caninum. None of the remaining 62 samples reacted with more than 1 parasite.

  20. Dual congenital transmission of Toxoplasma gondii and Sarcocystis neurona in a late-term aborted pup from a chronically infected southern sea otter (Enhydra lutris nereis).

    Science.gov (United States)

    Shapiro, Karen; Miller, Melissa A; Packham, Andrea E; Aguilar, Beatriz; Conrad, Patricia A; Vanwormer, Elizabeth; Murray, Michael J

    2016-03-01

    Toxoplasma gondii and Sarcocystis neurona are protozoan parasites with terrestrial definitive hosts, and both pathogens can cause fatal disease in a wide range of marine animals. Close monitoring of threatened southern sea otters (Enhydra lutris nereis) in California allowed for the diagnosis of dual transplacental transmission of T. gondii and S. neurona in a wild female otter that was chronically infected with both parasites. Congenital infection resulted in late-term abortion due to disseminated toxoplasmosis. Toxoplasma gondii and S. neurona DNA was amplified from placental tissue culture, as well as from fetal lung tissue. Molecular characterization of T. gondii revealed a Type X genotype in isolates derived from placenta and fetal brain, as well as in all tested fetal organs (brain, lung, spleen, liver and thymus). This report provides the first evidence for transplacental transmission of T. gondii in a chronically infected wild sea otter, and the first molecular and immunohistochemical confirmation of concurrent transplacental transmission of T. gondii and S. neurona in any species. Repeated fetal and/or neonatal losses in the sea otter dam also suggested that T. gondii has the potential to reduce fecundity in chronically infected marine mammals through parasite recrudescence and repeated fetal infection.

  1. MANAGEMENT OF ACUTE RENAL FAILURE WITH DELAYED HYPERCALCEMIA SECONDARY TO SARCOCYSTIS NEURONA-INDUCED MYOSITIS AND RHABDOMYOLYSIS IN A CALIFORNIA SEA LION (ZALOPHUS CALIFORNIANUS).

    Science.gov (United States)

    Alexander, Amy B; Hanley, Christopher S; Duncan, Mary C; Ulmer, Kyle; Padilla, Luis R

    2015-09-01

    A 3-yr-old captive-born California sea lion (Zalophus californianus) developed Sarcocystis neurona-induced myositis and rhabdomyolysis that led to acute renal failure. The sea lion was successfully managed with fluid therapy, antiprotozoals, antibiotics, anti-inflammatories, antiemetics, gastroprotectants, and diuretics, but developed severe delayed hypercalcemia, a syndrome identified in humans after traumatic or exertion-induced rhabdomyolysis. Treatment with calcitonin was added to the management, and the individual recovered fully. The case emphasizes that animals with rhabdomyolysis-induced renal failure risk developing delayed hypercalcemia, which may be life threatening, and calcium levels should be closely monitored past the resolution of renal failure.

  2. A protozoal-associated epizootic impacting marine wildlife: mass-mortality of southern sea otters (Enhydra lutris nereis) due to Sarcocystis neurona infection.

    Science.gov (United States)

    Miller, Melissa A; Conrad, Patricia A; Harris, Michael; Hatfield, Brian; Langlois, Gregg; Jessup, David A; Magargal, Spencer L; Packham, Andrea E; Toy-Choutka, Sharon; Melli, Ann C; Murray, Michael A; Gulland, Frances M; Grigg, Michael E

    2010-09-20

    During April 2004, 40 sick and dead southern sea otters (Enhydra lutris nereis) were recovered over 18km of coastline near Morro Bay, California. This event represented the single largest monthly spike in mortality ever recorded during 30 years of southern sea otter stranding data collection. Because of the point-source nature of the event and clinical signs consistent with severe, acute neurological disease, exposure to a chemical or marine toxin was initially considered. However, detailed postmortem examinations revealed lesions consistent with an infectious etiology, and further investigation confirmed the protozoan parasite Sarcocystis neurona as the underlying cause. Tissues from 94% of examined otters were PCR-positive for S. neurona, based on DNA amplification and sequencing at the ITS-1 locus, and 100% of tested animals (n=14) had elevated IgM and IgG titers to S. neurona. Evidence to support the point-source character of this event include the striking spatial and temporal clustering of cases and detection of high concentrations of anti-S. neurona IgM in serum of stranded animals. Concurrent exposure to the marine biotoxin domoic acid may have enhanced susceptibility of affected otters to S. neurona and exacerbated the neurological signs exhibited by stranded animals. Other factors that may have contributed to the severity of this epizootic include a large rainstorm that preceded the event and an abundance of razor clams near local beaches, attracting numerous otters close to shore within the affected area. This is the first report of a localized epizootic in marine wildlife caused by apicomplexan protozoa.

  3. A protozoal-associated epizootic impacting marine wildlife: Mass-mortality of southern sea otters (Enhydra lutris nereis) due to Sarcocystis neurona infection

    Science.gov (United States)

    Miller, M.A.; Conrad, P.A.; Harris, M.; Hatfield, B.; Langlois, G.; Jessup, David A.; Magargal, S.L.; Packham, A.E.; Toy-Choutka, S.; Melli, A.C.; Murray, M.A.; Gulland, F.M.; Grigg, M.E.

    2010-01-01

    During April 2004, 40 sick and dead southern sea otters (Enhydra lutris nereis) were recovered over 18 km of coastline near Morro Bay, California. This event represented the single largest monthly spike in mortality ever recorded during 30 years of southern sea otter stranding data collection. Because of the point-source nature of the event and clinical signs consistent with severe, acute neurological disease, exposure to a chemical or marine toxin was initially considered. However, detailed postmortem examinations revealed lesions consistent with an infectious etiology, and further investigation confirmed the protozoan parasite Sarcocystis neurona as the underlying cause. Tissues from 94% of examined otters were PCR-positive for S. neurona, based on DNA amplification and sequencing at the ITS-1 locus, and 100% of tested animals (n= 14) had elevated IgM and IgG titers to S. neurona. Evidence to support the point-source character of this event include the striking spatial and temporal clustering of cases and detection of high concentrations of anti- S. neurona IgM in serum of stranded animals. Concurrent exposure to the marine biotoxin domoic acid may have enhanced susceptibility of affected otters to S. neurona and exacerbated the neurological signs exhibited by stranded animals. Other factors that may have contributed to the severity of this epizootic include a large rainstorm that preceded the event and an abundance of razor clams near local beaches, attracting numerous otters close to shore within the affected area. This is the first report of a localized epizootic in marine wildlife caused by apicomplexan protozoa. ?? 2010 Elsevier B.V.

  4. Strains of Sarcocystis neurona exhibit differences in their surface antigens, including the absence of the major surface antigen SnSAG1.

    Science.gov (United States)

    Howe, Daniel K; Gaji, Rajshekhar Y; Marsh, Antoinette E; Patil, Bhagyashree A; Saville, William J; Lindsay, David S; Dubey, J P; Granstrom, David E

    2008-05-01

    A gene family of surface antigens is expressed by merozoites of Sarcocystis neurona, the primary cause of equine protozoal myeloencephalitis (EPM). These surface proteins, designated SnSAGs, are immunodominant and therefore excellent candidates for development of EPM diagnostics or vaccines. Prior work had identified an EPM isolate lacking the major surface antigen SnSAG1, thus suggesting there may be some diversity in the SnSAGs expressed by different S. neurona isolates. Therefore, a bioinformatic, molecular and immunological study was conducted to assess conservation of the SnSAGs. Examination of an expressed sequence tag (EST) database revealed several notable SnSAG polymorphisms. In particular, the EST information implied that the EPM strain SN4 lacked the major surface antigen SnSAG1. The absence of this surface antigen from the SN4 strain was confirmed by both Western blot and Southern blot. To evaluate SnSAG polymorphisms in the S. neurona population, 14 strains were examined by Western blots using monospecific polyclonal antibodies against the four described SnSAGs. The results of these analyses demonstrated that SnSAG2, SnSAG3, and SnSAG4 are present in all 14 S. neurona strains tested, although some variance in SnSAG4 was observed. Importantly, SnSAG1 was not detected in seven of the strains, which included isolates from four cases of EPM and a case of fatal meningoencephalitis in a sea otter. Genetic analyses by PCR using gene-specific primers confirmed the absence of the SnSAG1 locus in six of these seven strains. Collectively, the data indicated that there is heterogeneity in the surface antigen composition of different S. neurona isolates, which is an important consideration for development of serological tests and prospective vaccines for EPM. Furthermore, the diversity reported herein likely extends to other phenotypes, such as strain virulence, and may have implications for the phylogeny of the various Sarcocystis spp. that undergo sexual stages

  5. The heptanucleotide motif GAGACGC is a key component of a cis-acting promoter element that is critical for SnSAG1 expression in Sarcocystis neurona.

    Science.gov (United States)

    Gaji, Rajshekhar Y; Howe, Daniel K

    2009-07-01

    The apicomplexan parasite Sarcocystis neurona undergoes a complex process of intracellular development, during which many genes are temporally regulated. The described study was undertaken to begin identifying the basic promoter elements that control gene expression in S. neurona. Sequence analysis of the 5'-flanking region of five S. neurona genes revealed a conserved heptanucleotide motif GAGACGC that is similar to the WGAGACG motif described upstream of multiple genes in Toxoplasma gondii. The promoter region for the major surface antigen gene SnSAG1, which contains three heptanucleotide motifs within 135 bases of the transcription start site, was dissected by functional analysis using a dual luciferase reporter assay. These analyses revealed that a minimal promoter fragment containing all three motifs was sufficient to drive reporter molecule expression, with the presence and orientation of the 5'-most heptanucleotide motif being absolutely critical for promoter function. Further studies should help to identify additional sequence elements important for promoter function and for controlling gene expression during intracellular development by this apicomplexan pathogen.

  6. The SnSAG merozoite surface antigens of Sarcocystis neurona are expressed differentially during the bradyzoite and sporozoite life cycle stages.

    Science.gov (United States)

    Gautam, A; Dubey, J P; Saville, W J; Howe, D K

    2011-12-29

    Sarcocystis neurona is a two-host coccidian parasite whose complex life cycle progresses through multiple developmental stages differing at morphological and molecular levels. The S. neurona merozoite surface is covered by multiple, related glycosylphosphatidylinositol-linked proteins, which are orthologous to the surface antigen (SAG)/SAG1-related sequence (SRS) gene family of Toxoplasma gondii. Expression of the SAG/SRS proteins in T. gondii and another related parasite Neospora caninum is life-cycle stage specific and seems necessary for parasite transmission and persistence of infection. In the present study, the expression of S. neurona merozoite surface antigens (SnSAGs) was evaluated in the sporozoite and bradyzoite stages. Western blot analysis was used to compare SnSAG expression in merozoites versus sporozoites, while immunocytochemistry was performed to examine expression of the SnSAGs in merozoites versus bradyzoites. These analyses revealed that SnSAG2, SnSAG3 and SnSAG4 are expressed in sporozoites, while SnSAG5 was appeared to be downregulated in this life cycle stage. In S. neurona bradyzoites, it was found that SnSAG2, SnSAG3, SnSAG4 and SnSAG5 were either absent or expression was greatly reduced. As shown for T. gondii, stage-specific expression of the SnSAGs may be important for the parasite to progress through its developmental stages and complete its life cycle successfully. Thus, it is possible that the SAG switching mechanism by these parasites could be exploited as a point of intervention. As well, the alterations in surface antigen expression during different life cycle stages may need to be considered when designing prospective approaches for protective vaccination. Copyright © 2011 Elsevier B.V. All rights reserved.

  7. Prevalence of antibodies to Trypanosoma cruzi, Toxoplasma gondii, Encephalitozoon cuniculi, Sarcocystis neurona, Besnoitia darlingi, and Neospora caninum in North American opossums, Didelphis virginiana, from southern Louisiana.

    Science.gov (United States)

    Houk, Alice E; Goodwin, David G; Zajac, Anne M; Barr, Stephen C; Dubey, J P; Lindsay, David S

    2010-12-01

    We examined the prevalence of antibodies to zoonotic protozoan parasites ( Trypanosoma cruzi, Toxoplasma gondii, and Encephalitozoon cuniculi) and protozoans of veterinary importance ( Neospora caninum, Sarcocystis neurona, and Besnoitia darlingi) in a population of North American opossums ( Didelphis virginiana) from Louisiana. Samples from 30 opossums were collected as part of a survey for T. cruzi in Louisiana. Frozen sera from these 30 opossums were examined using an indirect immunofluorescent antibody test (IFAT) against in vitro-produced antigenic stages of these protozoans. Additionally, 24 of the 30 samples were examined using hemoculture, and all 30 were examined in the modified direct agglutination test (MAT) for antibodies to To. gondii. The prevalences of reactive IFAT samples were as follows: 60% for T. cruzi, 27% for To. gondii, 23% for E. cuniculi, 17% for S. neurona, 47% for B. darlingi, and 0% for N. caninum. Hemoculture revealed that 16 (67%) of 24 samples were positive for T. cruzi, compared to 18 of 30 (60%) by IFAT. The sensitivity and specificity for the IFAT compared to hemoculture was 100% for each. The modified direct agglutination test revealed that 9 (30%) of the 30 samples from opossums had antibodies to To. gondii , compared to 8 (27%) using the IFAT. The sensitivity and specificity of the IFAT compared to the MAT was 100% and 72%, respectively.

  8. Inhibitory Activities of Epidermal Growth Factor Receptor Tyrosine Kinase-Targeted Dihydroxyisoflavone and Trihydroxydeoxybenzoin Derivatives on Sarcocystis neurona, Neospora caninum, and Cryptosporidium parvum Development

    Science.gov (United States)

    Gargala, G.; Baishanbo, A.; Favennec, L.; François, A.; Ballet, J. J.; Rossignol, J.-F.

    2005-01-01

    Several gene sequences of parasitic protozoa belonging to protein kinase gene families and epidermal growth factor (EGF)-like peptides, which act via binding to receptor tyrosine kinases of the EGF receptor (EGFR) family, appear to mediate host-protozoan interactions. As a clue to EGFR protein tyrosine kinase (PTK) mediation and a novel approach for identifying anticoccidial agents, activities against Sarcocystis neurona, Neospora caninum, and Cryptosporidium parvum grown in BM and HCT-8 cell cultures of 52 EGFR PTK inhibitor isoflavone analogs (dihydroxyisoflavone and trihydroxydeoxybenzoine derivatives) were investigated. Their cytotoxicities against host cells were either absent, mild, or moderate by a nitroblue tetrazolium test. At concentrations ranging from 5 to 10 μg/ml, 20 and 5 analogs, including RM-6427 and RM-6428, exhibited an in vitro inhibitory effect of ≥95% against at least one parasite or against all three, respectively. In immunosuppressed Cryptosporidium parvum-infected Mongolian gerbils orally treated with either 200 or 400 mg of agent RM-6427/kg of body weight/day for 8 days, fecal microscopic oocyst shedding was abolished in 6/10 animals (P of 0.05, respectively). After RM-6427 therapy (200 mg/kg/day for 8 days), the reduction in the ratio of animals with intracellular parasites was nearly significant in ileum (P = 0.067) and more marked in the biliary tract (P < 0.0013) than after nitazoxanide or paromomycin treatment (0.05 < P < 0.004). RM-6428 treatment at a regimen of 400 mg/kg/day for 12 days inhibited oocyst shedding, measured using flow cytometry from day 4 (P < 0.05) to day 12 (P < 0.02) of therapy, when 2/15 animals had no shedding (P < 0.0001) and 11/15 were free of gut and/or biliary tract parasites (P < 0.01). No mucosal alteration was microscopically observed for treated or untreated infected gerbils. To our knowledge, this report is the first to suggest that the isoflavone class of agents has the potential for

  9. A new trivalent SnSAG surface antigen chimera for efficient detection of antibodies against Sarcocystis neurona and diagnosis of equine protozoal myeloencephalitis.

    Science.gov (United States)

    Yeargan, Michelle; de Assis Rocha, Izabela; Morrow, Jennifer; Graves, Amy; Reed, Stephen M; Howe, Daniel K

    2015-05-01

    Enzyme-linked immunosorbent assays (ELISAs) based on the SnSAG surface antigens of Sarcocystis neurona provide reliable detection of infection by the parasite. Moreover, accurate serodiagnosis of equine protozoal myeloencephalitis (EPM) is achieved with the SnSAG ELISAs by measuring antibodies in serum and cerebrospinal fluid (CSF) to reveal active infection in the central nervous system. Two independent ELISAs based on recombinant (r)SnSAG2 or a chimeric fusion of SnSAG3 and SnSAG4 (rSnSAG4/3) are currently used together for EPM serodiagnosis to overcome varied antibody responses in different horses. To achieve reliable antibody detection with a single ELISA instead of 2 separate ELISAs, rSnSAG2 was fused with rSnSAG4/3 into a single trivalent protein, designated rSnSAG2/4/3. Paired serum and CSF from 163 horses were tested with all 3 ELISAs. When the consensus antibody titers obtained with the rSnSAG2 and rSnSAG4/3 ELISAs were compared to the single SAG2/4/3 ELISA titers, Spearman rank correlation coefficients of ρ = 0.74 and ρ = 0.90 were obtained for serum and CSF, respectively, indicating strong agreement between the tests. When the rSnSAG2 and rSnSAG4/3 consensus serum-to-CSF titer ratio was compared to the rSnSAG2/4/3 serum-to-CSF titer ratio, the Spearman correlation coefficient was ρ = 0.87, again signifying strong agreement. Importantly, comparing the diagnostic interpretation of the serum-to-CSF titer ratios yielded a Cohen kappa value of 0.77. These findings suggest that the single ELISA based on the trivalent rSnSAG2/4/3 will provide serologic and diagnostic results that are highly comparable to the consensus of the 2 independent ELISAs based on rSnSAG2 and rSnSAG4/3. © 2015 The Author(s).

  10. Accurate antemortem diagnosis of equine protozoal myeloencephalitis (EPM) based on detecting intrathecal antibodies against Sarcocystis neurona using the SnSAG2 and SnSAG4/3 ELISAs.

    Science.gov (United States)

    Reed, S M; Howe, D K; Morrow, J K; Graves, A; Yeargan, M R; Johnson, A L; MacKay, R J; Furr, M; Saville, W J A; Williams, N M

    2013-01-01

    Recent work demonstrated the value of antigen-specific antibody indices (AI and C-value) to detect intrathecal antibody production against Sarcocystis neurona for antemortem diagnosis of equine protozoal myeloencephalitis (EPM). The study was conducted to assess whether the antigen-specific antibody indices can be reduced to a simple serum : cerebrospinal fluid (CSF) titer ratio to achieve accurate EPM diagnosis. Paired serum and CSF samples from 128 horses diagnosed by postmortem examination. The sample set included 44 EPM cases, 35 cervical-vertebral malformation (CVM) cases, 39 neurologic cases other than EPM or CVM, and 10 non-neurologic cases. Antibodies against S. neurona were measured in serum and CSF pairs using the SnSAG2 and SnSAG4/3 (SnSAG2, 4/3) ELISAs, and the ratio of each respective serum titer to CSF titer was determined. Likelihood ratios and diagnostic sensitivity and specificity were calculated based on serum titers, CSF titers, and serum : CSF titer ratios. Excellent diagnostic sensitivity and specificity was obtained from the SnSAG2, 4/3 serum : CSF titer ratio. Sensitivity and specificity of 93.2 and 81.1%, respectively, were achieved using a ratio cutoff of ≤100, whereas sensitivity and specificity were 86.4 and 95.9%, respectively, if a more rigorous cutoff of ≤50 was used. Antibody titers in CSF also provided good diagnostic accuracy. Serum antibody titers alone yielded much lower sensitivity and specificity. The study confirms the value of detecting intrathecal antibody production for antemortem diagnosis of EPM, and they further show that the antigen-specific antibody indices can be reduced in practice to a simple serum : CSF titer ratio. Copyright © 2013 by the American College of Veterinary Internal Medicine.

  11. Prevalence of antibodies to Trypanosoma cruzi, Leishmania infantum, Encephalitozoon cuniculi, Sarcocystis neurona, and Neospora caninum in capybara, Hydrochoerus hydrochaeris, from São Paulo State, Brazil

    OpenAIRE

    2010-01-01

    Little is known about the importance of capybara. Hydrochoerus hydrochaeris, as reservoirs for parasites of zoonotic or veterinary importance. Sera from 63 capybaras, from 6 counties in the state of Sao Paulo, Brazil, were examined for antibodies to Trypanosoma cruel, Leishmania infantum, Encephalitozoon cuniculi. Sarcacystis neurona, and Neospora caninum using an indirect immunofluorescent antibody test. Five (8%) of the 63 capybaras had antibodies to T cruzi epimastigotes. None of the sampl...

  12. Sarcocyst development in raccoons (Procyon lotor) inoculated with different strains of Sarcosytis neurona culture-derived merozoites

    Science.gov (United States)

    Sarcocystis neurona is considered the major etiologic agent of equine protozoal myeloencephalitis (EPM), a neurological disease in horses. Raccoon (Procyon lotor) is considered the most important intermediate host in the life cycle of S. neurona in the USA; S. neurona sarcocysts do mature in raccoon...

  13. Diversity of Sarcocystis spp shed by opossums in Brazil inferred with phylogenetic analysis of DNA coding ITS1, cytochrome B, and surface antigens.

    Science.gov (United States)

    Valadas, Samantha Y O B; da Silva, Juliana I G; Lopes, Estela Gallucci; Keid, Lara B; Zwarg, Ticiana; de Oliveira, Alice S; Sanches, Thaís C; Joppert, Adriana M; Pena, Hilda F J; Oliveira, Tricia M F S; Ferreira, Helena L; Soares, Rodrigo M

    2016-05-01

    Although few species of Sarcocystis are known to use marsupials of the genus Didelphis as definitive host, an extensive diversity of alleles of surface antigen genes (sag2, sag3, and sag4) has been described in samples of didelphid opossums in Brazil. In this work, we studied 25 samples of Sarcocystis derived from gastrointestinal tract of opossums of the genus Didelphis by accessing the variability of sag2, sag3, sag4, gene encoding cytochrome b (cytB) and first internal transcribed spacer (ITS1). Reference samples of Sarcocystis neurona (SN138) and Sarcocystis falcatula (SF1) maintained in cell culture were also analyzed. We found four allele variants of cytB, seven allele variants of ITS1, 10 allele variants of sag2, 13 allele variants of sag3, and 6 allele variants of sag4. None of the sporocyst-derived sequences obtained from Brazilian opossums revealed 100% identity to SN138 at cytB gene, nor to SN138 or SF1 at ITS1 locus. In addition, none of the sag alleles were found identical to either SF1 or SN138 homologous sequences, and a high number of new sag allele types were found other than those previously described in Brazil. Out of ten sag2 alleles, four are novel, while eight out of 13 sag3 alleles are novel and one out of six sag4 alleles is novel. Further studies are needed to clarify if such a vast repertoire of allele variants of Sarcocystis is the consequence of re-assortments driven by sexual exchange, in order to form individuals with highly diverse characteristics, such as pathogenicity, host spectrum, among others or if it only represents allele variants of different species with different biological traits.

  14. Molecular characterization and development of Sarcocystis speeri sarcocysts in gamma interferon gene knockout mice

    Science.gov (United States)

    The North American opossum (Didelphis virginiana) is the definitive host for at least three named species of Sarcocystis: S. falcatula, S. neurona, and S. speeri. It appears that there may be additional undescribed species of Sarcocystis in D. virginiana feces. The South American opossums (D. albive...

  15. Genetic assemblage of Sarcocystis spp. in Malaysian snakes

    Science.gov (United States)

    2013-01-01

    Background Sarcocystis species are protozoan parasites with a wide host range including snakes. Although there were several reports of Sarcocytis species in snakes, their distribution and prevalence are still not fully explored. Methods In this study, fecal specimens of several snake species in Malaysia were examined for the presence of Sarcocystis by PCR of 18S rDNA sequence. Microscopy examination of the fecal specimens for sporocysts was not carried as it was difficult to determine the species of the infecting Sarcocystis. Results Of the 28 snake fecal specimens, 7 were positive by PCR. BLASTn and phylogenetic analyses of the amplified 18S rDNA sequences revealed the snakes were infected with either S. nesbitti, S. singaporensis, S. zuoi or undefined Sarcocystis species. Conclusion This study is the first to report Sarcocystis infection in a cobra, and S. nesbitti in a reticulated python. PMID:24010903

  16. Detection of Sarcocystis spp. infection in bobcats (Lynx rufus)

    Science.gov (United States)

    Verma, S. K.; Calero-Bernal, R.; Lovallo, M. J.; Sweeny, A. R.; Grigg, M. E.; Dubey, J. P.

    2015-01-01

    The protozoan Sarcocystis neurona is an important cause of severe clinical disease of horses (called equine protozoal myeloencephalitis, EPM), marine mammals, companion animals, and several species of wildlife animals in the Americas. The Virginia opossum (Didelphis virginiana) is its definitive host in the USA and other animals act as intermediate or aberrant hosts. Samples of tongue and heart from 35 bobcats hunted for fur and food from Mississippi State, USA in February, 2014 were used for the present study. Muscles were examined for Sarcocystis infection by microscopic examination of either unfixed muscle squash preparations or pepsin digests, by histopathology of fixed samples, and by molecular methods. Sarcocystis-like bradyzoites were found in digests of 14 hearts and 10 tongues of 35 bobcats. In histological sections, sarcocysts were found in 26 of 35 bobcats; all appeared relatively thin-walled similar to S. felis sarcocysts under light microscope at 1000x magnification. S. neurona-like sarcocysts having thickened villar tips were seen in unstained muscle squash of tongue of two bobcats and PCR-DNA sequencing identified them definitively as S. neurona-like parasite. DNA extracted from bradyzoites obtained from tongue and heart muscle digests was analyzed by PCR-DNA sequencing at the ITS1 locus. Results indicated the presence of S. neurona-like parasite in 26 of 35 samples. ITS1 sequences identical to S. dayspi were identified in 3 bobcats, 2 of which were also co-infected with S. neurona-like parasite. The high prevalence of sarcocysts in bobcat tissues suggested an efficient sylvatic cycle of Sarcocystis spp. in the remote regions of Mississippi State with the bobcat as a relevant intermediate host. PMID:26138150

  17. Sarcocysts of an unidentified species of Sarcocystis in the sea otter (Enhydra lutris)

    Science.gov (United States)

    Dubey, J.P.; Lindsay, D.S.; Rosenthal, B.M.; Thomas, N.J.

    2003-01-01

    The number of Sarcocystis species that infect sea otters (Enhydra lutris) is unknown. Sea otter tissues were recently shown to harbor sarcocysts of S. neurona and of unidentified species of Sarcocystis. Whereas sarcocysts of S. neurona have walls 1a??3 I?m thick with type 9 villar protrusions, ultrastructure of a distinct thin-walled sarcocyst (0.5a??0.7 I?m thick) lacking villar protrusions, but instead exhibiting minute type 1 undulations on the sarcocyst wall, is described in this report. Parasites characterized from a sea otter infection were inferred to be related to, but distinct from, other species belonging to Sarcocystis, based on sequencing and phylogenetic analysis of a portion of the beta subunit of the plastid-encoded RNA polymerase gene.

  18. The red fox (Vulpes vulpes) and the arctic fox (Vulpes lagopus) are definitive hosts of Sarcocystis alces and Sarcocystis hjorti from moose (Alces alces).

    Science.gov (United States)

    Dahlgren, Stina S; Gjerde, Bjørn

    2010-09-01

    The aim of this study was to determine whether foxes might act as definitive hosts of Sarcocystis alces in moose. In 2 experiments, 6 silver foxes (Vulpes vulpes) and 6 blue foxes (Vulpes lagopus) were fed muscle tissue from moose containing numerous sarcocysts of S. alces, and euthanazed 7-28 days post-infection (p.i.). Intestinal mucosal scrapings and faecal samples were screened microscopically for Sarcocystis oocysts/sporocysts, which were identified to species by means of species-specific primers and sequence analysis targeting the ssu rRNA gene. All foxes in both experiments became infected with Sarcocystis; the oocysts were fully sporulated by 14 days p.i., containing sporocysts measuring 14-15 x 10 microm. Molecular identification revealed that the oocysts/sporocysts belonged to 2 species, S. alces and Sarcocystis hjorti, although sarcocysts of S. hjorti were only identified in moose subsequent to the infection of foxes. In the first experiment, all 8 foxes also became infected with a Hammondia sp. derived from moose, shedding unsporulated, subspherical oocysts, measuring 10-12 microm in diameter, from 6-7 days p.i. onwards. The study proved that canids (the red fox and arctic fox) are definitive hosts for S. alces and S. hjorti, as had been inferred from the phylogenetic position of these species.

  19. An outbreak of Sarcocystis calchasi encephalitis in multiple psittacine species within an enclosed zoological aviary.

    Science.gov (United States)

    Rimoldi, Guillermo; Speer, Brian; Wellehan, James F X; Bradway, Daniel S; Wright, Lewis; Reavill, Drury; Barr, Bradd C; Childress, April; Shivaprasad, H L; Chin, Richard P

    2013-11-01

    A total of 5 psittacine birds in an enclosed zoological exhibit, including 2 princess parrots and 3 cockatoos of 2 different species, developed severe central nervous system clinical signs over a 2-3-month period and died or were euthanized. Histologically, all birds had a lymphoplasmacytic and histiocytic encephalitis with intralesional protozoa consistent with a Sarcocystis species in addition to intramuscular tissue sarcocysts. By immunohistochemical staining, merozoites in brain and tissue cysts in muscle did not react with polyclonal antisera against Sarcocystis falcatula, Sarcocystis neurona, Toxoplasma gondii, and Neospora caninum, or with a monoclonal antibody to S. neurona. Transmission electron microscopy on sarcocyst tissue cyst walls from 2 birds was morphologically consistent with Sarcocystis calchasi. Polymerase chain reaction (PCR) amplification and sequencing of partial 18S ribosomal RNA from muscle tissue cysts and brain schizonts from 3 birds was consistent with a clade containing S. calchasi and Sarcocystis columbae but could not distinguish these closely related Sarcocystis species. However, PCR amplification and sequencing of the internal transcribed spacer 1 RNA segment in the brain from 2 birds and muscle from 2 birds specifically identified the isolates as S. calchasi. The current report documents that multiple psittacine species are susceptible intermediate hosts of S. calchasi, and that infection can cause encephalitis resulting in significant morbidity and mortality in psittacine aviaries.

  20. Sarcocystis cruzi (Apicomplexa: Sarcocystidae no cachorro-do-mato (Cerdocyon thous Sarcocystis cruzi (Apicomplexa: Sarcocystidae in the crab-eating fox (Cerdocyon thous

    Directory of Open Access Journals (Sweden)

    Janaina S. Rodrigues

    2008-11-01

    Full Text Available Esporocistos de Sarcocystis foram identificados nas amostras fecais de um cachorro-do-mato. Eles foram dados por via oral para um bezerro em aleitamento, sendo observados cistos com morfologia compatível com os de Sarcocystis cruzi na musculatura cardíaca e esquelética, três meses após a infecção. Musculatura cardíaca deste bezerro foi dada para um segundo cão doméstico livre de coccídios, que eliminou esporocistos compatíveis com os de Sarcocystis em suas fezes, tendo com períodos pré-patente e patente 11 e 12 dias após a infecção respectivamente. Para comparar a morfologia dos esporocistos e cistos, um segundo cão, também livre de coccídios, foi alimentado com musculatura cardíaca de um bovino infectando naturalmente e positivo para cistos de S. cruzi. Esporocistos compatíveis com os eliminados pelo primeiro cão foram encontrados nas fezes. Apesar dos esporocistos eliminados pelo cachorro-do-mato serem significativamente diferentes dos eliminados pelos cães infectados experimentalmente, pode se considerar com base na morfologia dos esporocistos, cistos e na transmissão biológica que a espécie encontrada nas fezes do cachorro-do-mato é Sarcocystis cruzi.Sporocysts of Sarcocystis were identified in feces samples of a crab-eating fox, and were orally given to a suckling calf; after 3 months of infection, sarcocysts morphologically similar to Sarcocystis cruzi were observed in cardiac and skeletal striated muscles. The cardiac muscles of this calf were orally given to a puppy free of coccidia, that shed sporocysts in its feces.with a prepatent and patent period of 11 and 12 days after infection, respectively. To compare the morphology of the sporocysts and cysts, a second puppy was fed on bovine cardiac muscles infected naturally, and sporocysts identical to those shed by the first dog were recovered from its feces. In spite of the significant difference between sporocysts found in the mucosa of the crab-eating fox and

  1. Sarcocystis heydorni, n. sp. (Apicomplexa: Sarcocystidae) with cattle (Bos taurus) and human (Homo sapiens) cycle.

    Science.gov (United States)

    Dubey, Jitender P; van Wilpe, Erna; Calero-Bernal, Rafael; Verma, Shiv Kumar; Fayer, Ronald

    2015-11-01

    Cattle (Bos taurus) are intermediate hosts for four species of Sarcocystis, namely Sarcocystis cruzi, Sarcocystis hirsuta, Sarcocystis hominis, and Sarcocystis rommeli. Of these four species, mature sarcocysts of S. cruzi are thin-walled (<1 μm), whereas S. hirsuta, S. hominis, and S. rommeli have thick walls (4 μm or more). Here, we describe a new species of Sarcocystis with thin-walled sarcocysts in cattle. Two newborn calves were fed with sporocysts from the feces of a human volunteer who had ingested raw beef. The calves were killed 111 and 222 days later. In addition to thick-walled sarcocysts of S. hominis, both calves were coinfected with a Sarcocystis species that had a thin-walled sarcocysts, distinct from S. cruzi. The sarcocysts were mature, microscopic, up to 80 μm wide, and up to 1060 μm long. By light microscopy, the sarcocyst wall was thin (<1 μm thick) and had minute protrusions. By transmission electron microscopy, the sarcocyst wall had short, conical villar protrusions (vp) that were up to 0.5 μm long and up to 0.5 μm wide, similar to type 29. The vp on the sarcocyst wall lacked microtubules but had six or more disc-shaped plaques. The ground substance layer was smooth, approximately 0.5 μm thick, and without microtubules. The bradyzoites were 8-11 μm long. The structure of the sarcocyst wall was distinct from any species of Sarcocystis reported from livestock. This unique species is named in honor of Dr. Alfred Otto Heydorn who provided the sporocysts.

  2. Modest genetic differentiation among North American populations of Sarcocystic neurona may reflect expansion in its geographic range

    Science.gov (United States)

    Sundar, N.; Asmundsson, I.M.; Thomas, N.J.; Samuel, M.D.; Dubey, J.P.; Rosenthal, B.M.

    2008-01-01

    Sarcocystis neurona is an important cause of neurological disease in horses (equine protozoal myeloencephalitis, EPM) and sea otters in the United States. In addition, EPM-like disease has been diagnosed in several other land and marine mammals. Opossums are its only definitive hosts. Little genetic diversity among isolates of S. neurona from different hosts has been reported. Here, we used 11 microsatellites to characterize S. neurona DNA isolated from natural infections in 22 sea otters (Enhydra lutris) from California and Washington and in 11 raccoons (Procyon lotor) and 1 striped skunk (Mephitis mephitis) from Wisconsin. By jointly analyzing these 34 isolates with 26 isolates previously reported, we determined that geographic barriers may limit S. neurona dispersal and that only a limited subset of possible parasite genotypes may have been introduced to recently established opossum populations. Moreover, our study confirms that diverse intermediate hosts share a common infection source, the opossum (Didelphis virginiana).

  3. Characterization of Sarcocystis from four species of hawks from Georgia, USA.

    Science.gov (United States)

    Yabsley, Michael J; Ellis, Angela E; Stallknecht, David E; Howerth, Elizabeth W

    2009-02-01

    During 2001 to 2004, 4 species of hawks (Buteo and Accipiter spp.) from Georgia were surveyed for Sarcocystis spp. infections by examining intestinal sections. In total, 159 of 238 (66.8%) hawks examined were infected with Sarcocystis spp. Samples from 10 birds were characterized by sequence analysis of a portion of the 18S rRNA gene (783 base pairs). Only 3 of the 10 sequences from the hawks were identical; the remainder differed by at least 1 nucleotide. Phylogenetic analysis failed to resolve the position of the hawk Sarcocystis species, but they were closely related several Sarcocystis species from raptors, rodents, and Sarcocystis neurona. The high genetic diversity of Sarcocystis suggests that more than 1 species infects these 4 hawk species; however, additional molecular or experimental work will be required to determine the speciation and diversity of parasites infecting these avian hosts. In addition to assisting with determining species richness of Sarcocystis in raptors, molecular analysis should be useful in the identification of potential intermediate hosts.

  4. Sarcocystis pantherophis, n. sp. from eastern rat snakes (Pantherophis alleghaniensis) definitive hosts and interferongamma gene knockout mice as experimental intermediate hosts

    Science.gov (United States)

    Here we report a new species, Sarcocystis pantherophisi with the Eastern rat snake (Pantherophis alleghaniensis) as natural definitive host and the interferon gamma gene knockout (KO) mouse as the experimental intermediate host. Sporocysts (n=15) from intestinal contents of the snake were 17.3 x 10....

  5. Intra-uterine exposure of horses to Sarcocystis spp. antigens

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    A.M. Antonello

    2016-04-01

    Full Text Available The aim of this study was to examine the intra-uterine exposure to Sarcocystis spp. antigens, determining the number of foals with detectable concentrations of antibodies against these agents in the serum, before colostrum ingestion and collect data about exposure of horses to the parasite. Serum samples were collected from 195 thoroughbred mares and their newborns in two farms from southern Brazil. Parasite specific antibody responses to Sarcocystis antigens were detected using the indirect immunofluorescent antibody test (IFAT and immunoblot analysis. In 84.1% (159/189 of the pregnant mares and in 7.4% (14/189 of foals we detected antibodies anti-Sarcocystis spp. by IFAT. All samples seropositive from foals were also positive in their respective mares. Serum samples of seropositive foals by IFAT, showed no reactivity on the immunoblot, having as antigens S. neurona merozoites. In conclusion, the intra-uterine exposure to Sarcocystis spp. antigens in horses was demonstrated, with occurrence not only in mares, but also in their foals, before colostrum ingestion these occurrences were reduced.

  6. Sarcocystis spp. Infection in two Red Panda Cubs (Ailurus fulgens).

    Science.gov (United States)

    Zoll, W M; Needle, D B; French, S J; Lim, A; Bolin, S; Langohr, I; Agnew, D

    2015-01-01

    Two neonatal male red panda (Ailurus fulgens) littermates were submitted for necropsy examination. One animal was found dead with no prior signs of illness; the other had a brief history of laboured breathing. Post-mortem examination revealed disseminated protozoal infection. To further characterize the causative agent, transmission electron microscopy (TEM), immunohistochemistry (IHC), polymerase chain reaction (PCR) and amplification and nucleic acid sequencing were performed. IHC was negative for Toxoplasma gondii and Neospora caninum, but was positive for a Sarcocystis spp. TEM of cardiac muscle and lung revealed numerous intracellular apicomplexan protozoa within parasitophorous vacuoles. PCR and nucleic acid sequencing of partial 18S rRNA and the internal transcribed spacer (ITS)-1 region confirmed a Sarcocystis spp. that shared 99% sequence homology to Sarcocystis neurona and Sarcocystis dasypi. This represents the first report of sarcocystosis in red pandas. The histopathological, immunohistochemical, molecular and ultrastructural findings are supportive of vertical transmission resulting in fatal disseminated disease. Copyright © 2015 Elsevier Ltd. All rights reserved.

  7. Transmission studies with Sarcocystis idahoensis of deer mice (Peromyscus maniculatus) and gopher snakes (Pituophis melanoleucus).

    Science.gov (United States)

    Bledsoe, B

    1980-04-01

    Transmission studies with Sarcocystis idahoensis of deer mice (Peromyscus maniculatus) and gopher snakes (pituophis melanoleucus) were conducted to determine host specificity of various stages of the parasite. Sporocysts were not passed by four dogs or four cats fed infected skeletal muscle from deer mice. Seven white mice (Mus musculus) and 34 white-footed mice (Peromyscus leucopus) were negative for sarcocysts and liver meronts following oral inoculation with S. idahoensis sporocysts; however, excystation of sporocysts occurred in two white-footed mice killed four hours post inoculation (PI). A gopher snake orally inoculated with sporocysts remained negative for coccidia for two months PI. Three deer mice orally inoculated and three intraperitoneally (IP) inoculated with tachyzoites from liver meronts developed sarcocysts in their skeletal muscles similar to those seen in deer mice orally inoculated with sporocysts. Liver meronts were not found. Ten deer mice orally inoculated and 10 deer mice inoculated IP with bradyzoites from S. idahoensis sarcocysts remained negative for sarcocysts and liver meronts at necropsy 17 days PI.

  8. Sarcocystis caninum and Sarcocystis svanai n. spp. (Apicomplexa: Sarcocystidae) Associated with Severe Myositis and Hepatitis in the Domestic Dog (Canis familiaris)

    Science.gov (United States)

    Dubey, J. P.; Sykes, J. E.; Shelton, G. D.; Sharp, N.; Verma, S. K.; Calero-Bernal, R.; Viviano, J.; Sundar, N.; Khan, A.; Grigg, M. E.

    2014-01-01

    There are several reports of Sarcocystis sarcocysts in muscles of dogs but these species have not been named. Additionally, there are 2 reports of Sarcocystis neurona in dogs. Here, we propose 2 new names, Sarcocystis caninum, and Sarcocystis svanai for sarcocysts associated with clinical muscular sarcocystosis in 4 domestic dogs (Canis familiaris), 1 each from Montana and Colorado in the USA, and 2 from British Columbia, Canada. Only the sarcocyst stage was identified. Most of the sarcocysts identified were S. caninum. Sarcocysts were studied using light microscopy, transmission electron microscopy, and PCR. Based on collective results 2 new species, Sarcocystis caninum and Sarcocystis svanai were designated. Sarcocystis caninum and Sarcocystis svanai were structurally distinct. Sarcocystis caninum sarcocysts were up to 1.2 mm long and up to 75 μm wide. By light microscopy, the sarcocyst wall was relatively thin and smooth. By transmission electron microscopy (TEM), the sarcocyst wall “type 9”, 1–2 μm thick, and contained villar protrusions that lacked microtubules. Bradyzoites in sections were 7–9 μm long. Sarcocysts of S. svanai were few and were identified by TEM. Sarcocystis svanai sarcocysts were “type 1”, thin walled (< 0.5 μm), and the wall lacked villar protrusions but had tiny blebs that did not invaginate. DNA was extracted either from infected frozen muscle biopsies or formalin-fixed paraffin-embedded sections. Dogs were either singly infected with S. caninum or multiply co-infected with S. caninum and S. svanai (the result of a mixed infection) based on multi-locus DNA sequencing and morphology. BLASTn analysis established that the sarcocysts identified in these dogs were similar to, but not identical to S. canis or S. arctosi, parasites found to infect polar bears (Ursus maritimus) or brown bears (Ursus arctosi), respectively. However, the S. caninum sequence showed 100% identify over the 18S rRNA region sequenced to that of S. arctica

  9. A review of Sarcocystis of domestic animals and of other coccidia of cats and dogs.

    Science.gov (United States)

    Dubey, J P

    1976-11-15

    The nomenclature, life cycles, and pathogenicity of Sarcocystis of domestic animals are reviewed. Sarcocystis had a 2-host life cycle, with carnivores as definitive hosts and herbivores as intermediate hosts. The following species are found in domestic animals (with the definitive hosts given in parentheses): 3 species in the ox: S cruzi (dog, wolf, coyote, raccoon, fox), S hirsuta (cat), S hominis (man, monkey); 2 species in the sheep: S ovicanis (dog), S tenella (cat); 3 species in the pig: S miescheriana (dog), S porcifelis n sp (cat), S porcihominis n sp (man); and 1 species in the horse: S bertrami (dog). Sarcocystis cruzi, S ovicanis, and S porcifelis are highly pathogenic to the ox, the sheep, and the pig, respectively. Clinical signs of acute bovine sarcocystosis are: anorexia, pyrexia (42 C, or more), anemia, cachexia, enlarged palpable lymph nodes, excessive salivation, and loss of hair at the tip of the tail. Anemia, anorexia, ataxia, and abortions are the chief clinical signs of acute ovine sarcocystosis. These signs are evident at the time of vascular endothelium is parasitized by schizonts. The schizonts disappear in about 1 month, and cysts are formed in the muscles. The cystic phase of sarcocystosis is virtually nonpathogenic. Carnivores shed sporocysts in their feces after ingesting the intramuscular cysts from the herbivores. Sarcocystis is nonpathogenic to the definitive host. Feline and canine coccidia are also reviewed. The following 11 species are found in cats: Toxoplasma gondii, Hammondia hammondi, Isospora felis, Isosporarivolta, Besnoitia besnoiti, Besnoitia sp, and 5 types of Sarcocystis (S hirsuta from the ox, S tenella from the sheep, S muris from the mouse, S porcifelis from the pig, and Sarcocystis sp from Grant's gazelle). The following 10 species are found in canine feces (Isospora canis, Isospora ohioensis, Isospora wallacei n sp; and 7 types of Sarcocystis (S cruzi from the ox, S ovicanis from the sheep, S bertrami and Sarcocystis

  10. Accipiter hawks (Accipitridae) confirmed as definitive hosts of Sarcocystis turdusi, Sarcocystis cornixi and Sarcocystis sp. ex Phalacrocorax carbo.

    Science.gov (United States)

    Mayr, Sylvia L; Maier, Kristina; Müller, Jana; Enderlein, Dirk; Gruber, Achim D; Lierz, Michael

    2016-08-01

    Sarcocystis is a large genus of protozoan parasites with complex heteroxenous life cycles. For many species, either the intermediate or the definitive host is still unknown. In this study, 116 Accipiter hawks (Eurasian sparrowhawks and northern goshawks) were investigated for the presence of Sarcocystis spp. in their intestinal tract or their faeces. To gain a wide distribution, samples were collected throughout Germany within 2 years. It was possible to detect Sarcocystis-like oocysts in 65 samples. Sequencing of the ITS region or species-specific PCR identified 33 samples as Sarcocystis turdusi/Sarcocystis sp. ex A. nisus (18), Sarcocystis calchasi (6), Sarcocystis columbae (3), Sarcocystis cornixi (3) and Sarcocystis sp. ex Phalacrocorax carbo (3). Besides the known infestation with S. columbae, S. sp. ex A. nisus and S. calchasi the Accipiter hawks were thereby confirmed as definitive host of S. turdusi, S. cornixi and S. sp. ex Phalacrocorax carbo for the first time.

  11. Las neuronas de la conciencia

    Directory of Open Access Journals (Sweden)

    Rodrigo Quian Quiroga

    2008-05-01

    Full Text Available El estudio de la conciencia ha sido descrito como uno de los grandes desafíos de la humanidad. Es por ello que los neurocientíficos se han dedicado a estudiar la percepción visual consciente de objetos. Un reciente estudio en humanos –implantados con electrodos intracraneales por motivos clínicos- mostró la presencia de neuronas que disparan exclusivamente cuando las imágenes son percibidas conscientemente.

  12. A report of intestinal sarcocystosis in the bullsnake (Pituophis melanoleucus sayi) and a re-evaluation of Sarcocystis sp. from snakes of the genus Pituophis.

    Science.gov (United States)

    Daszak, P; Cunningham, A

    1995-07-01

    We report a severe enteric infection of Sarcocystis sp. from a wild-caught bullsnake (Pituophis melanoleucus sayi). The animal was collected in October 1988 by a commercial dealer, imported into the United Kingdom during November 1988 and purchased by the London Zoo, in December 1988. The animal was not fed after capture and was anorexic from the time of purchase to the time of death in January 1989. On necropsy, the animal was emaciated and the mucosa of the proximal intestine was markedly thickened. The lamina propria was packed with oocysts, and enterocytes were parasitized by an organism which closely resembled Sarcocystis roudabushi and Sarcocystis idahoensis, two bisporocystid coccidia described previously from Pituophis melanoleucus. We propose that Sarcocystis idahoensis and Sarcocystis roudabushi are synonymous since both occur in the same host species, both invade the intestinal lamina propria and entreocytes, and sporocyst measurement ranges of both species overlap. This is the first report of death believed to be due to sarcocytosis in a naturally-infected definitive host.

  13. Neuronas espejo y el aprendizaje en anestesia

    OpenAIRE

    Bautista, Jhon; Navarro, José Ricardo

    2011-01-01

    Las neuronas espejo fueron descritas inicialmente en primates de la especie Macaca nemestrina hacia el año 1990 por el neurofisiólogo Giacomo Rizzolatti y su grupo de la Universidad de Parma, en Italia. Son neuronas motoras que activan cuando el individuo observa la acción concreta para la que están predeterminadas sin generar ningún tipo de actividad motora. En la actualidad se considera que estas neuronas participan en procesos de adaptación al entorno social ya que permiten no solamente co...

  14. Neuronas espejo y el aprendizaje en anestesia

    OpenAIRE

    Bautista, Jhon; Navarro, José Ricardo

    2011-01-01

    Las neuronas espejo fueron descritas inicialmente en primates de la especie Macaca nemestrina hacia el año 1990 por el neurofisiólogo Giacomo Rizzolatti y su grupo de la Universidad de Parma, en Italia. Son neuronas motoras que activan cuando el individuo observa la acción concreta para la que están predeterminadas sin generar ningún tipo de actividad motora. En la actualidad se considera que estas neuronas participan en procesos de adaptación al entorno social ya que permiten no solamente co...

  15. Transplantation of Cardicola opisthorchis (Trematoda: Aporocotylidae) sporocysts into the intermediate host, Terebella sp. (Polychaeta: Terebellidae).

    Science.gov (United States)

    Sugihara, Yukitaka; Yamada, Toshiyuki; Iwanaga, Shunsuke; Kanai, Kinya

    2017-02-01

    Cardicola opisthorchis is a blood fluke pathogen significantly affecting cultured Pacific bluefin tuna Thunnus orientalis in Japan. It is known that the intermediate host of C. opisthorchis is a terebellid polychaete Terebella sp. In order to study the intrapolychaete larval development of C. opisthorchis, we transplanted sporocysts, which contained a large number of cercariae, of C. opisthorchis obtained from Terebella sp. into sporocyst-free Terebella sp., which had been maintained at 20°C. The transplanted sporocysts switched from cercarial to sporocystal production by 17days after transplantation (d.a.t.) and daughter sporocysts were released into the polychaete body cavity at 25d.a.t. Subsequently, the released daughter sporocysts produced daughter sporocysts again. Thereafter, daughter sporocysts that contained cercariae appeared at 38d.a.t. and gradually increased. At 51d.a.t., 136 sporocysts that had multiplied from the original two transplanted sporocysts were observed in the body of one polychaete, and cercariae were released from daughter sporocysts inside the polychaete body cavity. Subsequently the cercariae were found to be released outside the polychaete at 57d.a.t. This is the first successful case of in situ observation of the development of a blood fluke within the intermediate host. Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.

  16. Multiple infection of amber Succinea putris snails with sporocysts of Leucochloridium spp. (Trematoda).

    Science.gov (United States)

    Ataev, G L; Zhukova, A A; Tokmakova, А S; Prokhorova, Е E

    2016-08-01

    Amber Succinea putris snails were collected in the Leningrad Region (Russia). Some of them were infected with trematodes Leucochloridium paradoxum, Leucochloridium perturbatum and Leucochloridium vogtianum. One snail had triple infection with all these species. Genotyping of sporocysts by ITS1-5.8S-ITS2 nucleotide sequences of ribosomal DNA (rDNA) and phylogenetic analysis were performed. The results confirmed the species identification of sporocysts of Leucochloridium based on the shape and colour of mature broodsacs. Sporocyst broodsacs could leave the host snail on their own, remaining viable in the environment for up to an hour. This ability of sporocysts may prevent the excessive infection of the molluscan host.

  17. Effects of different sizes of glass beads on the release of sporocysts from Eimeria tenella oocysts.

    Science.gov (United States)

    You, Myung-Jo

    2014-06-01

    The oocyst wall is severed by means of mechanical injury or chemical agents. This study reports the percentage of in vitro sporocyst release following mechanical shaking in the presence of varying sizes of glass beads. Glass beads measured 0.5, 1, and 3 mm in diameter and were shaken with the oocysts for different times ranging from 5 sec to 5 min. Approximately 80% of sporocysts were released with 5 min of shaking in the presence of 3 mm glass beads, as well as 30 sec with 0.5 mm beads and 1 mm glass beads. The release of sporocysts of E. tenella was most efficient using 1 mm glass beads and treatment times of 30 sec to 1 min. Therefore, the use of 1 mm glass beads with 30 sec to 1 min of agitation is recommended in order to maximize sporocyst release and recovery and to improve the yield of viable sporozoites for use in biochemical, tissue culture, and immunological applications of coccidia.

  18. Molecular evidence of Sarcocystis species in captive snakes in Japan.

    Science.gov (United States)

    Abe, Niichiro; Matsubara, Katsuki; Tamukai, Kenichi; Miwa, Yasutsugu; Takami, Kazutoshi

    2015-08-01

    Sarcocystis nesbitti, using snakes as the definitive host, is a causative agent of acute human muscular sarcocystosis in Malaysia. Therefore, it is important to explore the distribution and prevalence of S. nesbitti in snakes. Nevertheless, epizootiological information of S. nesbitti in snakes remains insufficient because few surveys have assessed Sarcocystis infection in snakes in endemic countries. In Japan, snakes are popular exotic pet animals that are imported from overseas, but the degree of Sarcocystis infection in them remains unclear. The possibility exists that muscular sarcocystosis by S. nesbitti occurs in contact with captive snakes in non-endemic countries. For a total of 125 snake faecal samples from 67 snake species collected at animal hospitals, pet shops and a zoo, this study investigated the presence of Sarcocystis using polymerase chain reaction (PCR) for the 18S ribosomal RNA gene (18S rDNA). Four (3.2%) faecal samples were positive by PCR. Phylogenetic analysis of the 18S rDNA sequences obtained from four amplification products revealed one isolate from a beauty snake (Elaphe taeniura), Sarcocystis zuoi, which uses rat snakes as the definitive host. The isolate from a Macklot's python (Liasis mackloti) was closely related with unidentified Sarcocystis sp. from reticulated pythons in Malaysia. The remaining two isolates from tree boas (Corallus spp.) were closely related with Sarcocystis lacertae, Sarcocystis gallotiae and unidentified Sarcocystis sp. from smooth snakes, Tenerife lizards and European shrews, respectively. This report is the first of a study examining the distribution of Sarcocystis species in captive snakes in Japan.

  19. Molecular characterisation of three regions of the nuclear ribosomal DNA unit and the mitochondrial cox1 gene of Sarcocystis fusiformis from water buffaloes (Bubalus bubalis) in Egypt.

    Science.gov (United States)

    Gjerde, Bjørn; Hilali, Mosaad; Mawgood, Sahar Abdel

    2015-09-01

    A total of 33 macroscopically visible (3-11 × 1-5 mm) sarcocysts of Sarcocystis fusiformis were excised from the oesophagus of 12 freshly slaughtered water buffalos in Giza, Egypt. Genomic DNA was extracted from the sarcocysts, and all isolates were characterised at the mitochondrial cytochrome c oxidase subunit I (cox1) gene through PCR amplification and direct sequencing, whereas a few selected isolates were characterised at the 18S and 28S ribosomal (r) RNA genes and the internal transcribed spacer 1 (ITS1) region of the nuclear rDNA unit following cloning. Among the 33 cox1 sequences (1,038-bp long), there was a total of 13 haplotypes, differing from each other by one to seven substitutions and sharing an identity of 99.3-99.9 %. In comparison, the sequence identity was 98.8-99.0 % among eight complete 18S rRNA gene sequences (1,873-1,879-bp long), 98.1-100 % among 28 complete ITS1 sequences (853-864-bp long) and 97.4-99.6 % among five partial 28S rRNA gene sequences (1,607-1,622 bp). At the three nuclear loci, the intraspecific (and intra-isolate) sequence variation was due to both substitutions and indels, which necessitated cloning of the PCR products before sequencing. Some additional clones of the 18S and 28S rRNA genes were highly divergent from the more typical clones, but the true nature of these aberrant clones could not be determined. Sequence comparisons and phylogenetic analyses based on either 18S rRNA gene or cox1 nucleotide sequences, placed S. fusiformis closest to Sarcocystis cafferi from the African buffalo, but only the analyses based on cox1 data separated the two taxa clearly from each other and showed that they were separate species (monophyletic clusters and 93 % sequence identity at cox1 versus interleaved sequences and 98.7-99.1 % sequence identity at the 18S rRNA gene). Two cats experimentally infected with sarcocysts of S. fusiformis started shedding small numbers of sporocysts 8-10 days post-infection (dpi) and were euthanized 15

  20. LAS NEURONAS DEL SEPTUM LATERAL MODIFICAN LA ACTIVIDAD DE LAS NEURONAS DEL NUCLEO TUBEROMAMILAR DEL HIPOTALAMO

    OpenAIRE

    2012-01-01

    El septum lateral (SL), es un núcleo del cerebro anterior, que, procesa la información sensorial afectiva procedente del hipocampo y dirige sus respuestas, importantes para la supervivencia, hacia las zonas del hipotálamo importantes para la motivación, como lo es el núcleo tuberomamilar del hipotálamo (TMN). El TMN contiene las neuronas histaminérgicas en el cerebro, la cual relacionamos con la vigilia y alerta en conductas motivadas y así puede dirigir y reforzar el comportamiento. El TM...

  1. ACOPLAMIENTO EXCITATORIO E INHIBITORIO DE NEURONAS PULSANTES ACOPLADAS

    Directory of Open Access Journals (Sweden)

    Francis Armando Segovia Chaves

    2012-05-01

    Full Text Available La información es representada como patrones de actividad neuronal o pulsos, lo que crea una diferencia significante entre las redes neuronales pulsantes y las redes neuronales clásicas. Una característica diferente de las redes neuronales pulsantes es que la información es codificada en patrones de actividad neuronal y estas se comunican usando trenes de pulsos en lugar de valores individuales. Además, este tipo de redes neuronales pulsantes trabajan con una gran cantidad de neuronas donde se requiere grandes recursos computacionales para ser simuladas. En el presente trabajo se realiza un análisis teórico de las redes neuronales pulsantes,  para el caso de dos neuronas acopladas. Se logra obtener teóricamente las condiciones para acoplamiento excitatorio e inhibitorio en las neuronas.

  2. Molecular differentiation of Sarcocystis buffalonis and Sarcocystis levinei in water buffaloes (Bubalus bubalis) from Sarcocystis hirsuta and Sarcocystis cruzi in cattle (Bos taurus).

    Science.gov (United States)

    Gjerde, Bjørn; Hilali, Mosaad; Abbas, Ibrahim E

    2016-06-01

    The purpose of the present study was to obtain sarcocysts of Sarcocystis buffalonis and Sarcocystis levinei from water buffaloes and characterize the isolates by molecular methods in order to determine whether the two species were genetically different from Sarcocystis hirsuta and Sarcocystis cruzi, respectively, from cattle, which had been characterized before. About 35 macroscopically visible (3-4 × 1-2 mm) and 20 barely visible (1-3 × 0.2 mm) sarcocysts were excised from the esophagus of 18 naturally infected and freshly slaughtered adult water buffaloes at three slaughterhouses in Egypt. Genomic DNA was extracted from the sarcocysts, and all isolates were first characterized at the mitochondrial cytochrome c oxidase subunit I gene (cox1) gene through PCR amplification and direct sequencing. Selected isolates were subsequently further characterized at the 18S and 28S ribosomal (r) RNA genes and the internal transcribed spacer 1 (ITS1) region of the nuclear rDNA unit by direct sequencing or cloning. Only six of the isolated macroscopic sarcocysts belonged to S. buffalonis, whereas the others belonged to Sarcocystis fusiformis. Twelve of the smaller cysts belonged to S. levinei and seven to Sarcocystis sinensis. The characterization of the sarcocysts of S. sinensis and some of the sarcocysts of S. fusiformis have been reported before. Fifteen additional sarcocyst isolates of S. fusiformis were characterized at cox1 in the present study and found to be identical or closely similar to previous isolates. At cox1, the sequence identity between the six isolates of S. buffalonis was 99.8-100 % (two haplotypes), whereas the identity between the 12 isolates of S. levinei was 99.0-100 % (10 haplotypes). The identity between cox1 sequences of S. buffalonis and S. hirsuta (n = 56) was 92.9-93.6 % (on average 93.4 %), and the identity between cox1 sequences of S. levinei and S. cruzi (n = 22) was 92.9-94.0 % (on average 93.5 %). The phylogenetic

  3. Estructura electrotónica de neuronas motoras de sanguijuela

    OpenAIRE

    2011-01-01

    Las neuronas son células con estructuras tridimensionales complejas adaptadas a su función. Poseen extensos árboles neuríticos, en los que pueden recibir señales de otras neuronas en distintos puntos de su estructura. Las neuritas funcionan como cables, cuyas propiedades morfológicas y las propiedades eléctricas de la membrana determinan cómo se propagarán las señales. Los registros electrofisiológicos intracelulares nos permiten conocer con gran precisión la evolución en el tiempo del potenc...

  4. Cytokines and mother sporocysts in susceptible and resistant Bulinus truncatus snails infected with Schistosoma haematobium.

    Science.gov (United States)

    El-Din, Abdel Hakim Saad; Gawish, Fathiya Ali; Abu El Einin, Hanaa Mohamed; Mansour, Shereen Mahfouz

    2014-08-01

    The presence of immunoreactive interleukin (IL-2), interferon gamma (IFN-γ) and tumor necrosis factor alpha (TNF-α) in addition to the citation of mother sporscytes in cephalopodal musculature in the susceptible and resistance Bulinus truncatus the specific intermediate host for the trematode Schistosoma haematobium were investigated,. Using ELISA tests, Results indicated that the concentration of IL-2-like activity in the susceptible and resistant snails decreased significantly after infection then persisted at low levels until the 4th week post exposure (WPE) in susceptible snails, while in resistant snails elevated during the second WPE, and returned to initial level at 3 and 4 WPE. Susceptible snails had low detectable levels of TNF-α and INF-γ like-activity after infection. However, the resistant snails had significant low levels of TNF-α and INF-γ like-activity from 3 WPE until the 4th WPE without any sign of normalization. Histological sections in the head- foot region of susceptible and resistance B. truncatus infected with S. haematobium, mother sporocysts exists from 1 to 7(day post exposure) DPE, in the susceptible snail the mother sporocysts were found as single, multiple and mature types. No mother sporocysts were appear in the lip and mantle of the snail on 2, 5, 7 DPE and on 1-3, 6 DPE respectively. In the resistant snails few mother sporocysts were found in the lip, mantle and tentacles. The results showed that schistosome-resistant Bulinus can be an alternative strategy for the control of schistosomiasis.

  5. [Clonal and population RAPD variation of cercariae obtained from Bucephalus polymorphus sporocysts (Trematoda: Bucephalidae)].

    Science.gov (United States)

    Korsunenko, A V; Tiutin, A V; Semenova, S K

    2009-01-01

    Three arbitrary primers produced 114 RAPD markers for 37 cercariae from nine Bucephalus polymorphus sporocysts obtained from three Dreissena polymorpha mollusks, which were collected in two water reservoirs of the Volga basin. Analysis of the RAPD patterns established a unique genotype for each cercaria. The topology of an UPGMA dendrogram did not reliably differentiate the cercaria according to the corresponding sporocysts. However, three groups of genotypes were isolated and corresponded to the host mollusks, indicating that each cercaria clone had a different genotype set. A within-sporocyst variation made the greatest contribution (53.0%) to the total RAPD diversity, while the contributions of within-host and between-host variations to the total diversity were equal (23.5%). Cercariae isolated from two mollusks of the Rybinsk Water Reservoir were more similar to each other than to cercariae from the geographically distant Gor'kovskoe Water Reservoir. Possible causes and distribution specifics of the observed genetic diversity of B. polymorphus are discussed.

  6. Interaction between primary and secondary sporocysts of Schistosoma mansoni and the internal defence system of Biomphalaria resistant and susceptible to the parasite

    Directory of Open Access Journals (Sweden)

    Ana Carolina Alves de Mattos

    2011-06-01

    Full Text Available The outcome of the interaction between Biomphalaria and Schistosoma mansoni depends on the response of the host internal defence system (IDS and the escape mechanisms of the parasite. The aim of this study was to evaluate the responsiveness of the IDS (haemocytes and soluble haemolymph factors of resistant and susceptible Biomphalaria tenagophila lineages and Biomphalaria glabrata lineages in the presence of in vitro-transformed primary sporocysts and secondary sporocysts obtained from infected B. glabrata. To do this, we assayed the cellular adhesion index (CAI, analysed viability/mortality, used fluorescent markers to evaluate the tegumental damage and transplanted secondary sporocysts. B. tenagophila Taim was more effective against primary and secondary sporocystes than the susceptible lineage and B. glabrata. Compared with secondary sporocysts exposed to B. tenagophila, primary sporocysts showed a higher CAI, a greater percentage of dead sporocysts and were labelled by lectin from Glycine max and Alexa-Fluor 488 fluorescent probes at a higher rate than the secondary sporocysts. However, the two B. tenagophila lineages showed no cercarial shedding after inoculation with secondary sporocysts. Our hypothesis that secondary sporocysts can escape the B. tenagophila IDS cannot be confirmed by the transplantation experiments. These data suggest that there are additional mechanisms involved in the lower susceptibilty of B. tenagophila to S. mansoni infection.

  7. Ultrastructure of Sarcocystis bertrami sarcocysts from naturally infected donkey (Equus asinus) from Egypt

    Science.gov (United States)

    There is considerable confusion concerning Sarcocystis species in equids. Little is known of Sarcocystis infections in donkeys (Equus asinus). Here we describe the structure of Sarcocystis bertrami-like from the donkey by light and transmission electron microscopy (LM, TEM). Nineteen sarcocysts fro...

  8. Modelos de neuronas artificiales en software para su uso en preparaciones de electrofisiología

    OpenAIRE

    2016-01-01

    Este proyecto tiene por objetivo la implementación y validación online o en tiempo real de circuitos híbridos compuestos por neuronas vivas de sistemas biológicos y neuronas electrónicas implementadas en software. En estos circuitos híbridos las neuronas vivas y las neuronas artificiales interactúan bidireccionalmente a través de sinapsis artificiales. El desarrollo de estos circuitos híbridos es de gran interés en el contexto de la investigación en neurociencia ya que permiten...

  9. Modelos de neuronas artificiales en software para su uso en preparaciones de electrofisiología

    OpenAIRE

    Cubillos Martínez, Jenniffer

    2016-01-01

    Este proyecto tiene por objetivo la implementación y validación online o en tiempo real de circuitos híbridos compuestos por neuronas vivas de sistemas biológicos y neuronas electrónicas implementadas en software. En estos circuitos híbridos las neuronas vivas y las neuronas artificiales interactúan bidireccionalmente a través de sinapsis artificiales. El desarrollo de estos circuitos híbridos es de gran interés en el contexto de la investigación en neurociencia ya que permiten...

  10. Field prevalence and laboratory susceptibility of southern Australian land snails to Brachylaima cribbi sporocyst infection

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    Butcher A.R.

    2003-06-01

    Full Text Available Brachylaima cribbi is a terrestrial trematode of birds and mammals with helic id and hygromild land snails reported as first and second Intermediate hosts. However, reports describing the first Intermediate host range of B. cribbi have been limited to those snail species present In a small number of geographical locations In South Australia. The natural first Intermediate host range, distribution and prevalence of B. cribbi In land snails In southern Australia were determined. A total of 6,432 introduced and native land snails were collected from eight geographical districts across 3,000 km of southern Australia and examined microscopically for B. cribbi sporocysts. Four Introduced European snails, Theba pisana, Cernuella virgata, Cochlicella acuta and Cochlicella barbara were natural first Intermediate hosts. Sporocyst-infected snails were detected In all districts from Victoria to the west coast of South Australia, a distance of over 1,300 km. Natural sporocyst infection was not observed in introduced European snails Microxeromagna armillata and Helix aspersa or In native Australian land snails Succinea australis and Strangesta gawleri. Egg feeding experiments in the laboratory with B. cribbi confirmed the susceptibility of those species of snails found to be natural first intermediate hosts. Of those species not found to be Infected In nature, only M. armillata could be Infected In the laboratory. Although this study has shown that five different species of European land snails are suitable first Intermediate hosts for B. cribbi there are as yet no reports of B. cribbi from these snails In Europe or from other countries where they have been introduced. Further Investigations are needed in Europe to clarify the origins of this parasite.

  11. Role of the endogenous antioxidant system in the protection of Schistosoma mansoni primary sporocysts against exogenous oxidative stress.

    Science.gov (United States)

    Mourão, Marina de Moraes; Dinguirard, Nathalie; Franco, Glória R; Yoshino, Timothy P

    2009-11-17

    Antioxidants produced by the parasite Schistosoma mansoni are believed to be involved in the maintenance of cellular redox balance, thus contributing to larval survival in their intermediate snail host, Biomphalaria glabrata. Here, we focused on specific antioxidant enzymes, including glutathione-S-transferases 26 and 28 (GST26 and 28), glutathione peroxidase (GPx), peroxiredoxin 1 and 2 (Prx1 and 2) and Cu/Zn superoxide dismutase (SOD), known to be involved in cellular redox reactions, in an attempt to evaluate their endogenous antioxidant function in the early-developing primary sporocyst stage of S. mansoni. Previously we demonstrated a specific and consistent RNA interference (RNAi)-mediated knockdown of GST26 and 28, Prx1 and 2, and GPx transcripts, and an unexpected elevation of SOD transcripts in sporocysts treated with gene-specific double-stranded (ds)RNA. In the present followup study, in vitro transforming sporocysts were exposed to dsRNAs for GST26 and 28, combined Prx1/2, GPx, SOD or green-fluorescent protein (GFP, control) for 7 days in culture, followed by assessment of the effects of specific dsRNA treatments on protein levels using semi-quantitative Western blot analysis (GST26, Prx1/2 only), and larval susceptibility to exogenous oxidative stress in in vitro killing assays. Significant decreases (80% and 50%) in immunoreactive GST26 and Prx1/2, respectively, were observed in sporocysts treated with specific dsRNA, compared to control larvae treated with GFP dsRNA. Sporocysts cultured with dsRNAs for GST26, GST28, Prx1/2 and GPx, but not SOD dsRNA, were significantly increased in their susceptibility to H(2)O(2) oxidative stress (60-80% mortalities at 48 hr) compared to GFP dsRNA controls ( approximately 18% mortality). H(2)O(2)-mediated killing was abrogated by bovine catalase, further supporting a protective role for endogenous sporocyst antioxidants. Finally, in vitro killing of S. mansoni sporocysts by hemocytes of susceptible NMRI B. glabrata

  12. Parasite distribution and early-stage encephalitis in Sarcocystis calchasi infections in domestic pigeons (Columba livia f. domestica).

    Science.gov (United States)

    Maier, Kristina; Olias, Philipp; Enderlein, Dirk; Klopfleisch, Robert; Mayr, Sylvia L; Gruber, Achim D; Lierz, Michael

    2015-01-01

    Pigeon protozoal encephalitis is a biphasic, neurologic disease of domestic pigeons (Columba livia f. domestica) caused by the apicomplexan parasite Sarcocystis calchasi. Despite severe inflammatory lesions of the brain, associated parasitic stages have only rarely been identified and the cause of the lesions is still unclear. The aim of this study was therefore to characterize the tissue distribution of S. calchasi within pigeons between the two clinical phases and during the occurrence of neurological signs. For this purpose, a semi-quantitative real-time polymerase chain reaction (PCR) was developed. Forty-five domestic pigeons were infected orally (via a cannula into the crop) with 200 S. calchasi sporocysts and euthanized in groups of three pigeons at intervals of 2 to 10 days over a period of 61 days. Tissue samples including brain and skeletal muscle were examined by histology, immunohistochemistry, and PCR. Schizonts were detected in the liver of one pigeon at day 10 post infection. A mild encephalitis was detected at day 20 post infection, around 4 weeks before the onset of neurological signs. At the same time, immature sarcocysts were present in the skeletal muscle. In seven pigeons a few sarcocysts were identified in the brain, but not associated with any lesion. These results suggest that the encephalitis is induced at a very early stage of the S. calchasi lifecycle rather than in the chronic phase of pigeon protozoal encephalitis. Despite the increasing severity of lesions in the central nervous system, the amount of sarcocysts did not increase. This supports the hypothesis of a delayed-type hypersensitivity response as the cause of the encephalitis. The study also demonstrated that S. calchasi DNA is detectable in tissues negative by histological methods, indicating a higher sensitivity of the real-time PCR.

  13. Survey on Sarcocystis in bovine carcasses slaughtered at the municipal abattoir of El-Kharga, Egypt

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    Ali Meawad Ahmed

    2016-12-01

    Full Text Available Aim: The main objectives of this study were to determine the incidence of Sarcocystis sp. infection in cattle and buffalo carcasses slaughtered at El-Kharga abattoir, New Valley Governorate, Egypt. Materials and Methods: The slaughtered animals were daily inspected for Sarcocystis macrocysts through a year (2015. Macroscopic Sarcocystis was detected from a total of 2120 cattle and buffalo carcasses. In addition, 100 meat samples were collected from female cattle and buffalo (50 each and were examined microscopically for sarcocystosis. Results: The overall incidence of Sarcocystis macrocyst among bovine carcasses was 159/2120 (7.5%. Total incidence in cattle was 149/2000 (7.45%, whereas it was 10/120 (8.33% in buffalo carcasses. Concerning gender, the overall prevalence of Sarcocystis infection was 127/1790 (7.09% in male and 32/330 (9.69% in females bovine carcasses. The highest detection rate of Sarcocystis lesions was from the esophagus (76.3% followed by throat muscles (35.3%, tongue (33.8%, and diaphragm muscles (18.71%. Macrocysts from cattle were identified to Sarcocystis hirsuta, whereas Sarcocystis fusiformis was identified from buffalo carcasses. By microscopic examination, 18 (36% of 50 female cattle carcasses harbor Sarcocystis sp., whereas 11 (22% of buffalo carcasses were harbored Sarcocystis microcysts. Conclusion: A high incidence of Sarcocystis infection was detected among slaughtered bovines in El-Kharga abattoir, Egypt. Sarcocystis macrocysts were a higher incidence in female elder animals macrocysts were identified to S. hirsuta in cattle and S. fusiformis in buffaloes. Sarcocystosis constitute a major cause of economic losses at El-Kharga abattoir. Beef meat may carry health risks to consumers.

  14. Hemiuroid trematode sporocysts are undetected by hemocytes of their intermediate host, the ark cockle Anadara trapezia: potential role of surface carbohydrates in successful parasitism.

    Science.gov (United States)

    Kawasaki, Minami; Delamare-Deboutteville, Jerome; Dang, Cecile; Barnes, Andrew C

    2013-12-01

    In order to establish a successful relationship with their hosts, parasites must subvert or evade immune defences. Cockle Anadara trapezia and Sydney Rock oyster (SRO) Saccostrea glomerata live in the same location but only ark cockles are infected by sporocysts of hemiuroid trematode. This provides an opportunity to explore differing interactions between the parasite and the immune system of susceptible and refractive hosts. Rapid migration and encapsulation of sporocysts was observed by SRO hemocytes but not by cockle hemocytes. This migration/encapsulation was inhibited by N-acetylglucosamine or N-acetylgalactosamine but not by the other sugars, implicating specific surface carbohydrates in immune detection. Effector responses of hemocytes were investigated in vitro in terms of production of reactive oxygen production (ROS). Hemocytes of both species strongly reacted to Zymosan, but only SRO hemocytes responded to live sporocysts. Neither species' hemocytes produced ROS in the presence of dead/fixed sporocysts, and there was no suppression of Zymosan-induced respiratory burst by sporocysts. This suggests that immune escape is mediated by avoiding encapsulation, perhaps through molecular mimicry. Membrane-shaving with proteases indicated that sporocyst surface proteins are not a key factors in hemocytic detection. Surface carbohydrates of SRO and cockle hemocytes and of sporocysts were profiled with a panel of biotinylated lectins. This revealed substantial differences between cockle and SRO hemocytes, but greater similarity between cockle hemocytes and sporocysts. Results suggest that surface carbohydrates play an integral role in hemocyte immunorecognition and that surface carbohydrate molecular mimicry is a potential strategy for immune evasion in cockles by hemiuroid trematode sporocysts.

  15. NEURONAS ESPEJO Y EL APRENDIZAJE EN ANESTESIA Learning anaesthesia and mirror neurons

    OpenAIRE

    John Bautista; José R Navarro

    2011-01-01

    Las neuronas espejo fueron descritas inicialmente en primates de la especie Macaca nemestrina hacia el año 1990 por el neurofisiólogo Giacomo Rizzolatti y su grupo de la Universidad de Parma, en Italia. Son neuronas motoras que activan cuando el individuo observa la acción concreta para la que están predeterminadas sin generar ningún tipo de actividad motora. En la actualidad se considera que estas neuronas participan en procesos de adaptación al entorno social ya que permiten no solamente co...

  16. Morphological and molecular characteristics of four Sarcocystis spp. in Canadian moose (Alces alces), including Sarcocystis taeniata n. sp.

    Science.gov (United States)

    Gjerde, Bjørn

    2014-04-01

    Individual sarcocysts were isolated from fresh or alcohol-fixed muscle samples of two moose from Alberta, Canada, and examined by light (LM) and scanning electron microscopy (SEM) and molecular methods, comprising polymerase chain reaction (PCR) amplification and sequencing of the complete18S rRNA gene and the partial cytochrome c oxidase subunit I gene (cox1). By LM, four sarcocyst types were recognized, and the sequencing results showed that each type represented a distinct species, i.e. Sarcocystis alces, Sarcocystis alceslatrans, Sarcocystis ovalis and Sarcocystis taeniata n. sp. The finding of S. alceslatrans and S. ovalis has been reported briefly previously, but further details are provided here, including the ultrastructure of sarcoysts of S. alceslatrans as seen by SEM. The species S. alces was found for the first time in Canadian moose, whereas the finding of S. taeniata is the first record of this species in any host. The sarcocysts of S. taeniata were sac-like and about 1,000-1,100 × 60-80 μm in size. By LM, the cysts had a thin and smooth wall with no visible protrusions, whereas SEM revealed that the cyst surface had sparsely but regularly distributed, thin ribbon-like protrusions, about 2 μm long and 0.2 μm wide, lying flat against the surface and leaving most of the cyst surface naked. Similar protrusions have previously been reported from Sarcocystis grueneri in reindeer, which was found by sequence comparisons and phylogenetic analyses to be the species most closely related to S. taeniata. The phylogenetic analyses further suggested that S. taeniata, like S. alces and S. alceslatrans, use canids as definitive hosts, whereas corvid birds are known definitive hosts for S. ovalis. In contrast to the three other species found, S. taeniata displayed considerable intra-specific and intra-isolate sequence variation (substitutions, insertions/deletions) in certain regions of the 18S rRNA gene.

  17. Molecular characterization of Sarcocystis species from Polish roe deer based on ssu rRNA and cox1 sequence analysis.

    Science.gov (United States)

    Kolenda, Rafał; Ugorski, Maciej; Bednarski, Michał

    2014-08-01

    Sarcocysts from four Polish roe deer were collected and examined by light microscopy, small subunit ribosomal RNA (ssu rRNA), and the subunit I of cytochrome oxidase (cox1) sequence analysis. This resulted in identification of Sarcocystis gracilis, Sarcocystis oviformis, and Sarcocystis silva. However, we were unable to detect Sarcocystis capreolicanis, the fourth Sarcocystis species found previously in Norwegian roe deer. Polish sarcocysts isolated from various tissues differed in terms of their shape and size and were larger than the respective Norwegian isolates. Analysis of ssu rRNA gene revealed the lack of differences between Sarcocystis isolates belonging to one species and a very low degree of genetic diversity between Polish and Norwegian sarcocysts, ranging from 0.1% for Sarcocystis gracilis and Sarcocystis oviformis to 0.44% for Sarcocystis silva. Contrary to the results of the ssu rRNA analysis, small intraspecies differences in cox1 sequences were found among Polish Sarcocystis gracilis and Sarcocystis silva isolates. The comparison of Polish and Norwegian cox1 sequences representing the same Sarcocystis species revealed similar degree of sequence identity, namely 99.72% for Sarcocystis gracilis, 98.76% for Sarcocystis silva, and 99.85% for Sarcocystis oviformis. Phylogenetic reconstruction and genetic population analyses showed an unexpected high degree of identity between Polish and Norwegian isolates. Moreover, cox1 gene sequences turned out to be more accurate than ssu rRNA when used to reveal phylogenetic relationships among closely related species. The results of our study revealed that the same Sarcocystis species isolated from the same hosts living in different geographic regions show a very high level of genetic similarity.

  18. Sarcocystis in moose (Alces alces): molecular identification and phylogeny of six Sarcocystis species in moose, and a morphological description of three new species.

    Science.gov (United States)

    Dahlgren, Stina S; Gjerde, Bjørn

    2008-06-01

    Muscle tissues from 34 moose from Southeastern Norway and two moose from Canada were examined. Sarcocysts were excised and morphologically classified by light microscopy, and some cysts were further examined by scanning electron microscopy or DNA amplification and sequencing at the small subunit (ssu) rRNA gene. In Norwegian moose, three sarcocyst types were recognized, yet five Sarcocystis species were found by sequence analysis. New names were proposed for three species which could be characterised by both morphological and molecular methods, i.e., Sarcocystis alces, Sarcocystis ovalis, and Sarcocystis scandinavica. S. alces was the most prevalent species, whereas S. scandinavica and the two unnamed species were rare and might either use another principal intermediate host or a rare definitive host. The five species in Norwegian moose were different from Sarcocystis alceslatrans isolated from a Canadian moose. Phylogenetic analyses based on complete ssu rRNA gene sequences revealed a close relationship between the six Sarcocystis species from moose and species from reindeer and Sika deer. We conclude that molecular methods are necessary for unequivocal species identification, as different cervid hosts harbour morphologically indistinguishable sarcocysts.

  19. Prevalence, morphology, and molecular characteristics of Sarcocystis spp. in domestic goats (Capra hircus) from Kunming, China.

    Science.gov (United States)

    Hu, Jun-Jie; Liu, Ting-Ting; Liu, Qiong; Esch, G W; Chen, Jin-Qing; Huang, Si; Wen, Tao

    2016-10-01

    Despite the importance of worldwide goat production, little is known about the prevalence of Sarcocystis spp. in domestic goats (Capra hircus) in China. The aims of the present study were to determine prevalence of Sarcocystis spp. in domestic goats in Kunming, China, as well as to identify parasite species based on morphological characteristics and DNA sequence analysis. Only microscopic sarcocysts of Sarcocystis spp. were detected in 174 of 225 goats (77.3 %). By light and transmission electron microscopy, two species, i.e., Sarcocystis capracanis and Sarcocystis hircicanis, were identified. Two sarcocysts from each of the two species were randomly selected for DNA extraction; the 18S rRNA gene (18S rRNA), the 28S rRNA gene (28S rRNA), and the mitochondrial cytochrome c oxidase subunit 1 (cox1) were amplified by the polymerase chain reaction (PCR) and subsequently sequenced. The results were compared with other previously sequenced Sarcocystis species retrieved from GenBank. There was little sequence variation between two isolates of the same species. S. capracanis was most closely related with Sarcocystis tenella; 18S rRNA, 28S rRNA, and mitochondrial cox1 sequences shared identities of 95.7-99.1, 95.3, and 92.3-93.2 % with those of S. tenella, respectively. Thus, mitochondrial cox1 sequences seem to perform better than 18S rRNA sequences or 28S rRNA sequences for identification of the two species. S. hircicanis was most closely related to Sarcocystis arieticanis, i.e., 18S rRNA and 28S rRNA sequences of the former species shared 97.2-97.4 and 95.6-96.1 % identities with those of latter, respectively. Phylogenetic analysis inferred from the three genetic markers yielded similar results and indicated the two species were within a group of Sarcocystis species with canines as known, or presumed, definitive hosts.

  20. El sistema de neuronas espejo y el procesamiento facial de las emociones: El caso del miedo

    Directory of Open Access Journals (Sweden)

    Aníbal Monasterio Astobiza

    2013-08-01

    Full Text Available Desde su descubrimiento en la corteza ventral premotora, área F5, del cerebro del macaco, las neuronas espejo se han convertido en el santo grial de la neurociencia sirviendo de base neurofisiológica para la empatía, imitación, entendimiento de las acciones e intenciones, lenguaje... Estudios recientes sugieren que el sistema de neuronas espejo contribuye también a procesar información emocional, pero niegan que la amígdala, región por excelencia responsable de procesar cierto tipo de emociones, sea parte de tal sistema. Parece ser que el sistema de neuronas espejo se reorganiza funcionalmente para compensar daños en la amígdala en algunos pacientes.

  1. Fenotipo celular de las neuronas sensitivas afectadas en la ataxia de Friedreich

    OpenAIRE

    Mollá Moliner, Belén

    2016-01-01

    La FRDA es una enfermedad caracterizada por la afectación primaria del ganglio dorsal. La falta de frataxina no afecta por igual a todos los tipos neuronales del ganglio dorsal, siendo las neuronas propioceptivas las más dañadas. Esto nos lleva a cuestionarnos porque este tipo neuronal es más sensible a una deficiencia de frataxina. Esta tesis doctoral se ha centrado en la investigación de la biología celular de frataxina en neuronas sensitivas del ganglio dorsal y las consecuencias fisiop...

  2. El sistema de neuronas espejo y el procesamiento facial de las emociones: El caso del miedo

    OpenAIRE

    Aníbal Monasterio Astobiza; Jesús Ezquerro Martínez

    2013-01-01

    Desde su descubrimiento en la corteza ventral premotora, área F5, del cerebro del macaco, las neuronas espejo se han convertido en el santo grial de la neurociencia sirviendo de base neurofisiológica para la empatía, imitación, entendimiento de las acciones e intenciones, lenguaje... Estudios recientes sugieren que el sistema de neuronas espejo contribuye también a procesar información emocional, pero niegan que la amígdala, región por excelencia responsable de procesar cierto tipo de emocion...

  3. Modelado de un Sistema de Neuronas Espejo en un Agente Autónomo Artificial

    OpenAIRE

    David Castillo Arceo; Esaú Escobar; Jorge Hermosillo; Bruno Lara

    2013-01-01

    La presente investigación está basada en el importante trabajo interdisciplinario desarrollándose en las ciencias cognitivas y que estudia tópicos tales como Neuronas Espejo, Reconocimiento de Comportamientos, Imit a ción, y Robótica Cognitiva. Abordando una perspectiva anclada en la Teoría de la Simulación y basado en modelos computacionales sobre Sistemas de Neuronas Espejo se ha diseñado un sistema, implemen tado en un Agente Autónomo Artificial. Dicho sistema d...

  4. El sistema de neuronas espejo y el procesamiento facial de las emociones: El caso del miedo

    OpenAIRE

    Aníbal Monasterio Astobiza; Jesús Ezquerro Martínez

    2013-01-01

    Desde su descubrimiento en la corteza ventral premotora, área F5, del cerebro del macaco, las neuronas espejo se han convertido en el santo grial de la neurociencia sirviendo de base neurofisiológica para la empatía, imitación, entendimiento de las acciones e intenciones, lenguaje... Estudios recientes sugieren que el sistema de neuronas espejo contribuye también a procesar información emocional, pero niegan que la amígdala, región por excelencia responsable de procesar cierto tipo de emocion...

  5. Sarcocystis fayeri in skeletal muscle of horses with neuromuscular disease.

    Science.gov (United States)

    Aleman, Monica; Shapiro, Karen; Sisó, Silvia; Williams, Diane C; Rejmanek, Daniel; Aguilar, Beatriz; Conrad, Patricia A

    2016-01-01

    Recent reports of Sarcocystis fayeri-induced toxicity in people consuming horse meat warrant investigation on the prevalence and molecular characterization of Sarcocystis spp. infection in horses. Sarcocysts in skeletal muscle of horses have been commonly regarded as an incidental finding. In this study, we investigated the prevalence of sarcocysts in skeletal muscle of horses with neuromuscular disease. Our findings indicated that S. fayeri infection was common in young mature horses with neuromuscular disease and could be associated with myopathic and neurogenic processes. The number of infected muscles and number of sarcocysts per muscle were significantly higher in diseased than in control horses. S. fayeri was predominantly found in low oxidative highly glycolytic myofibers. This pathogen had a high glycolytic metabolism. Common clinical signs of disease included muscle atrophy, weakness with or without apparent muscle pain, gait deficits, and dysphagia in horses with involvement of the tongue and esophagus. Horses with myositis were lethargic, apparently painful, stiff, and reluctant to move. Similar to humans, sarcocystosis and cardiomyopathy can occur in horses. This study did not establish causality but supported a possible association (8.9% of cases) with disease. The assumption of Sarcocysts spp. being an incidental finding in every case might be inaccurate.

  6. Comparison of rDNA sequences from colchicine treated and untreated sporocysts of Phyllodistomum folium and Bucephalus polymorphus (Digenea).

    Science.gov (United States)

    Stunzenas, Virmantas; Cryan, Jason R; Molloy, Daniel P

    2004-09-01

    The most frequently used antimitotic agent in cytogenetic studies is colchicine. We investigated whether the initial treatment of trematodes for karyological analysis with colchicine would have mutagenic or degradational effect on rDNA sequences. Dreissena polymorpha is the intermediate host of Phyllodistomum folium and Bucephalus polymorphus, and the sporocyst stage of these trematode species develop, respectively, in the gills and gonads of this mussel. Sporocysts of P. folium and B. polymorphus were obtained from D. polymorpha collected from waterbodies in Belarus and in Lithuania. 5.8S and 28S rDNA genes, ITS1 and ITS2 of P folium and B. polymorphus were sequenced and compared, and no nucleotide sequence differences between colchicine treated and untreated trematodes were found. Based on these results, we conclude that colchicine treatment for 3-5 h has no mutagenic or degradational effect on rDNA sequences. During the course of this investigation, two genetically different P. folium samples were noted in Belarus.

  7. First Molecular Identification of Sarcocystis ovicanis (Protozoa, Apicomplexa in the Brain of Sheep in Iran.

    Directory of Open Access Journals (Sweden)

    Mitra Salehi

    2014-06-01

    Full Text Available The objective of the present study was to survey the presence of Sarcocystis in sheep's brain in North Khorasan Province.In general, 80 samples of sheep's brain were collected from slaughtered sheep in slaughterhouses of North Khorasan Province. Tissue digestion method was used for observing bradyzoites in tissues. Histopathological processing tracing Sarcocystis and ensuing structural change in the brain tissue were conducted. PCR analysis was conducted on all the brain samples. Sequencing was done for one PCR product. Genotype was identified by Blast search and homology analysis.Sarcocystis spp. was found in one of the brain samples (1.25% using tissue digestion method. The presence of bradyzoite was also confirmed in the prepared histopathological sections. PCR analysis was positive in one of samples. Genotyping of one sample proved that Sarcocystis species was Sarcocystis ovicanis and the nucleotide sequence of this parasite was deposited in the GenBank database under accession number No.KF489431.Sarcocystis ovicanis can involve brain tissue of sheep and consequently causes clinical symptoms.

  8. El sistema de neuronas espejo y el procesamiento facial de las emociones: El caso del miedo

    National Research Council Canada - National Science Library

    Aníbal Monasterio Astobiza; Jesús Ezquerro Martínez

    2013-01-01

    Desde su descubrimiento en la corteza ventral premotora, área F5, del cerebro del macaco, las neuronas espejo se han convertido en el santo grial de la neurociencia sirviendo de base neurofisiológica para la empatía...

  9. COMPARTIMENTACIÓN INTRACELULAR DEL ACETATO EN NEURONAS DURANTE LA PRELACTANCIA

    Directory of Open Access Journals (Sweden)

    B. Barrios-Socha

    2006-06-01

    Full Text Available En la transición a la vida extrauterina, el recién nacido sufre un período de ayuno (prelactancia que transcurre entre el cese de la nutrición placentaria y la instauración de la lactancia. El gasto de energía por las neuronas es tan alto en estas circunstancias, que la glucogenólisis es incapaz de restablecer los niveles de glucosa en la sangre. En consecuencia, durante la prelactancia debe haber otros sustratos energéticos y lipogénicos, que adicionalmente ayuden a mantener la síntesis de neurotransmisores.Este trabajo establece la importancia de acetato en el metabolismo oxidativo y del lipogénico en neuronas durante la prelactancia. Se determinaron las velocidades de oxidación y lipogénesis en cultivos quiescentes de neuronas fetales de rata incubadas con acetato (5 mM, [1- 14C]-acetato, [2- 14C]-acetato y [U- 14C]-acetato(200-300dpm/nmol Adicionalmente, se utilizaron inhibidores enzimáticos como el dicloroacetato(1 mM y el aminooxiacetato (5 mM, e inhibidores del transporte como el α-ciano-4-hidroxicinnamato(2 mM, butilmalonato (5 mM y 1,2,3-bencenotricarboxilato (5 mM.Los resultados en su conjunto indican que las neuronas pueden metabolizar acetato más como sustrato energético que lipogénico, lo que nos permite pensar que este sustrato puede llegar a ser más importante para ayudar a mantener el metabolismo oxidativo, favoreciendo el reciclaje de carbonos en la prelactancia.Adicionalmente, se evidenció con el uso de [1-14C]-acetato una alta actividad anaplerótica sobre todo cuando las neuronas requieren mantener los reservorios de oxalacetato y acetil-CoA para mantener la respiración. Estos resultados señalan a la acetil-CoA sintetasa (AceCS2 y la enzima málica (mME mitocondriales, como enzimas claves para mantener el funcionamiento de las neuronas en la prelactancia.Con el uso de [2-14C]-acetato, los resultados sugieren que las neuronas tienen un alto requerimiento de carbonos, principalmente para la síntesis de

  10. Phylogenetic relationships between Sarcocystis species from reindeer and other Sarcocystidae deduced from ssu rRNA gene sequences

    DEFF Research Database (Denmark)

    Dahlgren, S.S.; Oliveira, Rodrigo Gouveia; Gjerde, B.

    2008-01-01

    were constructed using Bayesian analysis and maximum likelihood estimations. All six Sarcocystis species from reindeer were placed together with other Sarcocystis species using an even-toed ungulate as their intermediate host. The three canine transmitted species, S. grueneri, S. rangi, S...

  11. Sarcocystis masoni, n. sp. (Apicomplexa: Sarcocystidae), and redescription of Sarcocystis aucheniae from llama (Lama glama), guanaco (Lama guanicoe) and alpaca (Vicugna pacos).

    Science.gov (United States)

    Moré, Gastón; Regensburger, Cristian; Gos, M Laura; Pardini, Lais; Verma, Shiv K; Ctibor, Juliana; Serrano-Martínez, Marcos Enrique; Dubey, Jitender P; Venturini, M Cecilia

    2016-04-01

    There is considerable confusion concerning the species of Sarcocystis in South American camelids (SAC). Several species names have been used; however, proper descriptions are lacking. In the present paper, we redescribe the macroscopic sarcocyst forming Sarcocystis aucheniae and describe and propose a new name, Sarcocystis masoni for the microscopic sarcocyst forming species. Muscles samples were obtained from llamas (Lama glama) and guanacos (Lama guanicoe) from Argentina and from alpacas (Vicugna pacos) and llamas from Peru. Individual sarcocysts were processed by optical and electron microscopy, and molecular studies. Microscopic sarcocysts of S. masoni were up to 800 µm long and 35-95 µm wide, the sarcocyst wall was 2·5-3·5 µm thick, and had conical to cylindrical villar protrusions (vp) with several microtubules. Each vp had 11 or more rows of knob-like projections. Seven 18S rRNA gene sequences obtained from sarcocysts revealed 95-96% identity with other Sarcocystis spp. sequences reported in the GenBank. Sarcocysts of S. aucheniae were macroscopic, up to 1·2 cm long and surrounded by a dense and laminar 50 µm thick secondary cyst wall. The sarcocyst wall was up to 10 µm thick, and had branched vp, appearing like cauliflower. Comparison of the 11 sequences obtained from individual macroscopic cysts evidenced a 98-99% of sequence homology with other S. aucheniae sequences. In conclusion, 2 morphologically and molecularly different Sarcocystis species, S. masoni (microscopic cysts) and S. aucheniae (macroscopic cysts), were identified affecting different SAC from Argentina and Peru.

  12. Sarcocystis nesbitti Infection in Human Skeletal Muscle: Possible Transmission from Snakes

    Science.gov (United States)

    Lau, Yee Ling; Chang, Phooi Yee; Tan, Chong Tin; Fong, Mun Yik; Mahmud, Rohela; Wong, Kum Thong

    2014-01-01

    Sarcocystis nesbitti is an intracellular protozoan parasite found as sarcocysts within muscle fibers of intermediate hosts (monkey and baboon). The definitive host is suspected to be the snake. We report two cases from a larger cohort of 89 patients who had fever, headache, and generalized myalgia after a trip to Pangkor Island, Malaysia. Sarcocysts were detected in skeletal muscle biopsy specimens by light and electron microscopy from these two patients. DNA sequencing based on the 18S ribosomal DNA region identified the Sarcocystis species as S. nesbitti. We also identified S. nesbitti sequences in the stools of a snake (Naja naja). Phylogenetic analysis showed that these sequences form a cluster with most of the other known Sarcocystis species for which the snake is a definitive host. We believe these two patients were likely to have symptomatic acute muscular sarcocystosis after S. nesbitti infection that may have originated from snakes. PMID:24420776

  13. Sarcocystis cruzi (Apicomplexa: Sarcocystidae) no cachorro-do-mato (Cerdocyon thous)

    OpenAIRE

    Janaina S. Rodrigues; Gisele S. Meireles; Paulo R. Carvalho Filho; Ribeiro, Carlos T.; Flausino,Walter; Lopes,Carlos Wilson G.

    2008-01-01

    Esporocistos de Sarcocystis foram identificados nas amostras fecais de um cachorro-do-mato. Eles foram dados por via oral para um bezerro em aleitamento, sendo observados cistos com morfologia compatível com os de Sarcocystis cruzi na musculatura cardíaca e esquelética, três meses após a infecção. Musculatura cardíaca deste bezerro foi dada para um segundo cão doméstico livre de coccídios, que eliminou esporocistos compatíveis com os de Sarcocystis em suas fezes, tendo com períodos pré-patent...

  14. Sarcocystis canis n. sp. (Apicomplexa: Sarcocystidae), the etiologic agent of generalized coccidiosis in dogs.

    Science.gov (United States)

    Dubey, J P; Speer, C A

    1991-08-01

    Sarcocystis canis n. sp. is proposed for the protozoon associated with encephalitis, hepatitis, and generalized coccidiosis in dogs. Only asexual stages are known in macrophages, neurons, dermal, and other cells of the body. The parasite is located free in the host cell cytoplasm without a parasitophorous vacuole; schizonts divide by endopolygeny. Schizonts are 5-25 x 4-20 microns and contain 6-40 merozoites. Merozoites are approximately 5-7 microns x 1 micron and do not contain rhoptries. The parasite is PAS-negative and reacts with Sarcocystis cruzi antiserum but not with Toxoplasma gondii, Neospora caninum, or Caryospora bigenetica antisera in an immunohistochemical test.

  15. cromo (VI en cultivos primarios de neuronas y astrocitos de rata

    Directory of Open Access Journals (Sweden)

    V Uroz Martínez

    2008-01-01

    Full Text Available El presente estudio pretende comparar la concentración letal 50 (CL , dosis que causa la muerte del 50% de las células de 50 metilmercurio, cadmio (II y cromo (VI en cultivos primarios de corteza de rata. Se emplearon hemisferios cerebrales de rata para preparar los cultivos primarios. Los cultivos primarios de neuronas fueron realizados a partir de ratas Wistar de 14-16 días de gestación, usando el medio Eagle modificado por Dulbecco. Para los cultivos primarios de astrocitos se emplearon ratas de un día de vida y el medio de cultivo de Waymouth. Se emplearon las tinciones de azul de metileno y azul tripano para cuantificar la muerte neuronal mediante citometría. La CL para neuronas y astrocitos se calculó mediante el 50 método de Reed-Muench. En cultivos de 24 horas, la CL para las 50 -6 -6 neuronas fue de 5 x 10 M para el metilmercurio, 3,7 x 10 M para el -6 cadmio (II y 5,34 x 10 M para el cromo (VI. En el caso de los -5 astrocitos, las CL en los cultivos de 24 horas fue de 1,46 x 10 M para 50 -5 -5 el metilmercurio, 3,73 x 10 M para el cadmio (II y 2,46 x 10 M para el cromo (VI. Estos resultados muestran una resistencia diez veces mayor aproximadamente de los astrocitos con respecto a las neuronas para estos tres compuestos.

  16. Neuro3d: software de reconstrucción tridimensional de neuronas

    OpenAIRE

    1997-01-01

    Se describe un proyecto de cooperación interdisciplinaria para construir un sistema de reconstrucción tridimensional de neuronas a partir de cortes observados al microscopio electrónico. Se presentan brevemente las partes constitutivas del sistema: adquisición de las imágenes, apareamiento, visualización e interfaz gráfica. Se presentan algunos resultados obtenidos.

  17. Modelado de un Sistema de Neuronas Espejo en un Agente Autónomo Artificial

    Directory of Open Access Journals (Sweden)

    David Castillo Arceo

    2013-01-01

    Full Text Available La presente investigación está basada en el importante trabajo interdisciplinario desarrollándose en las ciencias cognitivas y que estudia tópicos tales como Neuronas Espejo, Reconocimiento de Comportamientos, Imit a ción, y Robótica Cognitiva. Abordando una perspectiva anclada en la Teoría de la Simulación y basado en modelos computacionales sobre Sistemas de Neuronas Espejo se ha diseñado un sistema, implemen tado en un Agente Autónomo Artificial. Dicho sistema deberá reconocer los movimientos de otro agente, basado en el aprendizaje de sus movimientos y las relaciones que surgen de éstos con la percepción del mundo. El diseño de este sistema se propone parta de dos supuestos: (1 El Sistemas de Neuronas Espejo visto como un acoplamiento de los Modelos Internos Inverso y Directo - siendo el segundo y su función de predictor lo que se hipotetiza es la función de las Neuronas Espejo - y (2 que la base para el re conocimiento de las conductas de otros está en la habilidad de los seres vivos de empatar en un lenguaje común las conductas propias, desarrolladas a lo largo de su experiencia, con las conductas ejercidas por otros. Presentamos un ejercicio donde nuestro Agente imita a otro para comprobar que el reconocimiento de las conductas de los otros es posible desde la perspectiva que se ha adoptado. Creemos que nuestro experimento es una prueba de concepto y presenta una base s ó lida para investigaciones futuras.

  18. Aborto ovino associado com infecção por Sarcocystis sp Ovine abortion associated with Sarcocystis sp. infection

    Directory of Open Access Journals (Sweden)

    Caroline A. Pescador

    2007-10-01

    Full Text Available Infecções por protozoários têm distribuição mundial e podem causar aborto, nascimentos prematuros e ou morte fetal em diversas espécies animais. Em julho de 2004, oito ovinos Corriedale apresentaram problemas reprodutivos caracterizados por aborto e natimortalidade no terço final da gestação. Dessas oito perdas, um natimorto macho foi enviado ao Setor de Patologia Veterinária para necropsia. Alterações macroscópicas não foram observadas durante a necropsia. Lesões histológicas foram observadas principalmente no cérebro e coração e se caracterizaram por encefalite não-supurativa multifocal acentuada associada à presença de protozoários no interior de células endoteliais e vasos sanguíneos e miocardite não-supurativa focal leve. Alguns desses organismos apresentaram formato de roseta. O teste de imunoistoquímica anti-Toxoplasma gondii foi negativo, mas houve reação cruzada com anticorpo anti-Neospora caninum. O exame de imunofluorescência direta para Leptospira sp. foi negativo. A bacteriologia aeróbica e micro-aeróbica não revelou crescimento significativo. Esses achados foram compatíveis com o diagnóstico de Sarcocystis sp.Protozoal infection has worldwide distribution and may cause abortion, premature parturition or fetal death in almost all domestic animals. In July 2004, eight Corriedale sheep showed abortion and stillbirth in the third trimester of gestation. Of these reproductive losses, one stillborn male was submitted to the Laboratory of Veterinary Pathology for necropsy investigation. The direct immunofluorescence test for Leptospira sp. was negative. No significant bacteria was isolated from lung and liver by aerobic and microaerobic cultures. Macroscopic lesions were not found in any fetal tissue. The histological lesions were observed mainly in the brain and heart and consisted primarily of severe multifocal nonsupurative encephalitis and nonsuppurative myocarditis. Schizonts of a protozoan

  19. NEURONAS ESPEJO Y EL APRENDIZAJE EN ANESTESIA Learning anaesthesia and mirror neurons

    Directory of Open Access Journals (Sweden)

    John Bautista

    2011-12-01

    Full Text Available Las neuronas espejo fueron descritas inicialmente en primates de la especie Macaca nemestrina hacia el año 1990 por el neurofisiólogo Giacomo Rizzolatti y su grupo de la Universidad de Parma, en Italia. Son neuronas motoras que activan cuando el individuo observa la acción concreta para la que están predeterminadas sin generar ningún tipo de actividad motora. En la actualidad se considera que estas neuronas participan en procesos de adaptación al entorno social ya que permiten no solamente comprender las acciones sino también las intenciones de otros individuos. Se les atribuye función en los procesos de aprendizaje simple a través de la observación y la imitación que pueden ser aprovechados en la enseñanza de la anestesiología.Mirror neurons were initially described in primates from the Macaca nemestrina species around 1990 by the neurophysiologist Giacomo Rizzolatti and his group from Parma University in Italy. They are motor neurons which become activated when an individual observes a concrete action for which they are predetermined without any type of motor activity being produced. It is currently considered that these neurons participate in adapting to the social setting since they lead to understanding other individuals' actions and intensions. A function has been ascribed to them regarding simple learning through observation and imitation which can be exploited in teaching anesthesiology.

  20. Sarcocystis spp. in sheep and goats: frequency of infection and species identification by morphological, ultrastructural, and molecular tests in Bahia, Brazil.

    Science.gov (United States)

    Bittencourt, Marta Vasconcelos; Meneses, Iris Daniela S; Ribeiro-Andrade, Müller; de Jesus, Rogério Fernando; de Araújo, Flábio Ribeiro; Gondim, Luís F Pita

    2016-04-01

    Sarcocystis spp. are cyst-forming coccidia that infect numerous animals species, including several livestock species. Despite the importance of sheep and goat production in Brazil, little it is known about the Sarcocystis species that infect small ruminants in the country and their potential impact on meat condemnation due to the presence of macroscopic cysts of the parasite. The aims of the present study were to determine the frequency of infection by Sarcocystis spp. in goats and sheep intended for human consumption in Bahia State, Brazil, as well as to identify the parasite species in selected samples. The entire tongue, esophagus, and heart were collected from 120 goats and 120 sheep. Tissues were examined for Sarcocystis spp. by macroscopic evaluation, light microscopy, electron microscopy, and molecular tests. Microscopic cysts of Sarcocystis spp. were detected in 95.8 % of sheep and 91.6 % of goats. Using either transmission electron microscopy or partial sequencing of the 18S region of the ribosomal DNA (rDNA) for species identification, Sarcocystis tenella and Sarcocystis arieticanis were observed in sheep and Sarcocystis capracanis in goats. Macroscopic cysts were not detected in the analyzed samples. We concluded that goats and sheep destined for human consumption in Bahia possess high frequencies of Sarcocystis infection. Carcass condemnation due to Sarcocystis macrocysts seems to be rare in the studied region. S. arieticanis and S. capracanis were confirmed for the first time by electron microscopy or by molecular tests in small ruminants from Brazil.

  1. CAMBIOS EN LAS PROPIEDADES DEL RECEPTOR DE GLICINA DURANTE EL DESARROLLO DE NEURONAS ESPINALES EN CULTIVO. EFECTOS CELULARES DE LA ACTIVACION.

    OpenAIRE

    TAPIA AMARO, JUAN CARLOS

    2002-01-01

    Evidencia experimental sugiere que el neurotransmisor inhibitorio glicina puede regular el crecimiento neurítico de neuronas embrionarias. Para evaluar esta hipótesis se propuso: 1) determinar cómo la activación del receptor de glicina en neuronas inmadur 216p.

  2. The resurrection of a species: Sarcocystis bovifelis Heydorn et al., 1975 is distinct from the current Sarcocystis hirsuta in cattle and morphologically indistinguishable from Sarcocystis sinensis in water buffaloes.

    Science.gov (United States)

    Gjerde, Bjørn

    2016-01-01

    In the mid-1970s, it was established through transmission experiments and ultrastructural studies of sarcocysts by transmission electron microscopy (TEM) that cattle was the intermediate host of three Sarcocystis spp. using dogs, cats and humans, respectively, as definitive hosts. The cat-transmitted species with microscopic sarcocysts was initially named Sarcocystis bovifelis, but it was soon renamed Sarcocystis hirsuta, since it was considered to be identical with a previously named species. In recent years, an apparently new species has been detected in cattle in several countries by molecular methods and TEM and found by both methods to be indistinguishable from Sarcocystis sinensis in water buffaloes. This species was recently named Sarcocystis rommeli. Beginning in August 2014, a thorough review of papers comprising TEM micrographs of thick-walled sarcocysts in cattle was made in order to determine whether S. sinensis-like sarcocysts had been reported previously under other designations. Surprisingly, the review showed that the species S. bovifelis Heydorn et al., 1975 as described from cattle in Germany was S. sinensis-like and that indistinguishable sarcocysts had also been found in cattle in New Zealand and Canada in the 1980s. However, in the New Zealand study, these small sarcocysts were erroneously thought to represent developmental stages of a species with ultrastructurally similar but macroscopic sarcocysts, since the macroscopic cysts were found to be infective for cats. Thus, in the late 1980s, the cat-transmitted S. bovifelis, after having been renamed S. hirsuta, was erroneously synonymised with a second cat-transmitted species in cattle and then slid into obscurity until recently being rediscovered as a S. sinensis-like species in cattle and then named S. rommeli. Following the erroneous synonymisation, the name S. hirsuta has consistently been used for a taxon with macroscopic sarcocysts, and this usage should be continued. The name S. bovifelis

  3. Sarcocystis heydorni, n. sp. (Apicomplexa: Protozoa) with cattle (Bos taurus) and human (Homo sapiens) cycle

    Science.gov (United States)

    Cattle (Bos taurus) are intermediate hosts for four species of Sarcocystis, S. cruzi, S. hirsuta, S. hominis, and S. rommeli. Of these four species, mature sarcocysts of S. cruzi are thin-walled (< 1µm) whereas S. hirsuta, S. hominis, and S. rommeli have thick walls (4 µm or more). Here we describe ...

  4. Detection of zoonotic protozoa Toxoplasma gondii and Sarcocystis suihominis in wild boars from Spain

    Science.gov (United States)

    Food safety regulations require the control of presence of protozoa in meats destined for human consumption. Wild boar (Sus scrofa) meat may constitute a source of zoonoses. A 23.8% (688/2881) seroprevalence of anti-Toxoplasma gondii antibodies, and 72.2% (662/910) Sarcocystis sarcocysts prevalence ...

  5. Sarcocystis arctica (Apicomplexa: Sarcocystidae): ultrastructural description and its new host record, the Alaskan wolf (Canis lupus

    Science.gov (United States)

    Sarcocystis sarcocysts are common in muscles of herbivores but are rare in muscles of carnivores. Here, we report sarcocysts in muscle of an Alaskan wolf (Canis lupus) from Alaska, USA for the first time. Sarcocysts extracted from tongue of the wolf were up to 900 µm long, slender, and appeared to h...

  6. Acute, fatal Sarcocystis calchasi-associated hepatitis in Roller pigeons (Columbia livia f. dom.) at Philadelphia Zoo

    Science.gov (United States)

    Four Roller pigeons (Columba livia f. dom.) at the Philadelphia Zoo died suddenly. Necropsy examination revealed macroscopic hepatitis. Microscopically, the predominant lesions were in liver, characterized with necrosis and mixed cell inflammatory response. Sarcocystis calchasi-like schizonts and fr...

  7. Study of Zoonotic Tissue Parasites (Hydatid Cyst, Fasciola, Dicrocoelium and Sarcocystis in Hamadan Abattoir

    Directory of Open Access Journals (Sweden)

    M. Fallah

    2010-10-01

    Full Text Available Introduction & Objectives: Zoonotic parasites are large groups of zoonoses among which the most important are hydatid cyst, liver trematodes and sarcocystis.These zoonoses are of considerable importance regarding both human health and economy. The objective of this study was to determine the prevalence of tissue zoonotic parasites and their epidemiologic status in Hamadan and to estimate the health and medical burden they impose on the society.Materials & Methods: In this cross sectional study, viscera (including liver, lung, kidney, heart,… and muscles of 2590 sheep, 420 cattle, and 490 goats were macroscopically inspected for hydatid cysts, liver flukes, cysticercus , and microscopically (for Sarcocystis in the Hamadan abattoir. The data were presented by descriptive tables and analyzed by 2 statistical test. Results: The infection rate for hydatid cyst, Fasciola, Dicrocoelium and Sarcocystis were found 12.3%, 4.9%, 6.5%, and 5.5% respectively. The high infection rates for hydatid cyst and Fasciola were found in cattle (16.2% and 9.5% and for Dicrocoelium and Sarcocystis were found in sheep (6.9%. Infection rate of lungs was higher (41.2% than liver (36.6% and liver and lung simultaneously were 22.2% in the infected animals. Infection to Sarcocystis and Cysticercus were not found in the cattle. Conclusion: This study indicated that infection rate of tissue zoonotic parasites are relatively high in the domestic animals of Hamadan , however, the rate is lower in comparison to the previous studies. These parasites had imposed considerable economic burden on the society through reduction in the dairy production and increased the risk of infection in the population as well. (Sci J Hamadan Univ Med Sci 2010;17(3: 5-12

  8. Cyst wall ultrastructure of two Sarcocystis spp. from European mouflon (Ovis ammon musimon) in Germany compared with domestic sheep.

    Science.gov (United States)

    Odening, K; Stolte, M; Walter, G; Bockhardt, I

    1995-10-01

    Muscle samples from six wild and two captive European mouflons (Ovis ammon musimon) in Germany as well as one domestic sheep from a German zoo were infected with sarcocysts (Sarcocystis: Sarcocystidae, Apicomplexa). Sarcocystis tenella and S. arieticanis were identified by light and electron microscopy. Both species are determined for the first time from wild sheep, and this is the first description of S. arieticanis from wild sheep.

  9. Mecanismos de regulación de la glucolisis en neuronas y su función en supervivencia celular

    OpenAIRE

    Rodriguez-Rodriguez, Patricia

    2013-01-01

    [ES] El mantenimiento de un correcto equilibrio en el metabolismo energético neuronal es esencial para la supervivencia celular. Existen datos que indican que la neurotransmisión glutamatérgica activa señales moleculares que afectan tanto a la captación de glucosa por las neuronas como a sus vias de metabolización. En esta tesis doctoral describimos un método sensible y específico para la determinación de flujos metabólicos por vía de las pentosas-fosfato y por glucolisis en neuronas a...

  10. Virus de rabia en cultivos de neuronas sensoriales de ratón adulto

    Directory of Open Access Journals (Sweden)

    H. Hurtado

    2000-02-01

    Full Text Available Introducción: Las neuronas sensoriales de los ganglios de la raíz dorsal (GRD del ratón adulto, son un modelo interesante en el estudio de la infección in vitro por virus de rabia. Su importancia radica puesto que es una de las vías que tiene el virus para llegar a sistema nervioso central. El virus de la rabia usualmente entra por la mordedura de un animal infectado, inicialmente llega al músculo, replicándose localmente, pasa a terminales nerviosas adyacentes, sube a través del sistema nervioso periférico y llega a los ganglio de la raíz dorsal. Durante el transporte del virus no hay síntomas y la enfermedad sólo se inicia con la llegada del virus al sistema nervioso central, donde la replicación del virus es seguida por su transporte en sentido centrífugo, teniendo un particular e inexplicable tropismo por las glándulas salivares y lacrimales. Objetivo: Describir el proceso de infección del virus de la rabia en neuronas GRD. Metodología: Cultivos de neuronas de GRD de ratón adulto fueron inoculados con virus de rabia cepa CVS, siendo observada la ultraestructura en tiempos progresivos de infección desde 5 minutos hasta 60 horas. Los resultados obtenidos en los que no se observaron viriones, nos llevaron a hacer un marcaje con inmunoperoxidasas para evidenciar este proceso. Para corroborar los resultados obtenidos fue necesario comparar ultraestructuralmente y con la técnica de inmunoperoxidasas la infección en tejido cerebral de ratones adultos inoculados experimentalmente. Resultados: Este estudio nos permite afirmar que la producción de partículas virales en neuronas de ganglio de raíz dorsal de ratón adulto, cultivadas in vitro, e inoculadas con virus de rabia es escasa, comparada con la gran cantidad de antígeno viral observada en vesículas de 0,5 mm localizadas en el citoplasma de estas mismas células. Los resultados más importantes del estudio revelan que las neuronas sensoriales de ratón adulto son

  11. EFECTO DEL COBRE SOBRE LA EXCITABILIDAD ELECTRICA DE NEURONAS PIRAMIDALES DE CA 1

    OpenAIRE

    VERA BUSCHMANN, JORGE ALEJANDRO

    2010-01-01

    El cobre es un metal esencial para los organismos aeróbicos y ha sido vinculado principalmente al metabolismo celular. Además, existen evidencias para proponer que este metal tiene un rol en la modulación de la excitabilidad neuronal. Sin embargo, esta hipótesis no ha sido demostrada directamente. En nuestro laboratorio encontramos que cobre en concentraciones que pueden alcanzarse en el espacio sináptico (0,01-0,1 μM), aumenta la tasa de disparos espontáneos de neuronas pir...

  12. COMPARTIMENTACIÓN INTERCELULAR DEL ACETATO EN NEURONAS Y ASTROCITOS DURANTE LA PRELACTANCIA

    Directory of Open Access Journals (Sweden)

    J. Tovar-Franco

    2005-12-01

    Full Text Available Durante el período perinatal el cerebro utiliza sustratos alternativos a la glucosa para mantener su desarrollo, pues en este momento sus niveles están disminuidos. El acetato es metabolizado por las neuronas y los astrocitos durante la prelactancia. La utilización del acetato por estas células puede verse mejorada por lasreacciones fijadoras de CO2, algunas de las cuales participan en el mantenimiento de los intermediarios del TCA, que son reducidos por la producción y liberación de aminoácidos, suministrando los recursos para la producción de energía y sustratos que son compartimentados intercelularmente.Se estudió el efecto de la fijación de CO2 en procesos metabólicos intercelulares donde está involucrado el acetato. En incubaciones con neuronas y astrocitos de 7 y 14 días de cultivo, utilizando acetato (5 mM y [14C]-bicarbonato de sodio (10 µ Ci (500-1000 dpm/nmol, se determinó la incorporación en metabolitos marcados en células y en sustratos estables liberados al medio. Adicionalmente, se realizaron experimentos similares utilizando inhibidores como el aminooxiacetato (AOA, dicloroacetato (DCA, α-ciano-4-hidroxicinnamato (α-CN, butilmalonato (BM y bencenotricarboxílato (BT, cuantificando porcromatografía de capa delgada la concentración en el medio de incubación de alanina, aspartato, glutamato y glutamina.Los resultados indican que las neuronas tienen una menor capacidad para fijar carbonos en estructuras celulares, durante la prelactancia, pero utilizan mejor el acetato vía acetil-CoA mitocondrial (AceCS2 para la producción de energía y aminoácidos. En los astrocitos, estas reacciones favorecen la utilización del acetato vía citrato liasa y Acetil-CoA citosólica (AceCS1 para la producción de estructuras y sustratos utilizados por las neuronas, que para la producción de aminoácidos.

  13. El uniportador de calcio mitocondrial en cultivos de neuronas de hipocampo de rata

    OpenAIRE

    García Casas, Paloma

    2015-01-01

    La captura de Ca2+ por parte de la mitocondria se debe principalmente a la apertura del Uniportador de Calcio Mitocondrial. La hipótesis del envejecimiento neuronal postula que durante el envejecimiento se produce una sobrecarga de Ca2+ mitocondrial que promueve la apoptosis celular (Fig. 7). Además, estudios previos de nuestro laboratorio han mostrado que la entrada de calcio a la mitocondria en neuronas jóvenes, maduras y envejecidas varía en respuesta a un estímulo con NMDA. To...

  14. COMPARTIMENTACIÓN INTERCELULAR DEL ACETATO EN NEURONAS Y ASTROCITOS DURANTE LA PRELACTANCIA

    OpenAIRE

    J. Tovar-Franco; F. Saavedra

    2005-01-01

    Durante el período perinatal el cerebro utiliza sustratos alternativos a la glucosa para mantener su desarrollo, pues en este momento sus niveles están disminuidos. El acetato es metabolizado por las neuronas y los astrocitos durante la prelactancia. La utilización del acetato por estas células puede verse mejorada por lasreacciones fijadoras de CO2, algunas de las cuales participan en el mantenimiento de los intermediarios del TCA, que son reducidos por la producción y liberación de aminoáci...

  15. COMPARTIMENTACIÓN INTERCELULAR DEL ACETATO EN NEURONAS Y ASTROCITOS DURANTE LA PRELACTANCIA

    OpenAIRE

    Tovar Franco, J.; Laboratorio de Neurobioquímica, Departamento de Nutrición y Bioquímica, Facultad de Ciencias, Pontificia Universidad Javeriana, Bogotá; Saavedra, F.; Laboratorio de Neurobioquímica, Departamento de Nutrición y Bioquímica, Facultad de Ciencias, Pontificia Universidad Javeriana, Bogotá

    2005-01-01

    Durante el período perinatal el cerebro utiliza sustratos alternativos a la glucosa para mantener su desarrollo, pues en este momento sus niveles están disminuidos. El acetato es metabolizado por las neuronas y los astrocitos durante la prelactancia. La utilización del acetato por estas células puede verse mejorada por las reacciones fijadoras de CO2, algunas de las cuales participan en el mantenimiento de los intermediarios del TCA, que son reducidos por la producción y liberación de aminoác...

  16. Caracterización del metabolismo del glucógeno en neuronas y su implicación en la tolerancia a la hipoxia

    OpenAIRE

    Sáez Martínez, Isabel

    2012-01-01

    La presencia de glucógeno en las neuronas ha sido motivo de controversia durante las pasadas décadas. Sin embargo, está aceptado que las neuronas expresan la maquinaria necesaria para sintetizar glucógeno, pero no para degradarlo. La presencia de la glucógeno sintasa (GS) en las neuronas es un misterio y no existe ningún estudio que analice cuál es su función fisiológica en este tipo neuronal. Recientemente se ha establecido un paralelismo entre la GS neuronal y el caballo de Troya, ya que mú...

  17. Neuronas Espejo y Teoría de la Mente en la explicación de la empatía

    OpenAIRE

    García García, Emilio; González Marqués, Javier; Maestú Unturbe, Fernando

    2011-01-01

    La empatía es la capacidad de una persona para vivenciar los pensamientos y sentimientos de los otros, reaccionando adecuadamente. Diferenciamos en la empatía dos componentes: cognitivo y emocional. El componente cognitivo comprende los pensamientos y sentimientos del otro. El componente afectivo comparte el estado emocional de otra persona. Comentamos dos teorías para explicar la empatía: las neuronas espejo y la Teoría de la Mente. Las neuronas espejo son un tipo particular de neuronas que ...

  18. ¿La neurotoxicidad del etanol depende del estadío de diferenciación neuronal? Estudio en cultivos primarios de neuronas corticales

    OpenAIRE

    Guadagnoli, Tamara

    2014-01-01

    El abuso de alcohol conduce a graves problemas sanitarios y sociales, tanto por la elevada incidencia de su consumo como por las diferentes patologías asociadas a él, entre las que merecen destacarse las producidas a nivel del Sistema Nervioso Central (SNC). Las neuronas son particularmente sensibles al efecto neurotóxico del etanol (EtOH). En este trabajo se demostró que las neuronas corticales en cultivo son suceptibles al daño inducido por el EtOH. Es sabido que no todas las neuronas son i...

  19. Identification and intraspecific genetic diversity of Sarcocystis rileyi from ducks, Anas spp., in Lithuania and Finland.

    Science.gov (United States)

    Prakas, P; Oksanen, A; Butkauskas, D; Sruoga, A; Kutkienė, L; Švažas, S; Isomursu, M; Liaugaudaitė, S

    2014-10-01

    Macroscopic Sarcocystis cysts were detected in the muscles of 28 Mallards ( Anas platyrhynchos ), 1 Eurasian Wigeon ( Anas penelope ), and 1 Common Teal ( Anas crecca ) hunted in Lithuania and Finland. According to the sequences of the 18S rRNA gene, 28S rRNA gene, and ITS-1 region, the macrocysts examined from all 30 ducks belonged to Sarcocystis rileyi. This parasite was found in the Eurasian Wigeon and the Common Teal for the first time. All S. rileyi isolates examined were identical to each other and differed from 2 S. rileyi isolates previously reported from 2 Mallards from the United States only by 1 nucleotide substitution within the ITS-1 region.

  20. Detection of Zoonotic Protozoa Toxoplasma gondii and Sarcocystis suihominis in Wild Boars from Spain.

    Science.gov (United States)

    Calero-Bernal, R; Pérez-Martín, J E; Reina, D; Serrano, F J; Frontera, E; Fuentes, I; Dubey, J P

    2016-08-01

    Food safety regulations require the control of the presence of protozoa in meats destined for human consumption. Wild boar (Sus scrofa) meat may constitute a source of zoonoses. A 23.8% (688/2881) seroprevalence of anti-Toxoplasma gondii antibodies and 72.2% (662/910) Sarcocystis sarcocysts prevalence were detected among wild boars hunted in Southwestern areas of Spain. Identity of Sarcocystis spp. was performed by RFLP-PCR and sequencing, detecting S. miescheriana (7/8) and the zoonotic S. suihominis (1/8). Risk assessment studies of these coccidian in meats destined to human consumption are needed. © 2015 Blackwell Verlag GmbH.

  1. Sarcocystis chloropusae (protozoa: Sarcocystidae) n. sp. from the common moorhen (Gallinula chloropus) from Egypt.

    Science.gov (United States)

    El-Morsey, A; El-Seify, M; Desouky, A Y; Abdel-Aziz, M M; Sakai, H; Yanai, T

    2015-07-01

    A new name Sarcocystis chloropusae is proposed for a parasite previously found in two of 25 common moorhen (Gallinula chloropus) from Brolos Lake, Egypt. Sarcocysts were microscopic, up to 650 μm long, the cyst wall was up to 4.5 μm thick, and contained villar protrusions that were up to 4 μm long and up to 2 μm wide. The villar protrusions were crowded, contained vesicles but lacked microtubules. The ground substance layer was smooth. The bradyzoites were up to 12 μm long and up to 2 μm wide. Molecular characterization and phylogenetic analysis of the (ITS-1) supported the conclusion that the Sarcocystis in G. chloropus is a distinct species.

  2. Eosinophilic myositis resulted from Sarcocystis infection in prime marbled beef of Japanese black cattle

    Directory of Open Access Journals (Sweden)

    Tohru Kimura

    Full Text Available Partial changes of color (greenish to brownish were found in prime marbled beef of Japanese black cattle. The disseminated lesions of the skeletal muscles were histopathologically examined in relation to Sarcocystis infection. The lesions in the muscles showed granulomas with inflammatory cell infiltration. The sarcocysts had a distinct wall, which was radically striated by palisading villar protrusions. The sarcocyst wall was surrounded by degenerative eosinophils and necrotic muscle fibers. In conclusion, eosinophilic myositis in prime marbled beef of Japanese black cattle resulted from Sarcocystis spp. infection. The muscular lesions were characterized by the presence of granulomas and capsulated sarcocysts surrounded by numerous eosinophils. [Vet. World 2011; 4(11.000: 500-502

  3. DNA extraction methods and multiple sampling to improve molecular diagnosis of Sarcocystis spp. in cattle hearts.

    Science.gov (United States)

    Bräunig, Patrícia; Portella, Luiza Pires; Cezar, Alfredo Skrebsky; Libardoni, Felipe; Sangioni, Luis Antonio; Vogel, Fernanda Silveira Flores; Gonçalves, Paulo Bayard Dias

    2016-10-01

    Molecular detection of Sarcocystis spp. in tissue samples can be useful for experimental and diagnostic purposes. However, the parasite spreads unevenly through tissues, forming tissue cysts, and the cystic wall is an obstacle in DNA extraction protocols. Therefore, adequate sampling and effective disruption of the cysts are essential to improve the accuracy of DNA detection by PCR. The aims of this study were to evaluate the suitability of four protocols for DNA extraction from cysts of Sarcocystis spp. present in bovine myocardium samples or after their harvest in phosphate-buffered saline (PBS) solution as well as determine the effects of single or multiple sampling on the accuracy of molecular diagnosis of sarcocystosis in cattle hearts. Cysts and myocardium samples from nine bovine hearts were randomly distributed to four DNA extraction protocols: kit, kit with modification, DNAzol, and cetyl-trimethyl ammonium bromide (CTAB). Samples were submitted to DNA extraction and PCR as replicates of each heart (simplicate, duplicate, and triplicate), and the probability of a true positive diagnostic was calculated. Among the protocols tested, the kit with modification was determined to be the most suitable for DNA extraction from cysts in PBS solution (92.6 % of DNA detection by PCR); DNAzol resulted in higher DNA detection frequency from bovine myocardium samples (48.1 %). Multiple sampling improved the molecular diagnosis of Sarcocystis spp. infection in cattle hearts, increasing at 22.2 % the rate of true positive diagnostic.

  4. Necrotizing meningoencephalitis caused by Sarcocystis falcatula in bare-faced ibis (Phimosus infuscatus).

    Science.gov (United States)

    Konradt, Guilherme; Bianchi, Matheus Viezzer; Leite-Filho, Ronaldo Viana; da Silva, Bruna Zafalon; Soares, Rodrigo Martins; Pavarini, Saulo Petinatti; Driemeier, David

    2017-02-01

    The infection by S. falcatula is commonly associated with respiratory disease in captive psittacine birds, with a few case reports of this protozoan causing encephalitis in wild birds. We describe the clinical, pathological, and molecular aspects of an infection by S. falcatula in a bare-faced ibis (Phimosus infuscatus). Clinically, wing paralysis and mild motor incoordination were observed. At necropsy, the telencephalic cortex showed multifocal to coalescing yellowish soft areas. Histologically, multifocal to coalescent nonsuppurative necrotizing meningoencephalitis of telencephalic cortex, cerebellum, and brainstem was observed. Necrotic areas showed multiple protozoan organism characteristics of Sarcocystis sp. schizonts in the cytoplasm of endothelial cells or lying free in the neuropil. Partial genetic sequences of the gene encoding cytochrome b (CYTB), the gene encoding the beta subunit of RNA polymerase (RPOB) and the first internal transcribed spacer (ITS-1) from Sarcocystis sp. schizonts revealed that the parasite had ITS-1 sequences that were 100% identical to the homologous alleles from Sarcocystis sp. shed by Didelphis albiventris in Brazil. RPOB and CYTB sequences were 100% identical to homologous of S. falcatula available in Genbank. Thus, this is the first report of necrotizing meningoencephalitis caused by S. falcatula in bare-faced ibis (P. infuscatus).

  5. Fatal hepatic sarcocystosis in a captive black bear (Ursus americanus) associated with Sarcocystis canis-like infection.

    Science.gov (United States)

    Davies, Jennifer L; Haldorson, Gary J; Bradway, Dan S; Britton, Ann P

    2011-03-01

    Fatal hepatic sarcocystosis was diagnosed in a 13-year-old captive black bear (Ursus americanus) with a history of acute onset of vomiting, polyuria, polydipsia, and bilirubinuria. Gross lesions included severe icterus, multisystemic hemorrhage, and gall bladder edema. The most significant microscopic lesion was severe necrotizing hepatitis with intralesional protozoa that reproduced by endopolygeny consistent with a Sarcocystis spp. Infrequent microglial nodules were randomly scattered within the white matter of the cerebral cortices, thalamus, and brainstem, but intralesional protozoal schizonts were not observed. In the liver, immunohistochemistry was positive for Sarcocystis spp. and negative for Toxoplasma gondii and Neospora spp. Positive staining was not observed in the brain. Genus-specific polymerase chain reaction (PCR) amplification of the 18S ribosomal RNA gene was performed on formalin-fixed, paraffin-embedded sections of liver and brain; in both tissues, PCR was positive for Sarcocystis spp. Sequence analysis of the PCR amplicons revealed 100% identity to the published sequences of Sarcocystis canis and Sarcocystis arctosi.

  6. Short communication: Genetic variants of Sarcocystis cruzi in infected Malaysian cattle based on 18S rDNA.

    Science.gov (United States)

    Ng, Yit Han; Fong, Mun Yik; Subramaniam, Vellayan; Shahari, Shahhaziq; Lau, Yee Ling

    2015-12-01

    Sarcocystis species are pathogenic parasites that infect a wide range of animals, including cattle. A high prevalence of cattle sarcocystosis has been reported worldwide, but its status is unknown in Malaysia. This study focused on utilizing 18S rDNA to identify Sarcocystis species in Malaysian cattle and to determine their genetic variants. In this study, only Sarcocystis cruzi was detected in Malaysian cattle. The intra-species S. cruzi phylogenetic tree analysis and principal coordinate analysis (PCoA), respectively displayed two minor groups among the parasite isolates. This finding was supported by high Wright FST value (FST=0.647). The definitive hosts (dogs) may play a fundamental role in the development of S. cruzi genetic variants. Additionally, the existence of microheterogeneity within the S. cruzi merozoites and/or distinct genetic variants arisen from independent merozoites in mature sarcocysts, possibly contributed to the existence of intra-species variations within the population.

  7. Sarcocystis spp. in llamas (Lama glama) in Southern Bolivia: a cross sectional study of the prevalence, risk factors and loss in income caused by carcass downgrades.

    Science.gov (United States)

    Rooney, A L; Limon, G; Vides, H; Cortez, A; Guitian, J

    2014-10-01

    Llamas (Lama glama) are intermediate hosts of the protozoan parasite Sarcocystis spp. This parasite is described as causing economic losses in the production of llama meat in South America. The aim of this study was to estimate prevalence, identify risk factors and explore spatial patterns of Sarcocystis in llamas in an area of the Bolivian High Plateau including estimating financial losses due to carcass downgrades as a result of the presence of Sarcocystis cysts. Information was collected from a local abattoir between 2006 and 2011 on 1196 llamas. Sarcocystis status was determined at meat inspection where any carcasses with one or more visible cysts were deemed Sarcocystis positive. A high prevalence was found, estimated to vary between 23.4% (95% CI 16.6-30.1) in 2007 and 50.3% (95% CI 44.4-56.3) in 2011. Period prevalence between 2006 and 2011 was estimated at 34.1% (95% CI 31.4-36.8). Age, sex and type (analogous to breed) were identified as risk factors for Sarcocystis using a mixed-effects logistic regression model adjusting for clustering by community and owner. Llamas over 4.5 years of age had an increased odds of being Sarcocystis positive (OR 19.31, 95% CI 9.10-40.98) as well as females (OR 1.75, 95% CI 1.13-2.68) and long haired type llamas (OR 1.90, 95% CI 1.26-2.87). An interaction between age and sex was detected indicating that the increased odds of disease from the youngest age group to the 2.5-4.5 years group was much more pronounced in females than in males. Spatial patterns of Sarcocystis were explored at district level by means of Standardised Morbidity Ratios and some spatial heterogeneity was revealed. Estimates of financial loss due to the disease were calculated using the difference in price paid for Sarcocystis positive and negative meat. Loss due to Sarcocystis varied per year but could be up to 20% of the annual income generated through the abattoir by sale of meat. Overall this study shows a high prevalence of Sarcocystis in the study

  8. Factores tróficos en neuronas dopaminérgicas mesencefálicas

    Directory of Open Access Journals (Sweden)

    G. Pinzón

    1994-12-01

    Full Text Available Desde su descubrimiento, se ha postulado, y en algunos casos comprobado, que los factores tróficos juegan un papel importante en el desarrollo, mantenimiento y regeneración del sistema nervioso. El conocimiento y la manipulación de estas sustancias ha servido para: a formular nuevas teorías acerca de la etiología de varios desórdenes neurodebeneraivos y b desarrollar nuevas altemativas terapéuticas para estas entidades. En la presente revisión, resumimos los principales efectos de diferentes factores tróficos sobre las neuronas dopaminérgicas de la substantia nigra en desarrollo, cuya degeneración en el adulto ocasiona la mayoría de los síntomas observados en la enfermedad de Parkinson.

  9. Molecular Analysis of Sarcocystis Spp. Isolated from Sheep (Ovis aries in Babol Area, Mazandaran Province, Northern Iran

    Directory of Open Access Journals (Sweden)

    Narges KALANTARI

    2016-03-01

    Full Text Available Background: To differentiate Sarcocystis macro-cyst-forming species in slaughtered sheep in Babol area, Mazandaran Province, sequence analysis of 18S rRNA gene was performed.Methods: Overall, 150 slaughtered sheep were examined macroscopically in slaughterhouse, Babol and intra-abdominal and diaphragm muscles tissues infected with macro-cyst of Sarcocystis spp. were collected in 2013. One macro-cyst was isolated from the infected muscles of each sheep. The partial 18S rRNA gene was amplified by PCR and sequenced afterward.Results: The rate of infection with macro-cyst producing Sarcocystis spp. was 33.3% (50 / 150. The partial 18S rRNA gene of Sarcocystis species was amplified at the expected PCR product size (~1100 bp from all 50 macroscopic cysts samples. From 30 sequences DNA samples, 20 samples (66.7%, six (20% and four (13.3% isolates were identified as S. gigantea, S. moulei and Sarcocystis spp., respectively. Eight and thirty-four variations in nucleotide position were seen in partial sequence of the18S rRNA gene of S. gigantea and S. moulei.Conclusion: Sheep can be considered as an alternative intermediate host for S. moulei. Furthermore, multiple alignments showed some variations in the consensus sequences of the isolates obtained in the current study compared with previously published isolates. To understand better the genetic diversity among Sarcocystis species complete sequences of the18S rRNA gene or sequence analysis of other genetic loci would be beneficial.

  10. Ultrastructure of the cysts of Sarcocystis rangi from skeletal muscle of reindeer (Rangifer tarandus tarandus

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    Bjørn Gjerde

    1985-05-01

    Full Text Available Mature muscle cysts of Sarcocystis rangi from Rangifer tarandus were examined by transmission electron microscopy. The long and slender cysts were located within skeletal muscle cells, and were bounded by a unit membrane, the cyst membrane. The cysts were provided with closely spaced flexible, hairlike surface processes, measuring up to 12.6 |im in length and 0.3 to 0.6 \\lm in diameter. The projections had a smooth surface, whereas the cyst membrane formed numerous hexagonally packed vesicular invaginations between the bases of the projections. The cyst membrane was reinforced by an underlying thin layer of electron-dense material, except at the points where it was invaginated. Cyst ground substance formed a thin layer at the periphery of the cysts, filled the core of the projections, and formed thin septa that divided the interior of the cysts into numerous compartments. Most compartments contained a large number of tightly packed cystozoites, whereas a few metrocytes were forund in each of a few compartments at the periphery of the cysts. Some of the cystozoites multiplied by endodyogeny. The metrocytes displayed a vacuolation of their cytoplasm. The cysts of S. rangi were similar in surface morphology to the sarcocysts of certain other Sarcocystis species reported from other intermediate hosts.Ultrastrukturen til cyster av Sarcocystis rangi frå skjelettmuskulaturen hos rein.Abstract in Norwegian / Samandrag: Muskelcyster av S. rangi frå rein vart undersøkt ved transmisjonselektronmikroskopi. Dei lange cystene låg intracellulært i skjelettmuskelceller, og var avgrensa av ein elementærmembran, cystemembranen. Cystene var utstyrt med talrike hårliknande overflateprosessar, som strekte seg langsetter cysteoverflata. Prcsessane var opptil 12.6 Hm lange, og målte 0.3 til 0.6 \\lm i diameter. Prosessane hadde ei glatt overflate, medan cystemembranen danna talrike regelmessige ordna, små invaginasjonar innimellom basis av prosessane

  11. Pervasive Environmental Contamination with Human Feces Results in High Prevalence of Zoonotic Sarcocystis Infection in Pigs in the Punjab, India.

    Science.gov (United States)

    Kaur, M; Singh, B B; Sharma, R; Gill, J P S

    2016-04-01

    Three species of Sarcocystis-S. miescheriana, S. suihominis, and S. porcifelis-have been recorded from pigs ( Sus scrofa ). Among these 3 species, the zoonotic species S. suihominis is of paramount importance and an important food safety issue. Previous studies indicate prevalence of porcine Sarcocystis species in India, but molecular evidence, among other evidence, is required for proper species differentiation. Myocardium from 250 stray and farm pigs destined for slaughter for human consumption were collected from slaughter shops located in urban slums in Punjab, northern India. Tissues were examined for Sarcocystis by using an intact cyst isolation method, pepsin acid digestion, Sarcocystis 18S ribosomal RNA polymerase chain reaction (PCR), and real-time quantitative PCR with melting curve analysis (qPCR-MCA). The combination of primers was used for 18S rRNA PCR amplification followed by sequencing. Ten representative samples were sequenced in both the directions from which 7 readable sequences were obtained for phylogenetic analysis. Sarcocystis cysts/zoites were recorded in 146 (58.4%), 169 (67.6%), 182 (72.8%), and 191 (76.4%) of samples by using intact cyst isolation, pepsin HCl digestion, conventional PCR, and qPCR-MCA, respectively. Molecularly, 1 S. miescheriana isolate and 6 isolates of the zoonotic species S. suihominis were recorded. This is the first study providing molecular identification for the presence of zoonotic species S. suihomonis in India. The prevalence of zoonotic S. suihominis in pork in India is worrisome and warrants intervention policies to stop the practice of rearing pigs under unhygienic conditions.

  12. Occurrence and Distribution of Sarcocystis Parasite Isolated from Sheep in Yazd Province, Iran

    Directory of Open Access Journals (Sweden)

    Bahador Hajimohammadi

    2014-11-01

    Full Text Available Introduction: Sarcocystis species are one of the most important meat borne parasites. Sarcocystosis causes several symptoms in human as well as numerous diseases with high economic impact in livestock. In current paper at first results of a pilot study for determination of disease agent in lamb of Yazd province central Iran is presented. Then status of parasite in red meat products in study region gets discussed. Materials and Methods: Muscles of 70 slaughtered Sheep from both sexes and different ages were investigated for presence of parasite cysts during September to October 2013. Carcass inspection with naked eye at industrial slaughterhouse of Yazd for macroscopic cysts, and pepsin-digestion method for microscopic cysts was performed on common infected sites of infection. Results: No macroscopic cyst was seen at inspection, however bradyzoites of parasite were observed in 97.14% of animals’ digested muscles. No significant difference between infection and age groups or sex of animals was observed. Conclusion: As humans are considered as final and intermediate host of different species of Sarcocystis, and parasite cysts present at microscopic sizes, transmission of infection from lamb meat should come into consideration. Hence public training of disease health importance, parasite cycle and methods of inactivation probable cysts in meat is recommended.

  13. Experimentos con una protección basada en redes de neuronas artificiales

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    Orlys Ernesto Torres Breffe

    2011-10-01

    Full Text Available En este trabajo se muestran los resultados de los experimentos físicos realizados con una protección basada totalmente en Redes de Neuronas Artificiales para un transformador eléctrico a escala de laboratorio. Se demuestra que unas Redes de Neuronas Artificiales entrenadas, con datos provenientes de regímenes simulados matemáticamente, opera correctamente con señales de regímenes provenientes de casos reales, al menos a escala de laboratorio y con niveles reducidos de intensidad. Se describe la instalación experimental, tanto desde el puntode vista de hardware como software utilizando la tecnología de National Instrument. Se entrenan diferentes tipos de Redes Neuronales y todas aprendieron a proteger correctamente. Estos experimentos establecen las pautas para el desarrollo de Relés Electrónicos Inteligentes que no se ajustarían, al menos con datos y valores de difícil comprensión como los actuales relés, sino que se entrenarían una vez mediante la simulación matemática y la experiencia práctica los haría cada vez mejores. In this work is shown the results of the physical experiments done with a protection totally based in Artificial Neural Networks for an electric transformer of the laboratory scale. Its demonstrated that some Artificial Neural Networks trained with data coming from a mathematically simulated regimens, it operates correctly with signals coming fromreal cases, at least to laboratory scale and with reduced levels of intensity. The experimental installation is described, so much from the hardware and software point of view, using the technology of National Instrument. Different types of Artificial Neural Nets are trained and all learned how to protect correctly. These experiments establish the rules forthe development of Intelligent Electronic Relays that would not be adjusted, at least with complex data and values like the current relays, they will be trained once from the mathematically simulation and the

  14. Reduced Levels of Nitric Oxide Metabolites in Cerebrospinal Fluid Are Associated with Equine Protozoal Myeloencephalitis

    Science.gov (United States)

    Njoku, Chinedu J.; Saville, William J. A.; Reed, Stephen M.; Oglesbee, Michael J.; Rajala-Schultz, Päivi J.; Stich, Roger W.

    2002-01-01

    Equine protozoal myeloencephalitis (EPM) is a disease of horses that is primarily associated with infection with the apicomplexan Sarcocystis neurona. Infection with this parasite alone is not sufficient to induce the disease, and the mechanism of neuropathogenesis associated with EPM has not been reported. Nitric oxide (NO) functions as a neurotransmitter, a vasodilator, and an immune effector and is produced in response to several parasitic protozoa. The purpose of this work was to determine if the concentration of NO metabolites (NOx−) in the cerebrospinal fluid (CSF) is correlated with the development of EPM. CSF NOx− levels were measured before and after transport-stressed, acclimated, or dexamethasone-treated horses (n = 3 per group) were experimentally infected with S. neurona sporocysts. CSF NOx− levels were also compared between horses that were diagnosed with EPM after natural infection with S. neurona and horses that did not have clinical signs of disease or that showed no evidence of infection with the parasite (n = 105). Among the experimentally infected animals, the mean CSF NOx− levels of the transport-stressed group, which had the most severe clinical signs, was reduced after infection, while these values were found to increase after infection in the remaining groups that had less severe signs of EPM. Under natural conditions, horses with EPM (n = 65) had a lower mean CSF NOx− concentration than clinically normal horses with antibodies (Abs) against S. neurona (n = 15) in CSF, and horses that developed ataxia (n = 81) had a significantly lower mean CSF NOx− concentration than horses that did not have neurologic signs (n = 24). In conclusion, lower CSF NOx− levels were associated with clinical EPM, suggesting that measurement of CSF NOx− levels could improve the accuracy of diagnostic tests that are based upon detection of S. neurona-specific Abs in CSF alone and that reduced NO levels could be causatively related to the development

  15. Inmunorreactividad de neuronas gabaergicas y glutamatergicas en la corteza y el cerebelo de ratones infectados con rabia

    OpenAIRE

    Rengifo Castillo, Aura Caterine

    2012-01-01

    La rabia es una enfermedad viral que produce cambios en la función neuronal. Estos cambios, entre otros, inducen alteraciones en el metabolismo de los neurotransmisores. Los signos clínicos de la rabia indican que se podría afectar el sistema GABA-glutamato y, por lo tanto, el balance entre la inhibición y excitación neuronal. El objetivo de este trabajo consistió en evaluar la inmunorreactividad de neuronas GABAérgicas y glutamatérgicas en la corteza y el cerebelo de ratones infectados co...

  16. RESONANCIA ELECTRICA EN EL RANGO THETA (8) EN NEURONAS DE LA CAPA II DEL NUCLEO CORTICAL ANTERIOR DE LA AMIGDALA

    OpenAIRE

    2010-01-01

    El complejo de la amígdala participa en procesar información sensorial relevante desde el punto de vista emocional. La información sensorial olfativa entra desde el bulbo olfatorio (OB) a este complejo a través de la corteza olfatoria, la cual incluye los núcleos corticales de la amígdala. En ratas las neuronas mitrales del OB y aquellas de la capa II del núcleo cortical anterior (ACo) y la corteza periamigdaloide división medial (P A Cm) presentan oscilaciones intrínsecas del potencial de...

  17. RESONANCIA ELECTRICA EN EL RANGO THETA (0) EN NEURONAS DE LA CAPA II DEL NUCLEO CORTICAL ANTERIOR DE LA AMIGDALA

    OpenAIRE

    2010-01-01

    El complejo de la amígdala participa en procesar información sensorial relevante desde el punto de vista emocional. La información sensorial olfativa entra desde el bulbo olfatorio (OB) a este complejo a través de la corteza olfatoria, la cual incluye los núcleos corticales de la amígdala. En ratas las neuronas mitrales del OB y aquellas de la capa II del núcleo cortical anterior (ACo) y la corteza periamigdaloide división medial (P A Cm) presentan oscilaciones intrínsecas del ...

  18. Avances en el desarrollo infantil temprano: desde neuronas hasta programas a gran escala

    Directory of Open Access Journals (Sweden)

    Rafael Pérez-Escamilla

    2017-03-01

    Full Text Available El desarrollo infantil temprano (DIT es la base del desarrollo económico y social de los países y de su capacidad de cumplir con los Objetivos de Desarrollo Sostenible (ODS. La gestación y los primeros 3 años de vida son fundamentales para que los niños tengan un desarrollo físico, psicosocial, emocional y cognitivo adecuado para el resto de sus vidas. La crianza y el cuidado cariñoso y sensible a las necesidades de los niños durante la gestación y la primera infancia son esenciales para el desarrollo de los billones de neuronas y trillones de sinapsis necesarias. El DIT requiere de acceso a buena nutrición y servicios de salud desde la gestación, crianza sensible de acuerdo a la etapa de desarrollo del niño, protección social y del bienestar del niño, y oportunidades de estimulación y aprendizaje temprano. Para mejorar el DIT a nivel nacional se recomiendan seis acciones con fuerte participación de la sociedad civil: expandir la voluntad política y financiamiento, crear un entorno de políticas favorables basadas en evidencia, construir capacidad con coordinación intersectorial, asegurar una gobernanza justa y transparente de los programas y servicios, aumentar apoyo a la investigación multidisciplinaria y promover el desarrollo de líderes. México ha logrado avances importantes en DIT bajo el liderazgo del Sector Salud, pero enfrenta retos significativos para implementar estas recomendaciones. La reciente creación de un marco nacional intersectorial favorable al DIT con apoyo de los organismos internacionales y la participación de la sociedad civil pueden ayudar a sobreponer estos retos.

  19. Ongoing outbreak of an acute muscular Sarcocystis-like illness among travellers returning from Tioman Island, Malaysia, 2011-2012.

    Science.gov (United States)

    Esposito, D H; Freedman, D O; Neumayr, A; Parola, P

    2012-11-08

    As of 4 November, 2012, 100 patients with an acute muscular Sarcocystis-like illness associated with travel to Tioman Island, Malaysia, have been identified. Thirty-five travelled there mostly during July and August 2011 and 65 mostly during July and August 2012, suggesting an ongoing outbreak. Epidemiological investigations are ongoing. Public health agencies and practicing clinicians should be aware of this rarely-reported disease in humans and consider it as differential diagnosis in travellers returning from Tioman Island.

  20. Morphological and molecular characterization of Sarcocystis arctica-like sarcocysts from the Arctic fox (Vulpes lagopus) from Alaska, USA.

    Science.gov (United States)

    Cerqueira-Cézar, Camila K; Thompson, Peter C; Verma, Shiv Kumar; Mowery, Joseph; Calero-Bernal, Rafael; Antunes Murata, Fernando H; Sinnett, David R; Van Hemert, Caroline; Rosenthal, Benjamin M; Dubey, Jitender P

    2017-07-01

    The muscles of herbivores commonly harbor sarcocysts of parasites belonging to species in the genus Sarcocystis, but such muscle parasites are rare in carnivores. Here, we report Sarcocystis arctica-like sarcocysts in muscles of Arctic foxes (Vulpes lagopus) from Alaska, USA, for the first time. The tongues of 56 foxes were examined for Sarcocystis infection using several methods. Sarcocystis bradyzoites were detected in pepsin digests of 13 (23.2%), and sarcocysts were found in histological sections stained with hematoxylin and eosin (HE) of 9 (16.0%). By light microscopy, sarcocysts were up to 4 mm long and up to 245 μm wide. In HE-stained sections, the sarcocyst wall appeared smooth and up to 1.5 μm thick without visible protrusions. By transmission electron microscopy, the sarcocyst wall had a wavy parasitophorous vacuolar membrane (pvm) folded as pleomorphic villar protrusions (vp), sometimes with anastomoses of villar tips. The vp and the ground substance (gs) layer were smooth and without microtubules. The gs was up to 2.0 μm thick. The total width of the wall including vp and the gs was up to 4.0 μm. The vp were up to 3.0 μm long and most closely resembled "type 9c." All sarcocysts were mature and contained numerous 8.1 × 2.1 μm sized bradyzoites. Molecular characterization (at 18S rDNA, 28S rDNA, ITS-1, and cox1) showed the highest affinity for S. arctica of the Arctic fox (V. lagopus) from Norway. In the present investigation, we provide evidence that sarcocysts are common in tongues of Alaskan Arctic foxes suggesting that these carnivores are serving as intermediate hosts, and we also provide ultrastructure of S. arctica from the Arctic fox for the first time.

  1. In the United States, negligible rates of zoonotic sarcocystosis occur in feral swine that, by contrast, frequently harbour infections with Sarcocystis miescheriana, a related parasite contracted from canids.

    Science.gov (United States)

    Calero-Bernal, R; Verma, S K; Oliveira, S; Yang, Y; Rosenthal, B M; Dubey, J P

    2015-04-01

    Transmission of pathogens between domestic and wild life animals plays an important role in epidemiology. Feral pig populations are increasing and expanding in the USA, and may constitute a risk to non-biosecure domestic pig facilities by serving as reservoirs for pathogens. We surveyed, for Sarcocystis infection, the myocardium of 1006 feral pigs (Sus scrofa) trapped or hunted in 29 states during the Comprehensive Feral Swine Disease Surveillance Program of the USDA's Animal and Plant Health Inspection Service, Wildlife Services unit during 2012-2014. Sarcocysts were detected in histological sections of 25% (251/1006) of myocardium with an average parasitic load/intensity of infection of 3.03 sarcocysts/section (1.5×0.7 cm), and higher prevalence of myocarditis in severe infections. Microscopic examination of pepsin digests of 147 hearts revealed a higher prevalence of Sarcocystis bradyzoites (49%, 72/147) than when diagnosed by histology. A fragment of Sarcocystis 18S rRNA was amplified and digested with a restriction endonuclease, revealing a pattern consistent with Sarcocystis miescheriana in all 44 selected samples. Sequencing 31 of these 44 isolates confirmed their correspondence to S. miescheriana. Thus, S. miescheriana infection, but not the zoonotic parasite Sarcocystis suihominis, appears to be prevalent and widespread in feral pigs in the USA.

  2. The Neurona at Home project: Simulating a large-scale cellular automata brain in a distributed computing environment

    Science.gov (United States)

    Acedo, L.; Villanueva-Oller, J.; Moraño, J. A.; Villanueva, R.-J.

    2013-01-01

    The Berkeley Open Infrastructure for Network Computing (BOINC) has become the standard open source solution for grid computing in the Internet. Volunteers use their computers to complete an small part of the task assigned by a dedicated server. We have developed a BOINC project called Neurona@Home whose objective is to simulate a cellular automata random network with, at least, one million neurons. We consider a cellular automata version of the integrate-and-fire model in which excitatory and inhibitory nodes can activate or deactivate neighbor nodes according to a set of probabilistic rules. Our aim is to determine the phase diagram of the model and its behaviour and to compare it with the electroencephalographic signals measured in real brains.

  3. Ultrastructural studies of sarcocystis cruzi (Hasselmann,1926 Wenyon, 1926 infection in cattle (Bos Taurus: Philippine cases

    Directory of Open Access Journals (Sweden)

    Claveria F.G

    2001-09-01

    Full Text Available This paper documents the first report of Sarcocysli s cruzi infection in domesticated cattle (Bos taurus in the Philippines. Fusiformshaped microscopic sarcocysts (183-578 μm long and 20-98 μm wide with distinct septae were found in the skeletal, striated and heart muscle. The sarcocyst wall or parasitophorous vacuolar membrane, 1.37-2.75 μm thick consisted of closely-packed villar protrusions 80-400 nm in dm. Middle and distal segments of VP were bent approximately 90 degrees parallel to the cyst wall surface. The villar core lacked microtubules, and at some points, the distal ends of the VP collectively formed conical tufts. Primary cyst wall had numerous 70-100 nm bubble-like undulations, and the ground substance was 0.25-0.5 μm in thickness. The ultrastructure of S. cruzi cyst wall typifies the Type 7 sarcocyst wall, and bears close similarities with the Philippine and the Vietnam strain of bubaline Sarcocystis levinei.

  4. Sarcocystis schneideri n. sp. (Sarcocystidae) infecting the barber skink Eumeces schneideri schneideri (Scincidae) Daudin, 1802. A light and ultrastructural study.

    Science.gov (United States)

    Bashtar, Abdel-Rahman; Al Aal, Zain Abd; Maarouf, Wael; Morsy, Kareem; Al Quraishy, Saleh

    2014-06-01

    The current study provides the first record of infection with Sarcocystis species in the barber skink Eumeces schneideri schneideri (Scincidae) captured from the north region of Egypt around the cities of El-Hamam and Al-Dabaa, Mersa Matruh Governorate, Egypt. Morphology of the parasite cysts was described using light and transmission electron microscopy. Five out of 80 (6.25%) of the examined skinks were found to be infected. The infection was recorded firstly by light microscopy as spindle-shaped cysts embedded in the muscle tissue. The cysts were microscopic and measured 250-900 μm in length × 50-100 μm in width (mean, 575 × 75 μm). The validity of this species was confirmed by means of ultrastructural characteristics of the primary cyst wall (0.28 μm thick) which revealed the presence of irregularly shaped crowded and osmiophilic knob-like projections underlined by a thin layer of ground substance measuring 0.15-0.17 μm (mean, 0.16 μm). This layer consisted mainly of fine, dense homogenous granules enclosing the developing metrocytes and merozoites that usually contain nearly all the structures of the apical complex and fill the interior cavity of the cyst. Several septa derived from the ground substance divided the cyst into compartments. The merozoites were banana-shaped and measured 3-5 μm in length and 1.5-2.5 in width with centrally or posteriorly located nuclei. The morphological and morphometric data obtained during study were compared with those recorded previously from organisms within the Scincidae family. It was observed that this parasite possessed some distinguishing characteristics from the comparable species, which should be considered as a new species of the Sarcocystis genus, and the proposed name was Sarcocystis schneideri n. sp. with new host and locality records in Egypt.

  5. Acute, fatal Sarcocystis calchasi-associated hepatitis in Roller pigeons (Columba livia f. dom.) at Philadelphia Zoo.

    Science.gov (United States)

    Trupkiewicz, J G; Calero-Bernal, R; Verma, S K; Mowery, J; Davison, S; Habecker, P; Georoff, T A; Ialeggio, D M; Dubey, J P

    2016-01-30

    Four Roller pigeons (Columba livia f. dom.) at the Philadelphia Zoo died suddenly. Necropsy examination revealed macroscopic hepatitis. Microscopically, the predominant lesions were in liver, characterized with necrosis and mixed cell inflammatory response. Sarcocystis calchasi-like schizonts and free merozoites were identified in liver. Transmission electron microscopy confirmed that schizonts were in hepatocytes. A few schizonts were in spleen. PCR using S. calchasi-specific primers confirmed the diagnosis. Neither lesions nor protozoa were found in brain and muscles. This is the first report of acute visceral S. calchasi-associated sarcocystosis in naturally infected avian hosts.

  6. EFECTO DE LA UTILIZACIÓN DE DIFERENTES SUSTRATOS COMPARTIMENTADOS POR NEURONAS Y ASTROCITOS, SOBRE LA CONCENTRACIÓN DE CALCIO EXTRA E INTRACELULAR

    Directory of Open Access Journals (Sweden)

    Elsa Guzmán de Aristizábal

    2003-06-01

    Full Text Available El mecanismo de intercambio de sustratos entre neuronas y astrocitos, no es claro y menos claro es, si los efectos metabólicos en las células receptoras, son resultado de señalización por calcio. Se plantea la posibilidad de que existan señales entre neuronas y astrocitos que relacionen su funcionamiento metabólico a través de las concentraciones de calcio. La concentración de calcio se midió por absorción atómica en el medio intra y extracelular de cultivos primarios de neuronas y astrocitos y posteriormente en el medio intra y extracelular después de una hora de incubación con lactato, glutamato, glutamina y acetato a concentraciones fisiológicas. Las comparaciones estadísticas se efectuaron con ANOVA y Duncan (p < 0.05. Se hicieron 3 replicaciones de cada experimento con 5 repeticiones. Los resultados permiten afirmar que al hacer incubaciones in vitro con los sustratos, se producen variaciones en las concentraciones de calcio extra é intracelular. El estrés metabólico puede estar influyendo en estas variaciones. Adicionalmente, se demuestra que los astrocitos son menos dependientes del calcio extracelular que las neuronas. Las variaciones del calcio intracelular pueden incrementar el metabolismo de estas células y acelerar el metabolismo mitocondrial. Se postula que cambios en la concentración de calcio afectan el metabolis-mo de células excitables en incubaciones in vitro usando diferentes sustratos.

  7. Cross-sectional survey in pig breeding farms in Hesse, Germany: seroprevalence and risk factors of infections with Toxoplasma gondii, Sarcocystis spp. and Neospora caninum in sows

    DEFF Research Database (Denmark)

    Damriyasa, I.M.; Bauer, C.; Edelhofer, R.

    2004-01-01

    A cross-sectional survey was performed to estimate the prevalences of antibodies to Toxoplasma gondii (ELISA, IFAT), Sarcocystis spp. (ELISA, using S. miescheriana as antigen) and Neospora caninum (ELISA, immunoblotting) in sows from breeding farms in southern Hesse, Germany. A total of 2041 plas...

  8. In the United States, negligible rates of zoonotic sarcocystosis occur in feral swine that, by contrast, frequently harbor infections with Sarcocystis meischeriana, a related parasite contracted from dogs

    Science.gov (United States)

    Transmission of pathogens between domestic and wild life animals plays important role in epidemiology. Feral pig populations are increasing and expanding in the USA, and may constitute a risk to non-biosecure domestic pig facilities by serving as reservoirs for pathogens. We surveyed, for Sarcocysti...

  9. Occurrence of Sarcocystis spp. in opossums (Didelphis aurita and Didelphis albiventris in regions of the State of São Paulo, Brazil

    Directory of Open Access Journals (Sweden)

    Renata Assis Casagrande

    2009-04-01

    Full Text Available O objetivo deste estudo foi de determinar a ocorrência de Sarcocystis spp. em D. albiventris e D. aurita em três regiões do Estado de São Paulo. Para tal, utilizou-se noventa e oito Didelphis mortos, sendo 66 D. aurita e 32 D. albiventris, e também 28 D. aurita e cinco D. albiventris vivos. O método de centrífugo-flutuação em solução de sacarose foi empregado para isolamento dos oocistos/esporocistos de Sarcocystis spp. do intestino delgado e das fezes. Encontrou-se Sarcocystis spp. no intestino delgado de 9,1% dos D. aurita (6/66, sendo que quatro destes também houve positividade nas fezes. Não houve diferença estatística significativa entre machos e fêmeas positivos (P= 0,522, e entre os positivos de diferentes origens do Estado de São Paulo (P= 0,627, quanto a ocorrência de Sarcocystis spp. Entretanto, houve diferença estatística significativa entre animais de vida livre e de cativeiro (P = 0.009, sendo que somente os de vida livre foram positivos. Entre adultos e filhotes positivos também houve diferença (P= 0,004, sendo os adultos mais parasitados que os filhotes. Das amostras provenientes dos 28 D. aurita vivos, encontrou-se Sarcocystis spp. em 7.1% (2/28 deles. Dos 32 D. albiventris, todos foram negativos para Sarcocystis spp. nas amostras de intestino delgado e fezes. Os cincos D. albiventris vivos também foram negativos. Sendo assim, pode-se observar que a ocorrência de Sarcocystis spp. em D. aurita e D. albiventris nestas três regiões do Estado de São Paulo é baixa para estas condições analisadas.

  10. Occurrence and first molecular characterization of Sarcocystis spp. in wild boars (Sus scrofa) and domestic pigs (Sus scrofa domesticus) in Romania: Public health significance of the isolates.

    Science.gov (United States)

    Imre, Kálmán; Sala, Claudia; Morar, Adriana; Imre, Mirela; Ciontu, Cătălin; Chisăliță, Ion; Dudu, Andreea; Matei, Marius; Dărăbuș, Gheorghe

    2017-03-01

    Domestic and wild pigs, as intermediate hosts, can harbor tissue cysts of three Sarcocystis species namely S. miescheriana, S. suihominis and S. porcifelis. Out of them, S. suihominis is zoonotic. Romania is a country with high consumption of raw and/or undercooked traditional pork products. This fact may greatly favor the acquiring of the zoonotic Sarcocystis infections by humans, as definitive host. Based on this consideration and in order to investigate the occurrence and public health significance of Sarcocystis spp. in two western counties (Caraş-Severin and Timiş) of Romania, a total of 165 heart samples from hunted wild boars (Sus scrofa, n=101) and home slaughtered domestic pigs (Sus scrofa domesticus, n=64) were screened using microscopic fresh examination and molecular methods. Microscopic examination revealed the presence of sarcocysts in 60.4% of wild boars, and 23.4% of domestic pigs. Genetic characterization of isolates through the PCR-RFLP procedure, targeting the 18S rRNA gene, was successfully achieved for all microscopically positive samples, indicating the presence of a single species, S. miescheriana, in both hosts. The identity of 13 selected S. miescheriana isolates was also confirmed through sequencing. The tested hosts older than 27 months were found to be significantly higher infected (p<0.05) with Sarcocystis than the 6 to ≤27months age group. Although the human infective S. suihominis has not been registered, for a more reliable epidemiological picture, further molecular studies enrolling a larger number of animals and diagnosis on human intestinal Sarcocystis infections are still necessary.

  11. A Survey on Sarcocystis Infection Rate in Slaughtered Cattle and Sheep by Macroscopic Inspection and Pepsin Digestion Methods in Hamadan Abattoir, Iran, 2014

    Directory of Open Access Journals (Sweden)

    F. Parandin

    2015-10-01

    Full Text Available Introduction & Objective: 130 heteroxenous species of sarcosytis with different life cycle and pathogenesis have been recognized. The pathogenic species for humans are S. hominis from cattle and S. suihominis from pig that humans are definitive and cattle and pig are intermedi-ate hosts. Some species of Sarcocystis can cause important economic loss and disease in livestock, and health issues in humans. The aim of this study was to determine the prevalence of Sarcocystis infection in slaughtered Cattle and sheep in Hamadan, west of Iran. Materials & Methods: In this cross sectional descriptive study a total of 324 cattle and 334 sheep carcasses were examined using naked eye inspection for macroscopic Sarcocysts, and digestion method, for microscopic types of parasite. Muscles from thigh, heart, tongue, esophagus, diaphragm and costal muscles were examined. All carcasses examined by naked eyes and tissues were minced and poured in digestion medium separately and sediment was examined microscopically. Results: The prevalence of microscopic Sarcocystis in cattle was detected in 100% and there was no macroscopic cyst in examined carcasses. However, the prevalence of microscopic Sarcocystis in the sheep was also 100% and the sarcocysts were found in the 48.34 % of esophagus and 29.49% of diaphragm muscles by naked eyes inspection. Conclusion: The digestion is found the most sensitive method for diagnosis of Sarcocystis. Al-though 100% of muscles were found infected but the majority of the cysts in the sheep and all in the cattle were as microcysts. That means, the meat should be cooked sufficiently irrespec-tive of meat inspection results. (Sci J Hamadan Univ Med Sci 2015; 22 (3: 210-216

  12. Morphologic identification of a new Sarcocystis sp. in the common moorhen (Gallinula chloropus ) (Aves: Gruiformes: Rallidae) from Brolos Lake, Egypt.

    Science.gov (United States)

    El-Morsey, Ahmed; El-Seify, Mahmoud; Desouky, Abdel-Razik Y; Abdel-Aziz, Mohamed M; Sakai, Hiroki; Yanai, Tokuma

    2014-01-01

    Sarcocystis species are among the most common and widespread protozoan parasites of mammals and birds. The current study provides the first record of infection with Sarcocystis species in the common moorhens from Brolos Lake, KafrElsheikh province, Egypt. Morphology of the parasite cysts was described using light and transmission electron microscopy. Out of 25 examined birds, sarcocysts were found in neck, thigh, and legs muscles of two birds. The cysts were microscopic and measured 150-650 μm in length×45-185 μm in width. Histologically, the sarcocyst wall appeared striated and characterized by the presence of radial spines. Ultrastructurally, it measured 2-4.5 μm in thickness and had irregularly shaped crowded finger-like villar protrusions that measured 1.5-4 μm in length and up to 0.4-2 μm in width with the presence of dense electron ground substance of 200-750 nm thick. Several septa derived from the ground substance were present and divided the cyst into compartments containing both bradyzoites and metrocytes. The bradyzoites were banana-shaped and measured 6-12 × 1-2 μm with centrally or posteriorly located nuclei. The ultrastructural features of the cyst wall belonged to type 10 cyst wall according the classification of Dubey et al. (1989) and Dubey and Odening (2001).

  13. EXPERIMENTOS CON UNA PROTECCION BASADA EN REDES DE NEURONAS ARTIFICIALES;EXPERIMENTS WITH A PROTECTION BASED ON ARTIFICIALS NEURONS NETWORKS

    Directory of Open Access Journals (Sweden)

    Orlys Ernesto - Torres Breffe y otros

    2011-11-01

    Full Text Available En este trabajo se muestran los resultados de los experimentos físicos realizados con una protección basadatotalmente en Redes de Neuronas Artificiales para un transformador eléctrico a escala de laboratorio. Se demuestraque unas Redes de Neuronas Artificiales entrenadas, con datos provenientes de regímenes simuladosmatemáticamente, opera correctamente con señales de regímenes provenientes de casos reales, al menos a escalade laboratorio y con niveles reducidos de intensidad. Se describe la instalación experimental, tanto desde el puntode vista de hardware como software utilizando la tecnología de National Instrument. Se entrenan diferentes tipos deRedes Neuronales y todas aprendieron a proteger correctamente. Estos experimentos establecen las pautas para eldesarrollo de Relés Electrónicos Inteligentes que no se ajustarían, al menos con datos y valores de difícilcomprensión como los actuales relés, sino que se entrenarían una vez mediante la simulación matemática y laexperiencia práctica los haría cada vez mejores.In this work is shown the results of the physical experiments done with a protection totally based in Artificial NeuralNetworks for an electric transformer of the laboratory scale. Its demonstrated that some Artificial Neural Networkstrained with data coming from a mathematically simulated regimens, it operates correctly with signals coming fromreal cases, at least to laboratory scale and with reduced levels of intensity. The experimental installation is described,so much from the hardware and software point of view, using the technology of National Instrument. Different typesof Artificial Neural Nets are trained and all learned how to protect correctly. These experiments establish the rules forthe development of Intelligent Electronic Relays that would not be adjusted, at least with complex data and valueslike the current relays, they will be trained once from the mathematically simulation and the practical

  14. Neuronas Espejo: un nuevo camino dentro de las Neurociencias : Aportes y aplicaciones, en el área de la reeducación y la rehabilitación

    OpenAIRE

    Figueroa Cuadrado, Emiliano

    2013-01-01

    El presente trabajo, pretende sumergirse en el mundo de las Neuronas Espejo. Dichas neuronas fueron descubiertas por un equipo de Neurobiólogos Italianos, de la Universidad de Parma, en el año 1995. Es el ultimo "gran descubrimiento" que se ha hecho en el ámbito de las Neurociencias; tanto que hasta algunos especialistas han llegado a decir, que tal descubrimiento estaba llamado a desempeñar en las Neurociencias, un papel semejante al que había tenido en Biología, la decodificación de la e...

  15. Adaptación y modificaciones de corta y larga duración en la actividad eléctrica de neuronas de la corteza cerebral in vitro.

    OpenAIRE

    Montoro Laseca, Rafael Jesús

    2017-01-01

    El sistema nervioso central lleva a cabo sus complejas funciones gracias a la actividad armónica de sus unidades básicas, las neuronas, que son células de una enorme sofisticación morfológica y funcional. Una neurona típica recibe decenas de miles de aferencias y es capaz de generar en cada instante la respuesta bioquímica y electrofisiológica adecuada que permite la transmisión a otras células de una información c...

  16. Regulación de las GTPasas de la familia Ras y la viabilidad de neuronas dopaminérgicas en respuesta a la señalización purinérgica

    OpenAIRE

    2015-01-01

    158 p. El ATP es una molécula natural cuya liberación descontrolada puede elevar su concentración extracelular a rango mM y promover la estimulación de receptores purinérgicos. Se sabe que esta estimulación tiene efectos citotóxicos sobre las neuronas dopaminérgicas, aunque se desconocen los eventos moleculares a los que implica. La muerte de estas neuronas está íntimamente relacionada con la Enfermedad de Parkinson, ya que conlleva una disminución de la síntesis de dopamina y consecuente ...

  17. Neuronas Espejo: un nuevo camino dentro de las Neurociencias : Aportes y aplicaciones, en el área de la reeducación y la rehabilitación

    OpenAIRE

    Figueroa Cuadrado, Emiliano

    2013-01-01

    El presente trabajo, pretende sumergirse en el mundo de las Neuronas Espejo. Dichas neuronas fueron descubiertas por un equipo de Neurobiólogos Italianos, de la Universidad de Parma, en el año 1995. Es el ultimo "gran descubrimiento" que se ha hecho en el ámbito de las Neurociencias; tanto que hasta algunos especialistas han llegado a decir, que tal descubrimiento estaba llamado a desempeñar en las Neurociencias, un papel semejante al que había tenido en Biología, la decodificación de la e...

  18. Mieloencefalite protozoária eqüina (Relato de caso.

    Directory of Open Access Journals (Sweden)

    R. C. Gonçalves

    2005-03-01

    Full Text Available RESUMO :O objetivo deste trabalho foi relatar um caso de mieloencefalite protozoária eqüina no Estado de São Paulo, Brasil. O diagnóstico se baseou nos sinais clínicos, no resultado positivo para anticorpos contra Sarcocystis neurona no soro e no líquor pela técnica de Western blot. Palavras chave: Mieloencefalite, Sarcocystis neurona, eqüinos. SUMMARY: The purpose of this work was to present a case of equine protozoal myeloencephalitis (EPM in the State of São Paulo, Brazil. The diagnosis was based on the clinical sings, the positive results of the serum and cerebrospinal fluid analysis (Western blot for antibodies against Sarcocystis neurona. Keywords: Myeloencephalitis, Sarcocystis neurona,

  19. Detection and characterization of diverse coccidian protozoa shed by California sea lions

    Directory of Open Access Journals (Sweden)

    Yvette A. Girard

    2016-04-01

    Full Text Available Tissue-cyst forming coccidia in the family Sarcocystidae are etiologic agents of protozoal encephalitis in marine mammals including the federally listed Southern sea otter (Enhydra lutris. California sea lions (Zalophus californianus, whose coastal habitat overlaps with sea otters, are definitive hosts for coccidian protozoa provisionally named Coccidia A, B and C. While Coccidia A and B have unknown clinical effects on aquatic wildlife hosts, Coccidia C is associated with severe protozoal disease in harbor seals (Phoca vitulina. In this study, we conducted surveillance for protozoal infection and fecal shedding in hospitalized and free-ranging California sea lions on the Pacific Coast and examined oocyst morphology and phenotypic characteristics of isolates via mouse bioassay and cell culture. Coccidia A and B were shed in similar frequency, particularly by yearlings. Oocysts shed by one free-ranging sea lion sampled at Año Nuevo State Park in California were previously unidentified in sea lions and were most similar to coccidia infecting Guadalupe fur seals (Arctocephalus townsendi diagnosed with protozoal disease in Oregon (USA. Sporulated Coccidia A and B oocysts did not replicate in three strains of mice or in African green monkey kidney cells. However, cultivation experiments revealed that the inoculum of fecally-derived Coccidia A and B oocysts additionally contained organisms with genetic and antigenic similarity to Sarcocystis neurona; despite the absence of detectable free sporocysts in fecal samples by microscopic examination. In addition to the further characterization of Coccidia A and B in free-ranging and hospitalized sea lions, these results provide evidence of a new role for sea lions as putative mechanical vectors of S. neurona, or S. neurona-like species. Future work is needed to clarify the distribution, taxonomical status, and pathogenesis of these parasites in sea lions and other marine mammals that share their the near

  20. Detection and characterization of diverse coccidian protozoa shed by California sea lions

    Science.gov (United States)

    Girard, Yvette A.; Johnson, Christine K.; Fritz, Heather M.; Shapiro, Karen; Packham, Andrea E.; Melli, Ann C.; Carlson-Bremer, Daphne; Gulland, Frances M.; Rejmanek, Daniel; Conrad, Patricia A.

    2015-01-01

    Tissue-cyst forming coccidia in the family Sarcocystidae are etiologic agents of protozoal encephalitis in marine mammals including the federally listed Southern sea otter (Enhydra lutris). California sea lions (Zalophus californianus), whose coastal habitat overlaps with sea otters, are definitive hosts for coccidian protozoa provisionally named Coccidia A, B and C. While Coccidia A and B have unknown clinical effects on aquatic wildlife hosts, Coccidia C is associated with severe protozoal disease in harbor seals (Phoca vitulina). In this study, we conducted surveillance for protozoal infection and fecal shedding in hospitalized and free-ranging California sea lions on the Pacific Coast and examined oocyst morphology and phenotypic characteristics of isolates via mouse bioassay and cell culture. Coccidia A and B were shed in similar frequency, particularly by yearlings. Oocysts shed by one free-ranging sea lion sampled at Año Nuevo State Park in California were previously unidentified in sea lions and were most similar to coccidia infecting Guadalupe fur seals (Arctocephalus townsendi) diagnosed with protozoal disease in Oregon (USA). Sporulated Coccidia A and B oocysts did not replicate in three strains of mice or in African green monkey kidney cells. However, cultivation experiments revealed that the inoculum of fecally-derived Coccidia A and B oocysts additionally contained organisms with genetic and antigenic similarity to Sarcocystis neurona; despite the absence of detectable free sporocysts in fecal samples by microscopic examination. In addition to the further characterization of Coccidia A and B in free-ranging and hospitalized sea lions, these results provide evidence of a new role for sea lions as putative mechanical vectors of S. neurona, or S. neurona-like species. Future work is needed to clarify the distribution, taxonomical status, and pathogenesis of these parasites in sea lions and other marine mammals that share their the near-shore marine

  1. Detection and characterization of diverse coccidian protozoa shed by California sea lions.

    Science.gov (United States)

    Girard, Yvette A; Johnson, Christine K; Fritz, Heather M; Shapiro, Karen; Packham, Andrea E; Melli, Ann C; Carlson-Bremer, Daphne; Gulland, Frances M; Rejmanek, Daniel; Conrad, Patricia A

    2016-04-01

    Tissue-cyst forming coccidia in the family Sarcocystidae are etiologic agents of protozoal encephalitis in marine mammals including the federally listed Southern sea otter (Enhydra lutris). California sea lions (Zalophus californianus), whose coastal habitat overlaps with sea otters, are definitive hosts for coccidian protozoa provisionally named Coccidia A, B and C. While Coccidia A and B have unknown clinical effects on aquatic wildlife hosts, Coccidia C is associated with severe protozoal disease in harbor seals (Phoca vitulina). In this study, we conducted surveillance for protozoal infection and fecal shedding in hospitalized and free-ranging California sea lions on the Pacific Coast and examined oocyst morphology and phenotypic characteristics of isolates via mouse bioassay and cell culture. Coccidia A and B were shed in similar frequency, particularly by yearlings. Oocysts shed by one free-ranging sea lion sampled at Año Nuevo State Park in California were previously unidentified in sea lions and were most similar to coccidia infecting Guadalupe fur seals (Arctocephalus townsendi) diagnosed with protozoal disease in Oregon (USA). Sporulated Coccidia A and B oocysts did not replicate in three strains of mice or in African green monkey kidney cells. However, cultivation experiments revealed that the inoculum of fecally-derived Coccidia A and B oocysts additionally contained organisms with genetic and antigenic similarity to Sarcocystis neurona; despite the absence of detectable free sporocysts in fecal samples by microscopic examination. In addition to the further characterization of Coccidia A and B in free-ranging and hospitalized sea lions, these results provide evidence of a new role for sea lions as putative mechanical vectors of S. neurona, or S. neurona-like species. Future work is needed to clarify the distribution, taxonomical status, and pathogenesis of these parasites in sea lions and other marine mammals that share their the near-shore marine

  2. Estudios del rol modulador de ghrelina sobre la actividad neuroendocrina: circuitos neuronales implicados en la activación de las neuronas CRF hipofisiotrópicas

    OpenAIRE

    2014-01-01

    En la presente Tesis Doctoral estudiamos los circuitos neuronales que median los efectos de la ghrelina sobre las neuronas CRF hipofisiotrópicas del NPV y el eje HHA. Esperamos que el esclarecimiento de estos circuitos pueda ayudar a entender cómo funcionan y cómo se integran la homeostasis energética y el estrés. Así como también, contribuir al desarrollo de futuras terapias que intenten manipular las acciones de la ghrelina. Facultad de Ciencias Exactas

  3. Efecto del 3-nitropropionato sobre el metabolismo del lactato y del acetato en neuronas y astrocitos crecidos in vitro en concentraciones perinatales

    OpenAIRE

    Tovar-Franco, RJairo Alfonso; Grupo de Neurobioquímica. Departamento de Nutrición y Bioquímica, Pontificia Universidad Javeriana. Cra. 7ª # 43-82, Bogotá D.C.; Criollo-Rayo, Ángel Alexandro; Departamento de Biología, Universidad del Tolima, Ibagué, Tolima

    2009-01-01

    Las reacciones anapleróticas son un mecanismo metabólico esencial para la continuidad postnatal del desarrollo cerebral, contribuyendo en procesos que requieren sustratos sintetizados a partir de intermediarios del ciclo de Krebs, sin embargo, se desconoce su papel en el neonato durante la prelactancia. Objetivo. Estimar la capacidad anaplerótica de neuronas y astrocitos crecidos in vitro. Materiales y métodos. Se midió el efecto del 3-nitropropionato (3-NPA)(2 mM), un inhibidor de Succinato ...

  4. Estudio comparativo de la toxicidad del metilmercurio, cadmio (II) y cromo (VI) en cultivos primarios de neuronas y astrocitos de rata

    OpenAIRE

    V Uroz Martínez; MJ Anadón-Baselga; M. Capó-Martí

    2008-01-01

    El presente estudio pretende comparar la concentración letal 50 (CL , dosis que causa la muerte del 50% de las células) de 50 metilmercurio, cadmio (II) y cromo (VI) en cultivos primarios de corteza de rata. Se emplearon hemisferios cerebrales de rata para preparar los cultivos primarios. Los cultivos primarios de neuronas fueron realizados a partir de ratas Wistar de 14-16 días de gestación, usando el medio Eagle modificado por Dulbecco. Para los cultivos primarios de as...

  5. Análisis de las Propiedades Integrativas de las Neuronas de la Región Ventral de la Sustancia Gris Periacueductal.

    OpenAIRE

    Sánchez Romero, Diego

    2016-01-01

    La sustancia gris central periacueductal (SGC) se localiza entre el romboencéfalo y el diencéfalo. Sus neuronas, de un tamaño relativamente pequeño, están densamente empaquetadas rodeando al acueducto mesencefálico. En los roedores, la SGC comienza caudalmente por delante del locus coeruleus donde el acueducto de Silvio se abre al cuarto ventrículo. Rostralmente se extiende hasta la comisura posterior donde se mezcla con la sustancia gris aso...

  6. Preliminary investigation on in vitro-cultivation and manipulation of Schistosoma japonicum sporocysts%日本血吸虫胞蚴的体外培养和操作初探

    Institute of Scientific and Technical Information of China (English)

    江艳; 龚仁敏; 杨艺; 李小红; 刘毅; 朱传刚; 陆珂; 郑浩

    2011-01-01

    目的 探究一种体外培养日本血吸虫胞蚴的新方法,并通过体外注射,感染阴性钉螺,培养阳性钉螺.方法 将日本血吸虫虫卵孵化的毛蚴与作为滋养层的草地夜蛾(Spodoptera frugiperda)卵巢细胞(sf9细胞)共培养,观察毛蚴的生长情况,并拍摄生长照片.用显微注射针将3~5只母胞蚴注射到钉螺体内,计算钉螺的存活率及尾蚴的阳性率,用钉螺逸出的尾蚴人工感染昆明鼠,检测尾蚴的活力,用组织化学染色法和PCR方法鉴定尾蚴的相关基因特性.结果 毛蚴培养至第12小时观察到纤毛板已脱落,培养2~3 d的虫体呈不断的伸缩运动,此后母胞蚴维持该状态并不转化成子胞蚴.3次实验的钉螺存活率依次为24.72%、28.23%和57.89%,活螺阳性率依次为4.55%、8.57%和14.29%.阳性钉螺释放的尾蚴具有感染性,且具有与日本血吸虫相同的基因特性.结论 体外培养毛蚴通过显微注射可以人工感染钉螺并逸出有感染活力的尾蚴,为日本血吸虫幼虫的体外操作提供一种新的方法.%Objective To explore a new method of in vitro cultivation of Schistosoma japonicum sporocysts,infection of negative snails through in vitro-injection,and cultivation of positive snails.Methods Isolated miracidia were directly cultivated in sf9 cells-conditioned medium,the growth of miracidia was observed and the growth picture was taken.3-5 mother sporocysts were inoculated into the snails body using a microscopic needle.The survival rate of the snails and the positive rate of cercariae were calculated.Kunming mice were infected with the cercariac and the activity of cercariae Was detected.The related gene characteristics of cercariae was identified by histochemical examination and PCR method.Results The pictures of miracidia were recorded after co-cultivation for 1 h,12 h,24 h and 3 d.The shedding of the cilia of miracidia occurred within 12 h,parasites exhibited continuous stretching movements after

  7. Estudio de migración de neuronas Pax6+ en el tálamo del pollo y del ratón

    OpenAIRE

    Domenech Hita, Jose Manuel

    2015-01-01

    OBJETIVO GENERAL El objetivo general de esta tesis es la caracterización de la migración protagonizada por un conjunto de neuronas Pax6+ en el tálamo del pollo y del ratón y su análisis comparativo. MATERIALES Y MÉTODOS Se utilizaron embriones de pollo (HH28 – HH38) para analizar mediante técnicas de inmunohistoquímica y de hibridación in situ con sondas de mRNA del gen Pax6 en secciones de vibratomo. También se llevaron a cabo marcajes mediante BDA y posterior cultivo organotípic...

  8. Caracterización de un modelo organotípico de cultivos de neuronas corticales de humano derivadas de trauma craneoencefálico

    Directory of Open Access Journals (Sweden)

    David Riascos

    2008-09-01

    Full Text Available Introducción: El trauma craneoencefálico (TEC es un problema de salud global que puede generar en los pacientes que lo padecen, muerte, discapacidad y/o alteraciones psiquiátricas con gran impacto sobre su desempeño posterior y sobre su ámbito familiar. En los últimos años se ha avanzado en el conocimiento de los mecanismos fisiopatológicos que subyacen al TCE. Sin embargo, esto no está completamente entendido, como tampoco hay claridad sobre los mecanismos de neuroprotección. Por esta razón cada vez más se buscan modelos que permitan aproximarse al estudio de este síndrome y de esta manera aproximarse a la neuroprotección.Objetivo: Caracterizar un modelo de cultivo organotípico de neuronas corticales humanas obtenidas de personas que sufrieron TCE y a las cuales se les practicó remoción de la contusión.Metodología: Se utilizó tejido cortical humano procedente de 4 individuos que sufrieron TCE y a los cuales se les removió la contusión. Se obtuvieron tajadas de corteza cerebral de 1,500-2,000 mm, las cuales se mantuvieron en un flujo continuo de LCRa a 2 ml/min y una mezcla gaseosa de O2 al 95% y CO2 al 5% con burbujeo permanente durante 2, 8 y 14 horas. Se tomó como tiempo cero el momento de obtención de la muestra. Después de cada tiempo se tomaron las tajadas, se cortaron en un vibrátomo de medio líquido a 50 mm y se procesaron inmunohistoquímicamente con los marcadores neuronales de degeneración NeuN y MAP2.Resultados: Los resultados indican que las muestras de corteza cerebral se pudieron mantener con cierto grado de integridad celular y laminar hasta las 2 horas de cultivo. Se observó que a partir de este tiempo se inicia un proceso de alteración de la citoarquitectura neuronal y laminar, determinada por la pérdida y alteración de la inmunorreactividad a los marcadores NeuN y MAP2. Además se encontró que hay vulnerabilidad celular que compromete en mayor medida a las neuronas localizadas en las l

  9. Genotyping of Toxoplasma gondii and Sarcocystis spp. in road-killed wild mammals from the Central Western Region of the State of São Paulo, Brazil

    Directory of Open Access Journals (Sweden)

    Virgínia Bodelão Richini-Pereira

    Full Text Available Abstract INTRODUCTION: Road-killed wild animals host zoonotic pathogens such as Toxoplasma gondii, offering a new opportunity for the epidemiological study of these infectious organisms. METHODS This investigation aimed to determine the presence of T. gondii and other apicomplexan parasites in tissue samples of 64 road-killed wild animals, using polymerase chain reaction (PCR. Positive samples were then typed by PCR-restriction fragment length polymorphism (RFLP using 7 markers: SAG1, 5′-3′SAG2, SAG3, BTUB, c29-6, PK1, and Apico. PCR-RFLP targeting 18S ribosomal RNA (rRNA genes was also performed on all samples to detect other apicomplexan parasites. RESULTS T. gondii DNA was detected in 16 tissue samples from 8 individual animals, as follows: 1 Cerdocyon thous (crab-eating fox, 1 Didelphis albiventris (white-eared opossum, 1 Lutreolina crassicaudata (lutrine opossum, 2 Myrmecophaga tridactyla (giant anteater, 1 Procyon cancrivorus (crab-eating raccoon, and 2 Sphiggurus spinosus (Paraguay hairy dwarf porcupine. Seven different T. gondii genotypes were identified, 6 of which were novel. Typing by 18S rRNA verified these 16 T. gondii-infected samples, and identified 1 Sarcocystis spp.-infected animal [Dasypus novemcinctus (nine-banded armadillo]. The amplified T. gondii (GenBank accession No. L37415.1 and Sarcocystis spp. 18S rRNA products were confirmed by sequencing. CONCLUSIONS Our results indicate that T. gondii is commonly present in wild mammals, which act as sources of infection for humans and animals, including other wild species. The approach employed herein proved useful for detecting T. gondii and Sarcocystis spp. in the environment and identifying their natural reservoirs, contributing to our understanding of host-parasite interactions.

  10. 化隆县家畜膈肌住肉孢子虫感染情况研究%Study on the Infection of Sarcocystis in Diaphragmatic Muscle of Yak and Sheep in Hualong County

    Institute of Scientific and Technical Information of China (English)

    康明; 李英; 石文辉; 席进桂花

    2013-01-01

    [目的]摸清化隆县牦牛和绵羊住肉孢子虫的感染情况.[方法]采用膈肌压片镜检法,对青海省化隆县6个乡(镇)的牦牛和绵羊膈肌中住肉孢子虫的感染情况进行研究.[结果]化隆县牦牛和绵羊膈肌中住肉孢子虫的感染率分别为40%和93.3%,感染寄生强度分别为11和41 个/g肉样.化隆县牦牛和绵羊中住肉孢子虫的感染情况较为严重.[结论]该研究可为今后住肉孢子虫的防治提供科学依据.%[Objective] The research aimed to investigate the infection situation of Sarcocystis in yak and sheep in Hualong County. [Method] Using microscope examination method of pressed diaphragmatic muscle, the infection situations of Sarcocystis in diaphragmatic muscle of yak and sheep in six towns (countrysides) of Hualong County were studied. [Result] The infection rate of Sarcocystis in diaphragm muscle of yak and sheep in Hualong County were 40% and 93.3% respectively. And the intensity of infection were 11 and 41 worms in each gram of meat sample. The infection of Sarcocystis in yak and sheep was serious in Hualong County. [Conclusion] The research could provide scientific basis for the control of Sarcocystis in future.

  11. Diagnóstico da esquistossomose mansônica mediante técnica de imunofluorescência com esporocistos em tecidos de planorbídeos Diagnosis of mansoni schistosomiasis by means of immunofluorescent technique using sporocysts in planorbid tissues

    Directory of Open Access Journals (Sweden)

    Ana Maria Aparecida Guaraldo

    1981-12-01

    Full Text Available Propõe-se uma técnica de imunofluorescência para diagnóstico da esquistossomose mansônica, adotando-se tecidos de Biomphalaria glabrata contendo esporocistos secundários de Schistosoma mansoni. A reação de imunofluorescência indireta é executada sobre cortes histológicos preparados por inclusão em parafina.An immunofluorescent technique is proposed for diagnosis of mansoni schistosomiasis using Biomphalaria glabrata tissue with secondary sporocysts. The indirect immunofluorescent reaction is carried out on histological sections prepared by embedding in paraffin.

  12. Detection of Neospora caninum in tissue sections using a murine monoclonal antibody.

    Science.gov (United States)

    Cole, R A; Lindsay, D S; Dubey, J P; Blagburn, B L

    1993-10-01

    A murine monoclonal antibody (MAb 6G7), isotype IgG2a, produced against tachyzoites of Neospora caninum (isolate NC-1) reacted specifically with tachyzoites of N. caninum in an indirect immunofluorescent antibody test. MAb 6G7 did not react with tachyzoites of Toxoplasma gondii, sporozoites of Isospora suis, Eimeria bovis, or E. tenella, or merozoites of E. bovis in the indirect immunofluorescent antibody test. MAb 6G7 reacted positively with both tachyzoites and bradyzoites of N. caninum in an avidin-biotin peroxidase complex immunohistochemical test on formalin-fixed paraffin-embedded tissues. No reaction was observed with the following: tachyzoites and bradyzoites of T. gondii, T. gondii-like parasites, or Hammondia hammondi; bradyzoites of Frenkelia microti; schizonts and merozoites of Sarcocystis-like organisms; schizonts, sarcocysts, and oocysts/sporocysts of S. cruzi; schizonts and merozoites of S. canis; schizonts of S. hirsuta, S. tenella, and S. capracanis; merozoites of S. neurona and S. neurona-like organisms, E. bovis, or Haemoproteus sp.; bradyzoites and merozoites of S. montanaensis; bradyzoites of S. odocoileocanis, S. cruzi, and S. tenella; meronts, sexual stages, and caryocysts of Caryospora sp. and C. bigenetica; micromerozoites, macromerozoites, and schizonts of Hepatozoon canis; sporozoites, sexual stages, and oocysts of Cryptosporidium parvum and C. baileyi; trophozoites of Monocystis lumbrici, Tritrichomonas foetus, and Balantidium coli; tissue cysts and bradyzoites of Besnoitia sp. and B. jellisoni; amastigotes of Leishmania sp.; and trophic theronts of Ichthyopthirius multifilis. MAb 6G7 reacted with tachyzoites and bradyzoites of N. caninum in natural and experimental infections in dogs, cattle, mice, rats, sheep, and goats, indicating that host origin of the tissues did not affect the performance of the test.

  13. Participación de los receptores muscarínicos en el efecto del β - amiloide (25-35) sobre las neuronas piramidales de la región CA3 del hipocampo. Estudio Electrofisiológico

    OpenAIRE

    Sanabria Castro, Alfredo

    2011-01-01

    [ES] El objetivo general de esta Tesis Doctoral es estudiar el efecto del péptido β - amiloide (25 - 35) y sus mecanismos de acción en neuronas piramidales pertenecientes a la región CA3 del hipocampo de rata por medio de técnicas electrofisiológicas de registro intracelular. [EN] The overall objective of this Thesis is to study the effect of β peptide - amyloid (25 - 35) and their mechanisms of action in pyramidal neurons belonging to the region of rat hippocampal CA3 through electrophysi...

  14. [Control of toxicity of Sarcocystis fayeri in horsemeat by freezing treatment and prevention of food poisoning caused by raw consumption of horsemeat].

    Science.gov (United States)

    Harada, Seiya; Furukawa, Masato; Tokuoka, Eisuke; Matsumoto, Kazutoshi; Yahiro, Shunsuke; Miyasaka, Jiro; Saito, Morihiro; Kamata, Yoichi; Watanabe, Maiko; Irikura, Daisuke; Matsumoto, Hiroshi; Sugita-Konishi, Yoshiko

    2013-01-01

    More than 27 outbreaks per year of food poisoning caused by consuming horse meat were reported in Kumamoto Prefecture (including Kumamoto City) from January 2009 to September 2011. It was found that the causative agent of the outbreaks was a protein with a molecular weight of 15 kDa that had originated from bradyzoites of Sarcocystis fayeri parasitizing the horse meat. Rabit ileal loop tests showed that pepsin treatment of homogenates of frozen horse meat containing the cysts of S. fayeri induced loss of toxicity, presumably by digestion of the proteinous causative agent(s). Slices of horse meat containing the cysts were frozen at below -20°C for various periods. The cysts were collected after thawing the slices, then treated in an artificial stomach juice containing pepsin. The bradyzoites of the cysts kept at -20°C for 48 hr or more completely disappeared. Simultaneously, the 15 kDa protein also disappeared in the frozen cysts. After notifying the public and recommending freezing treatment of horse meat, no subsequent cases of food poisoning were reported. This indicates that freezing of horse meat is effective to prevent the occurrence of food poisoning caused by consuming raw horse meat containing S. fayeri.

  15. First identification of Sarcocystis tenella (Railliet, 1886) Moulé, 1886 (Protozoa: Apicomplexa) by PCR in naturally infected sheep from Brazil.

    Science.gov (United States)

    da Silva, Rodrigo Costa; Su, Chunlei; Langoni, Helio

    2009-11-12

    Sarcocystis tenella is a dog-sheep protozoan parasite, causing a widespread enzootic muscle parasitosis and neurological disease mainly in lambs. This parasite is pathogenic to sheep and important to the economical production of sheep. The present study was initially aimed to determine Toxoplasma gondii infection and the occurrence of co-infection with other Apicomplexa parasites in 602 Brazilian sheep. Twenty of these sheep were positive with antibodies to T. gondii by MAT and IFAT-IgG tests, positive with PCR-RFLP genotyping at multiple loci, and parasites were isolated from mice infected with sheep tissue samples. Two additional sheep born in Brazil, a 2-year-old female Polwarth (Ideal) sheep, a breed originated from Australia (#1), and a 1-year-old male Corriedale sheep, a breed originated from New Zealand and Australia (#2) were positive to T. gondii antibodies by serum tests, and PCR, but negative for bioassay in mice. In genotyping at 12 loci, sheep #1 sample and #2 presented positive results only for some markers. PCR-RFLP of 18S ribosomal RNA (18S rRNA) was performed in all 22 animals to identify the possibility of co-infection of T. gondii with other Apicomplexa parasites, such as S. tenella, Neospora caninum and Hammondia hammondi, resulting in a T. gondii profile for the first 20 animals and a unique genotyping profile for sheep #1 and #2, identical to S. tenella. The 18S rRNA PCR products (approximately 310 bp) were sequenced and blasted to GenBank database at NCBI. Both samples were identical to S. tenella 18S rRNA gene (GenBank accession number L24383-1). These results suggest the existence of co-infection of S. tenella with T. gondii in ewes from Brazil.

  16. Enolasa específica de neurona en dos recién nacidos con depresión ligera al nacer Neuron- specific Enolase in two newborns presenting with moderate depression at birth

    Directory of Open Access Journals (Sweden)

    Raisa Bu-Coifiu Fanego

    2009-03-01

    Full Text Available INTRODUCCIÓN. La enolasa específica de neurona es una isoenzima que se vierte al torrente sanguíneo después de un episodio de daño neuronal. En los procesos de hipoxia neonatal estos valores enzimáticos en suero suelen estar alterados. El objetivo del presente artículo fue estudiar la enolasa específica de neurona en suero de 2 recién nacidos con Apgar bajo y determinar si, en el seguimiento durante un año, dichos pacientes presentaban trastornos del desarrollo psicomotor. MÉTODOS. Se tomaron muestras de suero al momento del nacimiento y a las 72 h siguientes. Se determinaron los niveles de enolasa específica de neurona por un método inmunoenzimático de tipo ELISA. Cada muestra fue evaluada por el método de reacción en cadena de la polimerasa para citomegalovirus, en el Instituto de Inmunología de Wuersburg (Alemania. También se cuantificaron anticuerpos contra citomegalovirus de clase IgM e IgG, en el Laboratorio de Neuroquímica de la Universidad Georg August de Goettingen (Alemania. Se recogieron los datos clínicos de interés de cada recién nacido y al año se citaron a estos pacientes y se les realizó un examen físico para evaluar su neurodesarrollo. RESULTADOS. Las cifras de enolasa estuvieron incrementadas tanto al nacimiento como a las 72 h, con anticuerpos anticitomegalovirus de clase IgG que fueron transferidos de la madre a través de la placenta. No se encontró presencia de este virus en el momento del nacimiento. En el examen físico y neurológico realizado al año se constató que los niños evolucionaban satisfactoriamente hasta esa fecha. CONCLUSIONES. Se recomienda extender el estudio hasta los 3 años de vida y aumentar el número de pacientes estudiados, con énfasis en aquellos casos cuyo Apgar es menor de 5 a los 5 min del nacimiento.INTRODUCTION: Neuron-specific Enolase of is an isoenzyme present in blood stream after a neuronal damage episode. In processes of neonatal hypoxia, these enzymatic values

  17. Non increased neuron-specific enolase concentration in cerebrospinal fluid during first febrile seizures and a year follow-up in pediatric patients No incrementos en la concentración de enolasa específica de neurona en el líquido cefalorraquídeo durante el primer ataque febril y al año en pacientes pediátricos

    Directory of Open Access Journals (Sweden)

    ALBERTO J. DORTA-CONTRERAS

    1998-09-01

    Full Text Available Febrile seizures are the commonest acute neurological disorder of early childhood. Studies suggested that febrile seizures are previous acute events from a more serious neurological problem. Due to neuron-specific enolase is generally accepted as a marker for neuropathological processes in the brain, 16 pediatric patients were studied during their first seizures and a year after it. Neuron-specific enolase in cerebrospinal fluid and blood were analysed by an immune enzyme assay. Non pathological neuron-specific enolase values were obtained in both periods in the group of patients. There were no significative differences when paired series statistics test was performed with 95% of confidence. Neuron-specific enolase appears not to be a marker for febrile seizures because its concentration not be increased in cerebrospinal fluid in this group of patients.Los ataques febriles constituyen el trastorno neurológico agudo más común en la infancia temprana. Existen estudios que sugieren que los ataques febriles son eventos agudos previos a problemas neurológicos más severos. Debido a que la enolasa específica de neurona está aceptada generalmente como marcador de procesos neuropatológicos en el cerebro, se estudiaran 16 pacientes pediátricos durante su primer ataque y al año de este. La enolasa específica de neurona en el líquido cefalorraquídeo y sangre fue analizada por una prueba inmunoenzimática. No se obtuvieron valores patológicos de enolasa específica de neurona en ambos períodos en el grupo de pacientes. No hubo diferencias significativas al aplicar el test de series apareadas con un 95% de confianza. La enolasa específica de neurona parece no ser un marcador para ataques febriles porque su concentración no se incrementa en este grupo de pacientes.

  18. Neuronas espejo, intersubjetividad y desarrollo temprano

    OpenAIRE

    Martínez, Mauricio Sebastián

    2009-01-01

    Clásicamente la capacidad que poseemos las personas, y algunos primates, para atribuir estados mentales (intenciones, deseos, creencias, etc.) se ha intentado explicar desde dos perspectivas. La primera de ellas, usualmente denominada inferencialista, asume que esta capacidad se basa en la capacidad de nuestro sistema cognitivo para realizar inferencias sobre los estados mentales propios y de las demás personas. La segunda, a la conocida como simulacionista, sostiene que nuestra capacidad par...

  19. Inmunomarcación de neuronas dopaminérgicas en cortes flotantes de hipotálamo de rata: preservación alternativa del tejido nervioso antes del corte Immunohistochemical Studies Of Dopaminergic Neurons On Free Floating Sections: Alternative Cryopreservation Method Of Nervous Tissue Before Cutting

    Directory of Open Access Journals (Sweden)

    Valeria Cholich

    2008-07-01

    Full Text Available Se realizó un estudio inmunohistoquímico de la enzima tirosina hidroxilasa (marcador de neuronas dopaminérgicas en el hipotálamo de ratas Wistar machos adultas en cortes flotantes de muestras fijadas por perfusión. Debido a que el número de cerebros que se procesaron fue superior al número que pueden ser cortados inmediatamente, el material debió almacenarse congelando los cerebros enteros a -80ºC. Pero por un desperfecto técnico del equipo de refrigeración, las muestras debieron trasladarse a -20ºC resultando en el deterioro de las mismas. Ante este inconveniente, los sucesivos cerebros fueron almacenados en sacarosa al 30% p/v en buffer fosfato salino (PBS con 0,01% de azida sódica y mantenidos a 4ºC durante tiempos variables (de semanas a meses hasta ser congelados con gas clorofluorado y cortados. Estos cerebros no mostraron alteración en la estructura morfológica del tejido. Esta metodología de preservación aquí descrita sería una alternativa de elección válida para aquellos laboratorios que no cuenten con un equipo de refrigeración de -80ºC.In central nervous system histological studies, free-floating sections of perfusion-fixed samples are frequently used. Samples storage may be performed freezing either the entire brain at -80ºC or sections at -20ºC. When studying hypothalamic tyrosine hydroxylase enzyme (dopaminergic neurons marker by immunohistochemistry in adult male Wistar rats, entire brains were stored at -80ºC. Due to an abrupt freezer technical failure, samples should be thawed to -20ºC with the resulting samples damage. To avoid this situation, subsequent brains were stored in 30% sucrose in saline phosphate buffer (PBS with 0.01% sodium azide and kept at 4ºC for different periods (weeks to months until they were frozen with chlorofluorade gas and cut. These brains showed no morphological alterations of tissue structure. This preservation method appeared to be an alternative valid option to

  20. Red foxes (Vulpes vulpes) in Ireland as hosts for parasites of potential zoonotic and veterinary significance.

    Science.gov (United States)

    Wolfe, A; Hogan, S; Maguire, D; Fitzpatrick, C; Vaughan, L; Wall, D; Hayden, T J; Mulcahy, G

    Intestinal washes, faecal flotations and serological examinations for antibodies to Toxoplasma gondii and Neospora caninum were used to assess the prevalence of parasites in carcases of foxes killed on roads or shot in the Dublin area and surrounding counties. The ascarids Uncinaria stenocephala and Toxocara canis were prevalent, as was the trematode Alaria alata. Taenia species, eggs of Capillaria species and sporocysts of Sarcocystis species were also found. Only one fox out of 70 examined was seropositive for N. caninum, whereas 24 of 51 were seropositive for T. gondii.

  1. Protozoal Meningoencephalitis in Sea Otters (Enhydra lutris): a Histopathological and Immunohistochemical Study of Naturally Occuring Cases

    Science.gov (United States)

    Thomas, N.J.; Dubey, J.P.; Lindsay, D.S.; Cole, R.A.; Meteyer, C.U.

    2007-01-01

    Protozoal meningoencephalitis is considered to be an important cause of mortality in the California sea otter (Enhydra lutris). Thirty nine of 344 (11.3%) California (CA) and Washington state (WA) sea otters examined from 1985 to 2004 had histopathological evidence of significant protozoal meningoencephalitis. The aetiological agents and histopathological changes associated with these protozoal infections are described. The morphology of the actively multiplicative life stages of the organisms (tachyzoites for Toxoplasma gondii and merozoites for Sarcocystis neurona) and immunohistochemical labelling were used to identify infection with S. neurona (n=22, 56.4%), T. gondii (n=5, 12.8%) or dual infection with both organisms (n=12, 30.8%). Active S. neurona was present in all dual infections, while most had only the latent form of T. gondii. In S. neurona meningoencephalitis, multifocal to diffuse gliosis was widespread in grey matter and consistently present in the molecular layer of the cerebellum. In T. gondii meningoencephalitis, discrete foci of gliosis and malacia were more widely separated, sometimes incorporated pigment-laden macrophages and mineral, and were found predominantly in the cerebral cortex. Quiescent tissue cysts of T. gondii were considered to be incidental and not a cause of clinical disease and mortality. Protozoal meningoencephalitis was diagnosed more frequently in the expanding population of WA sea otters (10 of 31, 32.3%) than in the declining CA population (29 of 313, 9.3%). Among sea otters with protozoal meningoencephalitis, those that had displayed neurological signs prior to death had active S. neurona encephalitis, supporting the conclusion that S. neurona is the most significant protozoal pathogen in the central nervous system of sea otters.

  2. Molecular phylogeny of Toxoplasmatinae: comparison between inferences based on mitochondrial and apicoplast genetic sequences

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    Michelle Klein Sercundes

    2016-03-01

    Full Text Available Abstract Phylogenies within Toxoplasmatinae have been widely investigated with different molecular markers. Here, we studied molecular phylogenies of the Toxoplasmatinae subfamily based on apicoplast and mitochondrial genes. Partial sequences of apicoplast genes coding for caseinolytic protease (clpC and beta subunit of RNA polymerase (rpoB, and mitochondrial gene coding for cytochrome B (cytB were analyzed. Laboratory-adapted strains of the closely related parasites Sarcocystis falcatula and Sarcocystis neurona were investigated, along with Neospora caninum, Neospora hughesi, Toxoplasma gondii (strains RH, CTG and PTG, Besnoitia akodoni, Hammondia hammondiand two genetically divergent lineages of Hammondia heydorni. The molecular analysis based on organellar genes did not clearly differentiate between N. caninum and N. hughesi, but the two lineages of H. heydorni were confirmed. Slight differences between the strains of S. falcatula and S. neurona were encountered in all markers. In conclusion, congruent phylogenies were inferred from the three different genes and they might be used for screening undescribed sarcocystid parasites in order to ascertain their phylogenetic relationships with organisms of the family Sarcocystidae. The evolutionary studies based on organelar genes confirm that the genusHammondia is paraphyletic. The primers used for amplification of clpC and rpoB were able to amplify genetic sequences of organisms of the genus Sarcocystisand organisms of the subfamily Toxoplasmatinae as well.

  3. Six new species of coccidia (Apicomplexa: Eimeriidae) from endangered Phelsuma spp. geckoes (Sauria: Gekkonidae) of the Black River Gorges National Park, Mauritius.

    Science.gov (United States)

    Daszak, Peter; Ball, Stanley J; Jones, Carl G; Streicker, Daniel G; Snow, Keith R

    2009-12-01

    of P. cepediana. These oocysts or sporocysts are significantly larger than the Cryptosporidium species so far described from reptiles, and likely represent excretion of spuriously ingested sporocysts of a Sarcocystis or Adelina coccidian.

  4. Characterization of IgG monoclonal antibody targeted to both tissue cyst and sporocyst walls of Toxoplasma gondii

    Science.gov (United States)

    Toxoplasma gondii infects approximately one third of the human population and animals habiting terrestrial and aquatic environments. Its environmentally resistant oocysts are excreted by felids, and the stage encysted in tissues (tissue cysts), are important in the horizontal transmission of T. gon...

  5. Endoparasites of American marten (Martes americana): Review of the literature and parasite survey of reintroduced American marten in Michigan.

    Science.gov (United States)

    Spriggs, Maria C; Kaloustian, Lisa L; Gerhold, Richard W

    2016-12-01

    The American marten (Martes americana) was reintroduced to both the Upper (UP) and northern Lower Peninsula (NLP) of Michigan during the 20th century. This is the first report of endoparasites of American marten from the NLP. Faeces from live-trapped American marten were examined for the presence of parasitic ova, and blood samples were obtained for haematocrit evaluation. The most prevalent parasites were Capillaria and Alaria species. Helminth parasites reported in American marten for the first time include Eucoleus boehmi, hookworm, and Hymenolepis and Strongyloides species. This is the first report of shedding of Sarcocystis species sporocysts in an American marten and identification of 2 coccidian parasites, Cystoisospora and Eimeria species. The pathologic and zoonotic potential of each parasite species is discussed, and previous reports of endoparasites of the American marten in North America are reviewed.

  6. Endoparasites of American marten (Martes americana: Review of the literature and parasite survey of reintroduced American marten in Michigan

    Directory of Open Access Journals (Sweden)

    Maria C. Spriggs

    2016-12-01

    Full Text Available The American marten (Martes americana was reintroduced to both the Upper (UP and northern Lower Peninsula (NLP of Michigan during the 20th century. This is the first report of endoparasites of American marten from the NLP. Faeces from live-trapped American marten were examined for the presence of parasitic ova, and blood samples were obtained for haematocrit evaluation. The most prevalent parasites were Capillaria and Alaria species. Helminth parasites reported in American marten for the first time include Eucoleus boehmi, hookworm, and Hymenolepis and Strongyloides species. This is the first report of shedding of Sarcocystis species sporocysts in an American marten and identification of 2 coccidian parasites, Cystoisospora and Eimeria species. The pathologic and zoonotic potential of each parasite species is discussed, and previous reports of endoparasites of the American marten in North America are reviewed.

  7. Equine Protozoal Myeloencephalitis: An Updated Consensus Statement with a Focus on Parasite Biology, Diagnosis, Treatment, and Prevention.

    Science.gov (United States)

    Reed, S M; Furr, M; Howe, D K; Johnson, A L; MacKay, R J; Morrow, J K; Pusterla, N; Witonsky, S

    2016-01-01

    Equine protozoal myeloencephalitis (EPM) remains an important neurologic disease of horses. There are no pathognomonic clinical signs for the disease. Affected horses can have focal or multifocal central nervous system (CNS) disease. EPM can be difficult to diagnose antemortem. It is caused by either of 2 parasites, Sarcocystis neurona and Neospora hughesi, with much less known about N. hughesi. Although risk factors such as transport stress and breed and age correlations have been identified, biologic factors such as genetic predispositions of individual animals, and parasite-specific factors such as strain differences in virulence, remain largely undetermined. This consensus statement update presents current published knowledge of the parasite biology, host immune response, disease pathogenesis, epidemiology, and risk factors. Importantly, the statement provides recommendations for EPM diagnosis, treatment, and prevention.

  8. First report of cerebellar abiotrophy in an Arabian foal from Argentina

    Science.gov (United States)

    Sadaba, S.A.; Madariaga, G.J.; Botto, C.M. Corbi; Carino, M.H.; Zappa, M.E.; García, P. Peral; Olguín, S.A.; Massone, A.; Díaz, S.

    2016-01-01

    Evidence of cerebellar abiotrophy (CA) was found in a six-month-old Arabian filly with signs of incoordination, head tremor, wobbling, loss of balance and falling over, consistent with a cerebellar lesion. Normal hematology profile blood test and cerebrospinal fluid analysis excluded infectious encephalitis, and serological testing for Sarcocystis neurona was negative. The filly was euthanized. Postmortem X-ray radiography of the cervical cephalic region identified not abnormalities, discounting spinal trauma. The histopathological analysis of serial transverse cerebellar sections by electron microscopy revealed morphological characteristics of apoptotic cells with pyknotic nuclei and degenerate mitochondria, cytoplasmic condensation and areas with absence of Purkinje cells, matching with CA histopathological characteristics. The indirect DNA test for CA was positive in the filly, and DNA test confirmed the CA carrier state in the parents and the recessive inheritance of the disease. To our knowledge this is the first report of a CA case in Argentina. PMID:28116251

  9. First report of cerebellar abiotrophy in an Arabian foal from Argentina

    Directory of Open Access Journals (Sweden)

    S.A. Sadaba

    2016-12-01

    Full Text Available Evidence of cerebellar abiotrophy (CA was found in a six-month-old Arabian filly with signs of incoordination, head tremor, wobbling, loss of balance and falling over, consistent with a cerebellar lesion. Normal hematology profile blood test and cerebrospinal fluid analysis excluded infectious encephalitis, and serological testing for Sarcocystis neurona was negative. The filly was euthanized. Postmortem X-ray radiography of the cervical cephalic region identified not abnormalities, discounting spinal trauma. The histopathological analysis of serial transverse cerebellar sections by electron microscopy revealed morphological characteristics of apoptotic cells with pyknotic nuclei and degenerate mitochondria, cytoplasmic condensation and areas with absence of Purkinje cells, matching with CA histopathological characteristics. The indirect DNA test for CA was positive in the filly, and DNA test confirmed the CA carrier state in the parents and the recessive inheritance of the disease. To our knowledge this is the first report of a CA case in Argentina.

  10. Diagnóstico diferencial de trombose aortoilíaca e mieloencefalite protozoária equina: relato de caso Differential diagnosis between aorto-iliac thrombosis and equine protozoal myeloencephalitis: case report

    Directory of Open Access Journals (Sweden)

    P.B. Escodro

    2010-10-01

    Full Text Available Relata-se o caso de uma égua de atividade de polo, que apresentou inicialmente claudicação leve no membro posterior esquerdo, a qual evoluiu para ataxia e atrofia da musculatura glútea do lado esquerdo, com diagnóstico de trombose aortoilíaca (TAI. A paciente foi tratada com suspeita de mieloencefalite protozoária equina, devido à semelhança dos sinais clínicos com essa doença, porém o líquido cefalorraquidiano apresentou-se negativo para anticorpos anti-Sarcocystis neurona. A palpação transretal indicou uma massa na bifurcação aortoilíaca esquerda. Na avaliação ultrassonográfica, visualizou-se imagem hiperecoica aderida ao endotélio vascular, sugerindo TAI atingindo a estenose de 70% da luz arterial.The case of a mare used for polo is reported. The animal showed clinical signs of soft lameness of the hindlimb, evolving to ataxia and gluteal muscle atrophy, with aorto-iliac thrombosis (AIT. The patient was treated with the suspect of equine protozoal myeloencephalitis (EPM, due to the resemblance of clinical signs. Cerebrospinal fluid analysis was negative for antibodies against Sarcocystis neurona. The transrectal examination indicated a mass in the left aorto-iliac bifurcation. In the ultrasonographic evaluation, a hyperechoic image adhered to the vascular endothelium was observed, suggesting (AIT, occupying 70% of arterial lumen. The present article has the objective of pointing out the importance of the differential diagnosis between AIT and EPM in horses with ataxia in hindlimbs and muscular atrophy.

  11. Coccidian parasites (Apicomplexa) from snakes in the southcentral and southwestern United States: new host and geographic records.

    Science.gov (United States)

    McAllister, C T; Upton, S J; Trauth, S E; Dixon, J R

    1995-02-01

    Four hundred thirty-five leptotyphlopid, colubrid, elapid, and viperid snakes were collected from various localities in Arkansas, New Mexico, Oklahoma, and Texas, and their feces were examined for coccidian parasites. Of these, 131 (30%) were passing oocysts or sporocysts of at least 1 coccidian; 88 (67%) of the infected snakes had only 1 species of coccidian when they were examined. Aquatic and semiaquatic snakes accounted for 48% of the infections, whereas strictly terrestrial snakes comprised the other 52%. There was more than a 2-fold difference in prevalence among these 2 groups as 63 of 129 (49%) of the aquatic and semiaquatic snakes versus 68 of 306 (22%) of the terrestrial snakes harbored coccidia. Most terrestrial snakes were infected by species of Caryospora and Sarcocystis that are either facultatively or obligatorily heteroxenous. The aquatic and semiaquatic species most often harbored eimerians. Attempts to transmit some of the Sarcocystis spp. experimentally from Crotalus atrox to Mus musculus, Peromyscus leucopus, Peromyscus maniculatus, or Microtus ochrogaster were unsuccessful. This report documents 27 new host and several distributional records for coccidians from snakes in the southcentral and southwestern United States.

  12. Prey choice and habitat use drive sea otter pathogen exposure in a resource-limited coastal system

    Science.gov (United States)

    Johnson, Christine K.; Tinker, M. Tim; Estes, James A.; Conrad, Patricia A.; Staedler, Michelle M.; Miller, Melissa A.; Jessup, David A.; Mazet, Jonna A.K.

    2014-01-01

    The processes promoting disease in wild animal populations are highly complex, yet identifying these processes is critically important for conservation when disease is limiting a population. By combining field studies with epidemiologic tools, we evaluated the relationship between key factors impeding southern sea otter (Enhydra lutris nereis) population growth: disease and resource limitation. This threatened population has struggled to recover despite protection, so we followed radio-tagged sea otters and evaluated infection with 2 disease-causing protozoal pathogens, Toxoplasma gondii and Sarcocystis neurona, to reveal risks that increased the likelihood of pathogen exposure. We identified patterns of pathogen infection that are linked to individual animal behavior, prey choice, and habitat use. We detected a high-risk spatial cluster of S. neurona infections in otters with home ranges in southern Monterey Bay and a coastal segment near San Simeon and Cambria where otters had high levels of infection with T. gondii. We found that otters feeding on abalone, which is the preferred prey in a resource-abundant marine ecosystem, had a very low risk of infection with either pathogen, whereas otters consuming small marine snails were more likely to be infected with T. gondii. Individual dietary specialization in sea otters is an adaptive mechanism for coping with limited food resources along central coastal California. High levels of infection with protozoal pathogens may be an adverse consequence of dietary specialization in this threatened species, with both depleted resources and disease working synergistically to limit recovery.

  13. Gene Discovery in the Apicomplexa as Revealed by EST Sequencing and Assembly of a Comparative Gene Database

    Science.gov (United States)

    Li, Li; Brunk, Brian P.; Kissinger, Jessica C.; Pape, Deana; Tang, Keliang; Cole, Robert H.; Martin, John; Wylie, Todd; Dante, Mike; Fogarty, Steven J.; Howe, Daniel K.; Liberator, Paul; Diaz, Carmen; Anderson, Jennifer; White, Michael; Jerome, Maria E.; Johnson, Emily A.; Radke, Jay A.; Stoeckert, Christian J.; Waterston, Robert H.; Clifton, Sandra W.; Roos, David S.; Sibley, L. David

    2003-01-01

    Large-scale EST sequencing projects for several important parasites within the phylum Apicomplexa were undertaken for the purpose of gene discovery. Included were several parasites of medical importance (Plasmodium falciparum, Toxoplasma gondii) and others of veterinary importance (Eimeria tenella, Sarcocystis neurona, and Neospora caninum). A total of 55,192 ESTs, deposited into dbEST/GenBank, were included in the analyses. The resulting sequences have been clustered into nonredundant gene assemblies and deposited into a relational database that supports a variety of sequence and text searches. This database has been used to compare the gene assemblies using BLAST similarity comparisons to the public protein databases to identify putative genes. Of these new entries, ∼15%–20% represent putative homologs with a conservative cutoff of p neurona: , , , , , , , , , , , , , –, –, –, –, –. Eimeria tenella: –, –, –, –, –, –, –, –, – , –, –, –, –, –, –, –, –, –, –, –. Neospora caninum: –, –, , – , –, –.] PMID:12618375

  14. Hepatic sarcocystosis in a striped dolphin (Stenella coeruleoalba) from the Spanish Mediterranean coast.

    Science.gov (United States)

    Resendes, A R; Juan-Sallés, C; Almeria, S; Majó, N; Domingo, M; Dubey, J P

    2002-02-01

    Fatal hepatic sarcocystosis was diagnosed in a striped dolphin (Stenella coeruleoalba) from the northeastern Spanish Mediterranean coast based on pathologic findings and the microscopic and ultrastructural characteristics of the intralesional parasite. Main gross lesions were icterus, subcutaneous hemorrhages, and hepatic congestion. The most prominent microscopic lesions consisted of severe acute multifocal to coalescing necrotizing hepatitis with cholestasis and intralesional protozoa. There was severe chronic pancreatitis with generalized distension of pancreatic ducts by hyaline plugs and adult trematodes. Only asexual stages of the protozoa were found. The parasite in the liver divided by endopolygeny. Schizonts varied in shape and size. Mature schizonts had merozoites randomly arranged or budding peripherally around a central residual body. Schizonts were up to 22 microm long, and merozoites were up to 6 microm long. Ultrastructurally, merozoites lacked rhoptries. This parasite failed to react by immunohistochemistry with anti-Toxoplasma gondii, anti-Neospora caninum and anti-Sarcocystis neurona antibodies. The microscopic and ultrastructural morphologies of the parasite were consistent with Sarcocystis canis, so far described only from animals in the Unites States. The life cycle and source of S. canis are unknown. The present report of S. canis-like infection in a sea mammal from Spain indicates that the definitive host for this parasite also exists outside of the United States.

  15. Fatal hepatic sarcocystosis in a puppy with eosinophilia and eosinophilic peritoneal effusion.

    Science.gov (United States)

    Allison, Robin; Williams, Philip; Lansdowne, Jennifer; Lappin, Michael; Jensen, Tracey; Lindsay, David

    2006-09-01

    A 3-month-old male Golden Retriever puppy was evaluated for lethargy and fever of 2-days duration. Results of a CBC and biochemical profile revealed marked eosinophilia (6.3 X 10(3)/microL; reference interval 0.1-1.2 X 10(3)/microL), moderate thrombocytopenia, and increased activities of alanine aminotransferase, aspartate aminotransferase, and creatine kinase. Hepatomegaly and peritoneal effusion were found using abdominal ultrasound. Peritoneal fluid analysis revealed eosinophilic inflammation (23,000 nucleated cells/microL with 88% eosinophils). Despite supportive treatment the puppy's condition deteriorated rapidly; euthanasia was requested, and a necropsy performed. Microscopically, there was marked necrosuppurative and eosinophilic hepatitis with vasculitis. Numerous hepatocytes contained protozoal organisms suspected to be Toxoplasma gondii or Neospora caninum. However, serum was negative for both T gondii and N caninum antibodies; polymerase chain reaction assay on hepatic tissue was negative for both organisms; and immunohistochemical evaluation of hepatic tissue using serum raised against T gondii, N caninum, and Sarcocystis neurona also was negative. Schizont morphology suggested that merozoites replicated by endopolygeny, forming rosettes around a central residual body. Transmission electron microscopy revealed that merozoites lacked rhoptries. These findings were consistent with a diagnosis of Sarcocystis canis, an apicomplexan parasite with an unknown life cycle.

  16. Cytokine gene signatures in neural tissue of horses with equine protozoal myeloencephalitis or equine herpes type 1 myeloencephalopathy.

    Science.gov (United States)

    Pusterla, N; Wilson, W D; Conrad, P A; Barr, B C; Ferraro, G L; Daft, B M; Leutenegger, C M

    2006-09-09

    This study was designed to determine the relative levels of gene transcription of selected pathogens and cytokines in the brain and spinal cord of 12 horses with equine protozoal myeloencephalitis (EPM), 11 with equine herpesvirus type 1 (EHV-1) myeloencephalopathy, and 12 healthy control horses by applying a real time pcr to the formalin-fixed and paraffin-embedded tissues. Total rna was extracted from each tissue, transcribed to complementary dna (cDNA) and assayed for Sarcocystis neurona, Neospora hughesi, EHV-1, equine GAPDH (housekeeping gene), tumour necrosis factor (TNF)-alpha, interferon (IFN)-gamma, interleukin (IL)-1beta, IL-2, IL-4, IL-6, IL-8, IL-10 AND IL-12 p40. S neurona cdna was detected in the neural tissue from all 12 horses with EPM, and two of them also had amplifiable cDNA of N hughesi. The relative levels of transcription of protozoal cdna ranged from 1 to 461 times baseline (mean 123). All the horses with ehv-1 myeloencephalopathy had positive viral signals by PCR with relative levels of transcription ranging from 1 to 1618 times baseline (mean 275). All the control horses tested negative for S neurona, N hughesi and EHV-1 cdna. The cytokine profiles of each disease indicated a balance between pro- and anti-inflammatory markers. In the horses with epm the pro-inflammatory Th1 cytokines (IL-8, TNF-alpha and IFN-gamma) were commonly expressed but the anti-inflammatory Th2 cytokines (IL-4, IL-6 AND IL-10) were absent or rare. In the horses with ehv-1 the proinflammatory cytokine IL-8 was commonly expressed, but IL-10 and IFN-gamma were not, and TNF-alpha was rare. Tissue from the control horses expressed only the gene GAPDH.

  17. Polyparasitism is associated with increased disease severity in Toxoplasma gondii-infected marine sentinel species.

    Directory of Open Access Journals (Sweden)

    Amanda K Gibson

    2011-05-01

    Full Text Available In 1995, one of the largest outbreaks of human toxoplasmosis occurred in the Pacific Northwest region of North America. Genetic typing identified a novel Toxoplasma gondii strain linked to the outbreak, in which a wide spectrum of human disease was observed. For this globally-distributed, water-borne zoonosis, strain type is one variable influencing disease, but the inability of strain type to consistently explain variations in disease severity suggests that parasite genotype alone does not determine the outcome of infection. We investigated polyparasitism (infection with multiple parasite species as a modulator of disease severity by examining the association of concomitant infection of T. gondii and the related parasite Sarcocystis neurona with protozoal disease in wild marine mammals from the Pacific Northwest. These hosts ostensibly serve as sentinels for the detection of terrestrial parasites implicated in water-borne epidemics of humans and wildlife in this endemic region. Marine mammals (151 stranded and 10 healthy individuals sampled over 6 years were assessed for protozoal infection using multi-locus PCR-DNA sequencing directly from host tissues. Genetic analyses uncovered a high prevalence and diversity of protozoa, with 147/161 (91% of our sampled population infected. From 2004 to 2009, the relative frequency of S. neurona infections increased dramatically, surpassing that of T. gondii. The majority of T. gondii infections were by genotypes bearing Type I lineage alleles, though strain genotype was not associated with disease severity. Significantly, polyparasitism with S. neurona and T. gondii was common (42% and was associated with higher mortality and more severe protozoal encephalitis. Our finding of widespread polyparasitism among marine mammals indicates pervasive contamination of waterways by zoonotic agents. Furthermore, the significant association of concomitant infection with mortality and protozoal encephalitis identifies

  18. Polyparasitism Is Associated with Increased Disease Severity in Toxoplasma gondii-Infected Marine Sentinel Species

    Science.gov (United States)

    Gibson, Amanda K.; Raverty, Stephen; Lambourn, Dyanna M.; Huggins, Jessica; Magargal, Spencer L.; Grigg, Michael E.

    2011-01-01

    In 1995, one of the largest outbreaks of human toxoplasmosis occurred in the Pacific Northwest region of North America. Genetic typing identified a novel Toxoplasma gondii strain linked to the outbreak, in which a wide spectrum of human disease was observed. For this globally-distributed, water-borne zoonosis, strain type is one variable influencing disease, but the inability of strain type to consistently explain variations in disease severity suggests that parasite genotype alone does not determine the outcome of infection. We investigated polyparasitism (infection with multiple parasite species) as a modulator of disease severity by examining the association of concomitant infection of T. gondii and the related parasite Sarcocystis neurona with protozoal disease in wild marine mammals from the Pacific Northwest. These hosts ostensibly serve as sentinels for the detection of terrestrial parasites implicated in water-borne epidemics of humans and wildlife in this endemic region. Marine mammals (151 stranded and 10 healthy individuals) sampled over 6 years were assessed for protozoal infection using multi-locus PCR-DNA sequencing directly from host tissues. Genetic analyses uncovered a high prevalence and diversity of protozoa, with 147/161 (91%) of our sampled population infected. From 2004 to 2009, the relative frequency of S. neurona infections increased dramatically, surpassing that of T. gondii. The majority of T. gondii infections were by genotypes bearing Type I lineage alleles, though strain genotype was not associated with disease severity. Significantly, polyparasitism with S. neurona and T. gondii was common (42%) and was associated with higher mortality and more severe protozoal encephalitis. Our finding of widespread polyparasitism among marine mammals indicates pervasive contamination of waterways by zoonotic agents. Furthermore, the significant association of concomitant infection with mortality and protozoal encephalitis identifies polyparasitism as

  19. Polyparasitism is associated with increased disease severity in Toxoplasma gondii-infected marine sentinel species.

    Science.gov (United States)

    Gibson, Amanda K; Raverty, Stephen; Lambourn, Dyanna M; Huggins, Jessica; Magargal, Spencer L; Grigg, Michael E

    2011-05-01

    In 1995, one of the largest outbreaks of human toxoplasmosis occurred in the Pacific Northwest region of North America. Genetic typing identified a novel Toxoplasma gondii strain linked to the outbreak, in which a wide spectrum of human disease was observed. For this globally-distributed, water-borne zoonosis, strain type is one variable influencing disease, but the inability of strain type to consistently explain variations in disease severity suggests that parasite genotype alone does not determine the outcome of infection. We investigated polyparasitism (infection with multiple parasite species) as a modulator of disease severity by examining the association of concomitant infection of T. gondii and the related parasite Sarcocystis neurona with protozoal disease in wild marine mammals from the Pacific Northwest. These hosts ostensibly serve as sentinels for the detection of terrestrial parasites implicated in water-borne epidemics of humans and wildlife in this endemic region. Marine mammals (151 stranded and 10 healthy individuals) sampled over 6 years were assessed for protozoal infection using multi-locus PCR-DNA sequencing directly from host tissues. Genetic analyses uncovered a high prevalence and diversity of protozoa, with 147/161 (91%) of our sampled population infected. From 2004 to 2009, the relative frequency of S. neurona infections increased dramatically, surpassing that of T. gondii. The majority of T. gondii infections were by genotypes bearing Type I lineage alleles, though strain genotype was not associated with disease severity. Significantly, polyparasitism with S. neurona and T. gondii was common (42%) and was associated with higher mortality and more severe protozoal encephalitis. Our finding of widespread polyparasitism among marine mammals indicates pervasive contamination of waterways by zoonotic agents. Furthermore, the significant association of concomitant infection with mortality and protozoal encephalitis identifies polyparasitism as

  20. BASES CELULARES Y MOLECULARES PARA EXPLICAR FILOGENETICAMENTE EL MODELO DE ACOPLAMIENTO METABOLICO GLIA-NEURONA.

    OpenAIRE

    BALMACEDA AGUILERA, CAROLINA IVETTE

    2009-01-01

    La glucosa es utilizada activamente para mantener la actividad metabólica del cerebro de los peces cartilaginosos, a pesar de ello, no existe información sobre la distribución y niveles de expresión de transportadores de glucosa en el cerebro de estos org 142p.

  1. Regulación de la dinámica mitocondrial en neuronas sometidas a excitotoxicidad

    OpenAIRE

    Martorell Riera, Alejandro

    2014-01-01

    Durante el ictus, los niveles elevados de glutamato extracelular, el principal neurotransmisor excitador en el sistema nervioso central, aumentan y se unen al receptor de NMDA promoviendo la excitotoxicidad. Esta situación genera que un flujo excesivo de Ca2+ pase a través del receptor de NMDA aumentando sus concentraciones intracelulares activando toda una serie de cascadas de señalización que pueden actuar directamente sobre las mitocondrias, promoviendo varios programas de mu...

  2. Estudios del ciclo vesicular en neuronas granulares de cerebelo de rata

    OpenAIRE

    2014-01-01

    Las sinapsis químicas son responsables de la transmisión de la información en el sistema nervioso central de mamíferos; estas se caracterizan por la presencia de pequeñas vesículas que contienen moléculas de neurotransmisor, denominadas vesículas sinápticas (SVs). (Sudhof, 2012). La llegada de un potencial de acción al compartimento presináptico, induce un influjo de calcio mediado por los canales de calcio activados por voltaje (CCAV) que promueve la fusión de estas SVs con la membrana plasm...

  3. 离体条件下球虫卵囊子孢子囊的释放%Studies on Sporocyst Releasing from Oocyst of Eimeria tenella in Vitro

    Institute of Scientific and Technical Information of China (English)

    安健; 王黎霞; 汪明; 张建军; 李翠莲; 高立娜

    2006-01-01

    利用柔嫩艾美耳球虫(Eimeria tenella)为试验虫株,盖玻片、载玻片为实验材料,用拇指适当施加压力时,在400倍的光学显微镜下,观察了柔嫩艾美耳球虫卵囊破裂和子孢子囊释放的过程,结果发现,卵囊在适当压力的作用下,在卵囊一端发生破裂,随后子孢子囊逐个从破裂口处溢出,溢出后的子孢子囊内含有2个子孢子,说明球虫卵囊虽然对常规的消毒剂抵抗力很强,但是在鸡的消化道内,尤其在肌胃内球虫卵囊很容易破裂而释放子孢子囊.

  4. Snyltelarve snyder sig vej til sangfuglens endetarm

    DEFF Research Database (Denmark)

    Buchmann, Kurt

    2013-01-01

    Leucochloridium paradoxum sporocysts in tentacles of the snail Succinea show pulsating movements. Moving sporocysts with infective parasite larvae looks like an insect larva. Birds eat the sporocysts and subsequently obtain intestinal infection with the adult fluke.......Leucochloridium paradoxum sporocysts in tentacles of the snail Succinea show pulsating movements. Moving sporocysts with infective parasite larvae looks like an insect larva. Birds eat the sporocysts and subsequently obtain intestinal infection with the adult fluke....

  5. Snyltelarve snyder sig vej til sangfuglens endetarm

    DEFF Research Database (Denmark)

    Buchmann, Kurt

    2013-01-01

    Leucochloridium paradoxum sporocysts in tentacles of the snail Succinea show pulsating movements. Moving sporocysts with infective parasite larvae looks like an insect larva. Birds eat the sporocysts and subsequently obtain intestinal infection with the adult fluke.......Leucochloridium paradoxum sporocysts in tentacles of the snail Succinea show pulsating movements. Moving sporocysts with infective parasite larvae looks like an insect larva. Birds eat the sporocysts and subsequently obtain intestinal infection with the adult fluke....

  6. Equine protozoal myeloencephalitis.

    Science.gov (United States)

    MacKay, R J; Granstrom, D E; Saville, W J; Reed, S M

    2000-12-01

    Recent advances in the understanding of the parasite life cycle, epidemiology, clinical signs, diagnosis, treatment, and prevention of EPM are reviewed. The NAHMS Equine '98 study and a controlled retrospective study from The Ohio State University College of Veterinary Medicine identified a number of risk factors associated with development of the disease. The national annual incidence of EPM was 1% or less depending on the primary use of the animals. Increased disease risk was associated with age (1-5 and > 13 years of age), season (lowest in winter months and increasing with ambient temperature), previous stressful events, the presence of opossums, the use of nonsurface water drinking systems, and failure to restrict wildlife access to feed. Horses that received treatment were 10 times more likely to improve, and those that improved were 50 times more likely to survive. A number of recent studies confirmed that horses can be experimentally infected with S. neurona; however, large numbers of sporocysts are apparently necessary to achieve infection, and clinical signs and abnormal CNS histology are only seen inconsistently. Results suggest that CNS infection and positive CSF immunoblot findings may be transient phenomena among naturally infected horses. Although immunosuppression may be involved in the development of EPM, some element of the immune response seems to be necessary for the development of clinical signs. Use of the standard immunoblot test for the detection of anti-S. neurona antibodies in CSF continues to provide the most useful adjunct to a detailed neurologic examination for the diagnosis of EPM. Test sensitivity and specificity were 89% in 295 horses euthanatized because of neurologic disease, of which 123 were confirmed cases of EPM. The PPV was 85%, and the NVP was 92%. A number of promising new EPM treatments are under investigation. In addition to standard SDZ/PYR therapy, toltrazuril, ponazuril, diclazuril, and NTZ have shown promise as

  7. Renal infection by a new coccidian genus in big brown bats (Eptesicus fuscus).

    Science.gov (United States)

    Wünschmann, Arno; Wellehan, James F X; Armien, Anibal; Bemrick, William J; Barnes, Donald; Averbeck, Gary A; Roback, Richard; Schwabenlander, Marc; D'Almeida, Edgar; Joki, Ron; Childress, April L; Cortinas, Roberto; Gardiner, Chris H; Greiner, Ellis C

    2010-02-01

    A novel coccidian parasite from the kidney of big brown bats (Eptesicus fuscus) is described. This coccidian (Nephroisospora eptesici nov. gen., n. sp.) was associated with a generally mild, focal or multifocal, well-demarcated cortical renal lesion less than 1 mm in diameter. The lesion represented cystic, dilated tubules with hypertrophied tubular epithelial cells and was present in the kidneys of 29 of 590 bats. Numerous coccidian parasites in various stages of development were present within the tubular epithelial cells and within the cyst lumina. Oocysts were collected from cystic dilated tubules. Thin-walled, sporulated ellipsoidal oocysts measuring an average of 18.9 x 20.8 microm were present in kidney tissue. The oocysts contained 2 sporocysts with 4 sporozoites. A polar body and a prominent oocyst residuum were present in the oocysts, but no micropyle, sporocyst residuum, or Stieda bodies were detected. Analysis of the 18S rRNA gene sequence put the parasite in the Sarcocystidae. The parasite is closely related to Besnoitia, Hammondia, Neospora, and Toxoplasma. Ultrastructural features, such as the presence of an apical complex in merozoites, support the identification of a coccidian. A new genus and species, Nephroisospora eptesicii, is proposed for this unusual coccidian in which the entire cycle is completed in the kidney of a single host; it has a membrane-like oocyst wall, sporogony occurs in the host rather than in the abiotic environment, and the positioning of the parasite by nucleic acid sequence indicates it to be closely allied to Sarcocystis and Besnoitia.

  8. Cytokine Gene Expression in Response to SnSAG1 in Horses with Equine Protozoal Myeloencephalitis

    Science.gov (United States)

    Spencer, Jennifer A.; Deinnocentes, Patricia; Moyana, Edith M.; Guarino, Anthony J.; Ellison, Siobhan E.; Bird, R. Curtis; Blagburn, Byron L.

    2005-01-01

    Equine protozoal myeloencephalitis (EPM) is a neurologic syndrome seen in horses from the Americas and is mainly caused by Sarcocystis neurona. Recently, a 29-kDa surface antigen from S. neurona merozoites was identified as being highly immunodominant on a Western blot. This antigen has been sequenced and cloned, and the expressed protein has been named SnSAG1. In a previous study, cell-mediated immune responses to SnSAG1 were shown to be statistically significantly reduced in horses with EPM in comparison to EPM-negative control horses. It therefore appears as though the parasite is able to induce immunosuppression towards parasite-derived antigens as parasite-specific responses are decreased. Isolated peripheral blood lymphocytes from 21 EPM (cerebrospinal fluid [CSF] Western blot)-negative horses with no clinical signs and 21 horses with clinical signs of EPM (CSF Western blot positive) were cocultured with SnSAG1 for 48 and 72 h, and the effect on cytokine production was investigated by means of reverse transcriptase PCR. Cytokines assayed include gamma interferon (IFN-γ), tumor necrosis factor alpha, interleukin (IL)-2, IL-4, and IL-6. β-Actin was used as the housekeeping gene. A Wilcoxon signed-rank test of the findings indicated that there was a statistically significant decrease in IFN-γ production after 48 h in culture for samples from horses with clinical disease. There was also a statistically significant increase in IL-4 production after 72 h in culture for samples from horses with EPM. These results further support the notion that this parasite is able to subvert the immune system in horses with clinical disease. PMID:15879026

  9. Seasonal and biogeographical patterns of gastrointestinal parasites in large carnivores: wolves in a coastal archipelago.

    Science.gov (United States)

    Bryan, Heather M; Darimont, Chris T; Hill, Janet E; Paquet, Paul C; Thompson, R C Andrew; Wagner, Brent; Smits, Judit E G

    2012-05-01

    Parasites are increasingly recognized for their profound influences on individual, population and ecosystem health. We provide the first report of gastrointestinal parasites in gray wolves from the central and north coasts of British Columbia, Canada. Across 60 000 km(2), wolf feces were collected from 34 packs in 2005-2008. At a smaller spatial scale (3300 km(2)), 8 packs were sampled in spring and autumn. Parasite eggs, larvae, and cysts were identified using standard flotation techniques and morphology. A subset of samples was analysed by PCR and sequencing to identify tapeworm eggs (n=9) and Giardia cysts (n=14). We detected ≥14 parasite taxa in 1558 fecal samples. Sarcocystis sporocysts occurred most frequently in feces (43·7%), followed by taeniid eggs (23·9%), Diphyllobothrium eggs (9·1%), Giardia cysts (6·8%), Toxocara canis eggs (2·1%), and Cryptosporidium oocysts (1·7%). Other parasites occurred in ≤1% of feces. Genetic analyses revealed Echinococcus canadensis strains G8 and G10, Taenia ovis krabbei, Diphyllobothrium nehonkaiense, and Giardia duodenalis assemblages A and B. Parasite prevalence differed between seasons and island/mainland sites. Patterns in parasite prevalence reflect seasonal and spatial resource use by wolves and wolf-salmon associations. These data provide a unique, extensive and solid baseline for monitoring parasite community structure in relation to environmental change.

  10. Daño nuclear en neuronas de cerebros de pacientes con enfermedad de Alzheimer y otras demencias

    Directory of Open Access Journals (Sweden)

    Francisco Lopera

    2000-02-01

    Full Text Available

    Introducción: La enfermedad de Alzheimer (EA es una entidad neurodegenerativa y es la causa más común de demencia. Recientemente se reportó en Antioquia (Colombia un grupo familiar con una mutación puntual en el codon 280 de la Presenilina 1 denominada E280A (sustitución de un ácido glutámico por una alanina, la cual produce un incremento en el acúmulo de b-Amiloide (bA de 42-43 aminoácidos y una patología cerebral severa. Durante los últimos años se ha propuesto que la muerte celular es uno de los factores principales de pérdida neuronal en la EA. Hasta el presente no se ha establecido el tipo de muerte celular implicadas en la pérdida neuronal. Por lo tanto el objetivo de esta investigación es establecer el tipo de muerte celular que ocurre en la EA y otras demencias tales como la Demencia Fronto Temporal (DFT, Huntington y Demencia Cerebro Vascular, con base en los siguientes criterios: 1. Fragmentación del ADN. 2. Cambios morfológicos nucleares. 3. Cambios citoplasmáticos y 4. Expresión de ciertas proteínas asociadas a muerte celular. Los resultados de esta investigación permitirán establecer una correlación entre los parámetros morfológicos e histoquímicos antes mencionados, entre placas de bA y ovillos neurofibrilares en la EA y con ovillos neurofibrilares en la DFT adicionalmente. Este trabajo nos permitirá determinar si existe un mecanismo común de muerte celular en las enfermedades neurodegenerativas con demencia.

    Objetivo General: Contribuir a la caracterización de los procesos de muerte celular en cerebros de pacientes con enfermedades neurodegenerativas

    Objetivos específicos: - Estandarizar un estudio cualitativo in situ para evaluar procesos de muerte celular neuronal en micro-secciones histológicas de las regiones cerebrales frontal, temporal, parietal, hipocampo, occipital y cerebelo de pacientes con la enfermedad de Alzheimer y otras demencias. - Establecer una correlación patológica entre la proporción de núcleos fragmentados y la presencia de placas seniles bA y ovillos neurofibrilares. - Establecer la correlación entre la expresión de las proteínas asociadas a muerte celular como Bax, p53, NF-kB, Par 4 y la fragmentación del ADN.

    Materiales y Métodos

    Preparaciones Histológicas:

    Secciones de tejido de cerebros humanos post-mortem de las regiones seleccionadas provenientes de pacientes con demencia, serán fijadas en formaldehido buferizado y embebidos en bloques de parafina. Secciones de 5mm serán adheridos a láminas precargadas. La deparafinización e hidratación se realizará de acuerdo a procedimientos estandares de histología (Gavrieli et al.,1992.

    Técnica de marcaje Tunel y Thioflavina:

    Las secciones serán marcadas in situ para TUNEL (terminal transferasemediated dUTP-fluorecent nick labeling tecnique de acuerdo al método descrito por Gavrieli et al., 1992 y al protocolo Promega de 1998. Adicionalmente, las láminas serán marcadas con Thioflavina-S para evidenciar las placas seniles bA y ovillos neurofibrilares (Smale et al., 1995. La evaluación semicuantitativa tanto de núcleos Tunel+, como de placas seniles y ovillos se realizarán de acuerdo a Mirra et al. 1991 y Troncoso et al. 1996 respectivamente.

    Inmunohistoquímica:

    Las microsecciones del cerebro, se incubarán con los anticuerpos primarios anti-p53, anti-p65(NF-kB, anti-Bax, anti-Par-4. Luego serán incubadas con anticuerpos secundarios anticonejo IgG conjugados con biotina, e incubadas con el sustrato extravidina peroxidasa. La cuantificación se realizará semi cuantitativamente de acuerdo a:(- no coloración,(+ coloración débil, (++ coloración moderada, (+++ coloración intensa. Adicionalmente, un registro microfotográfico se realizará y los datos se tabularán en tablas.

  11. Mapeo espacio-temporal de la conectividad postsináptica en neuronas jóvenes del hipocampo adulto

    OpenAIRE

    Temprana, Silvio Gabriel

    2016-01-01

    Las células granulares en desarrollo en el giro dentado adulto (nCGs) atraviesan un periodo crítico de exacerbada excitabilidad y plasticidad sináptica antes de alcanzar la madurez. Se desconoce el impacto que estas nuevas unidades de procesamiento tienen en el circuito preexistente del giro dentado. En este trabajo combinamos la utilización de optogenética, electrofisiología en rodajas y quemogenética in vivo para activar nCGs de diferentes edades y analizar el reclutamiento de sus redes pos...

  12. Capacidad anaplerótica de las neuronas y los astrocitos, utilizando lactato y acetato en condiciones perinatales

    Directory of Open Access Journals (Sweden)

    Angel Alexandro Criollo Rayo

    2005-03-01

    Full Text Available En la transición a la vida extrauterina, el niño recién nacido para por un período crítico de vulnerabilidad y ayuno (prelactancia que transcurre enrre el cese de la nutrición placentaria y la instauración de la lactancia.

  13. PARTICIPACION DE LOS TRANSPORTADORES DE MONOCARBOXILATOS EN EL MECANISMO SENSOR DE GLUCOSA BASADO EN UNA INTERACCION METABOLICA GLIA-NEURONA

    OpenAIRE

    CORTES CAMPOS, CHRISTIAN GONZALO

    2011-01-01

    El control de los niveles de glucosa sistémica y la ingesta alimenticia son dos procesos estrechamente relacionados y altamente regulados, que involucran a órganos periféricos y al sistema nervioso central. Se ha establecido que regiones específicas del cerebro, el hipotálamo y el núcleo arqueado (NA), son capaces de detectar y responder a cambios en la concentración de glucosa, desencadenando respuestas neuroendocrinas que regulan la ingesta alimenticia. Sin embargo, los mecanismos cel...

  14. Formacion de neuronas nuevas en el hipocampo adulto: neurogenesis [the new neuron formation in the adult hippocampus: neurogenesis

    OpenAIRE

    Ramirez-Rodriguez, G.; Benitez-King, G; Kempermann, G

    2007-01-01

    New neuron formation in the adult brain was an interesting finding that extended the knowledge about brain plasticity. In 1966 Joseph Altman reported the incorporation of tritiated thymidine to neural cell DNA. This finding indicated the proliferation event in the adult brain. After twenty years of this finding, new information was generated that confirmed the new neuron formation in the adulthood. In this review, we will mention different aspects of the new neuron formation process called...

  15. Formacion de neuronas nuevas en el hipocampo adulto: neurogenesis [the new neuron formation in the adult hippocampus: neurogenesis

    OpenAIRE

    2007-01-01

    New neuron formation in the adult brain was an interesting finding that extended the knowledge about brain plasticity. In 1966 Joseph Altman reported the incorporation of tritiated thymidine to neural cell DNA. This finding indicated the proliferation event in the adult brain. After twenty years of this finding, new information was generated that confirmed the new neuron formation in the adulthood. In this review, we will mention different aspects of the new neuron formation process called...

  16. RNG1 is a Late Marker of the Apical Polar Ring in Toxoplasma gondii

    Science.gov (United States)

    Tran, Johnson Q.; de Leon, Jessica C.; Li, Catherine; Huynh, My-Hang; Beatty, Wandy; Morrissette, Naomi S.

    2010-01-01

    The asexually proliferating stages of apicomplexan parasites cause acute symptoms of diseases such as malaria, cryptosporidiosis and toxoplasmosis. These stages are characterized by the presence of two independent microtubule organizing centers (MTOCs). Centrioles are found at the poles of the intranuclear spindle. The apical polar ring (APR), a MTOC unique to apicomplexans, organizes subpellicular microtubules which impose cell shape and apical polarity on these protozoa. Here we describe the characteristics of a novel protein that localizes to the APR of Toxoplasma gondii which we have named ring-1 (RNG1). There are related RNG1 proteins in Neospora caninum and Sarcocystis neurona but no obvious homologs in Plasmodium spp., Cryptosporidium spp. or Babesia spp. RNG1 is a small, low-complexity, detergent-insoluble protein that assembles at the APR very late in the process of daughter parasite replication. We were unable to knock-out the RNG1 gene, suggesting that its gene product is essential. Tagged RNG1 lines have also allowed us to visualize the APR during growth of Toxoplasma in the microtubule-disrupting drug oryzalin. Oryzalin inhibits nuclear division and cytokinesis although Toxoplasma growth continues, and similar to earlier observations of unchecked centriole duplication in oryzalin-treated parasites, the APR continues to duplicate during aberrant parasite growth. PMID:20658557

  17. DISCOVERY OF THREE NOVEL COCCIDIAN PARASITES INFECTING CALIFORNIA SEA LIONS (ZALOPHUS CALIFORNIANUS), WITH EVIDENCE OF SEXUAL REPLICATION AND INTERSPECIES PATHOGENICITY

    Science.gov (United States)

    Colegrove, Kathleen M.; Grigg, Michael E.; Carlson-Bremer, Daphne; Miller, Robin H.; Gulland, Frances M. D.; Ferguson, David J. P.; Rejmanek, Daniel; Barr, Bradd C.; Nordhausen, Robert; Melli, Ann C.; Conrad, Patricia A.

    2016-01-01

    Enteric protozoal infection was identified in 5 stranded California sea lions (Zalophus californianus). Microscopically, the apical cytoplasm of distal jejunal enterocytes contained multiple stages of coccidian parasites, including schizonts with merozoites and spherical gametocytes, which were morphologically similar to coccidians. By histopathology, organisms appeared to be confined to the intestine and accompanied by only mild enteritis. Using electron microscopy, both sexual (microgametocytes, macrogamonts) and asexual (schizonts, merozoites) coccidian stages were identified in enterocytes within parasitophorous vacuoles, consistent with apicomplexan development in a definitive host. Serology was negative for tissue cyst-forming coccidians, and immunohistochemistry for Toxoplasma gondii was inconclusive and negative for Neospora caninum and Sarcocystis neurona. Analysis of ITS-1 gene sequences amplified from frozen or formalin-fixed paraffin-embedded intestinal sections identified DNA sequences with closest homology to Neospora sp. (80%); these novel sequences were referred to as belonging to coccidian parasites ‘‘A,’’ ‘‘B,’’ and ‘‘C.’’ Subsequent molecular analyses completed on a neonatal harbor seal (Phoca vitulina) with protozoal lymphadenitis, hepatitis, myocarditis, and encephalitis showed that it was infected with a coccidian parasite bearing the ‘‘C’’ sequence type. Our results indicate that sea lions likely serve as definitive hosts for 3 newly described coccidian parasites, at least 1 of which is pathogenic in a marine mammal intermediate host species. PMID:21495828

  18. Enteric bacterial pathogen detection in southern sea otters (Enhydra lutris nereis) is associated with coastal urbanization and freshwater runoff

    Science.gov (United States)

    Miller, Melissa A.; Byrne, Barbara A.; Jang, Spencer S.; Dodd, Erin M.; Dorfmeier, Elene; Harris, Michael D.; Ames, Jack; Paradies, David; Worcester, Karen; Jessup, David A.; Miller, Woutrina A.

    2009-01-01

    Although protected for nearly a century, California’s sea otters have been slow to recover, in part due to exposure to fecally-associated protozoal pathogens like Toxoplasma gondii and Sarcocystis neurona. However, potential impacts from exposure to fecal bacteria have not been systematically explored. Using selective media, we examined feces from live and dead sea otters from California for specific enteric bacterial pathogens (Campylobacter, Salmonella, Clostridium perfringens, C. difficile and Escherichia coli O157:H7), and pathogens endemic to the marine environment (Vibrio cholerae, V. parahaemolyticus and Plesiomonas shigelloides). We evaluated statistical associations between detection of these pathogens in otter feces and demographic or environmental risk factors for otter exposure, and found that dead otters were more likely to test positive for C. perfringens, Campylobacter and V. parahaemolyticus than were live otters. Otters from more urbanized coastlines and areas with high freshwater runoff (near outflows of rivers or streams) were more likely to test positive for one or more of these bacterial pathogens. Other risk factors for bacterial detection in otters included male gender and fecal samples collected during the rainy season when surface runoff is maximal. Similar risk factors were reported in prior studies of pathogen exposure for California otters and their invertebrate prey, suggesting that land-sea transfer and/or facilitation of pathogen survival in degraded coastal marine habitat may be impacting sea otter recovery. Because otters and humans share many of the same foods, our findings may also have implications for human health. PMID:19720009

  19. Pathology produced by, prevalence, of, and probable life-cycle of a species of Sarcocystis in the domestic fowl.

    Science.gov (United States)

    Munday, B L; Humphrey, J D; Kila, V

    1977-01-01

    Sarcosporidiosis was found to be the cause of a severe myositis in 3 fowls in Papua New Guinea and 2 in Australia. This represented 3.8% of a series of fowls examined in Papua New Guinea. The overall prevalence of infection in these birds was 45%. Both epidemiological and experimental evidence suggested that the dog was the definitive host for this particular type of sarcocyst.

  20. Diagnosis and isolation of Toxoplasma gondii in horses from Brazilian slaughterhouses Diagnóstico e isolamento de Toxoplasma gondii em equídeos de frigoríficos brasileiros

    Directory of Open Access Journals (Sweden)

    Fernanda Evers

    Full Text Available This study aimed to investigate anti-Toxoplasma gondii antibodies and to isolate the parasite from the brains of horses processed at slaughterhouses in Brazil. We collected brain and blood samples from 398 horses of various ages, from six Brazilian states. Serum samples were evaluated by indirect fluorescent antibody test (IFAT cut-off titre ≥ 1:64, and brains were submitted to mouse bioassay. Among the 398 horses, positivity for T. gondii was identified in 46 (11.6% by IFAT and in 14 (3.5% by mouse bioassay. In 12 of those 14 bioassays, mice were positive only by IFAT (cut-off titre ≥ 1:16, T. gondii being isolated in the remaining two. Using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP analysis of 18S rDNA to differentiate among T. gondii, Neospora caninum, and Sarcocystis neurona, we found that two of the 14 brains were positive for T. gondii only. For genotyping of the two isolates and the PCR-positive brain, we performed PCR-RFLP based on 13 markers, and SAG2 all samples were Toxoplasma gondii type I. Collectively, IFAT of horse sera and mouse bioassay identified positivity in 60 (15% of the samples. Our results show that some horses sent to slaughter in Brazil have been exposed to T. gondii.O objetivo do estudo foi investigar anticorpos anti-Toxoplasma gondii e isolar o parasita do cérebro de equídeos abatidos em matadouros-frigoríficos no Brasil. Colheram-se amostras de 398 cérebros e sangue de equídeos machos e fêmeas de idades variadas, provenientes de seis estados brasileiros. As amostras de soro foram avaliadas pelo teste de imunofluorescência indireta (IFI para T. gondii (ponto de corte ≥ 64, e os fragmentos de cérebros foram submetidos ao bioensaio em camundongos. Por meio da IFI, 46 (11,6% equídeos foram soropositivos. Pelo bioensaio em camundongos, 14 (3,5% cérebros de equídeos testados foram positivos. Em doze dos bioensaios, os camundongos foram positivos somente pela IFI (ponto

  1. SURVEY FOR INFECTIOUS DISEASE IN THE SOUTH AMERICAN FUR SEAL (ARCTOCEPHALUS AUSTRALIS) POPULATION AT PUNTA SAN JUAN, PERU.

    Science.gov (United States)

    Jankowski, Gwen; Adkesson, Michael J; Saliki, Jeremiah T; Cárdenas-Alayza, Susana; Majluf, Patricia

    2015-06-01

    The Peruvian population of the South American fur seal ( Arctocephalus australis ) is a distinct evolutionarily significant unit that is endangered. One of the largest rookeries for this species in Peru is located within the Punta San Juan marine protected area (15°22'S, 75°12'W). To better understand the current health status of this population, exposure to 10 pinniped pathogens was evaluated in adult female fur seals (n=29) via serology and polymerase chain reaction (PCR) techniques in November 2010. The results suggest this population is naïve to canine and phocine distemper viruses (serum neutralization test), five Leptospira interrogans serovars (microscopic agglutination test), and Brucella canis (card test). Indirect fluorescent antibody testing for Toxoplasma gondii , Neospora caninum , and Sarcocystis neurona was also uniformly negative. PCR testing of nasal swabs using previously described Mycoplasma spp. primers was positive in 37.9% (11/29) of samples. One animal was positive via card test for Brucella abortus , whereas 53.7% (15/28) were positive or suspect using a marine Brucella competitive enzyme-linked immunosorbent assay. Antibody to phocine herpesvirus-1 (PHV-1) was identified in 85.7% (24/28) of the sampled population by serum neutralization testing. Overall, exposure to Mycoplasma spp., Brucella spp., and PHV-1 was observed, but results demonstrated low to no exposure to many key pinniped pathogens. The expansion of human populations, agriculture, and industry along the Peruvian coast may lead to increased pathogen exposure from human, domestic, and wild animal sources. The naïve nature of this key population of South American fur seals raises concerns about potential risk for disease outbreaks.

  2. Assessment of clinical pathology and pathogen exposure in sea otters (Enhydra lutris) bordering the threatened population in Alaska

    Science.gov (United States)

    Goldstein, T.; Gill, V.A.; Tuomi, Pamela A.; Monson, Daniel H.; Burdin, A.; Conrad, P.A.; Dunn, J.L.; Field, C.; Johnson, Chad; Jessup, David A.; Bodkin, J.; Doroff, A.M.

    2011-01-01

    Northern sea otter (Enhydra lutris kenyoni) abundance has decreased dramatically over portions of southwest Alaska, USA, since the mid-1980s, and this stock is currently listed as threatened under the Endangered Species Act. In contrast, adjacent populations in south central Alaska, USA, and Russia have been stable to increasing during the same period. Sea otters bordering the area classified in the recent decline were live-captured during 2004–2006 at Bering Island, Russia, and the Kodiak Archipelago, Alaska, USA, to evaluate differences in general health and current exposure status to marine and terrestrial pathogens. Although body condition was lower in animals captured at Bering Island, Russia, than it was at Kodiak, USA, clinical pathology values did not reveal differences in general health between the two regions. Low prevalences of antibodies (>5%) were found in Kodiak, USA, and on Bering Island, Russia, to Toxoplasma gondii, Sarcocystis neurona, and Leptospira interrogans. Exposure to phocine herpesvirus-1 was found in both Kodiak, USA (15.2%), and Bering Island, Russia (2.3%). Antibodies to Brucella spp. were found in 28% of the otters tested on Bering Island, Russia, compared with only 2.7% of the samples from Kodiak, USA. Prevalence of exposure to Phocine distemper virus (PDV) was 41% in Kodiak, USA, but 0% on Bering Island, Russia. Archived sera from southwest and south-central Alaska dating back to 1989 were negative for PDV, indicating exposure occurred in sea otters in Kodiak, USA, in recent years. Because PDV can be highly pathogenic in naïve and susceptible marine mammal populations, tissues should be examined to explore the contribution of this virus to otter deaths. Our results reveal an increase in exposure to pathogens in sea otters in Kodiak, Alaska, USA, since the 1990s.

  3. Pathogen exposure and blood chemistry in the Washington population of northern sea otters (Enhydra lutris kenyoni)

    Science.gov (United States)

    White, C. LeAnn; Schuler, Krysten L.; Thomas, Nancy J.; Webb, Julie L.; Saliki, Jeremiah T.; Ip, Hon S.; Dubey, J.P.; Frame, Elizabeth R.

    2013-01-01

    Northern sea otters (Enhydra lutris kenyoni) from Washington State, United States were evaluated in 2011 to determine health status and pathogen exposure. Antibodies to Brucella spp. (10%) and influenza A virus (23%) were detected for the first time in this population in 2011. Changes in clinical pathology values (serum chemistries), exposure to pathogens, and overall health of the population over the last decade were assessed by comparing 2011 data to the data collected on this population in 2001–2002. Several serum chemistry parameters were different between study years and sexes but were not clinically significant. The odds of canine distemper virus exposure were higher for otters sampled in 2001–2002 (80%) compared to 2011 (10%); likelihood of exposure significantly increased with age. Prevalence of exposure to Sarcocystis neurona was also higher in 2001–2002 (29%) than in 2011 (0%), but because testing methods varied between study years the results were not directly comparable. Exposure to Leptospira spp. was only observed in 2001–2002. Odds of Toxoplasma gondii exposure were higher for otters sampled in 2011 (97%) than otters in 2001–2002 (58%). Substantial levels of domoic acid (n = 2) and saxitoxin (n = 2) were found in urine or fecal samples from animals sampled in 2011. No evidence of calicivirus or Coxiella burnetii exposure in the Washington population of northern sea otters was found in either 2001–2002 or 2011. Changes in exposure status from 2001–2002 to 2011 suggest that the Washington sea otter population may be dealing with new disease threats (e.g., influenza) while also increasing their susceptibility to diseases that may be highly pathogenic in naïve individuals (e.g., canine distemper).

  4. Chagas disease in a Texan horse with neurologic deficits.

    Science.gov (United States)

    Bryan, Laura K; Hamer, Sarah A; Shaw, Sarah; Curtis-Robles, Rachel; Auckland, Lisa D; Hodo, Carolyn L; Chaffin, Keith; Rech, Raquel R

    2016-01-30

    A 10-year-old Quarter Horse gelding presented to the Texas A&M University Veterinary Teaching Hospital with a six month-history of ataxia and lameness in the hind limbs. The horse was treated presumptively for equine protozoal myeloencephalitis (EPM) based on clinical signs but was ultimately euthanized after its condition worsened. Gross lesions were limited to a small area of reddening in the gray matter of the thoracic spinal cord. Histologically, trypanosome amastigotes morphologically similar to Trypanosoma cruzi, the agent of Chagas disease in humans and dogs, were sporadically detected within segments of the thoracic spinal cord surrounded by mild lymphoplasmacytic inflammation. Ancillary testing for Sarcocystis neurona, Neospora spp., Toxoplasma gondii and Leishmania spp. was negative. Conventional and real time polymerase chain reaction (PCR) of affected paraffin embedded spinal cord were positive for T. cruzi, and sequencing of the amplified T. cruzi satellite DNA PCR fragment from the horse was homologous with various clones of T. cruzi in GenBank. While canine Chagas disease cases have been widely reported in southern Texas, this is the first report of clinical T. cruzi infection in an equid with demonstrable amastigotes in the spinal cord. In contrast to previous instances of Chagas disease in the central nervous system (CNS) of dogs and humans, no inflammation or T. cruzi amastigotes were detected in the heart of the horse. Based on clinical signs, there is a potential for misdiagnosis of Chagas disease with other infectious diseases that affect the equine CNS. T. cruzi should be considered as a differential diagnosis in horses with neurologic clinical signs and histologic evidence of meningomyelitis that originate in areas where Chagas disease is present. The prevalence of T. cruzi in horses and the role of equids in the parasite life cycle require further study. Copyright © 2015 Elsevier B.V. All rights reserved.

  5. Prevalence of Muscular Sarcosporidiosis in Slaughtered Domestic Pigs in Perak, Peninsular Malaysia

    Science.gov (United States)

    Zainalabidin, Fazly Ann; Noorazmi, Muhamad Syamsul Naim; Bakri, Wan Normaziah Wan Omar; Sathaya, Geethamalar; Ismail, Mohd Iswadi

    2017-01-01

    Sarcosporidiosis is a disease caused by intracellular protozoan parasites, namely, Sarcocystis spp. In pigs, three species of Sarcocystis spp. have been recognised, including Sarcocystis meischeriana, Sarcocystis porcifelis and Sarcocystis suihominis. The aim of this study is to determine the prevalence of muscular sarcosporidiosis in pigs using the pepsin digestion technique. A total of 150 fresh heart, oesophagus and thigh muscle samples from 50 Yorkshire and Landrace pigs were collected from two local abattoirs in Perak from May to August 2014. All the fresh muscle samples were thoroughly examined for macrocyst-forming Sarcocystis spp. and processed using the peptic digestion technique to detect bradyzoites. The results from the muscle samples showed that 58% (29 out of 50) of the pigs were positive for Sarcocystis spp. These findings highlight the importance of implementing stringent measures for screening pigs in abattoirs for Sarcocystis spp. infection because this infection in pigs is a public health concern. PMID:28228924

  6. La atorvastatina protege las neuronas gabérgicas y dopaminérgicas del sistema nigroestriatal en un modelo experimental de isquemia cerebral focal transitoria en ratas

    Directory of Open Access Journals (Sweden)

    Angélica María Sabogal

    2014-06-01

    Full Text Available Introducción. La isquemia cerebral es la tercera causa de muerte y la primera de discapacidad permanente en el mundo. La atorvastatina es un fármaco neuroprotector prometedor para el tratamiento de la apoplejía; sin embargo, su acción sobre las poblaciones neuronales del sistema nigroestriatal después de la isquemia aún se desconoce. Objetivo. Evaluar el efecto de la atorvastatina sobre poblaciones gabérgicas y dopaminérgicas en regiones exofocales en un modelo de oclusión transitoria de la arteria cerebral media. Materiales y métodos. Se utilizaron 28 ratas Wistar macho de ocho semanas de edad. Los ejemplares con isquemia simulada y los ejemplares sometidos a isquemia fueron tratados con atorvastatina (10 mg/kg y carboximetilcelulosa (placebo administrados por medio de sonda a las 6, 24, 48 y 72 horas después de la reperfusión. Se analizó la inmunorreacción de la descarboxilasa del ácido glutámico y de la tirosina hidroxilasa en el globo pálido, el putamen caudado y la sustancia negra. Resultados. Los datos confirmaron el daño neurológico y la pérdida celular en el putamen caudado. Se incrementó la inmunorreacción de la tirosina hidroxilasa en el globo pálido medial y la sustancia negra pars reticulata, disminuyendo la inmunorreacción de la descarboxilasa del ácido glutámico en el globo pálido lateral de los animales isquémicos tratados con placebo; sin embargo, el tratamiento con atorvastatina pudo revertirla, lo que logró una disminución significativa de la tirosina hidroxilasa en el globo pálido medial y la sustancia negra pars reticulata y aumentando los niveles de descarboxilasa del ácido glutámico en el globo pálido lateral. Conclusión. Nuestros datos sugieren que la atorvastatina en el tratamiento posterior a la isquemia ejerce neuroprotección en las zonas exofocales, modulando las poblaciones neuronales gabérgicas y dopaminérgicas del sistema nigroestriatal, lo que podría prevenir trastornos neurológicos.

  7. Efecto del 3-nitropropionato sobre el metabolismo del lactato y del acetato en neuronas y astrocitos crecidos in vitro en concentraciones perinatales

    Directory of Open Access Journals (Sweden)

    Jairo Alfonso Tovar- Franco

    2009-04-01

    Full Text Available 3-Nitropropionate effect on the lactate and acetate metabolism of neurons and astrocytes grown in vitro with perinatal concentrations.Anaplerotic reactions are an essential metabolic mechanism for the postnatal continuity of the brain development, contributing in processesthat require substrates synthesized from Krebs cycle intermediates; however, their role during the presuckling period in the neonate isunknown. Objective. To estimate the anaplerotic capacity of neurons and astrocytes grown in vitro under perinatal conditions. Materials andmethods. The effect of 3-nitropropionate (3-NPA(2 mM an inhibitor of the succinate dehydrogenase (SDH on the oxidative andlipogenic metabolism of 14C-derived from acetate and lactate in perinatal concentrations. The results were compared with its respectivecontrols without inhibitor. Results. In spite of the presence of 3-NPA, respiratory activity with lactate was 40% in neurons and 73% inastrocytes, the lipogenesis was 53% in neurons and 52% in astrocytes. With acetate, the oxidation in neurons was 15% and 63% inastrocytes, lipogenesis was maintained in astrocytes but in neurons it increased up to 174% (p<0.05. Conclusions. These results demonstratethat in spite the oxalacetate depletion generated by 3-NPA, neurons as well as astrocytes are able to maintain the energetic metabolism andthe lipid synthesis using lactate or acetate thanks to the anaplerotic activity in the presuckling period. Additionally, astrocytes showed acapacity of buffering the effects of 3-NPA on the oxidation process greater than the neuron capacity. Neurons and astrocytes revealed abetter capacity of directing acetate for lipid synthesis, activating the cytosolic acetyl-CoA synthetase pathway.

  8. Análisis de la especificación de las neuronas Va en la Cuerda Nerviosa Ventral de Drosophila melanogaster

    OpenAIRE

    Gabilondo Olmedo, Hugo

    2014-01-01

    Tesis doctoral inédita leída en la Universidad Autónoma de Madrid, Facultad de Ciencias, Departamento de Biología Molecular. Fecha de lectura: 18-06-2014 Durante el desarrollo embrionario, cada una de las células originadas a partir de los progenitores neurales, conocidos como neuroblastos (NB), adquiere un destino celular concreto que responde a diferentes requerimientos funcionales y estructurales, como los establecidos a lo largo del eje Antero-Posterior (A-P) del individuo. La...

  9. Extracción de conocimiento en bases de datos astronómicas mediante redes de neuronas artificiales : aplicaciones en la misión Gaia

    OpenAIRE

    2016-01-01

    [Resumen] En la llamada era de las TIC, las capacidades de los sistemas de adquisición de datos han aumentado enormemente, de forma que resulta complicado almacenar toda la información que producen, así como su análisis posterior. Esta explosión de datos ha aparecido recientemente en el campo de la Astronomía, donde cada vez se observan un número mayor de objetos, con mayor periodicidad. Un ejemplo de esto es la próxima misión Gaia, que observará múltiples propiedades de hasta ...

  10. Neuropsicología y Educación. De las neuronas espejo a la teoría de la mente

    OpenAIRE

    2008-01-01

    Las recientes investigaciones en Neurociencias y particularmente en Neuropsicología ofrecen aportaciones de gran interés para la educación. El cerebro es la conquista evolutiva que hace posibles los aprendizajes y enseñanza. Una conquista clave en el proceso de hominización fue la capacidad mentalista, que resulta esencial en los procesos de aprendizaje-enseñanza. El ser humano dispone de unas capacidades mentales que le permiten interpretar y predecir la conducta de los otros. Gracias a la T...

  11. Caracterización de un modelo organotípico de cultivos de neuronas corticales de humano derivadas de trauma craneoencefálico

    OpenAIRE

    David Riascos; Francisco Guzmán; Efraín Buriticá; Mauricio Palacios; Martha Isabel Escobar; Hernán Pimienta

    2008-01-01

    Introducción: El trauma craneoencefálico (TEC) es un problema de salud global que puede generar en los pacientes que lo padecen, muerte, discapacidad y/o alteraciones psiquiátricas con gran impacto sobre su desempeño posterior y sobre su ámbito familiar. En los últimos años se ha avanzado en el conocimiento de los mecanismos fisiopatológicos que subyacen al TCE. Sin embargo, esto no está completamente entendido, como tampoco hay claridad sobre los mecanismos de neuroprotección. Por esta razón...

  12. Demostración del ingreso del virus de la rabia a la corteza cerebral a través de las neuronas piramidales de la capa V

    Directory of Open Access Journals (Sweden)

    Hernán J. Pimienta J.

    2005-03-01

    Full Text Available En condiciones naturales el virus de la rabia (VR penetra en la piel o los músculos, con la saliva unyectada por un animal infectado y entra en contacto con receptores localizados en el sistema nervioso periférico.

  13. Valoración de las neuronas NADPH-d en la corteza visual : estudio experimental en rata Wístar

    OpenAIRE

    2013-01-01

    Las células NADPH-diaforasa (nicotinamida adenin dinucleotido fosfatasa reducida), son células que están directamente relacionadas con la enzima óxido nítrico sintetasa (ONS), productora del óxido nítrico (ON) neuronal. Se ha podido comprobar que la NADPH-diaforasa y la ONS se han localizado en las mismas poblaciones neuronales y que su actividad es paralela a la producción de ON y GMPc. (1). De manera que, si localizamos las células NADPH-diaforasa positivas, podremos localizar indirectamen...

  14. Identificación de receptores nicotínicos funcionales en neuronas del núcleo dorsal del rafé /

    OpenAIRE

    2011-01-01

     tesis que para obtener el grado de Doctor en Ciencias Biomédicas, presenta Luis Manuel Galindo Charles ; asesor Stefan Mihailescu. 69 páginas : ilustraciones, diagramas. Doctorado en Ciencias Biomédicas UNAM, Facultad de Medicina, 2011

  15. Uticaj elektromagnetnog polja (2 mT, 50 Hz) na spontanu bioelektričnu aktivnost neurona antenalnog lobusa adulta Morimus funereus (Insecta, Coleoptera)

    OpenAIRE

    2013-01-01

    Spoljašnja magnetna polja (MP) narušavaju ravnotežu bioloških sistema, čak i tokom kraćeg vremena izlaganja, što za posledicu ima poremećaje na različitim nivoima organizacije. Na ovaj način nastali poremaćaji akumuliraju se u organizmima, što je jedan od razloga za traženje objašnjenja bioloških efekata MP. S druge strane, veoma važna činjenica koja nas usmerava na što bolje razumevanje ove problematike je potreba za zaštitom ljudskog zdravlja zbog uvođenja novih tehnologija u...

  16. Extracción de conocimiento en bases de datos astronómicas mediante redes de neuronas artificiales: aplicaciones en la misión Gaia

    Science.gov (United States)

    Fustes Villadóniga, Diego

    2014-02-01

    In the so-called IT era, the capabilities of data acquisition systems have increased to such an extent that it has become difficult to store all the information they produce, and analyse it. This explosion of data has recently appeared in the field of Astronomy, where an increasing number of objects are being observed on a regular basis. An example of this is the upcoming Gaia mission, which will pick up multiple properties of a billion stars, whose information will have a volume of approximately a petabyte. The analysis of a similar amount of information inevitably requires the development of new data analysis methods to extract all the knowledge it contains. This thesis is devoted to the development of data analysis methods to be integrated in the Gaia pipeline, such that knowledge can be extracted from the data collected by the mission. In order to analyze the data from the Gaia mission, the European Space Agency organized the Data Processing and Analysis Consortium (DPAC) which is composed of hundreds of scientists and engineers. DPAC is divided into eight Coordination Units (CUs). This thesis is dedicated to algorithm development in CU8, which is responsible for source classification and astrophysical parameters (AP) estimation. Methods based on Artificial Neural Networks (ANNs) are developed to perform the tasks related to two different work packages in CU8: the GSP-Spec package (GWP-823), and the OA package (GWP-836). The GSP-Spec package is responsible for estimating stellar APs by means of the Radial Velocity Spectrograph (RVS) spectrum. This work presents the development of one of the GSP-Spec modules, which is based on the application of feed-forward ANNs. A methodology is described, based on the optimization of genetic algorithms and aimed at obtaining an optimal set of configuration parameters for the ANN in each case, depending on the signal to noise ratio (SNR) in the RVS spectrum and on the type of star to parameterize. Furthermore, in order to improve the AP estimates, wavelet signal processing techniques, applied to the RVS spectrum, are studied. Despite the effectiveness shown by ANNs in estimating APs, in principle they lack the ability to provide an uncertainty value on these estimates, making it impossible to determine their reliability. Because of this, a new architecture for the ANN is presented in which the inputs and outputs are reversed, so that the ANN estimates the RVS spectrum from the APs. Such an architecture is called Generative ANN (GANN) and is applied to the AP estimation of a set of simulated RVS spectra for the Gaia mission, where it is more effective than the conventional ANN model, in the case of faint stars with low SNR. Finally, the GANN can be applied for obtaining the posterior probability of each of the APs according to the RVS spectrum, allowing for their more complete analysis. Given the nature of the Gaia mission, which is the first astronomical mission that will observe, in an unbiased way, the entire sky up to magnitude 20, a large number of outliers are expected. The OA package in CU8 handles the processing of this type of objects, which are defined as those that could not be reliably classified by the methods in the upstream classification packages. OA methods are based on the unsupervised learning of all outliers. Such learning has two parts: clustering and dimensionality reduction. The Self-Organizing Map (SOM) algorithm is selected as a basis for this learning. Its effectiveness is demonstrated when it is applied, with an optimal configuration, to the Gaia simulations. Furthermore, the algorithm is applied to real outliers from the SDSS catalog. Since a subsequent identification of the clusters obtained by the SOM is necessary, two different methods of identification are applied. The first method is based on the similarity between the SOM prototypes and the Gaia simulations, and the second method is based on the recovery of stored classifications in the SIMBAD catalog by cross-matching celestial coordinates. Thanks to the visualization of the SOM planes, and to both methods of identification, it is possible to distinguish between valid observations and observational artifacts. Furthermore, the method allows for the selection of objects of interest for follow-up observations, in order to determine their nature.

  17. Experimental Infection of Sarcocystis suihominis in Pig and Human Volunteer in Guangxi%广西猪人肉孢子虫实验感染研究

    Institute of Scientific and Technical Information of China (English)

    李锦辉; 林珍; 杜进发; 覃业新

    2007-01-01

    目的 研究确定广西是否存在人-猪相互感染的肉孢子虫病.方法 采用人-猪-人循环感染方法.取自然感染病例的粪便,用薛氏糖漂浮法收集肉孢子虫孢子囊(10000个以上),拌入饲料,用吞食法感染猪.取含成熟肉孢子虫包囊的新鲜生猪肉,剁碎,用吞食法感染志愿者(含包囊数约71 000个以上).观察感染后症状及肉孢子虫在宿主体内发育情况.结果 人感染后约5 h出现腹胀,8~36 h腹泻水样便13次,呕吐4次,畏寒、发热(体温达38.5℃)、头昏、头痛、关节及肌肉酸痛、腰痛、上腹部隐痛,腿部抽筋,全身乏力,食欲明显减退.感染后第10天粪检查见未孢子化的孢子囊,第12天检出孢子化的孢子囊,孢子囊平均大小为11.9(8.8~14.5) μm×9.2(7.5~12.5) μm.猪感染后第5~8 天轻度厌食,疲乏无力、便秘、毛疏松,第17天恢复正常.包囊平均大小为299.2(175~575) μm×62.3(30~102.5) μm.缓殖子大小为11.5(9.5~13.5) μm×4.1(2.8~5.0) μm.人感染后第46天口服乙酰螺旋霉素(0.2 g/次,4次/d,连服15 d),服药后第30天粪检孢子囊阴转.结论 广西存在猪-人相互感染的肉孢子虫病.

  18. Intestinal Coccidia

    Directory of Open Access Journals (Sweden)

    MJ Ggaravi

    2007-06-01

    intestinal parasite is in most parts of the world. Sometimes it is noun traveller diarrhea Syndrom. The egg shapes of Oocyst are disporic tetrazoic. It is transmitted by vegetables and fruits. Trophozoite pass through schizogony step and repeats it several times. In the end of the cycle gametogony is done and the sexual forms will be repelled the human intestine. Symptoms are persistent diarrhoea, epigastric pain, headache, fever, vomitting and leanness, especially when physiologic disorder condition is seen in patient or they are in traveling. Misdiagnosis is a problem in laboratories but floatation method with zinc sulfate or sugar syrup is recommended. Sarcocystis: Sporocyst of S.hominis and S. suihominis is in the human feces, and the cyst form is in pig and cow muscles. It founds in tha tongue, pharynx and oesophagus muscles of habitant buffalo in Iran. Because of the large size of the cyst (1cm, it is seen with naked eyes and the risk of human infection is rare. If human eats raw or uncooked cow and pig meat, he will be infected with it. Sexual cycle is in the human body and sporocyst is repelled by the intestine. The disease may or may not have any symptoms. The symptoms are diarrhoea, stomach cramp, jejenuom and ileum necrosis. Diagnosis is based on concentrated floatation. The prevalence rate is too much in domestic animals.

  19. Calibración automática de modelos neuronales para su uso en circuitos híbridos

    OpenAIRE

    Reyes Sánchez, Manuel

    2016-01-01

    Este proyecto tiene como objetivo la calibración automática en tiempo real de modelos neuronales para su uso en circuitos híbridos, compuestos por neuronas vivas procedentes de sistemas biológicos y neuronas software. Estas conexiones se realizan por medio de sinapsis artificiales bidireccionales entre las neuronas vivas y las neuronas artificiales. La calibración automática supone un paso importante en este tipo de conexiones dada la corta vida útil durante la cual pueden util...

  20. Structural and evolutionary adaptation of rhoptry kinases and pseudokinases, a family of coccidian virulence factors

    Science.gov (United States)

    2013-01-01

    Background The widespread protozoan parasite Toxoplasma gondii interferes with host cell functions by exporting the contents of a unique apical organelle, the rhoptry. Among the mix of secreted proteins are an expanded, lineage-specific family of protein kinases termed rhoptry kinases (ROPKs), several of which have been shown to be key virulence factors, including the pseudokinase ROP5. The extent and details of the diversification of this protein family are poorly understood. Results In this study, we comprehensively catalogued the ROPK family in the genomes of Toxoplasma gondii, Neospora caninum and Eimeria tenella, as well as portions of the unfinished genome of Sarcocystis neurona, and classified the identified genes into 42 distinct subfamilies. We systematically compared the rhoptry kinase protein sequences and structures to each other and to the broader superfamily of eukaryotic protein kinases to study the patterns of diversification and neofunctionalization in the ROPK family and its subfamilies. We identified three ROPK sub-clades of particular interest: those bearing a structurally conserved N-terminal extension to the kinase domain (NTE), an E. tenella-specific expansion, and a basal cluster including ROP35 and BPK1 that we term ROPKL. Structural analysis in light of the solved structures ROP2, ROP5, ROP8 and in comparison to typical eukaryotic protein kinases revealed ROPK-specific conservation patterns in two key regions of the kinase domain, surrounding a ROPK-conserved insert in the kinase hinge region and a disulfide bridge in the kinase substrate-binding lobe. We also examined conservation patterns specific to the NTE-bearing clade. We discuss the possible functional consequences of each. Conclusions Our work sheds light on several important but previously unrecognized features shared among rhoptry kinases, as well as the essential differences between active and degenerate protein kinases. We identify the most distinctive ROPK-specific features

  1. Caryospora uptoni n. sp. (Apicomplexa: Eimeriidae) from red-tailed hawks (Buteo jamaicensis borealis).

    Science.gov (United States)

    Lindsay, D S; Blagburn, B L

    1986-10-01

    Oocysts of Caryospora uptoni n. sp. were described from the feces of red-tailed hawks, Buteo jamaicensis borealis. Sporulated oocysts were spherical or subspherical and measured 28.1 by 26.4 micron. The oocyst wall was composed of a yellowish outer layer and brownish inner layer and was about 1.5 micron thick. Neither micropyle, polar granules, nor oocyst residuum were present. A single, spherical sporocyst 18.2 by 17.9 micron was present; a Stieda body was absent. A spherical eccentrically located sporocyst residuum was present in many sporocysts, but it degenerated to form a dispersed granular residuum in other sporocysts. Eight randomly arranged sporozoites, 12.6 by 4.2 micron, were present in each sporocyst; they contained a centrally or slightly posteriorly located nucleus.

  2. Classical Conditioning of Hippocampal Theta Patterns in the Rat.

    Science.gov (United States)

    1976-08-01

    associated with changes in performance of learned tasks , 1,4,5, 8,9 there have been very few studies of neurona l plasticity of the hippocampus It self...rapid development of a conditioned hippocampal theta response to a visual sti mulus demonstrates tha t there is considerable neurona l plasticity in the

  3. Use of Monoclonal Antibodies to Study the Structural Basis of the Function of Nicotinic Acetylcholine Receptors on Electric Organ and Muscle and to Determine the Structure of Nicotinic Acetylcholine Receptors on Neurons

    Science.gov (United States)

    1989-09-30

    of chicken neurona .4receptor subunits. Sequences of al and a2 are from Net .Ot al. -l Sequences of a3 and a4 were determintl from clones described...Sucrose gradient analysis of neurona & nicotinic receptors was conducted as follows. Chicken ind rat brain receptors were extracted from crude

  4. REGULACION DE LA EXPRESION DEL GEN BCL-2 POR LA VIA DE TRANSDUCCION SE SEÑALES WNT/-CATENINA EN NEURONAS Y CARACTERIZACION DE LA EXPRESION DE LOS GENES WNT EN EL HIPOCAMPO DE RATA.

    OpenAIRE

    FUENTEALBA ALDAY, RODRIGO ESTEBAN

    2005-01-01

    Se ha demostrado que la producción y acumulación del péptido í3-amiloide (A0) es clave en la enfermedad de Alzheimer (EA) dadas las características neurotóxicas intrínsecas de este péptido. Una de las actividades quinasa desreguladas por AJ3 en la EA y as 132p.

  5. Retracción a largo plazo del árbol dendrítico de neuronas piramidales córtico-faciales por lesiones periféricas del nervio facial

    Directory of Open Access Journals (Sweden)

    Diana Urrego

    2011-06-01

    Esta reorganización morfológica cortical persistente podría ser el sustrato fisiopatológico de algunas de las secuelas funcionales que se observan en los pacientes con parálisis facial periférica.

  6. Experience in Surgery of Intracranial Astrocytic Tumors Assisted by Electromagnetic Neurona Vigation:Report of 54 Cases%54例神经导航引导下星形细胞肿瘤切除术的经验

    Institute of Scientific and Technical Information of China (English)

    张学新

    2008-01-01

    背景与目的:神经导航外科是微侵袭神经外科的重要组成部分,本研究评价神经导航在颅内星形细胞肿瘤显微手术中的应用价值.方法:回顾性分析哈尔滨医科大学肿瘤医院神经外科于2004年9月至2007年4月应用神经导航系引导进行颅内星形细胞肿瘤切除术的54例病例资料.结果:用神经导航系统进行星形细胞肿瘤及其周围解剖结构定位准确,平均注册误差(1.42±0.46)mm.术后近期复查,CT或MRI证实肿瘤全切36例(78%),次全切除10例,大部切除8例.所有肿瘤全切患者术后增强CT或MRI检查未发现肿瘤残留病灶.结论:神经导航定位精确,有助于手术计划的精确实施.实时导航颅内星形细胞肿瘤显微手术,有助于达到微侵袭效果和提高肿瘤全切除率.

  7. ENSEÑANZA DE LAS CIENCIAS BIOLÓGICAS, DESDE UN ENFOQUE ANATÓMICO, FISIOLÓGICO Y BIOFÍSICO. LA NEURONA Y SUS RESPUESTAS ELÉCTRICAS COMO MODELO DE TRABAJO

    OpenAIRE

    Hugo Molina Arroyo; Montserrat Vázquez Balbuena

    2014-01-01

    A partir del año 2008, la Benemérita Universidad Autónoma de Puebla implementa el Modelo Universitario Minerva (MUM), modelo fundamentado en el humanismo crítico y el construccionismo sociocultural, apostando por la implementación de nuevas TIC‟s en los procesos de aprendizaje, investigación y gestión. En este sentido la Escuela de Biología llevó a cabo una restructuración en su programa de estudios lo que permite garantizar, en todo momento, que el estudiante comprenda desde un punto de vist...

  8. ENSEÑANZA DE LAS CIENCIAS BIOLÓGICAS, DESDE UN ENFOQUE ANATÓMICO, FISIOLÓGICO Y BIOFÍSICO. LA NEURONA Y SUS RESPUESTAS ELÉCTRICAS COMO MODELO DE TRABAJO

    Directory of Open Access Journals (Sweden)

    Hugo Molina Arroyo

    2014-07-01

    Full Text Available A partir del año 2008, la Benemérita Universidad Autónoma de Puebla implementa el Modelo Universitario Minerva (MUM, modelo fundamentado en el humanismo crítico y el construccionismo sociocultural, apostando por la implementación de nuevas TIC‟s en los procesos de aprendizaje, investigación y gestión. En este sentido la Escuela de Biología llevó a cabo una restructuración en su programa de estudios lo que permite garantizar, en todo momento, que el estudiante comprenda desde un punto de vista comparativo, al individuo y sus sistemas pasando por tejido y llegando hasta niveles de organización biológica celular y molecular a través del estudio de los movimientos transmembrana. Para cumplir con este objetivo los estudiantes deben cursar en orden jerárquico las materias de Morfología Animal, Fisiología Animal y finalmente Biofísica (entre otras. La experiencia aquí aportada gira en torno a la implementación, dentro de las materias antes mencionadas, de la utilización de la plataforma virtual “Moodle” y de “simuladores”, herramientas mediante las cuales se fortalece el entorno de aprendizaje de los jóvenes universitarios.

  9. Meningoencephalitis associated with disseminated sarcocystosis in a free-ranging moose (Alces alces) calf.

    Science.gov (United States)

    Ravi, Madhu; Patel, Jagdish; Pybus, Margo; Coleman, James K; Childress, April L; Wellehan, James F X

    2015-08-01

    A wild moose (Alces alces) calf was presented for necropsy due to severe neurologic signs. Histopathologic examination revealed multisystemic inflammation with intralesional mature and immature schizonts. Schizonts in the brain reacted positively to Sarcocystis spp. polyclonal antibodies. Gene sequencing of PCR-amplified DNA identified the species as Sarcocystis alceslatrans.

  10. Evidence for the presence of an autoimmune component to the chronic muscle wasting disease characteristic of calves infected with Aarcocystis cruzi

    Science.gov (United States)

    Infection with Sarcocystis spp. often resolves in a progressive decline in muscle integrity. The underlying cause for this has remained undetermined. Previously, we described the presence of proinflammatory muscle protein nitration (PMPN) in calves (ScI) chronically infected with Sarcocystis cruzi. ...

  11. Análisis de corrientes en una red neuronal conectada mediante Gap junctions

    OpenAIRE

    Yustres Díaz, Miguel

    2015-01-01

    La conexión de neuronas mediante sinapsis eléctricas proporciona una mayor velocidad de transmisión sináptica y la capacidad de sincronizar grupos de células para coordinar su actividad. Este tipo de sinapsis permite el intercambio de información continua entre neuronas, no solo cuando se producen potenciales de acción. Dependiendo de la magnitud del acoplamiento, esta sincronización afecta a la actividad sub-umbral y a los potenciales de acción. Un exceso en la sincronización de las neuronas...

  12. Caryospora uptoni and Frenkelia sp.-like coccidial infections in red-tailed hawks (Buteo borealis).

    Science.gov (United States)

    Lindsay, D S; Blagburn, B L

    1989-07-01

    The feces from 16 red-tailed hawks (Buteo borealis) were examined by fecal flotation for the presence of coccidial oocysts or sporocysts. Oocysts of Caryospora uptoni were found in five (31%), sporocysts of a Frenkelia sp.-like coccidium were found in eight (50%), and mixed infections with both species of coccidia were found in three (19%) red-tailed hawks. Neither oocysts nor sporocysts were found in six (38%) red-tailed hawks. Sexual stages of C. uptoni were found in the duodenum and jejunum of a naturally infected red-tailed hawk. Sexual stages were located in enterocytes on the distal three-fourths of the villi. This study shows that over 60% of red-tailed hawks may be passing coccidial oocysts/sporocysts in their feces and provides morphological information for diagnosing C. uptoni infections in histological sections.

  13. [SEASONAL CHANGES IN THE BIOLOGY OF LEUCOCHLORIDIUM PARADOXUM (TREMATODA, LEUCOCHLORIDIOMORPHIDAE)].

    Science.gov (United States)

    Ataev, G L; Tokmakova, A S

    2015-01-01

    Infection of molluscs Succinea putris by trematodes Leucochloridium paradoxum was studied in the region of Vyritsa (Leningrad Province) during the period of 2008-2014. On the basis of the obtained data, seasonal dynamics of infection of molluscs can be presented as follows. Infection of S. putris occurs during the whole warm period from May to August. Young sporocysts of L. paradoxum overwinter and the metacercariae that develop in their extensions mature during spring becoming infective for birds. In the second half of summer, sporocysts start degenerating and die in late August-September. Each sporocyst can form 2-3 mature broodsacs (maximum 5) simultaneously. In cases of multiple infections, their number can reach 19. Several cases of independent release of sporocysts from molluscs were observed. They survive in environment for about an hour, retaining the ability to infect definitive hosts. Additionally, birds can be infected by pecking of horns of infected snails.

  14. Seven new species of Eimeria Schneider, 1875 (Apicomplexa: Eimeriidae) from colubrid snakes of Guatemala and a discussion of what to call ellipsoid tetrasporocystic, dizoic coccidia of reptiles.

    Science.gov (United States)

    Asmundsson, I M; Duszynski, D W; Campbell, J A

    2006-06-01

    During a survey of Guatemalan herpetofauna in the summers of 1998-2000, 29 presumed new species of Eimeria Schneider, 1875 were found, seven of which have a distinct elongate-ellipsoidal shape (L/W ratio >or= 1.7) and are described herein. Six of the seven new species are similar in oöcyst length, width and L/W ratio and sporocyst length, width and L/W ratio, lack a micropyle, oöcyst residuum, Stieda body, sub-- and parastieda bodies, have a polar granule and sporocyst residuum, and their sporocysts appear to have dehiscence sutures. The seventh is slightly smaller and has sporocysts with a Stieda body. The new species are: E. coniophanes n. sp - whose sporulated oöcysts from Coniophanes fissidens are 29.2x14.9 (27-31x13-16) microm, with sporocysts 10.0 x 7.8 microm; E. coniophis n. sp. -from Conophis lineatus are 32.0x16.5 (30-34x14-18) microm, with sporocysts 10.2 x 8.9microm; E. dryomarchoni n. sp. - from Drymarchon corais are 32.2x17.7 (31-34x17-19) microm, with sporocysts 10.7 x 8.6 microm; E. leptophis n. sp. - from Leptophis mexicanus are 29.5x17.0 (28-31x16-18) microm, with sporocysts 10.0 x 9.1 microm; E. oxybelis n. sp. - from Oxybelis aeneus are 31.8x16.5 (29-33x15-18) microm, with sporocysts 10.3 x 8.8 microm; and E. scaphiodontophis n. sp. - from Scaphiodontophis annulatus are 30.0x15.3 (28-33x14-16) microm, with sporocysts 9.9 x 7.9 microm. Sporulated oöcysts of E. siboni n. sp. from Sibon nebulata are 24.3x14.2 (21-27x13-16) microm, with sporocysts 10.0 x 7.1 microm and with a Stieda body. We conclude that until all aspects of each life-cycle are known, it is prudent at this time to name all tetrasporocystic dizoic coccidia from snakes as members of Eimeria rather than place some of them in Choleoeimeria Paperna & Landsberg, 1989.

  15. LA TIROSINA QUINASA C-ABL EN LA ENFERMEDAD DE ALZHEIMER: SU FUNCION EN LA MUERTE NEURONAL Y EN LAS ALTERACIONES DEL CITOESQUELETO.

    OpenAIRE

    CANCINO LOBOS, GONZALO IGNACIO

    2009-01-01

    Los mecanismos por los cuales las neuronas mueren en las enfermedades neurodegenerativas son sólo parcialmente conocidos y pobremente entendidos. Se ha descrito que tanto el envejecimiento como las enfermedades neurodegenerativas se caracterizan por una m 158p.

  16. Bases neurobiológicas de la conciencia: aspectos neuroanatómicos, cognitivos y evolutivos

    National Research Council Canada - National Science Library

    Ricardo R. García

    2012-01-01

    ... temas más controvertidos en el amplio dominio de las neurociencias. Tradicionalmente, la conciencia ha sido entendida como la experiencia subjetiva y privada que surge de la actividad de neuronas...

  17. Preguntas y respuestas sobre la epilepsia

    OpenAIRE

    Bardají Fandos, Teodosia

    2006-01-01

    ¿Cuál de las siguientes afirmaciones define mejor la crisis convulsiva? a. Es el resultado de una descarga brusca, anormal por su intensidad e hipersincronía de un grupo de neuronas cerebrales. b. Es la descarga brusca de un grupo de neuronas cerebrales que se repite crónicamente. c. Es la repetición crónica de crisis...

  18. Copying the development: mirror neurons in child development

    OpenAIRE

    Demian Arturo Herrera Morban; Nathalia Caridad Montero Cruz

    2016-01-01

    Resumen Desde la vida intrauterina nuestro cerebro está siendo expuesto a factores internos y externos que generan cambios epigenéticos que afectan las redes neuronales y por tanto modifican las propiedades de las neuronas espejo del infante en desarrollo. Consideramos que cambios en las neuronas espejo pueden jugar un papel en las patologías del neuro-desarrollo del infante donde no es observada una lesión estructural cerebral.

  19. Copying the development: mirror neurons in child development

    Directory of Open Access Journals (Sweden)

    Demian Arturo Herrera Morban

    2016-06-01

    Full Text Available Resumen Desde la vida intrauterina nuestro cerebro está siendo expuesto a factores internos y externos que generan cambios epigenéticos que afectan las redes neuronales y por tanto modifican las propiedades de las neuronas espejo del infante en desarrollo. Consideramos que cambios en las neuronas espejo pueden jugar un papel en las patologías del neuro-desarrollo del infante donde no es observada una lesión estructural cerebral.

  20. Circadian regulation of daily rhythms in orexinergic neurons in diurnal and nocturnal rodents

    Directory of Open Access Journals (Sweden)

    Gladys S. Martínez

    2009-01-01

    Full Text Available El trabajo que se presenta aquí se centra en la regulación diferencial que ejerce el sistema nervioso central sobre ritmos circadianos en una especie diurna, Arvicanthis niloticus, o rata Nile grass y una especie nocturna, Rattus norvegicus, o rata de laboratorio. En Nile grass, las neuronas que expresan orexina (ORX mostraron un ritmo endógeno diario en la expresión de Fos, ritmo que correlaciona con el ciclo de sueño y vigilia de esta especie y que es opuesto en comparación con el ritmo visto en ratas de laboratorio. En Nile grass las neuronas de ORX reciben proyecciones sustanciales desde neuronas del núcleo supraquiasmático (SCN que expresan el péptido vasoactivo intestinal (VIP. En contraste, en ratas de laboratorio se encontraron muy pocas fibras positivas para VIP adyacentes a neuronas de ORX. Esta diferencia entre especies sugiere un control directo por parte del SCN sobre neuronas que expresan ORX en Nile grass y una regulación más indirecta en ratas de laboratorio. Estos resultados son consistentes con la hipótesis según la cual las diferencias entre especies diurnas y nocturnas se deben a diferencias en las funciones de regiones que reciben eferencias del SCN tales como las neuronas de ORX y el hipotálamos dorsomedial (DMH

  1. Why our brains cherish humanity: Mirror neurons and colamus humanitatem

    Directory of Open Access Journals (Sweden)

    John R. Skoyles

    2009-11-01

    Full Text Available El sentido común dice que estamos aislados. Después de todo, nuestros cuerpos están separados físicamente. Pero la obra Colamus humanitatem de Séneca y la observación de que “ningún hombre es una isla”, que hizo John Donne, sugieren que no estamos ni completamente aislados ni separados. Un descubrimiento reciente de la neurociencia, el de las neuronas espejo, sostiene que el cerebro y la mente no son construidos ni funcionan alejados de lo que pasa en otros individuos. ¿Qué son las neuronas espejo? Son células cerebrales que procesan tanto lo que le pasa como lo que hace un individuo, y, por así decirlo, su “reflexión” percibida cuando esa misma cosa le pasa a, o es hecha por, otro individuo. Por lo tanto, las neuronas espejo se activan cuando una persona realiza una acción específica y cuando percibe la misma acción realizada por otro. El descubrimiento de las neuronas espejo indica que es preciso revisar radicalmente nuestras nociones sobre la naturaleza humana, ya que estas neuronas ofrecen un medio por el cual no concebimos estar tan separados como pensamos. A diferencia de otros simios, los humanos están adaptados a interactuar de forma similar no verbal, cuando están juntos. De manera particular, nuestras caras han evolucionado para mostrar movimientos ágiles y rápidos. Mientras esto usualmente explica cómo se logra la comunicación no verbal, una mejor descripción sería la comunicación no verbal  basada en las neuronas espejo. El autor sostiene que valoramos la humanidad, colamus humanitatem, porque las neuronas espejo y nuestra interfaz interpersonal adaptada de espejo desdibujan las fronteras que nos separan.

  2. A new Eimeria species (Protozoa: Eimeriidae) from caribou in Ameralik, West Greenland.

    Science.gov (United States)

    Skirnisson, K; Cuyler, C

    2016-04-01

    Fecal samples of 11 calves shot in the Ameralik area, West Greenland, in August-September 2014 were examined for coccidian parasites. The calves belonged to a population of interbreeding indigenous caribou Rangifer tarandus groenlandicus and feral semi-domestic Norwegian reindeer Rangifer tarandus tarandus. Two coccidian species were found: Eimeria rangiferis and a coccidium that was identified and described as a new species. The latter's sporulated oocyst is spherical or slightly subspherical. Average size is 25.6 × 24.8 μm. The oocyst has two distinct walls. Wall thickness is ∼1.4 μm. The unicolored outer wall is brown, the inner wall is dark gray. The oocysts contain a small polar granule but are devoid of a microphyle. The oocysts enclose four ovoid-shaped sporocysts with a rounded end opposite to the Stieda body. The average size of sporocysts is 15.2 × 7.8 μm. Sporocysts contain a granular sporocyst residuum that forms a spherical cluster between the sporocysts, one large refractile body is present in each sporozoite. The spherical form easily distinguishes oocysts of the new species from the seven previously described eimerid species in R. tarandus. This is the first eimerid described as a new species to the sciences from caribou in the Nearctic.

  3. Buyanghuanwu recipe inhibits neurona 1 apoptosis after cerebra 1 ischemia/reperfusion injury possibly through the p38MAPK/COX2 signa 1 pathway in rats%补阳还五汤对大鼠脑缺血/再灌注后p38MAPK磷酸化、COX2表达的影响

    Institute of Scientific and Technical Information of China (English)

    孙立倩; 赵雅宁; 李建民; 崔建忠; 张宇新

    2010-01-01

    目的 探讨补阳还五汤对脑缺血再灌注后神经细胞凋亡的作用及机制.方法 大脑中动脉线栓法制作大鼠局灶性脑缺血/再灌注损伤模型.原位缺口末端标记法(TUNEL)检测大鼠脑缺血/再灌注区神经细胞的凋亡,免疫组织化学和Westem Blot法检测p38MAPK和COX2蛋白表达,术后2、4及7 d对大鼠综合运动能力评分.结果 模型组TUNEL阳性细胞数量、p38MAPK和COX2蛋白表达水平明显升高,神经功能损害严重;补阳还五汤能够明显减少TUNEL阳性细胞数量,降低p38MAPK和COX2蛋白表达水平,改善神经功能状态.结论 补阳还五汤能减少脑缺血再灌注后神经细胞凋亡,其机制与抑制p38MAPK磷酸化、COX2蛋白表达有关.

  4. Sistematización morfo-funcional del complejo motor facial del perro. Análisis de las neuronas de origen de los ramos periféricos del nervio facial, identificadas por transporte axónico retrógrado de peroxidasa.

    OpenAIRE

    Prats Galino, Alberto

    1987-01-01

    El núcleo o complejo motor del nervio facial es un centro nervioso situado entre el bulbo raquídeo y la protuberancia, en la vecindad de la superficie ventrolateral troncoencefálica. Esta masa celular inerva la musculatura derivada del segundo arco branquial (arco hioideo), que comprende la totalidad de músculos faciales superficiales y ciertos músculos faciales profundos. Las fibras branquiomotoras faciales, después de un complicado trayecto intraencefálico e intrapetroso, emergen del cr...

  5. Molecular and experimental evidence refuse the life cycle of Proctoeces lintoni (Fellodistomidae) in Chile.

    Science.gov (United States)

    Oliva, Marcelo E; Valdivia, Isabel M; Cárdenas, Leyla; George-Nascimento, Mario; Gonzalez, Karen; Guiñez, Ricardo E; Cuello, Diego

    2010-02-01

    The mussel Perumitylus purpuratus has been described as the first intermediate host for the digenea Proctoeces lintoni (Fellodistomidae) in the Chilean coast. The study of more than 3000 specimens of P. purpuratus, taken off northern Chile revealed the absence of sporocysts. Experimental infection of mussels with eggs obtained from the known host for P. lintoni was unsuccessful. We analyze the V4 region of the SSU rRNA of living sporocysts and cercariae obtained from P. purpuratus from central Chile in order to confirm the proposed life cycle for this digenea. Our results demonstrated that sporocysts and cercariae obtained from P. purpuratus do not belong to P. lintoni but to an undescribed digenea from the Chilean coast.

  6. Caryospora peneireiroi n. sp. (Apicomplexa: Eimeriidae) in the common kestrel, Falco tinnunculus (Falconiformes: Falconidae), in mainland Portugal.

    Science.gov (United States)

    Cardozo, Sergian Vianna; Berto, Bruno Pereira; Caetano, Inês; Maniero, Viviane Camara; Fonseca, Isabel Pereira da; Lopes, Carlos Wilson Gomes

    2016-06-07

    The common kestrel Falco tinnunculus Linnaeus, 1758, is a widespread raptor, native in Europe, Asia and Africa, and vagrant in the Americas. In the current work, 27 fecal samples were collected from common kestrels kept in the Lisbon Center for Wild Animal Recovery, located at Monsanto Forest Park, Lisbon, Portugal. Five (19%) of them were found to be passing an undescribed species of Caryospora in their feces. The oocysts of Caryospora peneireiroi n. sp. were ellipsoidal with a bilayered wall and measured 47.1 × 37.6 µm with a shape index of 1.25. No micropyle, oocyst residuum or polar granule was present. The sporocysts were subspherical, measuring 25.1 × 24.3 µm. Stieda, sub-Stieda and para-Stieda bodies were absent. The sporocyst residuum was composed of many homogenous globules scattered throughout the periphery of the sporocyst. This is the fourth caryosporan species reported from F. tinnunculus.

  7. Caryospora peneireiroi n. sp. (Apicomplexa: Eimeriidae in the common kestrel, Falco tinnunculus (Falconiformes: Falconidae, in mainland Portugal

    Directory of Open Access Journals (Sweden)

    Sergian Vianna Cardozo

    2016-01-01

    Full Text Available Abstract The common kestrel Falco tinnunculus Linnaeus, 1758, is a widespread raptor, native in Europe, Asia and Africa, and vagrant in the Americas. In the current work, 27 fecal samples were collected from common kestrels kept in the Lisbon Center for Wild Animal Recovery, located at Monsanto Forest Park, Lisbon, Portugal. Five (19% of them were found to be passing an undescribed species of Caryospora in their feces. The oocysts of Caryospora peneireiroi n. sp. were ellipsoidal with a bilayered wall and measured 47.1 × 37.6 µm with a shape index of 1.25. No micropyle, oocyst residuum or polar granule was present. The sporocysts were subspherical, measuring 25.1 × 24.3 µm. Stieda, sub-Stieda and para-Stieda bodies were absent. The sporocyst residuum was composed of many homogenous globules scattered throughout the periphery of the sporocyst. This is the fourth caryosporan species reported from F. tinnunculus.

  8. A new species of Caryospora (Apicomplexa: Eimeriidae) from the bald eagle, Haliaeetus leucocephalus (Accipitriformes: Accipitridae), from Kansas.

    Science.gov (United States)

    McAllister, Chris T; Duszynski, Donald W; McKown, Richard D

    2013-04-01

    Between March 1989 and February 1994, 4 bald eagles ( Haliaeetus leucocephalus ) from various localities in Kansas were examined for coccidia. One (25%) of the bald eagles was found to be passing an undescribed species of Caryospora in its feces. Oocysts of Caryospora hanebrinki n. sp. are ellipsoidal to ovoidal with a bilayered wall and measure 48.1 × 42.1 μm with a shape index of 1.2. A micropyle, oocyst residuum, and polar granule were absent. Sporocysts are spheroidal, 24.8 μm wide. Stieda, substieda, and parastieda bodies were absent; a spheroidal sporocyst residuum is present; it measures 17.5 μm and is composed of many intact homogenous globules with a few dispersed in a loose spiral around the sporocysts. This is the first caryosporan documented from the bald eagle and is the largest known Caryospora from raptors.

  9. Coccidia of the collared peccary (Tayassu tajacu) in southern Texas with descriptions of three new species of Eimeria (Apicomplexa: Eimeriidae).

    Science.gov (United States)

    Wilber, P G; Hellgren, E C; Gabor, T M

    1996-08-01

    In February 1993, fresh fecal samples were collected from 47 collared peccaries (Tayassu tajacu) killed by hunters at the Chaparral Wildlife Management Area, southern Texas, USA. Five species of coccidia (Eimeria chaparralensis n. sp. [9/47, 19%], Eimeria dicotylensis n. sp. [21/47, 21%], Eimeria pecari n. sp. [2/47, 4%], Eimeria sp. [1/47, 2%], and Klossia sp. [1/47, 2%]) were observed. Measurements are in micron. Sporulated oocysts of E. chaparralensis are rough-walled, elongate ovoidal, 43.3 x 28.5 (37-52 x 26-35); sporocysts are elongate ellipsoidal 21.8 x 9.0 (16-27 x 7-12); micropyle (approximately 4.9), Stieda, and substieda body are present; sporocyst residuum is present in newly sporulated oocysts; polar granule and oocyst residuum are absent. Sporulated oocysts of E. dicotylensis are smooth-walled, ovoidal, 25.7 x 20.1 (23-29 x 17-23); sporocysts are ellipsoidal 13.0 x 6.9 (11-17 x 6-9); micropyle and oocyst residuum are absent; polar body sometimes present; Stieda body and sporocyst residuum always present. Sporulated oocysts of E. pecari are smooth-walled, elongate ellipsoidal, 26.8 x 18.1 (22-31 x 15-21); sporocysts are elongate ellipsoidal 16.4 x 5.9 (13-22 x 4-7); micropyle (approximately 5.8) with collar, Stieda body, substieda body, and sporocyst residuum are present; polar granule and small oocyst residuum sometimes present. There were no sex or age differences in prevalences of infection, and there were no positive or negative associations between any species of eimerian. The majority of hosts were infected with a single species of Eimeria. Overall prevalence of infection with eimerians was 23/47 (49%).

  10. Description of the Oocysts of Three New Species of Eimeria (Apicomplexa: Eimeriidae from Iguanid Lizards (Sauria: Iguanidae of Central and South America

    Directory of Open Access Journals (Sweden)

    Daszak P

    1998-01-01

    Full Text Available Three new species of Eimeria are described from iguanid lizards of Central and South America. The oocysts of each species have no micropyles or residua and the sporocysts lack Stieda bodies, but all have a sporocyst residuum. Eimeria sanctaluciae n.sp. was found in the St. Lucia tree lizard, Anolis luciae, collected from the Maria Islands, Lesser Antilles. The oocysts are spherical to subspherical, averaging 17.3 x 16.5 µm, with a single layered colourless wall; about 60% contain polar granules. The sporocysts are ellipsoidal and average 7.7 x 5.5 µm. Eimeria liolaemi n.sp. was recovered from the blue-gold swift, Liolaemus taenius, from Chile. The oocysts are spherical to subspherical, measuring 21 x 20.1 µm with a single-layered colourless wall. The sporocysts are subspherical and average 7.4 x 6.8 µm. Eimeria caesicia n.sp. is described from the Brazilian collared iguanid, Tropidurus torquatus. The oocysts measure 27.4 x 23.7 µm, are spherical to subspherical, with a bilayered wall, the outer surface of which appears pale blue in colour, the thin, inner wall appearing brown, when viewed by direct light under the optical microscope. The sporocysts are subspherical and average 9.4 x 7.2 µm. Unnamed polysporocystid oocysts with dizoic sporocysts are reported from the faeces of the lesser St. Vincent tree lizard, Anolis trinitatis and the possibility of spurious parasitism briefly discussed. In addition, oocysts of an unnamed Isospora sp. with a smooth oocyst wall which closely resembles I. reui were recovered from A. trinitatis.

  11. The red-tailed hawk, Buteo jamaicensis, a native definitive host of Frenkelia microti (Apicomplexa) in North America.

    Science.gov (United States)

    Upton, S J; McKown, R D

    1992-01-01

    Oral inoculation of prairie voles, Microtus ochrogaster, with coccidian sporocysts isolated from the feces of a red-tailed hawk, Buteo jamaicensis, in Kansas, USA, resulted in formation of Frenkelia microti (Apicomplexa: Sarcocystidae) tissue cysts in the brains of the voles. Five additional isolates of morphologically similar sporocysts collected from red-tailed hawks or other Buteo spp. in Kansas failed to result in detectable infections in rodents. These results are the first to verify that red-tailed hawks are natural definitive host in North America for F. microti.

  12. Frenkelia sp.-like infection in the small intestine of a red-tailed hawk.

    Science.gov (United States)

    Lindsay, D S; Ambrus, S I; Blagburn, B L

    1987-10-01

    Developmental stages of a Frenkelia sp.-like coccidium were observed in tissue sections of the duodenum, jejunum, and ileum of a naturally infected red-tailed hawk (Buteo jamaicensis borealis) that died and was examined at necropsy. Developmental stages were located in the lamina propria of these tissues. Thirty sporulated sporocysts measured 11.1 X 8.1 microns in tissue sections. Four sporozoites were present in each sporulated sporocyst. The coccidial infection was not a contributing factor in the death of this red-tailed hawk.

  13. First report of human intestinal sarcocystosis in Cambodia.

    Science.gov (United States)

    Khieu, Virak; Marti, Hanspeter; Chhay, Saomony; Char, Meng Chuor; Muth, Sinuon; Odermatt, Peter

    2017-10-01

    Human intestinal sarcocystosis (HIS), caused by Sarcocystis species, is acquired by eating undercooked meat from sarcocyst-containing cattle (S. hominis, S. heydorni) and pigs (S. suihominis). We report on the detection of human intestinal Sarcocystis infections in a cross-sectional survey of Strongyloides stercoralis in early 2014, in Rovieng District, Preah Vihear Province, northern Cambodia. Among 1081 participants, 108 (10.0%) were diagnosed with Sarcocystis spp. oocysts in stool samples. Males had a significantly higher risk of infection than females (OR: 1.9, 95% CI: 1.3-2.9, p=0.001). None of the reported symptoms (abdominal discomfort, diarrhea, muscle pain and itching skin) occurring in the two weeks preceding the examinations were associated with a Sarcocystis infection. Many Sarcocystis cases were found among those who had participated in a wedding celebration and Chinese New Year festivities, where they had consumed raw or insufficiently cooked beef (83.3%) and pork (38.9%) based dishes. This report documents the first HIS cases in Cambodia. Copyright © 2017 Elsevier B.V. All rights reserved.

  14. MODELANDO EL CRECIMIENTO DE NEURITAS

    Directory of Open Access Journals (Sweden)

    Oscar Ávila

    2007-01-01

    Full Text Available El funcionamiento adecuado del sistema nervioso de un organismo, aun desde su estado embrionario, requiere que las neuronas establezcan conexiones específicas con otras neuronas o tejidos. Dado que una red neuronal contiene un número inmenso de neuronas, encontrar el camino correcto para cada una de ellas es claramente un fenómeno complejo, en el que participan muchos procesos. En este artículo estudiamos el crecimiento de neuritas in vitro, y nos enfocamos en los efectos que tienen diversos factores químicos en el medio de cultivo. Construimos un modelo teórico para explicar las diferencias encontradas en medios químicos diferentes. Simulaciones numéricas reproducen las observaciones y permiten predecir la forma como actúan diversas substancias químicas en el crecimiento y la conexión de neuritas.

  15. Regulación neurotrófica de las propiedades de disparo y de la sinaptología aferente sobre las motoneuronas axotomizadas del núcleo motor ocular externo

    OpenAIRE

    Davis López de Carrizosa, María América

    2010-01-01

    La teoría trófica de las conexiones neuronales establece que durante el desarrollo embrionario los órganos diana son esenciales para la supervivencia y diferenciación de las neuronas que los inervan, rescatando a estas células del proceso natural de la muerte ... celular programada. El descubrimiento del factor de crecimiento nervioso (NGF, del inglés nerve growth factor) demostró que esta acción de los órganos diana sobre las neuronas está mediada por unas moléculas solubles denominadas ...

  16. PAPEL DE LA PROTEINA SIRT 1 EN LA DENDRITOGENESIS NEURONAL: NEUROPROTECCION CONTRA AGREGADOS DEL PEPTIDO A BETA

    OpenAIRE

    ALLARD GARROTE, CLAUDIO ANDRES; ALLARD GARROTE; CLAUDIO ANDRES

    2013-01-01

    La arborización dendrítica es requerida para la apropiada conectividad neuronal. La proteína SIRTl, es una desacetilasa de histonas dependiente de NAD+, a la cual se le asocian funciones relacionadas con el envejecimiento, longevidad y respuesta a estrés. En neuronas a la proteína SIRTl se le relaciona con la diferenciación neuronal, neurogénesis y neuroprotección. En el presente estudio, se evaluó el papel de SIRTl en el desarrollo dendrítico en cultivo de neuronas hipocampales. La sobree...

  17. Efecto de la pérdida de la inervación dopaminérgica del núcleo subtalámico sobre la conducta motora de ratas

    OpenAIRE

    Nancy Pavón-Fuentes; Lisette Blanco-Lezcano; Lourdes Lorigados-Pedre; Lázaro Álvarez-González; Lisis Martínez-Martí; Raúl Macías-González

    2010-01-01

    Actualmente la enfermedad de Parkinson es considerada como un trastorno del sistema nervioso central que afecta a los ganglios basales. Las características anatomopatológicas más prominentes de esta enfermedad son: degeneración de las células dopaminérgicas de la substantia nigra pars compacta (SNc), la existencia de gliosis y la presencia de cuerpos eosinófilos de inclusión. La relevancia fisiológica de la modulación directa de las neuronas del núcleo subtalámico (NST) por neuronas dopaminér...

  18. Dynamics of spontaneous activity in the cerebral cortex across brain states

    OpenAIRE

    Jercog, Daniel Alejandro

    2013-01-01

    [spa] La actividad espontánea en la corteza cerebral cambia en diferentes estados cerebrales. Durante estados desincronizados (e.g. estado de vigilia, sueño MOR), las poblaciones de neuronas en los potenciales de acción en una manera aparentemente estocástica y no correlacionada. Por el contrario, durante estados sincronizados (e.g. sueño de ondas lentas, anestesia) las neuronas corticales muestran la alternancia entre periodos de reposo (DOWN) y los períodos de actividad (UP) de manera coher...

  19. Procesamiento de la información propioceptiva en el núcleo cuneatus

    OpenAIRE

    Leiras González, Roberto

    2013-01-01

    Se estudiaron los mecanismos implicados en la transmisión de la información propioceptiva en el núcleo cuneatus medio-ventral (mvCN) de gatos anestesiados, utilizando técnicas estándar de registro extracelular combinadas con estimulación eléctrica y microiontoforesis. Se demostró, mediante registros dobles de neuronas del mvCN y del cuneatus rostro-ventral (rvCN), que la microestimulación en el rvCN induce un efecto dual sobre las neuronas de proyección del mvCN. El GABA y la glicina eliminar...

  20. Propiedades neuroprotectoras de los esteroides sexuales

    OpenAIRE

    Veiga, Sergio; García-Segura, Luis M.; Azcoitia, I.

    2004-01-01

    [ES]El sistema nervioso es una diana de las hormonas esteroides y también un tejido esteroidogénico, y produce esteroides que actúan de una forma paracrina o autocrina sobre neuronas y glía. Los esteroides formados en el tejido nervioso se denominan neuroesteroides, para diferenciarlos, por su origen, de los esteroides periféricos, aunque tienen la misma estructura molecular que éstos. Desarrollo. Se analiza la capacidad de las neuronas y las células de glía de sintetizar esteroides, y se des...

  1. Spinal cord injury: Role of endothelial differentiation gene family lysophosphatidic acid receptors

    OpenAIRE

    Santos Nogueira, Eva

    2015-01-01

    El daño tisular secundario que se produce tras una lesión de la médula espinal contribuye de manera significativa a las pérdidas funcionales que se observan pacientes que padecen este tipo de afectación. Aunque la regeneración axonal y la sustitución de las neuronas dañadas tras el traumatismo medular son objetivos importantes para reparar estas lesiones, el desarrollo de estrategias experimentales que tengan como meta evitar el daño secundario sobre axones, neuronas, mielina y las células gl...

  2. El espejo de la acción y la encarnación de la cognición

    OpenAIRE

    Yorio, Alberto A.

    2009-01-01

    En este trabajo se comentan algunas evidencias que sugieren que los “engramas motores” y el “patrón de inervación motora”·clásicamente postulados como mecanismos independientes de la codificación de las “praxias”, tienen una existencia real y son funciones complementarias de una misma red de neuronas (“neuronas espejo”), que se localiza en la circunvolución supramarginal ubicada en el lóbulo parietal inferior izquierdo, cuya lesión ocasiona el trastorno neuropsicológico conocido como “apraxia...

  3. Neuroprotección en un nuevo modelo de animal transgénico

    OpenAIRE

    Mejías Estévez, Rebeca María

    2006-01-01

    El objetivo general de este proyecto fue analizar en un modelo de parkinsonismo experimental en ratones, si el aumento del poder reductor de forma selectiva en las neuronas dopaminérgicas nigrostriatales (neuronas DNS9, mediante la sobre-expresión del enzima glucosa-6-fosfato deshidrogenada (G6PD), les confiere protección. Además nos interesó estudiar algunos aspectos relacionados con la regulación de la expresión de dicho enzima en células excitables. Los objetivos específicos de este tra...

  4. Técnicas de conectividad cerebral y transferencia de información aplicado al estudio de la esquizofrenia

    OpenAIRE

    DE LA IGLESIA VAYÁ, MARIA DE LOS DESAMPARADOS

    2011-01-01

    Santiago Ramón y Cajal demostró que el sistema nervioso y el cerebro estaban formados por células, al igual que el resto de los tejidos vivos. Esas células fueron llamadas neuronas y las conexiones entre ellas, la sinapsis, son fundamentales para su funcionamiento y comunicación. Todo lo que ocurre dentro del cerebro puede describirse como un entramado de corrientes eléctricas y reacciones bioquímicas entre neuronas. A partir del siglo XIX, la observación y estudio de síndromes o enfermeda...

  5. Fisiología del nucleo motor ocular externo en el gato

    OpenAIRE

    1982-01-01

    Los propósitos del presente trabajo experimental son:A). Estudiar la actividad eléctrica de las neuronas del núcleo motor ocular externo principal durante distint ... Específicamente se analiza la conducta de motoneuronas e interneuronas del núcleo motor ocular externo principal durante posiciones mantenidas del ojo en la órbita, así como durante movimiento sacádicos voluntarios o inducidos por estimulación visual o vestibular. Para ello, se realiza el registro extracelular de las neuronas ob...

  6. Modelado de circuitos neuronales empleando técnicas de programación orientada a bloques

    OpenAIRE

    Perea Paizal, Julia

    2015-01-01

    El presente trabajo consiste en la implementación de un modelo del circuito completo del arco reflejo basado en la neurona biológica y en el estudio de su comportamiento dinámico. El circuito reflejo modular básico está compuesto por un receptor y su fibra aferente, una o más neuronas medulares intercalares, una motoneurona y un efector y su músculo. Las propiedades de cualquier reflejo son una función de las características de los receptores que inician el estímulo y de la naturaleza de los ...

  7. Why our brains cherish humanity: Mirror neurons and colamus humanitatem

    OpenAIRE

    Skoyles, John R.

    2009-01-01

    El sentido común dice que estamos aislados. Después de todo, nuestros cuerpos están separados físicamente. Pero la obra Colamus humanitatem de Séneca y la observación de que “ningún hombre es una isla”, que hizo John Donne, sugieren que no estamos ni completamente aislados ni separados. Un descubrimiento reciente de la neurociencia, el de las neuronas espejo, sostiene que el cerebro y la mente no son construidos ni funcionan alejados de lo que pasa en otros individuos. ¿Qué son las neuronas e...

  8. Regulación de la formación de especies reactivas de oxígeno por la cadena respiratoria mitocondrial en células neurales

    OpenAIRE

    2016-01-01

    [ES]Para conocer la función fisiológica de las especies reactivas de oxígeno (ROS) en cerebro, es necesario analizar la contribución de los diferentes tipos de células neurales en la formación de ROS. En la Tesis Doctoral hemos evaluado la capacidad de las neuronas y astrocitos de generar ROS de forma espontánea. Hemos observado que la producción de ROS es mayor (desde 1.5 a 10 veces) en astrocitos que en neuronas, en cultivos primarios de ratas Wistar y ratones C57BL6, con independencia...

  9. Efecto de la infección por el virus de la rabia sobre la expresión de parvoalbúmina, calbindina y calretinina en la corteza cerebral de ratones.

    Directory of Open Access Journals (Sweden)

    Orlando Torres-Fernández

    2004-03-01

    Full Text Available Algunas manifestaciones clínicas de la rabia, así como los resultados de experimentos con cultivos celulares y animales de laboratorio han llevado a sugerir que el virus de la rabia afecta la neurotransmisión gabaérgica. En la corteza cerebral existen diferentes tipos de neuronas que sintetizan el neurotransmisor GABA. Éstas se pueden identificar con marcadores neuronales, entre los que se destacan tres proteínas ligadoras de calcio: la parvoalbúmina (PV, la calbindina (CB y la calretinina (CR. El virus de la rabia se disemina a través de la corteza cerebral pero se desconocen sus posibles efectos citopáticos sobre las neuronas gabaérgicas. Para evaluar el efecto de la rabia sobre estas neuronas, se estudió mediante inmunohistoquímica la expresión de PV, CB y CR en la corteza frontal de ratones normales y ratones infectados con virus 'calle' o virus 'fijo' de la rabia. La PV se expresó en neuronas multipolares dispersas regularmente entre las capas II y VI, y en botones sinápticos que bordeaban el soma de las neuronas piramidales. La inmunorreactividad a CB se manifestó en dos franjas corticales: la primera, en las capas supragranulares II y III en neuronas con somas redondeados e inmersos en un neuropilo intensamente marcado; la segunda, en las capas infragranulares V y VI en neuronas multipolares dispersas y rodeadas por un neuropilo menos reactivo. La CR se expresó en neuronas bipolares con somas fusiformes distribuidas en las seis capas corticales, pero concentradas principalmente en las capas II y III. Hubo una característica común en las muestras infectadas con los dos tipos de virus: la inmunotinción a PV fue más intensa que en las muestras normales. La infección derivada del virus 'calle' no causó alteraciones adicionales en la expresión de las tres proteínas. En contraste, la infección con virus 'fijo' produjo una reducción notable del número de neuronas CB+, así como de la inmunorreactividad a CB en el

  10. Macrophages facilitate the excystation and differentiation of Toxoplasma gondii sporozoites into tachyzoites following oocyst internalization

    Science.gov (United States)

    Toxoplasma gondii is a common parasite of humans and domestic animals, which is transmitted via oocysts in cat faeces or tissue cysts in contaminated meat. The oocyst and sporocyst walls are multilayered polymeric structures that protect the infective sporozoites from deleterious physical and chemic...

  11. Eimeria galateai sp. n. from the Paradise Kingfisher, and Eimeria duncani sp. n. from the Sacred Kingfisher in Papua New Guinea.

    Science.gov (United States)

    Varghese, T

    1977-05-01

    Eimeria galateai sp. n. from the paradise kingfisher (Tanysiptera galatea Gray) and Eimeria duncani sp. n. from the sacred kingfisher (Halcyon sancta Vigors & Horsfield) have been described from Papua New Guinea. Four of 11 paradise kingfishers were infected with E. galateai oocysts, measuring 13 (11-16) X 9 (8-11) micron. The oocysts were ovoid with nipple-like protrusion at one pole. Micropyle and polar granule were absent, while oocyst residuum (5 X 4 micron) was present. Sporocysts, measuring 5 (4-6) X 2 micron, were elongate-ovoid, and had a distinct convex Stieda body; the sporocyst residuum was absent. Two of 9 sacred kingfishers were infected with ovoid-truncated, 22 (19-25) X 16 (12-18) micron oocysts of E. duncani. Polar granule (5 X 2) was present in the oocysts, but there was no micropyle or oocyst residuum. Sporocysts were ovoid, measuring 9 (8-10) X 5 (4-6) micron, with a prominent Stieda body, and granular sporocyst residuum. Eimeria galateai and E. duncani are the first species of this genus to be described from birds of the order Coraciiformes.

  12. Four new coccidia (Apicomplexia: Eimeriidae) from anoles (Lacertilia: Polychrotidae) in the Dominican Republic.

    Science.gov (United States)

    Cisper, G L; Huntington, C; Smith, D D; Powell, R; Parmerlee, J S; Lathrop, A

    1995-04-01

    Fecal samples from 25 Anolis armouri, 2 Anolis bahorucoensis, 48 Anolis cybotes, and 21 Anolis olssoni (Lacertilia: Polychrotidae) from southern Hispaniola were examined for coccidian oocysts. Two eimerians and 2 isosporans are herein described as new species. Sporulated oocysts of Eimeria schwartzi n. sp. from A. armouri are ellipsoidal, 22.7 (20.8-25.0) x 15.7 (14.6-17.7) microns, with spherical to subspherical sporocysts, 7.9 (6.2-9.4) x 7.4 (6.2-8.3) microns. Sporulated oocysts of Isospora reui n. sp. from A. bahorucoensis are spherical to subspherical, 18.2 (15.6-20.0) x 17.8 (15.6-19.8) microns, with ovoid sporocysts, 11.9 (10.4-12.7) x 8.5 (7.5-9.4) microns. Sporulated oocysts of Isospora hendersoni n. sp. from A. armouri and A. cybotes are spherical to subspherical, 23.2 (20.8-26.0) x 21.1 (18.4-23.9) microns, with ellipsoidal sporocysts, 14.7 (12.5-15.6) x 10.0 (9.2-11.4) microns. Sporulated oocysts of Eimeria avilae n. sp. from A. olssoni are cylindrical, 29.3 (26.0-33.3) x 15.9 (13.5-18.9) microns, with ellipsoidal sporocysts 10.2 (9.4-11.4) x 6.8 (5.2-8.0) microns.

  13. Zoonotic parasites from exotic meat in Malaysia.

    Science.gov (United States)

    Fazly, Z A; Nurulaini, R; Shafarin, M S; Fariza, N J; Zawida, Z; Muhamad, H Y; Adnan, M; Premaalatha, B; Erwanas, A I; Zaini, C M; Ong, C C; Chandrawathani, P

    2013-09-01

    Four zoonotic parasites, Sarcocystis spp., Toxoplasma gondii, Trichinella spp. and Taenia spp were screened in exotic meats. A total of forty-six (n=46) meat samples from various species of exotic animals were received from all the 14 states in Malaysia from January 2012 to April 2012. All exotic meat samples were examined macroscopically and histologically for the four zoonotic parasites. Results by histological examination of exotic meats showed the presence of Sarcocystis and Toxoplasma cysts at 8.7% (n=4) and 4.3% (n=2) respectively. No Trichinella spp. and Taenia spp. were found.

  14. HISTOLOGICAL STUDIES ON THE DEVELOPMENT OF EURYTREMA COELOMATICUM IN THE SNAILS BRADYBAENA SIMILARIS FERUSSAC%腔阔盘吸虫在贝类宿主体中发育的组织学研究

    Institute of Scientific and Technical Information of China (English)

    杨玉荣

    2001-01-01

    目的 为了解腔阔盘吸虫在贝类宿主体内发育的组织学情况。方法用腔阔盘吸虫(Eurytrema coelomaticum)虫卵人工感染同型阔纹锅牛Bradybaena similaris Ferussac后在不同时间里固定蜗牛,经石蜡包埋,连续切片、苏木精伊红复染,观察腔阔盘吸虫在蜗牛体内的发育变化。结果与结论感染后5~12天为早期母胞蚴阶段,感染15天母胞蚴体内开始出现子胞蚴的胚球,29天的母胞蚴增大明显,胚球数目增多;40天的母胞蚴布满肠壁周围,胚球两端拉长;47天的母胞蚴体内的子胞蚴胚球增大明显,已出现内外囊壁的分化,内囊壁包围着胚细胞组成的中心区域;感染91天的子胞蚴体内出现尾蚴胚体;118天的子胞蚴体内的尾蚴已经成熟,子胞蚴移向呼吸腔。%Aim This paper reported the histological development of Eurytrema coelomaticum in the snails Bradybaena sirnilaris Ferussac. Method Snails were infected experimentally by feeding Eurytrema oelomaticum eggs, 5 ~ 6 snails were fixed in Bouin' s fluid at intervals of 3 ~ 6 days postinfection, the entire animal was dehydrated in thanol - toluol series, embedded in paraffin,serially sectioned at 10μm, and stained with Enlirch's hematoxylin - eosin. Results and Conclusion the germinal cells in the mother sporocyst stretched and scattered in 5 ~ 12days postinfection snails, and the number of germninal cells increased. In the 15 days postin fection snails, germinal cells created a large space around hemselves and germinal balls were presented in mother sporocyst, each become a daughter sporocyst. At 29 days postinfection mother sporocyst enlarged obviously, the mumber of germinal balls ncreased. At 40 days postinfection, mother sporocyst scattered all over the intestine wall. The germinal balls lengthened at the both sides. By 47days postinfection, the germinal balls in mother sporocyst enlarged significantly, daughter sporocyst balls present

  15. Desenvolvimento de Eurytrema coelomaticum (Giard & Billet (Digenea, Dicrocoeliidae em Bradybaena similaris (Férussac (Gastropoda, Xanthonychidae Development of Eurytrema coelomaticum (Giard & Billet (Digenea, Dicrocoeliidae in Bradybaena similaris (Férussac (Gastropoda, Xanthonychidae

    Directory of Open Access Journals (Sweden)

    Solange Viana Paschoal Blanco Brandolini

    2001-06-01

    Full Text Available To follow the larval developmenl of Eurytrema coelomaticum (Giard & Billet, 1892 in Bradybaena similaris (Férussac, 1821 snails were separated in three classes using the shell diameter: Class A (14.5-10.2 mm, Class B (10.1-6.9 mm and Class C (6.8-2.6 mm. Only snails belonging to classes A and B acquired the infection. Specimens of E. coelomaticum removed from the pancreatic ducts were exposed to three physiological solutions: Earle, Locke and saline 0.85%, to obtain eggs for the experimental infections, The Locke solution induced the best egg release. The route of migration the intramolluscan development of E. coelomaticum was studied with the aid of histology. The minimal period of intramolluscan developmenl, ending at the expelling of daughter sporocysts, was 107 days for the snails infected in March, and 79 days for the snails infected in November. The Student "t" test and the Chi-square test showed a significant difference (α = 5% between the two periods, although the mean temperature registered during the experiments did not significantly differed (α = 5%. The elimination of daughter sporocysts occurred through the snail's pneumostome, and always at night. Most sporocysts were eliminated at intervals that varied between one to three days, without regularity. The time of elimination of the daughter sporocysts was different for the two infection period studied: 12 weeks for the snails infected in March, and three weeks for those infected in November. Positive correlation between the number of sporocysts expelled by the snail host and higher temperatures registered in the laboratory was observed. This correlation was more evident in November infection.

  16. Morphological and molecular characterization of Choleoeimeria pogonae n. sp. coccidian parasite (Apicomplexa: Eimeriidae, 1989, Paperna and Landsberg) in a western bearded dragon (Pogona minor minor).

    Science.gov (United States)

    Yang, Rongchang; Brice, Belinda; Ryan, Una

    2016-01-01

    A new species, Choleoeimeria pogonae n. sp. is described from a Western bearded dragon (Pogona minor minor) in Western Australia. Sporulated oocysts (n = 48) were cylindroidal in shape. Oocyst length, 27.0 (26.0-28.3) μm, oocyst width, 15.2 (14.0-16.5) μm, oocyst length/width ratio (L/W) 1.8 (1.6-1.9), each with 4 sporocysts (Eimeria-like) and a polar granule, but lacking a micropyle and oocyst residuum. Sporocysts are ovoidal in shape, sporocyst length, 10.0 (9.0-11.0) μm, sporocyst width 8.5 (7.0-9.5) μm, sporocyst L/W ratio, 1.2 (1.1-1.3). Stieda, substieda and parasubstieda bodies were all absent. Molecular analysis was conducted at the 18S rRNA and cytochrome c oxidase I (COI) loci. Phylogenetic analysis of 18S sequences revealed that C. pogonae n. sp. grouped together with another four Choleoeimeria spp. and exhibited 99.1%-99.4% genetic similarity. At the COI locus, C. pogonae n. sp. was in an independent clade and had the highest similarity (80.4%) to Eimeria cf. mivati from a chicken (Gallus gallus domesticus). According to the morphological and molecular data, this isolate is a new species of coccidian parasite. This study further supports the taxonomy of Choleoeimeria spp. as a new genus based on molecular phylogenetic analysis. Crown Copyright © 2015. Published by Elsevier Inc. All rights reserved.

  17. Vulnerabilidad selectiva neuronal: la rabia como modelo de estudio

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    Orlando Torres Fernández

    2005-03-01

    Full Text Available La vulnerabilidad selectiva neuronal puede ser definida, anatómicamente, por la vulnerabilidad diferencial de circuitos y neuroquímicamnete, por la vulnerabilidad de las neuronas que expresan firentes proteínas en partícular.

  18. Efecto de un tratamiento ototóxico en la ultraestructura coclear

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    Sandra Rodríguez Salgueiro

    2007-01-01

    Full Text Available La sordera es una de las discapacidades más comunes mundialmente, con una incidencia en Cuba de 2,1 por cada 1 000 habitantes. La mayoría de las sorderas son de origen sensorineural, debido a la muerte de las células ciliadas cocleares, localizadas en el órgano de Corti, lo que conduce a la degeneración de las neuronas del ganglio espiral. En un trabajo previo por Microscopia Óptica, usando un modelo de ototoxicidad en ratas, el órgano de Corti se afectó a partir de las 2 semanas de sordera, mientras que la densidad de neuronas del ganglio espiral disminuyó significativamente solo a partir de las 8 semanas. Con el objetivo de precisar el comienzo de los cambios degenerativos inducidos por ototoxicidad, se estudiaron por Microscopia Electrónica las células del órgano de Corti y las neuronas del ganglio espiral en cócleas de ratas sordas, tomadas a las 2, 4, 8 y 16 semanas de sordera y cócleas de ratas sanas. Se produjeron alteraciones en las células de sostén del órgano de Corti desde las 2 semanas. Las neuronas tipo I del ganglio espiral sufrieron cambios degenerativos que fueron aumentando con el tiempo de sordera a partir de las 4 semanas, hasta su sustitución por neuronas patológicas (tipo III a las 16 semanas. La banda de mielina de los procesos periféricos que inervan el órgano de Corti presentó signos de degeneración desde las 4 semanas. Los resultados indican que el daño ultraestructural de las neuronas del ganglio espiral y sus procesos periféricos, inducido por el deterioro del órgano de Corti, comienza antes de que disminuya la densidad de estas neuronas y sus dendritas.

  19. Comparación de tres técnicas de trazado retrógrado para la identificación del origen espinal del nervio ciático en ratón.

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    Myriam L. Velandia

    2002-12-01

    Full Text Available En el presente trabajo se compararon tres técnicas para la aplicación de dos tipos de trazadores retrógrados fluorescentes (Dil y Fluorogold, con el fin de identificar las neuronas motoras y sensoriales que contribuyen con fibras al nervio ciático en ratones adultos. Se ensayó la aplicación de cristales directamente en el nervio, la inyección intraneural y la impregnación del nervio seccionado usando una cámara de silicona. La localización específica de las neuronas motoras en la médula espinal y las neuronas sensoriales en los ganglios de la raíz dorsal que aportan al nervio ciático de ratón se logró aplicando el Fluorogold mediante una cámara en el cabo proximal de los nervios previamente seccionados. Al utilizar el trazador Dil, la misma técnica no permitió hacer la identificación específica de las neuronas. Se encontró que al nervio ciático de ratón podrían contribuir el ganglio de la raíz dorsal más rostrales que los informados para ratas. Estos resultados muestran que la metodología de aplicación de neurotrazadores en cápsula y la descalcificación de tejidos es útil para la localización de neuronas de ganglios de raíz dorsal y de la médula espinal que componen el nervio ciático de ratón adulto, lo que en el futuro permitirá obtener mayor información sobre la neuroanatomía básica del ratón.

  20. An outbreak of sarcocystosis in psittacines and a pigeon in a zoological collection in Brazil.

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    Ecco, R; Luppi, M M; Malta, M C C; Araújo, M R; Guedes, R M C; Shivaprasad, H L

    2008-12-01

    This report describes an outbreak of acute pulmonary sarcocystosis in different species of captive psittacines and in a Luzon bleeding-heart pigeon (Gallicolumba luzonica) in a zoological collection in Brazil. A majority of the birds were found dead and had exhibited no previous clinical signs. Grossly, pulmonary congestion and edema were the most-common findings. Enlarged and congested livers and spleens were also frequently observed. Microscopically, there was edema, fibrin exudation, congestion, and perivascular and interstitial lymphoplasmacytic infiltration associated with numerous sinuous schizonts of Sarcocystis sp. in the lungs. Mild to moderate myocarditis, hepatitis, splenitis, and interstitial nephritis were also observed in the birds. Immunohistochemistry confirmed Sarcocystis sp. in the capillaries of lungs, hearts, livers, and spleens of most of the birds, but also in the pancreas, kidney, intestine, proventriculus, and brain of a few birds. The probable source of Sarcocystis sp. in these birds was the wild opossum (Didelphis albiventris), a common inhabitant of a local forest that surrounds the Belo Horizonte Zoo (Fundação Zoo-Botânica). This is the first documentation of Sarcocystis infection in psittacines and a pigeon from Brazil.

  1. Developmental biology of Cystoisospora (Apicomplexa: Sarcocystidae) monozoic tissue cysts

    Science.gov (United States)

    Tissue cyst stages are an intriguing aspect of the developmental cycle and transmission of members of the Family Sarcocystidae. Tissue cyst stages of the genera Toxoplasma, Hammondia, Neospora, Besnoitia, and Sarcocystis contain many infectious stages (bradyzoites).The tissue cyst stage of Cystoisos...

  2. Observations on some Avian Coccidia (Apicomplexa: Eimeriidae in Amazonian Brazil

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    Ralph Lainson

    1994-09-01

    Full Text Available Oocysts of Eimeria porphyrulae n. sp. are described in faeces of Porphyrula martinica (Aves: Gruiformes: Rallidae. They are ellipsoidal to oval, 22.4 x 17.7 (20.0-23.7 x 16.2-18.7 µm, shape-index (length/width 1.3. Oocyst wall about 1.25 µm thick, colourless, with two layers: inner one prominently striated. Micropyle and sub-micropylar granule present: no oocyst residuum. Sporocysts 17.5 x 9.0 (17.0-19.0 x 8.0-10.0 µm, shape-index 1.9, with inconspicuous Stieda/sub-Stieda bodies. Sporocyst residuum of scattered granules, sometimes a compact mass: sporozoites with two refractile bodies. Eimeria crypturelli n. sp. is described in faeces of Crypturellus soiu (Tinamiformes: Tinamidae. Oocysts ellipsoidal-oval, 20.75 x 14.5 (17.5-25.0 x 11.25-21.25 µm, shape-index 1.4. Oocysts wall about 1.25 µm thick and bi-layered: inner layer faintly striated. Micropyle present, with oocyst residuum immediately below: single polar body rarely present. Sporocysts 13.0 x 7.5 (12.5-13.75 x 7,5-8.1 µm, shape-index 1.7, with a Stieda body but seemingly no sub-Stieda. Sporocyst residuum compact: sporozoites with two refractile bodies. Isospora cacici n. sp. is recorded from faeces of Cacicus cela cela (Passeriformes: Icteridae. Oocysts subspherical-spherical, 26.5 x 23.7 (22.5-27.5 x 20.0-26.2 µm, shape-index 1.1. Wall a single, colourless layer about 1.5 µm thick. No micropyle or oocyst residuum: 1-2 polar bodies. Sporocysts ellipsoidal, 17.7 x 12.5 (17.5-18.75 x 11.25-13.75 µm, shape-index 1.4, with pronounced Stieda/sub-Stieda bodies: residuum compact and sporozoites with two refractile bodies. Isospora thraupis n. sp. is described from faeces of Thraupis palmarum melanoptera (Passeriformes: Thraupidae. Oocysts subspherial-spherical, 19.9 x 19.0 (18.7-21.2 x 18.75-20.0 µm, shape-index 1.0. Wall about 0.6 µm thick, smooth, colourless and a single layer: no micropyle, oocyst residuum or polar bodies. Sporocysts 14.2 x 9.2 (13.7-16.2 x 8.7-10.0 µm, shape

  3. Isospora streperae n. sp. (Apicomplexa: Eimeriidae) from a grey currawong (Strepera versicolour plumbea) (Passeriformes: Artamidae) in Western Australia.

    Science.gov (United States)

    Yang, Rongchang; Brice, Belinda; Habsi, Khalid Al; Elliot, Aileen; Ryan, Una

    2015-01-01

    A new species, Isospora streperae n. sp., (Apicomplexa: Eimeriidae) is described from a single grey currawong bird (Strepera versicolour) (subspecies S. v. plumbea) in Western Australia. Sporulated oocysts (n = 32) are spherical to subspherical, with smooth colourless bilayered oocyst wall, 1.0 µm thick (outer layer 0⋅8 µm, inner 0.2 µm thick). Oocyst with a polar granule, an oocyst residuum and two spheroidal to subspheroidal sporocysts. Oocyst length, 23.8 (20.4-25.0) µm; oocyst width, 22.5 (20.0-24.6) µm; a shape index of 1.06, with Stieda, substieda bodies. Micropyle is absent. Sporocysts with compressed sporocyst residuum and four sporozoites. Sporocyst length, 14.4 (12.5-15.2) µm; sporocyst width, 11.2 (10.6-14.0) µm, sporocyst L/W ratio, 1.29. Necropsy of the bird identified haemorrhaging along the ileum and jejunum, which is where Isospora oocysts were also mostly detected. Molecular analysis was conducted at three loci; the 18S, 28S ribosomal RNA and the mitochondrial cytochrome oxidase (COI) gene. At the 18S locus, I. streperae n. sp. exhibited 99.5% and 99.4% similarity respectively to an Isospora sp. (MS-2003) from a Southern cape sparrow (Passer melanurus melanurus) and Isospora dovati from a domestic pigeon (Columba livia domestica). At the 28S locus, I. streperae n. sp. exhibited 96.9% similarity to an Isospora sp. (MS-2003) from a grosbeak starling (Scissirostrum dubium) and 95.8% similarity with the Isospora sp. (MS-2003) from a Southern cape sparrow. At the COI locus, I. streperae n. sp. exhibited 95.0% similarity to Isospora sp. from a yellow-necked mouse (Apodemus flavicollis) from the Czech Republic. Based on morphological and molecular data, this isolate is a new species of Isospora, which is named Isospora streperae n. sp. after its host, the grey currawong (Strepera versicolour plumbea). Crown Copyright © 2014. Published by Elsevier Inc. All rights reserved.

  4. Hemolivia mauritanica (Haemogregarinidae: Apicomplexa infection in the tortoise Testudo graeca in the Near East with data on sporogonous development in the tick vector Hyalomna aegyptium

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    Paperna I.

    2006-12-01

    Full Text Available Testudo graeca tortoises were collected in the northern and southern Golan Heights (Israeli occupied territory of south Syria, and various locations in Israel and Palestine. Hyalomma aegyptium ticks were found only on Golan Height tortoises, and only the tortoises and ticks from the northern Golan Heights were infected with Hemolivia mauritanica. Tortoises became infected after ingesting infected ticks. Male ticks carrying sporocysts, which remain attached to tortoises for extended durations, apparently served as the source for dissemination of new infections among tortoises. Sporogenesis followed the pattern observed in the two other known species of Hemolivia, though there was some evident variation in fine-structural detail. The sutural slit detected in the H. mauritanica mature sporocyst wall was reminiscent of the suture characteristic of Coccidia of heterothermic vertebrate hosts; it could be a common ancestral character for both hemogregarines and Coccidia.

  5. Hepatozoon kisrae n. sp. infecting the lizard Agama stellio is transmitted by the tick Hyalomma cf. aegyptium

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    Paperna I.

    2002-03-01

    Full Text Available Hepatozoon kisrae n. sp. was found infecting a starred lizard at a site in southeastern Samaria, Palestine. These lizards were also hosts to the ixodid tick Hyolomma cf. aegyptium, which was demonstrated to be the vector of this hemogregarine. Hepatozoon and tick infections occurred in lizards within a very restricted locality; at a second site, nearby, ticks occurred without Hepatozoon infection. Micro- and macromeronts occurred mainly in the lungs, while cyst-like merogonic stages, mainly dizoic, occurred in the liver. Mature intraerythrocytic gametocytes were stout and encapsulated. Development from oocysts to sporocysts took place in the tick hemocoel, and was examined by transmission electron microscopy. Lizards were successfully infected when fed on sporocyst-infected ticks or viscera of infected lizards. Ticks become infected when fed on infected lizards; sporogony was complete when the ticks reached adult stage, over 40 days after initial attachment.

  6. Malabsorption syndrome observed in the common octopus Octopus vulgaris infected with Aggregata octopiana (Protista: Apicomplexa).

    Science.gov (United States)

    Gestal, C; Páez de la Cadena, M; Pascual, S

    2002-08-15

    Octopus vulgaris infected with Aggregata octopiana were collected from an open-water culture system in the Ría of Aldán (NW Spain). Digestive tract infection values were determined with the use of a Neubauer chamber by counting the number of A. octopiana sporocysts. After determining enzyme activity values by the colorimetric Api-Zym system Biomerieux, one representative enzyme of glycosidases, peptid hydrolases and phosphoric hydrolases showing high activity was spectrophotometrically analysed. The enzymes were maltase and leucine-aminopeptidase (LAP) involved in the absorption process, and acid phosphatase, a lysosomic enzyme, respectively. Enzymatic activity of maltase and LAP decreased significantly, with increased sporocyst counts. However, acid phosphatase activity increased with severity of infection, indicating the presence of degradative enzymes from phagocytic cells in the infected area. A detrimental effect on gastrointestinal function may result from a decrease or malfunction of absorption enzymes. The results suggest a malabsorption syndrome resulting from parasitic infection.

  7. Eimeria auratae n. sp. (Apicomplexa: Eimeriidae) infecting the lizard Mabuya aurata in Saudi Arabia.

    Science.gov (United States)

    Alyousif, M S; AL-Rasheid, K A

    2001-03-01

    Eimeria auratae n. sp. was described from the gall bladder of the lizard Mabuya aurata collected at Al-Hofuf village, eastern region, Saudi Arabia. Morphology of sporulated as well as non-sporulated oocysts were studied. Sporulated oocysts were ellipsoidal 22-31.5x13.5-21.8 (27.7x18.5) microm with smooth brownish-yellow bilayered wall, 1.1 (0.9-1.3) microm. Micropyle, polar granule and oocyst residuum were absent. Sporocysts were ellipsoidal 10.5-12.8x7.5-9 (11.8x8.5) microm. Sporocyst residuum was present but Stieda body was absent. Sporozoites were crescent-shaped, blunt at one end and slightly tapered at the other. Eimeria species from Scincidae were compared.

  8. A new coccidian, Isospora rheae sp. nov. (Apicomplexa, Eimeriidae, from Rhea americana (Aves, Rheidae from South America

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    Samira S.M. Gallo

    2014-12-01

    Full Text Available A new species of coccidian (Protozoa: Apicomplexa: Eimeriidae obtained from rheas, Rhea americana, is reported in Brazil. Oocysts of Isospora rheae sp. nov. are spherical to subspheroidal, measuring 22.6 × 21.0 µm, and have a double and smooth wall that is approximately 1.7 µm thick. The micropyle, oocyst residuum and polar granule are absent. Sporocysts are slightly ovoid, measuring 13.9 × 9.6 µm. The Stieda body is flattened, the substieda body is pointed, irregular and wavy and the sporocyst residuum is composed of scattered granules of varying sizes. Sporozoites have an oblong refractile body and one nucleus. This is the first description of an isosporid coccidian infecting birds of the family Rheidae.

  9. Eimeria pileata n. sp. (Apicomplexa: Eimeriidae) from the rufous-capped brush finch Atlapetes pileatus Wagler (Passeriformes: Emberizidae) in Mexico.

    Science.gov (United States)

    Soriano-Vargas, Edgardo; Medina, Juan Pablo; Salgado-Miranda, Celene; García-Conejo, Michele; Galindo-Sánchez, Karla Patrícia; Janczur, Mariusz Krzysztof; Berto, Bruno Pereira; Lopes, Carlos Wilson Gomes

    2015-11-01

    A new coccidian species (Protista: Apicomplexa: Eimeriidae) collected from the rufous-capped brush finch Atlapetes pileatus Wagler in the Nevado de Toluca Natural Protected Area, Mexico. Oöcysts of Eimeria pileata n. sp. are ellipsoidal, measuring on average 16.5 × 14.1 μm, with a smooth, bi-layered wall. Micropyle and oöcyst residuum are absent, but a polar granule is present. Sporocysts are ellipsoidal, measuring on average 9.0 × 5.4 μm. Stieda and sub-Stieda bodies are both present. A sporocyst residuum is present as a compact mass of granules. This is the third description of an eimeriid coccidian infecting passerines.

  10. Isospora celata n. sp. (Apicomplexa: Eimeriidae) from the orange-crowned warbler Oreothlypis celata (Say) (Passeriformes: Parulidae) in Mexico.

    Science.gov (United States)

    Berto, Bruno Pereira; Medina, Juan Pablo; Salgado-Miranda, Celene; García-Conejo, Michele; Janczur, Mariusz Krzysztof; Lopes, Carlos Wilson Gomes; Soriano-Vargas, Edgardo

    2014-11-01

    A new coccidian species (Protista: Apicomplexa: Eimeriidae) is described from the orange-crowned warbler Oreothlypis celata (Say) collected in the Nevado de Toluca National Park, Mexico at 3,000 metres above sea level. Isospora celata n. sp. has subspheroidal oöcysts, measuring 28.4 × 26.4 μm, with smooth, bi-layered wall c.1.2 μm thick. Micropyle and polar granule are absent, but oöcyst residuum is present as a compact mass. Sporocysts are ovoidal, 18.2 × 12.8 µm. Stieda body knob-like and sub-Stieda body irregular and barely discernible. Sporocyst residuum is composed of granules of different sizes. Sporozoites are vermiform with one refractile body and a nucleus. This is the third description of an isosporoid coccidian infecting a New World warbler.

  11. Isospora cardellinae n. sp. (Apicomplexa: Eimeriidae) from the red warbler Cardellina rubra (Swainson) (Passeriformes: Parulidae) in Mexico.

    Science.gov (United States)

    Salgado-Miranda, Celene; Medina, Juan Pablo; Zepeda-Velázquez, Andrea Paloma; García-Conejo, Michele; Galindo-Sánchez, Karla Patricia; Janczur, Mariusz Krzysztof; Soriano-Vargas, Edgardo

    2016-10-01

    A new coccidian species (Protozoa: Apicomplexa: Eimeriidae) collected from the red warbler Cardellina rubra (Swainson) is reported from the Nevado de Toluca National Park, Mexico. Isospora cardellinae n. sp. has subspherical oöcysts, measuring on average 26.6 × 25.4 μm, with smooth, bi-layered wall, c.1.3 μm thick. Micropyle, oöcyst residuum, and polar granule are absent. Sporocysts are ovoidal, measuring on average 19.0 × 12.0 µm, with a knob-like Stieda body, a trapezoidal sub-Stieda body and sporocyst residuum composed of scattered spherules of different sizes. Sporozoites are vermiform with one refractile body and a nucleus. This is the fourth description of an isosporoid coccidian infecting a New World warbler.

  12. Some remarks on the distribution and dispersion of Coccidia from icterid birds in South America: Isospora guaxi n. sp. and Isospora bellicosa Upton, Stamper & Whitaker, 1995 (Apicomplexa: Eimeriidae) from the red-rumped cacique Cacicus haemorrhous (L.) (Passeriformes: Icteridae) in southeastern Brazil.

    Science.gov (United States)

    da Silva, Lidiane Maria; Rodrigues, Mariana Borges; de Pinho, Irlane Faria; do Bomfim Lopes, Bruno; Luz, Hermes Ribeiro; Ferreira, Ildemar; Lopes, Carlos Wilson Gomes; Berto, Bruno Pereira

    2017-01-01

    A new species of coccidian, Isospora guaxi n. sp., and Isospora bellicosa Upton, Stamper & Whitaker, 1995 (Protozoa: Apicomplexa: Eimeriidae) are recorded from red-rumped caciques Cacicus haemorrhous (L.) in the Parque Nacional do Itatiaia, Brazil. Isospora guaxi n. sp. has sub-spheroidal oöcysts, measuring on average 30.9 × 29.0 μm, with smooth, bi-layered wall c.1.9 μm thick. Micropyle and oöcyst residuum are absent, but a polar granule is present. Sporocysts are ellipsoidal, measuring on average 19.3 × 13.8 μm. Stieda body is knob-like and sub-Stieda body is prominent and compartmentalized. Sporocyst residuum is composed of scattered granules. Sporozoites are vermiform, with one refractile body and a nucleus. Isospora bellicosa has sub-spheroidal to ovoidal oöcysts, measuring on average 27.1 × 25.0 μm, with smooth, bi-layered wall c.1.5 μm thick. Micropyle and oöcyst residuum are absent, but one or two polar granules are present. Sporocysts are ellipsoidal, measuring on average 18.1 × 10.9 μm. Stieda body is knob-like and sub-Stieda body is rounded to rectangular. Sporocyst residuum is composed of a cluster of compact or diffuse granules. Sporozoites are vermiform, with one refractile body and a nucleus. Isospora bellicosa was originally described from the Peruvian meadowlark Sturnella bellicosa deFilippi, a trans-Andean icterid which is allopatric with the cis-Andean C. haemorrhous. Therefore, in conclusion, this current study reveals the dispersion of coccidia from Icteridae across the Andes Mountains, besides describing the sixth isosporoid coccidium infecting an icterid bird.

  13. Two new species of Eimeria Schneider, 1875 (Apicomplexa: Eimeriidae) from emerald tree skinks, Lamprolepis smaragdina (Lesson) (Sauria: Scincidae) from Papua New Guinea and the Philippines.

    Science.gov (United States)

    McAllister, Chris T; Seville, R Scott; Duszynski, Donald W; Bush, Sarah E; Fisher, Robert N; Austin, Christopher C

    2013-10-01

    Two new species of Eimeria Schneider, 1875, from emerald tree skinks, Lamprolepis smaragdina (Lesson) are described from specimens collected in Papua New Guinea (PNG) and the Philippines. Oöcysts of Eimeria nuiailan n. sp. from the only L. smaragdina from PNG are ovoidal, with a smooth, colourless, bi-layered wall, measure 23.7 × 19.1 μm, and have a length/width (L/W) ratio of 1.3; both micropyle and oöcyst residuum are absent, but a fragmented polar granule is present. Sporocysts are ovoidal to ellipsoidal, 11.9 × 7.0 μm, L/W 1.7, and the wall is composed of two valves joined by a longitudinal suture; neither Stieda nor sub-Stieda bodies are present; a sporocyst residuum is present as a compact mass of granules. Sporozoites are elongate, 14.6 × 2.6 μm, and contain anterior and posterior refractile bodies with a nucleus between them. Oöcysts of Eimeria auffenbergi n. sp. from L. smaragdina collected in the Philippines are ovoidal, with a smooth, colourless, bi-layered wall, measure 19.9 × 15.8 μm, L/W 1.3; both micropyle and oöcyst residuum are absent, but one to four polar granules are present. Sporocysts are ovoidal to ellipsoidal, 10.3 × 5.8 μm, L/W 1.8, and the wall is composed of two valves joined by a longitudinal suture; neither Stieda nor sub-Stieda bodies are present; a sporocyst residuum is composed of dispersed granules.

  14. Schistosoma mansoni in susceptible and resistant snail strains Biomphalaria tenagophila: in vivo tissue response and in vitro hemocyte interactions.

    Directory of Open Access Journals (Sweden)

    Rafael Nacif-Pimenta

    Full Text Available Schistosomiasis is a parasitic disease that is highly prevalent, especially in developing countries. Biomphalaria tenagophila is an important invertebrate host of Schistosoma mansoni in Brazil, with some strains (e.g. Cabo Frio being highly susceptible to the parasite, whereas others (e.g. Taim are completely resistant to infection. Therefore, B. tenagophila is an important research model for studying immune defense mechanisms against S. mansoni. The internal defense system (IDS of the snail comprises hemocytes and hemolymph factors acting together to recognize self from non-self molecular patterns to eliminate the threat of infection. We performed experiments to understand the cellular defenses related to the resistance and/or susceptibility of B. tenagophila to S. mansoni. During the early stages of infection, fibrous host cells of both snail strains were arranged as a thin layer surrounding the sporocysts. However, at later stages of infection, the cellular reactions in resistant snails were increasingly more intense, with thicker layers surrounding the parasites, in contrast to susceptible strains. All parasites were damaged or destroyed inside resistant snails after 10 h of infection. By contrast, parasites inside susceptible snails appeared to be morphologically healthy. We also performed experiments using isolated hemocytes from the two strains interacting with sporocysts. Hemocyte attachment started as early as 1 h after initial infection in both strains, but the killing of sporocysts was exclusive to hemocytes from the resistant strain and was time course dependent. The resistant strain was able to kill all sporocysts. In conclusion, our study revealed important aspects of the initial process of infection related to immune defense responses of strains of B. tenagophila that were resistant to S. mansoni compared with strains that were susceptible. Such information is relevant for the survival or death of the parasites and so is important

  15. Two new species of Eimeria (Apicomplexa: Eimeriidae) from emerald tree skinks, Lamprolepis smaragdina (Sauria: Scincidae) from Papua New Guinea and the Philippines

    Science.gov (United States)

    McAllister, Chris T.; Seville, R. Scott; Duszynski, Donald W.; Bush, Sarah E.; Fisher, Robert N.; Austin, Christopher C.

    2014-01-01

    Two new species of Eimeria Schneider, 1875, from emerald tree skinks, Lamprolepis smaragdina (Lesson) are described from specimens collected in Papua New Guinea (PNG) and the Philippines. Oöcysts of Eimeria nuiailan sp. n. from the only L. smaragdina from PNG are ovoidal, with a smooth, colourless, bilayered wall, measure 23.7 × 19.1 μm, and have a length/width (L/W) ratio of 1.3; both micropyle and oöcyst residuum are absent, but a fragmented polar granule is present. Sporocysts are ovoidal to ellipsoidal, 11.9 × 7.0 μm, L/W 1.7, and the wall is composed of 2 valves joined by a longitudinal suture; neither Stieda nor sub-Stieda bodies are present; a sporocyst residuum is present as a compact mass of granules. Sporozoites are elongate, 14.6 × 2.6 μm, and contain anterior and posterior refractile bodies with a nucleus between them. Oöcysts of Eimeria auffenbergi sp. n. from both L. smaragdina we collected in the Philippines are ovoidal, with a smooth, colorless, bilayered wall, measure 19.9 × 15.8 μm, L/W 1.3; both micropyle and oöcyst residuum are absent, but 1–4 polar granules are present. Sporocysts are ovoidal to ellipsoidal, 10.3 × 5.8 μm, L/W 1.8, and the wall is composed of 2 valves joined by a longitudinal suture; neither Stieda nor sub-Stieda bodies are present; a sporocyst residuum is composed of dispersed granules. PMID:24048748

  16. Larval stages of Neoplagioporus elongatus (Goto and Ozaki, 1930) (Opecoelidae: Plagioporinae), with notes on potential second intermediate hosts.

    Science.gov (United States)

    Yano, Ayaka; Urabe, Misako

    2017-04-01

    The morphology of sporocysts and cercariae of Neoplagioporus elongatus (Goto and Ozaki, 1930) is described for the first time. A cotylomicrocercous cercaria obtained from the sorbeoconch snail Semisulcospira nakasekoae was confirmed to be the cercaria of N. elongatus, based on the degree of sequence identity of the COI gene to that of adult worms. Freshwater annelids (oligochaetes and leeches) and some aquatic insects (odonates) were demonstrated experimentally to be potential second intermediate hosts.

  17. Two new species of Eimeria Schneider, 1875 (Apicomplexa: Eimeriidae) from emerald tree skinks, Lamprolepis smaragdina (Lesson) (Sauria: Scincidae) from Papua New Guinea and the Philippines

    Science.gov (United States)

    McAllister, Chris T.; Seville, R. Scott; Duszynski, Donald W.; Bush, Sarah E.; Fisher, Robert N.; Austin, Christopher C.

    2013-01-01

    Two new species of Eimeria Schneider, 1875, from emerald tree skinks, Lamprolepis smaragdina (Lesson) are described from specimens collected in Papua New Guinea (PNG) and the Philippines. Oöcysts of Eimeria nuiailan n. sp. from the only L. smaragdina from PNG are ovoidal, with a smooth, colourless, bi-layered wall, measure 23.7 × 19.1 μm, and have a length/width (L/W) ratio of 1.3; both micropyle and oöcyst residuum are absent, but a fragmented polar granule is present. Sporocysts are ovoidal to ellipsoidal, 11.9 × 7.0 μm, L/W 1.7, and the wall is composed of two valves joined by a longitudinal suture; neither Stieda nor sub-Stieda bodies are present; a sporocyst residuum is present as a compact mass of granules. Sporozoites are elongate, 14.6 × 2.6 μm, and contain anterior and posterior refractile bodies with a nucleus between them. Oöcysts of Eimeria auffenbergi n. sp. from L. smaragdina collected in the Philippines are ovoidal, with a smooth, colourless, bi-layered wall, measure 19.9 × 15.8 μm, L/W 1.3; both micropyle and oöcyst residuum are absent, but one to four polar granules are present. Sporocysts are ovoidal to ellipsoidal, 10.3 × 5.8 μm, L/W 1.8, and the wall is composed of two valves joined by a longitudinal suture; neither Stieda nor sub-Stieda bodies are present; a sporocyst residuum is composed of dispersed granules.

  18. Two new species of Eimeria (Apicomplexa, Eimeriidae) from tree skinks, Prasinohaema spp. (Sauria: Scincidae), from Papua New Guinea

    Science.gov (United States)

    McAllister, Chris T.; Duszynski, Donald W.; Fisher, Robert N.; Austin, Christopher C.

    2014-01-01

    Between September 1991 and June 1992, feces from 4 species of tree skinks, Prasinohaema spp. from Papua New Guinea, were collected and examined for coccidia. Two species, P. flavipes and P. prehensicauda were found to harbor eimerians which are described as new. Oocysts of Eimeria krausi sp. nov. from P. flavipes were ellipsoidal to subspheroidal with a smooth bilayered wall and measured (L × W) 19.2 × 16.9 μm, with a length/width (L/W) ratio of 1.1. Micropyle and oocyst residuum were absent but a fragmented polar granule was present. Sporocysts were ellipsoidal, 9.7 × 6.7 μm, L/W of 1.5. Stieda, subStieda and paraStieda bodies were absent. The sporocyst residuum was composed of many small granules in a compact mass between sporozoites. The sporozoites were sausage-shaped, 11.7 × 2.7 μm, in situ, with an ellipsoidal posterior refractile body and a spheroidal anterior refractile body. Oocysts of Eimeria greeri sp. nov. from P. prehensicauda were ellipsoidal with a smooth bilayered wall, (L × W) 23.0 × 18.3 μm, with a L/W of 1.3. Micropyle and oocyst residuum were absent but a fragmented polar granule was present. Sporocysts were ellipsoidal, 9.7 × 8.4 μm, with a L/W of 1.2. Stieda, subStieda and paraStieda bodies were absent. The sporocyst residuum was composed of many large granules in a compact mass between sporozoites. The sporozoites were sausage-shaped, with an ellipsoidal posterior refractile body and a spheroidal anterior refractile body. We document here the first report of coccidia from skinks of the genus Prasinohaema.

  19. Two new species of Eimeria (Apicomplexa: Eimeriidae from Asian geoemydid turtles Kachuga tentoria and Melanochelys trijuga (Testudines: Geoemydidae

    Directory of Open Access Journals (Sweden)

    Široký P.

    2005-03-01

    Full Text Available Coprological examination of ten Pink-ringed tent turtles Kachuga tentoria circumdata, recently imported from India, and three Burmese black turtles Melanochelys trijuga edeniana, imported from Myanmar, revealed the presence of two new species of Eimeria. Oocysts of Eimeria kachua n. sp. from K. t. circumdata are broadly oval to subspherical, 15.3 (13-18 × 13.9 (12-16 μm, with polar granule and subspherical oocyst residuum. Sporocyst elongatelly oval to spindle-shaped, 8.7 (7.5-10 × 4.9 (4-6 μm, with a knoblike Stieda body, covered with fine membranous cupola-like structures. Thin walled oocysts of Eimeria patta n. sp. from M. t. edeniana, have an irregular shape, influenced by the position of sporocysts, frequently with lobular irregularities, 12.6 (11-16 × 9.1 (7.5-12 μm. Sporocysts are oval to ellipsoidal, 5.8 (5-7 × 4.2 (3.5-5 μm.

  20. Description of Eimeria motelo sp. n. (Apicomplexa: Eimeriidae from the yellow footed tortoise, Geochelone denticulata (Chelonia: Testudinidae, and replacement of Eimeria carinii Lainson, Costa & Shaw, 1990 by Eimeria lainsoni nom. nov.

    Directory of Open Access Journals (Sweden)

    Lada Hurková

    2000-12-01

    Full Text Available Eimeria motelo sp. n. is described from faeces of the yellow-footed tortoise, Geochelone denticulata (L.. Oocysts are irregularly ellipsoidal or cylindrical, with slightly expressed lobed protrusions and irregularities at the poles, possibly caused by wrinkling of the oocyst wall, 17 (15-19 × 9.4 (8.5-11 µm, shape index (length/width being 1.81 (1.45-2. The oocyst wall is smooth, single-layered, 0.5 µm thick with no micropyle. There are no polar bodies. Sporocysts are ellipsoidal, 8.9 (7.5-10 × 4.4 (4-5 µm, shape index 2.03 (1.7-2.5. A sporocyst residuum is present, composed of many granules of irregular size. The sporozoites are elongate, lying lengthwise in the sporocysts. Comparison with other species of the genus Eimeria parasitising members of family Testudinidae indicates that the presently described coccidium represents a new species. The name of Eimeria carinii Lainson, Costa & Shaw, 1990 is found to be preoccupied by a homonym, Eimeria carinii Pinto 1928 given to a coccidium from Rattus norvegicus. Therefore, it is replaced by Eimeria lainsoni nom. nov.

  1. Fatal coccidiosis by Isospora icterus (Upton & Whitaker, 2000) in captive Campo Troupial (Icterus jamacaii) in Brazil.

    Science.gov (United States)

    Marques, Marcus V R; Vilela, Daniel A da R; Andrade, Emily A G; Galvão, Carolina Z; de Resende, José S; Junior, Francisco C F; Andery, Danielle A; Ecco, Roselene; Preis, Ingred Sales; Martins, Nelson R S

    2011-12-01

    An outbreak of coccidiosis by Isospora icterus (I. icterus, Upton & Whitaker, 2000) in captive Campo Troupial (Icterus jamacaii) (Gmelin, 1788) at the Wild Animals Triage Center (IBAMA, Belo Horizonte, Brazil) is described. Clinical history and the necropsy findings documented diarrhea with diffuse necrotic enteritis. Sporulated oocysts (n = 100) had a bilayered wall, were subspherical, and measured 30.1 (27.5-32.5) microm in length and 28.5 (26.2-30.0) microm in width. A polar body but no micropyle was present and the length/width ratio was 1.1 (1.00-1.2). Each oocyst contained two ellipsoidal sporocysts measuring 17.6 (15.0-20.0) microm in length and 12.9 (12.5-15.0) microm in width, with a length/width ratio of 1.4 (1.2-1.5), and with Stieda and sub-Stieda bodies. Each sporocyst contained four sporozoites with granular sporocyst residuum. Oocysts were compatible with those from I. icterus, previously described in Campo Troupial.

  2. Molecular differentiation of bovine sarcocysts.

    Science.gov (United States)

    Akhlaghi, Majedeh; Razavi, Mostafa; Hosseini, Arsalan

    2016-07-01

    Cattle are common intermediate hosts of Sarcocystis, and the prevalence in adult bovine muscle is close to 100 % in most regions of the world. Three Sarcocystis spp. are known to infect cattle as intermediate hosts, namely, S. cruzi, S. hirsuta, and S. hominis. The aim of the present study was the molecular identification and differentiation of these three species, Neospora caninum and Besnoitia by PCR and RFLP methods. Tissue samples were obtained from diaphragmatic muscle of 101 cattle slaughtered in Shiraz, Fars Province, Iran, for both smear preparation and DNA extraction. The samples were digested by Pepsin, washed three times with PBS solution before taking smears, fixed in absolute methanol and stained with 10 % Giemsa. The slides were examined microscopically for Sarcocystis bradyzoites and DNA was extracted from 100 mg of Sarcocystis-infected meat samples. Since the primers also bind to 18S rRNA gene of some tissue cyst-forming coccidian protozoa, DNA was also extracted from 100 μl of tachyzoite-containing suspension of N. caninum and Besnoitia isolated from goat to compare RFLP pattern. Polymerase chain reaction (PCR) was performed on DNA of samples which were microscopically positive for Sarcocystis. Five restriction enzymes Dra1, EcoRV, RsaI, AvaI, and SspI were used for RFLP and DNA of one sample from protozoa was sequenced. Based on the RFLP results, 87 (98.9 %) DNA samples were cut with DraI, indicating infection by S. cruzi. One sample (1.1 %) of PCR products of infected samples was cut only with EcoRV which showed S. hominis infection. Forty-eight samples (53.3 %) of PCR products were cut with both DraI, EcoRV, or with DraI, EcoRV, and RsaI while none of them was cut with SspI, which shows the mixed infection of both S. cruzi and S. hominis and no infection with S. hirsuta. It seems by utilizing these restriction enzymes, RLFP could be a suitable method not only for identification of Sarcocystis species but also for differentiating them

  3. Utilización del patrón de restricción del DNA codificante para el RNA Ribosomal de la subunidad pequeña para la caracterización de Apicomplexa

    Directory of Open Access Journals (Sweden)

    López Adelaida

    1996-12-01

    Full Text Available Los Apicomplexos constituyen un phylum de protozoarios que se caracterizan por ser parásitos obligados de una gran variedad de huéspedes vertebrados e invertebrados. Hoy en día hay fuertes polémicas en tomo a su clasificación taxonómica, sus relaciones filogenéticas, y los patrones de coevolución con sus hospederos. El gen que codifica para el ARN ribosomal de la subunidad pequeña (ARN-SURp se utiliza como marcador molecular para resolver estas inquietudes. A partir del ADN de las especies de la familia Sarcocystidae (Sarcocystis cruzi, Sarcocystis sp. de Didelphis marsupialis y Sarcocystis sp. de Columbina talpacoti y Toxoplasma gondii, y de especies de la familia Plasmodiidae (Plasmodium de Anolis chloris, P. simium, y P. falciparumi, se amplificó por PCR el gen que codifica para el ARN de la subunidad ribosomal pequeña (ARN- SURp usando los iniciadores P5-P3, 0009-2134 Y566R-567R. Se compararon
    los patrones de restricción Hind III, Eco RI, Sau 3AI y Alw 261 del DNA ribosomal. La prueba de riboprini mostró que además de discriminar entre familias permite caracterizar diferencias a nivel de género y especie.Apicomplexa is a Protozoa phylum in which all members are obliged parasites of a wide range of vertebrate and invertebrate hosts. There is an ongoing controversy on
    systematics, phylogenetic relationships and parasite - host coevolution patterns. The SSU ribosomal gen has been used as a molecular marker in order to solve these issues.
    From DNA of the species of the Sarcocystidae family (Sarcocystis cruzi, Sarcocystis sp. from Didelphis marsupialis, Sarcocystis sp. from Columbina talpacoti and Toxoplasma
    gondii, and from the species of the Plasmodiidae family (Plasmodium from Anolis ehloris, P. simium, and P. falciparum, the SSU ribosomal DNA fragemnt was
    amplified by PCR, using the pair of primers P5-P3, 0009-2134 and 566R-567R. Hind III, Eco RI, Sau 3AI and Alw 261 restriction pattems were compared

  4. INTERACCIÓN ENTRE LAS CÉLULAS GLIALES Y NEURONALES Y SU PAPEL EN LA MUERTE Y SOBREVIVENCIA NEURONAL

    OpenAIRE

    2004-01-01

    El cerebro está conformado por neuronas y células gliales, la relación entre estos dos tipos de células es fundamental para mantener la homeostasis cerebral. La excitabilidad de las células nerviosas depende en gran medida del ácido glutámico, el principal neurotransmisor excitador en el cerebro de mamíferos. La síntesis y el metabolismo del ácido glutámico, involucra una estrecha relación entre las neuronas y las células gliales. Una alteración entre los sistemas neuro-gliales glutamartérgic...

  5. ELECTRICITY DEMAND FORECASTING USING A SARIMAMULTIPLICATIVE SINGLE NEURON HYBRID MODEL

    Directory of Open Access Journals (Sweden)

    JUAN DAVID VELÁSQUEZ HENAO

    2013-01-01

    Full Text Available La combinación de modelos SARIMA y redes neuronales son una aproximación común para pronosticar series de tiempo no lineales. Mientras la metodología SARIMA es usada para capturar las componentes lineales en la serie de tiempo, las redes neuronales artifi ciales son aplicadas para pronosticar las no-linealidades remanentes en los residuos del modelo SARIMA. En este artículo, se propone un modelo simple no lineal para el pronóstico de series de tiempo obtenido por la combinación de un modelo SARIMA y una neurona simple multiplicativa que usa las mismas entradas del modelo SARIMA. Para evaluar la capacidad de la nueva aproximación, la demanda mensual de electricidad en el mercado de energía de Colombia es pronosticada y comparada con los modelos SARIMA y la neurona simple multiplicativa.

  6. Papel de la conexina43 en el control de la proliferación de astrocitos y células de glioma

    OpenAIRE

    Herrero González, Sandra

    2009-01-01

    [ES] El sistema nervioso central (SNC) está formado por distintos tipos de células: las neuronas y las células de la glía. Las neuronas son las células responsables de la transmisión de la información gracias a su capacidad de transmitir el impulso nervioso. Aunque ésta constituye, sin duda, la función más relevante del SNC, las células no neuronales, es decir, las células de la glía, desempeñan también una función muy importante. Las células de la glía son de diferentes clases, distinguiéndo...

  7. Esclerosis lateral amiotrófica: ¿es el astrocito la célula primariamente dañada?

    Directory of Open Access Journals (Sweden)

    Roberto E. Sica

    2013-12-01

    Full Text Available La esclerosis lateral amiotrófica (ELA es considerada una enfermedad primaria de las motoneuronas. Ninguno de los procesos que conforman su patogenia ha probado ser su causa. Tampoco pudo demostrarse que factores ambientales la originen. Las neuronas mueren por apoptosis, hecho que abre la posibilidad de que ello sea debido a cambios en su ambiente, sin que constituyan el blanco directo de la noxa que ocasiona la enfermedad. El examen del medio que circunda a las motoneuronas encuentra a los astrocitos como responsables de su bienestar. Éstos son células plásticas, adaptan su función al tipo de neurona con la que se relacionan, cada población astrocitaria es única; si fuera afectada, las neuronas que le son dependientes padecerían. En el caso de las motoneuronas, esta circunstancia llevaría a la alteración de la producción astrocitaria de neurotransmisores y transportadores y a la carencia de nutrientes y factores tróficos que le suministran. Para explicar por qué en la ELA los síntomas se trasladan de un grupo muscular al vecino, observación correlacionada con lo que ocurre en las neuronas motoras corticales y espinales, la hipótesis aquí sostenida sugiere que el factor causante migra de un astrocito a otro, lesionándolos y privando a las motoneuronas del cuidado que le prodigan. También propone que una proteína del astrocito se pliega defectuosamente, transformándose en infecciosa e induciendo el plegamiento errado de sus similares normales, trasladándose entre los astrocitos protoplásmicos y a los astrocitos fibrosos que rodean la vía piramidal, utilizando para ello las sinapsis de hendidura.

  8. La difícil decisión de ventilación mecánica en esclerosis lateral amiotrófica: A propósito de dos casos.

    OpenAIRE

    Rey de Castro Mujica, Jorge; PORTOCARRERO URDAY, Alexandra; VALDEZ FERNANDEZ-BACA, Luis Manuel

    2012-01-01

    Esclerosis Lateral Amiotrófica (ELA) es una enfermedad progresiva y debilitante, invariablemente fatal que afecta a las neuronas motoras, en la que las funciones cognitivas del paciente permanecen intactas y habitualmente en las fases avanzadas se presenta insuficiencia respiratoria ventilatoria requiriendo alguna modalidad de soporte ventilatorio. Dos casos con diagnóstico de ELA forma bulbar se beneficiaron de esta intervención terapéutica en nuestra ciudad.

  9. Neuroligin-1 performs neurexin-dependent and neurexin-independent functions in synapse validation

    OpenAIRE

    2009-01-01

    Postsynaptic neuroligins are thought to perform essential functions in synapse validation and synaptic transmission by binding to, and dimerizing, presynaptic α- and β-neurexins. To test this hypothesis, we examined the functional effects of neuroligin-1 mutations that impair only α-neurexin binding, block both α- and β-neurexin binding, or abolish neuroligin-1 dimerization. Abolishing α-neurexin binding abrogated neuroligin-induced generation of neuronal synapses onto transfected non-neurona...

  10. La difícil decisión de ventilación mecánica en esclerosis lateral amiotrófica: A propósito de dos casos

    OpenAIRE

    Rey De Castro Mujica, Jorge; PORTOCARRERO URDAY, Alexandra; Luis Manuel VALDEZ FERNANDEZ-BACA

    2006-01-01

    Esclerosis Lateral Amiotrófica (ELA) es una enfermedad progresiva y debilitante, invariablemente fatal que afecta a las neuronas motoras, en la que las funciones cognitivas del paciente permanecen intactas y habitualmente en las fases avanzadas se presenta insuficiencia respiratoria ventilatoria requiriendo alguna modalidad de soporte ventilatorio. Dos casos con diagnóstico de ELA forma bulbar se beneficiaron de esta intervención terapéutica en nuestra ciudad.

  11. La difícil decisión de ventilación mecánica en esclerosis lateral amiotrófica: A propósito de dos casos

    Directory of Open Access Journals (Sweden)

    Jorge REY DE CASTRO MUJICA

    2006-10-01

    Full Text Available Esclerosis Lateral Amiotrófica (ELA es una enfermedad progresiva y debilitante, invariablemente fatal que afecta a las neuronas motoras, en la que las funciones cognitivas del paciente permanecen intactas y habitualmente en las fases avanzadas se presenta insuficiencia respiratoria ventilatoria requiriendo alguna modalidad de soporte ventilatorio. Dos casos con diagnóstico de ELA forma bulbar se beneficiaron de esta intervención terapéutica en nuestra ciudad.

  12. Red Neuronal Creciente Usando Perturbación Simultánea Growing Cell Neural Network using Simultaneous Perturbation

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    G. Sánchez

    2004-01-01

    Full Text Available Este artículo propone una red neuronal de tipo perceptron multicapas (MLP que optimiza tanto su matriz de pesos como el número de neuronas ocultas. Inicialmente el sistema propuesto usa un número reducido de neuronas ocultas, optimizándose la matriz de pesos mediante un algoritmo de perturbación simultánea. Una vez que la red converge se analiza su funcionamiento y si este no es el esperado se agrega una neurona oculta. Este proceso se repite hasta obtener el funcionamiento deseado. Los resultados obtenidos muestran que el sistema propuesto presenta un funcionamiento muy similar al de un MLP convencional, cuando éste tiene un número óptimo de nodos en la capa oculta y disminuye la complejidad computacional durante la etapa de entrenamiento.This paper proposes a multilayer perceptron neural network (MLP which optimizes both the matrix weights and the numbers of hidden neurons. Initially, the proposed system uses a reduced number of hidden neurons, optimizing the matrix weights by using a simultaneous perturbation algorithm. Once the network converges, its function is analyzed and if this is not as expected, a hidden neuron is added. This process is repeated until achieving the desired functioning. The results obtained show that the proposed system functions similarly to that of a conventional MLP when this has an optimal number of nodes in the hidden layer, decreasing the computational complexity during the training step.

  13. difusividad, masa, humedad, volumen y sólidos en yacón (Smallantus sonchifolius deshidratado osmóticamente

    Directory of Open Access Journals (Sweden)

    Julio Rojas Naccha

    2012-01-01

    Full Text Available Se evaluó la capacidad predictiva de la Red Neuronal Artificial (RNA en el efecto de la concentración (30,40, 50 y 60 % p/p y temperatura (30, 40 y 50°C de la solución de fructooligosacaridos (FOS en la masa,humedad, volumen y sólidos en cubos de yacón osmodeshidratados, y en el coeficiente de difusividad efectivamedia del agua, con y sin encogimiento. Se aplicó la RNA del tipoFeedforwardcon los algoritmos deentrenamientoBackpropagationy de ajuste de pesosLevenberg-Marquardt, usando la topología: error metade 10-5, tasa de aprendizaje de 0.01, coeficiente de momento de 0.5, 2 neuronas de entrada, 6 neuronas desalida, una capa oculta con 18 neuronas, 15 etapas de entrenamiento y funciones de transferencialogsig-purelin. El error promedio global por la RNA fue 3.44% y los coeficientes de correlación fueron mayores a0.9. No se encontraron diferencias significativas entre los valores experimentales con losvalores predichos porla RNA y con los valores predichos por un modelo estadístico de regresión polinomial de segundo orden (p >0.95.Palabras clave:Red Neuronal Artificial (RNA, difusividad efectiva, yacón, deshidratación osmótica

  14. PARASITES TRANSMITTED TO HUMAN BY INGESTION OF DIFFERENT TYPES OF MEAT, EL-MINIA CITY, EL-MINIA GOVERNORATE, EGYPT.

    Science.gov (United States)

    Abdel-Hafeez, Ekhlas Hamed; Kamal, Amany Mohamed; Abdelgelil, Noha Hamed; Abdel-Fatah, Mohamed

    2015-12-01

    Meat-borne parasites are Sarcocystis species, Toxoplasma gondii, Taenia saginata, Taenia solium and Trichinella spiralis. A total of 300 animals including 100 cattle, 100 goat, and 100 pigs, slaughtered in El-Minia governmental slaughterhouses. From each animal, five samples were taken from different muscles (esophageal, tongue and cardiac) and different organs (liver and brain). Meat samples were examined macroscopic and microscopic (direct, homogenization and H&E staining) for detection of the above-mentioned parasites. Serum samples were subjected to IHA for detection of T gondii specific antibodies. This study revealed that Sarcocystis species were the highest parasites that could be detected, with overall prevalence of 80%, which was statistically significant (P pigs were infected with C. cellulosae, but without statistical significant (P < or = 0.5).

  15. HISTOPATHOLOGICAL SURVEY OF PROTOZOA, HELMINTHS AND ACARIDS OF IMPORTED AND LOCAL PSITTACINE AND PASSERINE BIRDS IN JAPAN

    OpenAIRE

    Tsai, Shinn-Shyong; HIRAI, Katsuya; ITAKURA, Chitoshi

    1992-01-01

    A total of 534 psittacine and passerine birds consisting of 241 imported and 293 local birds were examined histologically. As a result, the following parasites were found : Giardia (86 cases), Knemido-coptes (26 cases), coccidia (10 cases), Ascaridia (6 cases), Cryptosporidium (5 cases), Sarcocystis (5 cases), tapeworm (4 cases), microfilaria (2 cases), Hexamita (1 case), and Spiroptera (1 case). High incidences of giardiasis and knemido-coptic infestation were detected in the local birds, bu...

  16. Suspected new wave of muscular sarcocystosis in travellers returning from Tioman Island, Malaysia, May 2014.

    Science.gov (United States)

    Tappe, D; Stich, A; Langeheinecke, A; von Sonnenburg, F; Muntau, B; Schäfer, J; Slesak, G

    2014-05-29

    In May 2014, six patients presented in Germany with a Sarcocystis-associated febrile myositis syndrome after returning from Tioman Island, Malaysia. During two earlier waves of infections, in 2011 and 2012, about 100 travellers returning to various European countries from the island were affected. While the first two waves were associated with travel to Tioman Island mostly during the summer months, this current series of infections is associated with travel in early spring, possibly indicating an upcoming new epidemic.

  17. Human Invasive Muscular Sarcocystosis Induces Th2 Cytokine Polarization and Biphasic Cytokine Changes, Based on an Investigation among Travelers Returning from Tioman Island, Malaysia.

    Science.gov (United States)

    Tappe, Dennis; Slesak, Günther; Pérez-Girón, José Vicente; Schäfer, Johannes; Langeheinecke, Andreas; Just-Nübling, Gudrun; Muñoz-Fontela, César; Püllmann, Kerstin

    2015-06-01

    Sarcocystis nesbitti is a parasite responsible for a biphasic eosinophilic febrile myositis syndrome in two recent outbreaks in Malaysia. We demonstrate Th2 cytokine polarization in infected travelers, an overall cytokine production decrease in the early phase of the disease suggestive of initial immunosuppression, and elevated levels of proinflammatory and chemotactic cytokines in the later myositic phase. Copyright © 2015, American Society for Microbiology. All Rights Reserved.

  18. Human and animal sarcocystosis in Malaysia:A review

    Institute of Scientific and Technical Information of China (English)

    Baha Latif; Azdayanti Muslim

    2016-01-01

    Sarcocystosis is a zoonotic disease caused by a coccidian intracellular protozoan parasite of the genus Sarcocystis. More than 200 Sarcocystis species have been recorded and the parasites are found in mammals, birds and reptiles. They require two hosts to complete their life cycle. In Malaysia, sarcocystosis was reported as a potential emerging food and water-borne disease after a series of large outbreak of human infections. There was not enough attention given before even though it was reported in both humans and animals. The first human case of invasive muscular sarcocystosis among local Malaysian was reported in 1975. Besides, a retrospective autopsy examination on 100 tongues revealed 21% positive cases. On top of that, a sero-epidemiological survey conducted in 243 subjects in West Malaysia showed that 19.7% had Sarcocystis antibodies. The clinical symptoms of muscular sarcocystosis were first described comprehensively in 1999. Meanwhile, many types of animals including livestock were found harbor the sarcocysts in their tissue. The first case of human intestinal sarcocystosis was reported in 2014. This review indicates that human sarcocystosis is currently endemic in Malaysia and parallel to that reported in animals. However, more studies and investigations need to be conducted since the source of human infection remains unknown.

  19. Sarcocystinae: nomina dubia and available names.

    Science.gov (United States)

    Frenkel, J K; Heydorn, A O; Mehlhorn, H; Rommel, M

    1979-02-28

    Examination of the original descriptions of the species of Sarcocystis in cattle, sheep, and swine, and of isosporid oocysts shed sporulated by dogs, cats, man, and other carnivores, has shown that it is not possible in most instances to identify unambiguously recently recognized taxa. The original descriptions are insufficient, and because no type specimens exist, could apply to two or more of the presently recognized taxa. We consider the following nomina dubia: Sarcocystis hirsuta S. miescheriana S. tenella S. cruzi S. bertrami Isospora bigemina (S. bigemina) I. hominis (S. hominis) I. buteonis (Frenkelia buteonis) Because the former type species, Sarcocystis miescheriana, is an indeterminate nomen dubium, we are proposing S. muris as the new type species. Historically, it was the first species described clearly and unambiguously even in the light of present knowledge, and the stages of its life cycle are probably completely known; it was the second species to be named. Old and recent descriptions are reviewed, and definitions are proposed for the following taxa: S. bovifelis S. bovicanis S. bovihominis S. ovifelis S. ovicanis S. muris (type species) S. suihominis S. suicanis S. equicanis Frenkelia microti F. glareoli for which neotypes will be prepared and deposited with designated institutions and curators. A new subfamily, Cystoisosporinae, is created.

  20. Subpoblaciones neuronales presentes en cultivos primarios de ganglio espinal y su relación con la infección in vitro por virus de rabia

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    Hernán Hurtado

    2000-02-01

    Full Text Available

    El virus de la rabia presenta un fuerte tropismo neuronal y que produce una encefalitis generalmente letal. En un accidente rábico clásico, producido por la mordedura de un animal infectado, el virus es captado por terminaciones nerviosas motoras, autonómicas o sensoriales. Si es captado por estas últimas, el virus se transporta retrógradamente hacia los somas neuronales ubicados en los ganglios espinales y de ahí pasa hasta el Sistema Nervioso Central en donde ejerce su acción patógena. Por este motivo los cultivos de ganglio espinal son un modelo relevante para estudiar la interacción entre el virus de la rabia y las neuronas sensoriales presentes en ellos. En estos cultivos se encuentran dos tipos de células, neuronas y células no neuronales (fibroblastos y células de Schwann. Al inocular los cultivos con virus de rabia cepa CVS (Challenge Virus Standard, a pesar de que las células no neuronales son la mayoría, las que se infectan en mayor proporción son las neuronas, lo que confirma el marcado neurotropismo del virus. Adicionalmente a esto, dentro de la población neuronal, parece existir una subpoblación con mayor susceptibilidad hacia la infección por el virus. Para comprobar esta hipótesis, se caracterizaron las subpoblaciones neuronales presentes en estos cultivos utilizando un criterio morfológico (diámetro neuronal y uno bioquímico (presencia de neuropéptidos como marcadores de subpoblaciones en el ganglio. Se realizó una técnica de doble inmunocitoquímica para virus rábico y los neuropéptidos Sustancia P (SP, Neuropéptido Y (NPY, Galanina (GAL, Péptido Relacionado con el Gen de la Calcitonina (CGRP y Péptido Intestinal Vasoactivo (VIP, que clásicamente se usan para la definición de subpoblaciones. El análisis morfométrico demostró que en nuestros cultivos el 85% de las neuronas presentes son de pequeño diámetro (<25

  1. Eimeria collieie n. sp. (Apicomplexa:Eimeriidae) from the western long-necked turtle (Chelodina colliei).

    Science.gov (United States)

    Yang, Rongchang; Brice, Belinda; Elloit, Aileen; Lee, Elvina; Ryan, Una

    2015-07-01

    A new species, Eimeria collieie n. sp., is described from the western long-necked turtle (Chelodina colliei). Sporulated oocysts (n = 35) are spherical to subspherical, with colourless single layer oocyst wall, 0.6 ± 0.2 (0.4-0.7) µm thick. Oocyst with elongated ellipsoid sporocysts. Oocyst length, 29.8 ± 0.4 (28.2-31.0) µm; oocyst width, 29.4 ± 0.3 (28.0-30.8) µm; oocyst length/width (L/W) ratio, 1.0 ± 0.03 (1.0-1.05). Micropyle, oocyst residuum and polar granule were absent. Sporocysts with sporocyst residuum and 2 sporozoites. Sporocyst length, 21.6 ± 0.4 (21.2-22.0) µm; sporocyst width, 6.0 ± 0.3 (5.7-6.3) µm; sporocyst L/W ratio, 3.6 ± 0.2 (3.4-3.8). Stieda, parastieda and substieda bodies were absent. Sporozoite length, 14.0 ± 0.2 (13.8-14.2) µm; sporozoite width, 2.6 ± 0.2 (2.4-2.8) µm; sporozoite L/W ratio, 5.46 ± 0.10 (5.4-5.6). Molecular analysis was conducted at three loci: the 18S and 28S ribosomal RNA (rRNA), and the mitochondrial cytochrome oxidase gene (COI). At the 18S rRNA locus, E. collieie n. sp. shared 96.4% and 98.3% genetic similarity to E. ranae (GenBank accession number: EU717219) and E. arnyi (AY613853) respectively. At the 28S rRNA locus, E. collieie n. sp. shared 91.6% genetic similarity to E. papillata (GenBank accession number: GU593706) and phylogenetic analysis at this locus placed E. collieie n. sp. in aseparateclade. At the COI locus, E. collieie n. sp. shared 92.7% genetic similarity to Eimeria setonicis (GenBankaccession number: KF225638) from a quokka (Setonix brachyurus) in Western Australia. Reptile-derived sequences were not available for the 28S rRNA and the COI loci. Based on morphological and molecular data, this isolate is a new species of coccidian parasite that, to date, has only been found in western long-necked turtles. Crown Copyright © 2015. Published by Elsevier Inc. All rights reserved.

  2. A new Caryospora coccidian species (Apicomplexa: Eimeriidae) from the laughing kookaburra (Dacelo novaeguineae).

    Science.gov (United States)

    Yang, Rongchang; Brice, Belinda; Ryan, Una

    2014-10-01

    A new Caryospora coccidian species is described from the laughing kookaburra (Dacelo novaeguineae). Sporulated oocysts (n=30) are ovoid in shape with a smooth, colourless, bilayered oocyst wall and measure 31.4×29.3 (30.0-32.0×28.0-31.0) μm with a shape index of 1.1. Oocysts contain one spheroidal to subspheroidal sporocyst, 21.2×20.6 (20.0-24.0×20.0-21.0) μm. A spheroidal shaped sporocyst residuum is present; micropyle, Stieda, substieda and parastieda bodies are absent. Vermiform sporozoites (n=8) are arranged either parallel or randomly in the sporocyst, measuring 17.0×4.8 (16.0-18.0×4.0-6.0) μm, with a L/W ratio of 3.5. There is a large spheroidal, posterior refractile body in the middle of the sporozoite. Morphologically, this new species is most similar to Caryospora. The prevalence of this parasite was 6.7% in birds sampled in the morning and 33.3% from those sampled after midday. Further molecular characterisation was conducted at two loci; the 18S and 28S ribosomal RNA (rRNA). At the 18S locus, the new species of Caryospora was most closely related to Besnoitia besnoiti (99.2% similarity) and Hammondia triffittae (98.8% similarity). Although, no 28S partial sequences from Caryospora were available in GenBank, the highest similarity was with B.besnoiti (91.3%). Based on morphological and molecular data, this coccidian parasite is a new species that to date has not been reported. The new coccidian parasite is named Caryospora daceloe n. sp. after its host D. novaeguineae (the laughing kookaburra). Crown Copyright © 2014. Published by Elsevier Inc. All rights reserved.

  3. Sequential histological changes in Biomphalaria glabrata during the course of Schistosoma mansoni infection

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    Queli Teixeira Lemos

    2001-07-01

    Full Text Available Biomphalaria glabrata, highly susceptible to Schistosoma mansoni, were seen to shed less and less cercariae along the time of infection. Histological examination kept a close correlation with this changing pattern of cercarial shedding, turning an initial picture of no-reaction (tolerance gradually into one of hemocyte proliferation with formation of focal encapsulating lesions around disintegrating sporocysts and cercariae, a change that became disseminated toward the 142nd day post miracidial exposure. Findings were suggestive of a gradual installation of acquired immunity in snails infected with S. mansoni.

  4. Two new species of Isospora (Apicomplexa: Eimeriidae) from skinks Emoia spp. (Sauria: Scincidae), from Fiji and Papua New Guinea

    Science.gov (United States)

    McAllister, Chris T.; Duszynski, Donald W.; Fisher, Robert N.

    2013-01-01

    Between September and October 1991 and again during September 1992, skinks (Emoia spp.) were collected from various localities on Fiji and Papua New Guinea (PNG) and examined for coccidians. One of 4 (25%) De Vis' emo skinks (Emoia pallidiceps) from PNG harbored an undescribed species of Isospora in its feces. Oocysts of Isospora grinbikpelapalai n. sp. were ellipsoidal to subspheroidal, 18.1 × 14.9 (17–20 × 14–16) μm, with a bilayered wall and a length/width index (L/W) of 1.2. Both micropyle and oocyst residuum were absent, but a prominent polar granule was present. Sporocysts were ovoidal, 10.7 × 7.6 (10–11 × 7–8) μm, with a L/W index of 1.4. Stieda and sub-Stieda bodies were present, but para-Stieda bodies were absent. The sporocyst residuum consisted of large scattered globules dispersed between sporozoites. Sporozoites were elongate with spheroidal anterior and posterior refractile bodies. Isospora grinbikpelapalai was also found in 1 of 2 (50%) Pope's emo skinks (Emoia popei) from PNG. One of 13 (8%) white-bellied copper-striped skinks (Emoia cyanura), from Fiji, was passing another undescribed species of Isospora in its feces. Oocysts of Isospora casei n. sp. were elongate, 31.8 × 21.3 (28–35 × 18–24) μm, with a bilayered wall and a L/W index of 1.5. Micropyle, oocyst residuum, and polar granule were all absent. Sporocysts were ovoidal, 15.3 × 10.6 (14–16 × 10–12) μm, with a L/W index of 1.4. Stieda and sub-Stieda bodies were present, but para-Stieda bodies were absent. The sporocyst residuum consisted of scattered globules among sporozoites or as a cluster surrounding sporozoites. Sporozoites were elongate with spheroidal anterior and posterior refractile bodies. Isospora casei was also found in 1 of 2 (50%) Fiji slender treeskinks (Emoia concolor) from Fiji. This represents the first report of coccidia from Emoia spp. and, to our knowledge, the initial documentation of reptilian coccidia from herpetofauna from Papua New Guinea.

  5. Two new species of coccidia (Apicomplexa: Eimeriidae) from leaf-tailed geckos, Uroplatus spp. (Sauria: Gekkonidae) from Madagascar, including a new host of Eimeria brygooi Upton & Barnard, 1987.

    Science.gov (United States)

    McAllister, Chris T; Scott Seville, R; Hartdegen, Ruston

    2016-10-01

    During May and June 2015, four common leaf-tailed geckos, Uroplatus fimbriatus (Schneider), five satanic leaf-tailed geckos, Uroplatus phantasticus (Boulenger), and four mossy leaf-tailed geckos, Uroplatus sikorae Boettger originally collected from Madagascar and housed at the Dallas Zoo, USA, had their faeces examined for coccidian parasites. Eight (62%) geckos were found to be passing oöcysts, including a new eimerian, a new isosporan and a previously described eimerian. Three of four (75%) U. fimbratus (type-host) and one of five (20%) U. phantasticus were infected with Eimeria schneideri n. sp.; oöcysts were subspheroidal to ellipsoidal with a bi-layered wall and measured (mean length × width, L × W) 15.1 × 13.5 µm, with a length/width (L/W) ratio of 1.1. A micropyle and oöcyst residuum were absent but one to many polar granules were present. Sporocysts were ovoidal, 6.9 × 5.3 µm, L/W = 1.3. Stieda, sub-Stieda and para-Stieda bodies were absent. A globular sporocyst residuum was present as dispersed granules. Four of five (80%) U. phantasticus harboured Isospora boulengeri n. sp.; oöcysts were subpheroidal to ellipsoidal with a bi-layered wall and measured 17.3 × 16.0 µm, L/W = 1.1. A micropyle and oöcyst residuum were absent but a polar granule was present. Sporocysts were ellipsoidal, 9.5 × 6.9 µm, L/W = 1.4. Stieda and sub-Stieda bodies were present but a para-Stieda body was absent. A globular sporocyst residuum was present with dispersed granules. In addition, one of four (25%) U. sikorae was infected with an eimerian indistinguishable from Eimeria brygooi Upton & Barnard, 1987, previously reported from Madagascar day gecko, Phelsuma grandis Gray and golddust day gecko, Phelsuma laticauda (Boettger) from Madagascar. These are the first coccidians described from Uroplatus spp.

  6. Klossiella equi in a donkey--a first case report from Iran.

    Science.gov (United States)

    Rezaie, A; Bahrami, S; Ansari, M

    2013-09-01

    Klossiella equi is the only known and rarely reported coccidian parasite of the renal paranchyma of equids. An aged male donkey (Equus asinus asinus) was submitted to necropsy department of veterinary hospital. In histopathological study of renal sections different developmental stages of parasite were observed. These stages were as follow: Trophozoites, microgametes, macrogametes, sporont, budding sporont, sporoblasts, free sporoblasts, mature sporoblast and sporocyst. Parasitic infection with K. equi was encountered in the donkey. According to literature review this is the first report of donkey klossiellosis in Iran.

  7. Prosthogonimus cuneatus (Digenea, Prosthogonimidae in Bithynia tentaculata mollusks in Ukraine

    Directory of Open Access Journals (Sweden)

    Y. P. Zhytova

    2011-01-01

    Full Text Available Parthenitae and larvae of Prosthogonimus cuneatus Rudolphi, 1809 in the fresh water mollusk Bithynia tentaculata s were firstly found in the eastern Polissya (the Psel river bend, Sumy oblast. The paper presents the morphological characteristics of the P. cuneatus cercariae. Comparative analysis of the dimensional data of P. cuneatus sporocysts and larvae with their parthenitae and larvae described by T. A. Krasnolobova (1961, L. F. Filimonova and V. I. Shalyapina (1980, and E. Arystanov (1986 from B. tentaculata, B. inflata and B.caerulans mollusks was made.

  8. Morphological and molecular characterization of Eimeria paludosa coccidian parasite (Apicomplexa:Eimeriidae) in a dusky moorhen (Gallinula tenebrosa, Gould, 1846) in Australia.

    Science.gov (United States)

    Yang, Rongchang; Brice, Belinda; Elloit, Aileen; Lee, Elvina; Ryan, Una

    2014-12-01

    An Eimeria species is described from a dusky moorhen (Gallinula tenebrosa). Sporulated oocysts (n = 40) are ovoid, with a pitted single-layered oocyst wall in young oocysts and a relatively smooth wall in the mature oocysts. Oocyst wall was 1.0 µm thick, oocysts measured 17.3 × 13.3 (16.3-17.9 × 12.7-13.9) µm, oocyst length/width (L/W) ratio, 1.3. Oocyst residuum was absent. A large polar granule was always observed in the centre of the micropyle and many small polar granules were observed when the focus was on the wall. Sporocysts are elongate-ovoid, 8.4 × 5.1 (8.0-8.9 × 4.9-5.5) µm, sporocyst L/W ratio, 1.6 (1.5-1.8), sporocyst residuum was present, composed of numerous granules in a spherical or ovoid mass. Each sporocyst contained 2 elongate sporozoites, 7.7 × 2.6 (7-10 × 2.2-3) µm. A spherical-ellipsoid posterior refractile body was found in the sporozoites. A nucleus is located immediately anterior to the posterior refractile body. When the oocyst measurements and features were compared with valid Eimeria species from hosts in the Rallidae family, this Eimeria species was identified as E. paludosa. This is the first report of E. paludosa in Australia and the dusky moorhen (Gallinula tenebrosa) in a new host for this species. Molecular analysis was conducted at three loci; the 18S and 28S ribosomal RNA genes and the mitochondrial cytochrome oxidase gene (COI). At the 18 S locus, E. paludosa shared 97.3% genetic similarity with Eimeria gruis (GenBank accession number: AB544336). It also shared 99.2% genetic similarity with Eimeria crecis (GenBank accession numbers: HE653904 and HE653905) and 98.5% similarity with Eimeria nenei (GenBank accession numbers: HE653906), both of which were identified from a corncrake (Crex crex) in the United Kingdom. At the 28S locus, E. paludosa shared 91.4% similarity with E. papillata from a chicken (Gallus gallus) in the USA. At COI locus, E. paludosa was in a clade by itself and shared 87.2% similarity with E

  9. Eimerid coccidia from capybaras (Hydrochoerus hydrochaeris in southern Bahia, Brazil Coccídios eimerídios em capivaras (Hydrochoerus hydrochaeris no sul da Bahia

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    George R. Albuquerque

    2008-07-01

    Full Text Available Two eimerid coccidia are reported in a capybara (Hydrochoerus hydrochaeris population kept in captivity in the south of Bahia, northeastern Brazil (14º 47' 57.89"S and 39º 10' 10.58" W. Oocysts of Eimeria ichiloensis are subspheroidal to ellipsoidal, 26.2 x 21.7mm with bi-layered wall, the outer yellow and sculptured and the inner, dark and smooth. Residuum is absent, but usually 2-3 polar granules are present. Sporocysts are ovoid, 12.0 x 7.6mm. Stieda body and sporocyst residuum are present. Oocysts of Eimeria trinidadensis are subspheroidal to ellipsoidal, 22.2 x 19.6mm with bi-layered wall, the outer yellow and smooth, and the inner dark and smooth. Residuum is absent, but one polar granule is present. Sporocysts are ovoid, 11.0 x 6.9mm. Stieda body and sporocyst residuum are present. Based on these descriptions and previous ones it can be concluded that these coccidea species are widely dispersed in capybaras in South America.Duas espécies de Eimeria foram relatadas em capivaras Hydrochaeris hydrochaeris cativas no sul da Bahia, nordeste do Brasil (14º 47' 57.89"S and 39º 10' 10.58" W. Os oocistos de Eimeria ichiloensis são sub-esferoidais a elipsoidais, 26,2 x 21,7mm. Apresentam parede dupla, sendo a externa amarela e esculpida e a interna, escura e lisa. Resíduo está ausente, mas usualmente 2-3 grânulos polares estão presentes. Os esporocistos são ovóides, 12,0 x 7,6mm. Corpo de Stieda e resíduo do esporocisto estão presentes. Oocistos de Eimeria trinidadensis são sub-esferoidais a elipsoidais, 22,2 x 19,6mm. Apresentam parede dupla, sendo a externa amarela e lisa e a interna, escura e lisa. Resíduo está ausente, mas um grânulo polar está presente. Os esporocistos são ovóides, 11,0 x 6,9mm. Corpo de Stieda e resíduo do esporocisto estão presentes. Baseado nestas descrições e em descrições prévias foi possível concluir que estas espécies estão amplamente dispersas em capivaras na América do Sul.

  10. Four new coccidia (Apicomplexa: Eimeriidae) from the Plateau zokor, Myospalax baileyi Thomas (Rodentia: Myospalacinae), a subterranean rodent from Haibei area, Qinghai Province, China.

    Science.gov (United States)

    Cao, Yi-Fan; Nie, Xu-Heng; Zhang, Tong-Zuo; Du, Shou-Yang; Duszynski, Donald W; Bian, Jiang-Hui

    2014-02-01

    Thirty-eight faecal samples from the Plateau zokor, Myospalax baileyi Thomas, collected in the Haibei Area, Qinghai Province, China, were examined for the presence of coccidia (Apicomplexa: Eimeriidae). Seventeen of 38 faecal samples (44.7%) were found to contain coccidian oöcysts representing four new species of Eimeria Schneider, 1875, and four of 17 (23.5%) infected zokors were concurrently infected with two or three of these eimerian species. The sporulated oöcysts of Eimeria myospalacensis n. sp. are ovoidal, 9.5-17.0 × 8.0-13.0 (mean 13.0 × 10.4) μm; a polar granule is present, oöcyst residuum is absent; sporocysts are ovoidal, 4.5-7.5 × 3.0-5.0 (mean 6.3 × 4.2) μm and have both a Stieda body and residuum. Oöcysts of Eimeria fani n. sp. are ellipsoidal to cylindroidal, 12.5-16.0 × 8.0-11.0 (mean 14.6 × 9.9) μm; a polar granule is present, but micropyle and residuum are lacking; sporocysts are ovoidal, 4.5-7.5 × 3.0-5.3 (mean 6.7 × 4.4) μm; a residuum and a Steida body are present. Oöcysts of Eimeria baileyii n. sp. are ellipsoidal, 15.0-23.0 × 12.0-18.0 (mean 18.2 × 13.7) μm; a polar granule is present but oöcyst residuum is absent; sporocysts are ovoidal, 8.0-11.0 × 5.0-7.0 (mean 9.5 × 5.9) μm and have both a Stieda body and residuum. Oöcysts of Eimeria menyuanensis n. sp. are ovoidal, 12.5-21.0 × 11.0-18.0 (mean 17.1 × 14.6) μm, with a distinct micropyle c.2.5 μm wide; a polar granule is present but a residuum is absent; sporocysts are ovoidal, 8.0-12.0 × 5.0-7.0 (mean 10.2 × 6.4) μm, and have both a Stieda body and residuum.

  11. The life cycle of Dendritobilharzia anatinarum cheatum, 1941 (Trematoda, Schistosomatidae

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    Antonio Cesar Rios Leite

    1982-12-01

    Full Text Available The life cycle of Dendritobilharzia anatinarum was completed experimentally in the laboratory. Cairina moschata domestica (domestic duck and Biomphalaria straminea served respectively as definitive and intermediate hosts. Eggs passed in duck faeces hatch miracidia in 10 minutes when placed in water. Eight days after the snail infection, the mother sporocyst contains daughter sporocysts ready to migrate. Cercariae are present within the daughter sporocysts 23 days after infection and emerge from the snail on the 25th day. They actively penetrate the skin of the duck and after a prepatent of 39 days, sexually mature trematodes are present in the blood vessels of the bird. The adult parasite is predominantly in the renal-portal system and to a lesser degree in the lungs and mesentery. A detailed morphological description of the egg. miracidium, sporocyst and cercaria is presented.O ciclo biológico de Dendritobilharzia anatinarum foi desenvolvido experimentalmente em laboratório. Patos domésticos Cairina (moschata domestica, e moluscos Biomphalaria straminea, foram os hospedeiros definitivo e intermediário, respectivamente. Os miracídios começaram a eclodir 10 minutos após a permanência dos ovos em água. Esporocistos primários continham esporocistos secundários aptos a migrar, após 8 dias da infecção dos moluscos. Decorridos 23 dias da infecção, esporocistos secundários já continham cercárias, as quais começaram a migrar dos moluscos no 25° dia. Após a penetração das cercárias nas aves, o período de pré-patência foi de 39 dias. Os parasitas adultos foram localizados nos vasos sanguíneos dos pulmões, mesentério e, principalmente, do sistema porta-renal. Detalhes morfológicos do ovo, miracídio, esporocisto e cercária são apresentados.

  12. Morphological and molecular characterization of Eimeria labbeana-like (Apicomplexa:Eimeriidae) in a domestic pigeon (Columba livia domestica, Gmelin, 1789) in Australia.

    Science.gov (United States)

    Yang, Rongchang; Brice, Belinda; Elloit, Aileen; Ryan, Una

    2016-07-01

    An Eimeria species is described from a domestic pigeon (Columba livia domestica). Sporulated oocysts (n = 35) were subspherical, with a smooth bi-layered oocyst wall (1.0 μm thick). Oocysts measured 20.2 × 16.1 (22.0-18.9 × 15.7-18.9) μm, oocyst length/width (L/W) ratio, 1.38. Oocyst residuum and a polar granule were present. The micropyle was absent. Sporocysts are elongate-ovoid, 13.0 × 6.1 (14.5-12.5 × 5.5-7.0) μm, sporocyst L/W ratio, 2.13 (2.0-2.2), sporocyst residuum was present, composed of numerous granules in a spherical or ovoid mass. Each sporocyst contained 2 banana-shaped sporozoites, 12.3 × 3.5 (11.8-13.0 × 3.3-3.6) μm. A spherical-ellipsoid posterior refractile body was found in the sporozoites. A nucleus was located immediately anterior to the posterior refractile body. Molecular analysis was conducted at three loci; the 18S and 28S ribosomal RNA genes and the mitochondrial cytochrome oxidase gene (COI). At the 18S locus, the new isolate shared 98.0% genetic similarity with three Isospora isolates from Japan from the domestic pigeon (Columba livia domestica). At the 28S locus, it grouped separately and shared 92.4% and 92.5% genetic similarity with Isospora anthochaerae (KF766053) from a red wattlebird (Anthochaera carunculata) from Australia and an Isospora sp. (MS-2003 - AY283845) from a Himalayan grey-headed bullfinch (Pyrrhula erythaca) respectively. At COI locus, this new isolate was in a separate clade and shared 95.6% and 90.0% similarity respectively with Eimeria tiliquae n. sp. from a shingleback skink in Australia and an Eimeria sp. from a common pheasant (Phasianus colchicus) from America. Based on the morphological data, this isolate is most similar to Eimeria labbeana. As no molecular data for E. labbeana is available and previous morphological data is incomplete, we refer to the current isolate as E. labbeana-like. Crown Copyright © 2016. Published by Elsevier Inc. All rights reserved.

  13. Las bases celulares de las oscilaciones neuronales

    OpenAIRE

    Mario Treviño; Rafael Gutiérrez

    2007-01-01

    Una de las características de los circuitos neuronales es que sus componentes, las neuronas, pueden presentar actividad eléctrica sincrónica y, gracias a ésta, generar actividad oscilatoria. Esta actividad se ha asociado a diversas funciones fisiológicas como el procesamiento de información sensorial, la memoria, el ciclo vigiliasueño y la conciencia. La actividad oscilatoria de un circuito neuronal está mediada por i) las propiedades intrínsecas de sus células, ii) la arquitectura de sus con...

  14. Estudio de la modulación del receptor µ opioide por el receptor dopaminérgico D4. Implicación en la adicción a morfina

    OpenAIRE

    Valderrama Carvajal, Alejandra

    2015-01-01

    La morfina se utiliza en el ámbito clínico por ser un potente analgésico, sin embargo produce efectos adversos como la adicción. La administración de morfina induce una liberación masiva de dopamina en el estriado, produciendo los efectos de refuerzo y consolidación de hábitos adictivos. La actividad de las neuronas dopaminérgicas de la sustancia negra compacta está regulada por proyecciones GABAérgicas de la sustancia negra reticular (SNr) y del caudado putamen (CPu). En ambas regiones se lo...

  15. Agregación de alfa-sinucleína y degeneración Parkinsoniana

    OpenAIRE

    Fernández-Espejo, Emilio

    2013-01-01

    La alfa-sinucleína es la proteína principal de los cuerpos de Lewy, marcador anatomopatológico de la enfermedad de Parkinson. Dicha proteína puede ver alterada su conformación y adquirir capacidad autoagregante, lo que se relaciona con el depósito de agregados proteináceos en las neuronas y podría constituir un factor fisiopatológico importante en dicha enfermedad. Los agregados poseen fibrillas de alfa-sinucleína alterada, y las moléculas se encuentran unidas entre sí por enlaces no...

  16. Inhibidores de fosfodiesterasas como potenciales fármacos para el tratamiento de enfermedades neurodegenerativas

    OpenAIRE

    García Fernández, Ana María

    2015-01-01

    Las enfermedades neurodegenerativas se caracterizan por una pérdida progresiva de neuronas en zonas específicas del sistema nervioso central. Entre estas patologías se encuentran la enfermedad de Alzheimer, la enfermedad de Parkinson y la esclerosis múltiple. A pesar de la etiología desconocida que presentan este tipo de patologías, se han identificado mecanismos comunes que podrían dar lugar a la muerte neuronal, tales como la excitotoxicidad, la neuroinflamación, el estrés oxidativo, o la a...

  17. Factor neurotrófico derivado del cerebro en tejido cerebral de ratas sanas

    OpenAIRE

    Teresa Serrano Sánchez; Lourdes Lorigados Pedre; Jorge Bergado Rosado; William Almaguer Melián; Jeffrey López Rojas; Esteban Alberti-Amador; Ivan Díaz Armesto; Jorge Felipe Montero León

    2009-01-01

    Hasta el presente se conocen cinco proteínas, estructuralmente relacionadas, que constituyen la familia de las neurotrofinas dentro de las que se encuentra el factor neurotrófico derivado del cerebro (FNDC), que tiene influencia sobre muchos tipos de neuronas en el sistema nervioso central, promoviendo en ellas su diferenciación, crecimiento y supervivencia. Esta proteína es importante en la neuroprotección, así como en los mecanismos de plasticidad sináptica. Teniendo en cuenta la importanci...

  18. Caracterización de la proliferación celular en las zonas subventriculares y de la evolución del infarto mediante espectroscopía de resonancia magnética en un modelo preclínico de isquemia cerebral

    OpenAIRE

    Jiménez Xarrié, Elena

    2014-01-01

    El ictus es una patología con una elevada incidencia en la población y los pacientes afectados sufren secuelas que les causan algún tipo de discapacidad. A nivel terapéutico, la posibilidad de incidir sobre la evolución de la enfermedad es a día de hoy aún escasa. Se ha descrito que la neurogénesis, la generación de nuevas neuronas con capacidad para migrar a la zona afectada, aumenta en las zonas subventriculares (ZSVs) y el hipocampo tras un infarto cerebral, en modelos animales y en humano...

  19. Alteraciones de los Astrocitos en el envejecimiento y en la enfermedad del Alzheimer

    OpenAIRE

    García-Matas, Silvia

    2009-01-01

    El tema de esta tesis ha sido el estudio de los mecanismos de neurodegeneración asociados al envejecimiento cerebral y el papel que desempeñan los astrocitos como neuroprotectores utilizando modelos animales in vitro e in vivo.Los astrocitos son las células más abundantes del sistema nervioso central y su función es muy importante, además de dar soporte trófico a las neuronas tienen una función anticitotóxica y modulan la actividad neuronal. El papel de los astrocitos y su activación en el e...

  20. Regulación de la utilización del aspartato por los astrocitos durante la prelactancia

    OpenAIRE

    Cecilia Espíndola; Ludis Morales; María Juliana Salamanca Ortiz; Jairo Alfonso Tovar-Franco

    2009-01-01

    En el período perinatal se incrementa la concentración de N-acetil-L-aspartato (NAA) producido por las neuronas, este sustrato es absorbido por los astrocitos e hidrolizado vía aspartoacilasa II (ASPA; EC 3.5.1.15) en acetato y aspartato. Se postula que el aspartato podría colaborar en suplir los requerimientos metabólicos de los astrocitos durante la prelactancia. Objetivos. Evaluar la capacidad de los astrocitos para utilizar el aspartato como sustrato metabólico en condiciones fisiológicas...

  1. ¿Qué es la optogenética? Aplicaciones futuras a la práctica clínica

    OpenAIRE

    Barrientos Duque, Marta A.

    2016-01-01

    RESUMEN: La optogenética es una técnica, desarrollada recientemente, que permite el control a través de la luz de la actividad de neuronas definidas genéticamente. Las células son primero modificadas genéticamente para expresar unas determinadas proteínas fotosensibles (opsinas), que son canales ionicos, bombas protónicas, o receptores acoplados a proteínas G. Luego, las células genéticamente modificadas son iluminadas con luz de una determinada longitud de onda, activando o inhibiendo los ca...

  2. Identificación y caracterización de la población total de las células ganglionares de la retina en rata : nuevos métodos de trazado, expresión de melanopsina y de factores de transcripción Brn3:estudio de la respuesta neuronal y microglial a la axotomía y efecto del envejecimiento en la retina

    OpenAIRE

    Nadal Nicolás, Francisco Manuel

    2015-01-01

    Introducción La retina es parte del sistema nervioso central (SNC) y se localiza en la cara interna del globo ocular. Su función principal es la fototransducción de las ondas electromagnéticas del espectro de la luz visible en energía eléctrica. Esta función es realizada por los fotorreceptores (conos y bastones). Tras su procesamiento, la información llega a las células ganglionares de retina (CGR). Las CGR son las únicas neuronas aferentes de la retina y transmiten la información visual ...

  3. POLIOMIELITIS PARALÍTICA. NUEVOS PROBLEMAS: EL SÍNDROME POSTPOLIO

    OpenAIRE

    Jesús Esteban

    2013-01-01

    En 1875 M Raymond describió la aparición de una atrofia y debilidad muscular progresiva en 3 individuos supervivientes de una poliomielitis aguda en la infancia. Jean-Martin Charcot, sugirió que la lesión inicial debía dejar a las neuronas de estos individuos más sensibles para desarrollar enfermedades medulares posteriores y que la nueva debilidad era consecuencia del sobreuso de los músculos afectos. En 1979, tras la publicación de la descripción realizada por un paciente de 57 años de las ...

  4. Aproximación a la fisiopatología de las anomalías neurológicas en la fenilcetonuria y evaluación de nuevas opciones terapéuticas

    OpenAIRE

    Pérez Dueñas, Belén

    2006-01-01

    [spa] El temblor en la fenilcetonuria es un trastorno del movimiento muy prevalente entre pacientes de diagnóstico precoz y tardío. Se trata de un temblor rápido y muy regular, localizado fundamentalmente en extremidades superiores, cuya amplitud aumenta con el movimiento sobre todo en los pacientes de diagnóstico tardío, en quienes puede causar una discapacidad para las tareas cotidianas. Los datos neurofisiológicos sugieren que el temblor está causado por una disfunción de circuitos neurona...

  5. Afectación retiniana en un modelo murino experimental de esclerosis múltiple

    OpenAIRE

    Jiménez Casares, Sandra

    2015-01-01

    La esclerosis múltiple (EM) es una enfermedad neurodegenerativa autoinmune adquirida, caracterizada por un proceso crónico de desmielinización inflamatoria que afecta de forma específica al sistema nervioso central (SNC) [1-6]. Es mediada por el ataque del sistema inmune a través de células T, contra antígenos del SNC. Hay destrucción o daño de la vaina de mielina (desmielinización), pérdida de oligodendrocitos y neuronas lo que lleva al aumento de la disfuncionalidad neurológica. Con el obje...

  6. Estrógenos y desarrollo del cerebro femenino en la adolescencia: anticoncepción de emergencia

    OpenAIRE

    Natalia López Moratalla; Tania Errasti Alcalá; Esteban Santiago

    2011-01-01

    En el periodo entre pubertad y madurez tiene lugar el proceso de maduración cerebral en el que los niveles hormonales inducen modificaciones en las neuronas y dirigen la arquitectura y funcionalidad estructural al modificar los patrones de desarrollo de diversa áreas cerebrales. El inicio de la pubertad trae consigo la invasión del cerebro femenino por niveles elevados de hormonas: oleadas cíclicas de estrógenos y progesterona que se suman a los esteroides producidos in situ. Los centros de c...

  7. Análisis de la capacidad vital forzada como indicador de inicio de ventilación no invasiva en enfermos con esclerosis lateral amiotrófica

    OpenAIRE

    Martínez González, Daniel

    2014-01-01

    La Esclerosis lateral amiotrófica (ELA) es una enfermedad neurodegenerativa de causa desconocida que se caracteriza por la pérdida de neuronas motoras en la médula espinal, el tronco cerebral y la corteza motora. Como consecuencia se produce un debilitamiento progresivo de los músculos de las extremidades, bulbares, torácicos y abdominales. La consecuencia directa de este hecho tiene repercusiones sobre la morbimortalidad en los pacientes con ELA. Ésta se constituye principalmente por problem...

  8. Regulación epigenética de la expresión estriatal del receptor de adenosina A(2A) en enfermedades neurológicas con trastorno motor asociado

    OpenAIRE

    Villar Menéndez, Izaskun

    2014-01-01

    La adenosina es un metabolito presente en todo el organismo con distintas funciones fisiológicas. En el sistema nervioso central, desempeña un importante papel como neuromodulador a través de la interacción con sus receptores de membrana: los receptores de adenosina A(1), A(2A), A(2B) y A(3), siendo los más abundantes en el cerebro el A(1 )y el A(2A). El receptor de adenosina A(2A) (A(2A)R) presenta una elevada expresión en el estriado, especialmente en las neuronas GABAérgicas medianas e...

  9. Desde la corteza auditiva a la cóclea: Progresos en el sistema eferente auditivo

    OpenAIRE

    Terreros H,Gonzalo; Wipe U,Bárbara; León I,Alex; Délano R,Paul H

    2013-01-01

    El sistema eferente auditivo está constituido por el sistema olivococlear y por vías descendentes que provienen de la corteza auditiva y se dirigen a la cóclea. El sistema olivococlear se divide en una porción medial y una lateral, con neuronas que inervan a las células ciliadas externas y a fibras del nervio auditivo respectivamente. El principal neurotransmisor de las sinapsis olivococleares es acetilcolina, y tanto las células ciliadas externas como las fibras del nervio auditivo poseen re...

  10. Desensibilización inducida por agonista del receptor TRPV1

    OpenAIRE

    2014-01-01

    El receptor TRPV1 es un canal catiónico capaz de activarse por calor, pH ácido, voltaje y por diferentes sustancias químicas entre las que destacan los agonistas vanilloides capsaicina y resiniferatoxina. En las neuronas aferentes nociceptivas o nociceptores, donde se expresa de forma abundante, TRPV1 actúa como un sensor polimodal cuya actividad se controla por multitud de mecanismos reguladores capaces de causar su sensibilización o desensibilización. La estimulación prolongada por sus agon...

  11. Functional and effective connectivity in MEG. Application to the study of epilepsy

    OpenAIRE

    Niso Galán, Julia Guiomar

    2014-01-01

    Nuestro cerebro contiene cerca de 1014 sinapsis neuronales. Esta enorme cantidad de conexiones proporciona un entorno ideal donde distintos grupos de neuronas se sincronizan transitoriamente para provocar la aparición de funciones cognitivas, como la percepción, el aprendizaje o el pensamiento. Comprender la organización de esta compleja red cerebral en base a datos neurofisiológicos, representa uno de los desafíos más importantes y emocionantes en el campo de la neurociencia. Se han propuest...

  12. Función de netirna-1 y semaforinas secretables en la guía neuronal y axonal en el hipocampo y el cerebelo

    OpenAIRE

    Guijarro Larraz, Patricia

    2006-01-01

    Los factores guía son proteínas esenciales en el proceso de guía de neuronas y axones que ocurre durante el desarrollo del sistema nervioso. Netrinas y Semaforinas componen dos de las cinco familias de factores guía existentes. En este trabajo, nosotros hemos estudiado el efecto quimiotáctico de Netrina1 y Semaforinas secretables Sema3A y Sema3F en la guía de interneuronas y sus axones durante el desarrollo del cerebelo y el hipocampo, así como la participación de Sema3A en el proceso de rege...

  13. INSULINA Y ENFERMEDAD DE ALZHEIMER: UNA DIABETES TIPO 3?

    Directory of Open Access Journals (Sweden)

    Andrés Jagua Gualdrón

    2007-03-01

    Full Text Available La enfermedad de Alzheimer es un trastorno degenerativo del sistema nervioso central cuya incidencia probablemente aumentará en los próximos años. Los resultados de investigaciones recientes relacionan esta enfermedad con trastornos en la señal de la insulina a nivel de las neuronas. ¿Es la Enfermedad de Alzheimer una diabetes tipo 3? En este documento presentamos una reseña breve de las evidencias que se levantan en torno a este modelo de la enfermedad.

  14. Plasticidad del sistema nervioso

    Directory of Open Access Journals (Sweden)

    L. M. Garcia-Segura

    1976-06-01

    Full Text Available En este trabajo se revisan los conocimientos más recientes sobre el fenómeno de la plasticidad del sistéma nervioso, tanto a nivel morfológico como a nivel fisiológico y molecular. Se estudian los cambios morfólogicos y fisiológicos de las neuronas frente a la experiencia. Tambien se considera la adaptación molecular del sistéma nervioso a la información que recibe como la base de todo tipo de plasticidad.

  15. Mecanismo de activación de P191NK4d y su papel como factor neuroprotector frente a la injuria genotóxica

    OpenAIRE

    Ogara, María Florencia

    2012-01-01

    La permanencia de la mayoría de las neuronas durante toda la vida del organismo necesaria para mantener sus funciones, y el hecho de que estas células no se dividan luego del desarrollo sugieren que, durante la evolución, se ha ejercido una fuerte presión sobre el sistema nervioso de modo de desarrollar diversos mecanismos que lo protejan contra la muerte celular. Las dramáticas consecuencias de la neurodegeneración enfatizan la importancia de estos mecanismos que promueven la supervivencia y...

  16. Redes neuronales modulares : topología, características y aplicación

    OpenAIRE

    Corte León, Héctor

    2012-01-01

    Trabajo de Fin de Máster. Máster Universitario en Física de Sistemas ComplejosEn este trabajo se muestra un modelo de red neuronal estocástica basada la versión original de Hopfield. El modelo además de poseer neuronas estocásticas, que cambian de estado de acuerdo a una regla probabilistica, posee aprendizaje mediante entrenamientos múltiples, adapatandose al uso que tenga la red, además posee olvido pasivo de forma que la red nunca llega a saturarse. Nuestro desarrollo se centra...

  17. Análisis genético y funcional de la frataxina y otras proteínas mitocrondriales relacionadas con ataxias cerebelosas.

    OpenAIRE

    González-Cabo, Pilar

    2005-01-01

    RESUMEN El déficit de frataxina es la causa principal de la ataxia de Friedreich, una enfermedad hereditaria neurodegenerativa que afecta a las neuronas sensitivas del ganglio dorsal y del tracto espinocerebelar. Desde que se describi¨® el gen responsable de la enfermedad y sobre todo gracias a la generaci¨®n de organismos modelos para su estudio, se han postulado diferentes funciones para la frataxina: homeostasis del hierro mitocondrial, almacenamiento del hierro, respuesta al estr¨¦s ox...

  18. Activación de la glía en procesos inflamatorios

    OpenAIRE

    González Martín, Adrián

    2014-01-01

    Hay cuatro tipos especiales de células gliales en el cerebro humano; astrocitos, oligodendrocitos, microglía y células ependimales. Aunque las células gliales componen más del 50% del total de la población en el cerebro, históricamente se ha pensado que unicamente servían como células de soporte para las neuronas. Sin embargo, ahora sabemos que varias células gliales tienen funciones críticas durante el desarrollo y el correcto funcionamiento del cerbro. Además, las células gliales son ...

  19. Propioceptores articulares y musculares

    OpenAIRE

    Vega, José A.

    1999-01-01

    La función de los mecanorreceptores de las articulaciones y músculos se considera asociada a la propiocepción. Sin embargo, existen evidencias de que la propiocepción no sólo depende del morfotipo de mecanorreceptor presente en dichos tejidos sino también de las propiedades de las neuronas sensitivas primarias y las fibras sensitivas asociadas a ellos, así como de su proyección sobre el asta posterior de la médula espinal. Este artículo resume las bases morfológicas de la propi...

  20. El síndrome de Kallmann. Correlación fenotipo-genotípica.

    OpenAIRE

    García Piñero, Alfonso José

    2015-01-01

    El Síndrome de Kallmann (SK) es una enfermedad genética del desarrollo, que asocia un hipogonadismo hipogonadotrópico (HH) congénito con pérdida total (anosmia) o parcial (hiposmia) del olfato. La alteración olfativa es secundaria a la aplasia o hipoplasia de las estructuras olfatorias (bulbos, tractos y surcos cerebrales olfatorios). El HH se debe a la deficiencia en la hormona liberadora de gonadotropinas hipotalámica (GnRH) como resultado del fallo en la migración de las neuronas productor...

  1. Detección de eventos en imagen de actividad neuronal para su uso en técnicas de estimulación dependiente de actividad

    OpenAIRE

    Taboada Pérez, Lourdes

    2015-01-01

    Este Proyecto Final de Carrera se sitúa dentro de las líneas de investigación desarrolladas por el Grupo de Neurocomputación Biológica (GNB) de la Escuela Politécnica Superior de la UAM. Los experimentos y estudios previos realizados por el GNB han servido como base y punto de partida para realizarlo. En este proyecto se desarrollarán algoritmos para detectar eventos significativos en la actividad de neuronas individuales empleando técnicas de tratamiento de imagen. Se pretende que estos a...

  2. Redes neuronales analógicas para la computación paralela masiva de señales en tiempo real

    OpenAIRE

    Cancelo, Gustavo Indalecio Eugenio

    1996-01-01

    En esta tesis se realiza un estudio sobre las posibilidades de la electrónica para modelar unidades y sistemas neuronales. En particular, se proponen implementaciones de redes neuronales analógicas. La primera a nivel microelectrónico, comprende el diseño de una neurona computacional con función de activación gaussiana. Primeramente, se demostrará que las unidades computacionales con función de activación gaussiana forman una base para aproximadores universales de funciones continuas y discon...

  3. Efecto de un tratamiento ototóxico en la ultraestructura coclear

    OpenAIRE

    Sandra Rodríguez Salgueiro; Odelsa Ancheta Niebla; Rosa María Coro Antich; Tania Valdés Prieto; Yahima Harvey Pedroso; Armando Alvaré Jaramillo; Pavel Prado Gutiérrez; Valia Rodríguez Rodríguez

    2007-01-01

    La sordera es una de las discapacidades más comunes mundialmente, con una incidencia en Cuba de 2,1 por cada 1 000 habitantes. La mayoría de las sorderas son de origen sensorineural, debido a la muerte de las células ciliadas cocleares, localizadas en el órgano de Corti, lo que conduce a la degeneración de las neuronas del ganglio espiral. En un trabajo previo por Microscopia Óptica, usando un modelo de ototoxicidad en ratas, el órgano de Corti se afectó a partir de las 2 semanas de sordera, ...

  4. El cerebro metafórico

    OpenAIRE

    Parra Rozo, Omar

    2012-01-01

    “Recordemos que la palabra psique significaba para los griegos “alma” y “mariposa”. La mariposa es metáfora del alma no sólo por su vuelo errabundo, aparente negación de la trayectoria inexorable, sino por su misma naturaleza metamórfica de oruga, crisálida y joya voladora”.Fernando SavaterLa estructura compleja del cerebro con sus millones de neuronas y sus infinitas conexiones tiende a compararse con una central telefónica, con una máquina cibernética, con un sistema organizacional holográ-...

  5. Importancia de la terapia física en la optimización de las manifestaciones incapacitantes y de la calidad de vida en pacientes con Esclerosis Lateral Amiotrófica: Revisión bibliográfica.

    OpenAIRE

    Olmo Treceño, Gema del

    2015-01-01

    La esclerosis lateral amiotrófica es la manifestación más frecuente de la enfermedad de la motoneurona. Se trata de una enfermedad neurodegenerativa, progresiva e incapacitante, caracterizada por la afectación de la primera y segunda neurona motora, con baja incidencia y prevalencia y escasa supervivencia. El tratamiento es sintomático, paliativo y multidisciplinar; el único medicamento que se prescribe es el riluzol, como tratamiento modificador de la acción del glutamato. ...

  6. Intervención sobre la señalización de receptores extrasinápticos y sinápticos de N-metil-Daspartato en la muerte neuronal excitotóxica

    OpenAIRE

    Guirao Salguero, Verónica

    2016-01-01

    [spa] La activación patológica de los receptores N-Metil-D-Aspartato (NMDARs), con la consiguiente desregulación del calcio intracelular, constituye la primera causa de muerte neuronal inducida por la isquemia (Arundine and Tymianski, 2004). Sin embargo, la actividad normal de estos receptores es crucial para la supervivencia y correcta funcionalidad de las neuronas. Lo que determina si la actividad de los NMDARs es neuroprotectora o inductora de muerte excitotóxica es la magnitud de la activ...

  7. Remodelado del calcio intracelular y susceptibilidad a la muerte neuronal en el envejecimiento y en la enfermedad de Alzheimer

    OpenAIRE

    Calvo Rodríguez, María

    2015-01-01

    a presente tesis doctoral se ha centrado en el estudio de la dishomeostasis del Ca2+ intracelular en el envejecimiento y en la Enfermedad de Alzhéimer como base para el desarrollo de nuevas estrategias eficaces en la prevención y/o el tratamiento de esta enfermedad. Nuestros resultados sugieren que el remodelado del Ca2+ intracelular, y particularmente la mayor captación de Ca2+ por la mitocondria, contribuyen a la mayor susceptibilidad a la muerte celular que aparece en las neuronas de hi...

  8. Agregación de alfa-sinucleína y degeneración Parkinsoniana

    OpenAIRE

    Fernández-Espejo, Emilio

    2013-01-01

    La alfa-sinucleína es la proteína principal de los cuerpos de Lewy, marcador anatomopatológico de la enfermedad de Parkinson. Dicha proteína puede ver alterada su conformación y adquirir capacidad autoagregante, lo que se relaciona con el depósito de agregados proteináceos en las neuronas y podría constituir un factor fisiopatológico importante en dicha enfermedad. Los agregados poseen fibrillas de alfa-sinucleína alterada, y las moléculas se encuentran unidas entre sí por enlaces no...

  9. Desarrollo neuromuscular en la atrofia muscular espinal

    OpenAIRE

    Martínez Hernàndez, Rebeca

    2012-01-01

    INTRODUCCIÓN: La atrofia muscular espinal (AME) es una enfermedad neuromuscular infantil caracterizada por la muerte de las neuronas motoras del asta anterior de la médula espinal. Como consecuencia de ello hay una degeneración y atrofia muscular, por lo que los pacientes mueren a menudo de insuficiencias respiratorias graves. La AME se clasifica en tres tipos principales según el grado de gravedad, la edad de aparición y las pautas motoras. Se trata de una enfermedad con patrón de herencia a...

  10. Redes neuronales analógicas para la computación paralela masiva de señales en tiempo real

    OpenAIRE

    Cancelo, Gustavo Indalecio Eugenio

    1996-01-01

    En esta tesis se realiza un estudio sobre las posibilidades de la electrónica para modelar unidades y sistemas neuronales. En particular, se proponen implementaciones de redes neuronales analógicas. La primera a nivel microelectrónico, comprende el diseño de una neurona computacional con función de activación gaussiana. Primeramente, se demostrará que las unidades computacionales con función de activación gaussiana forman una base para aproximadores universales de funciones continuas y discon...

  11. La teoría neuronal: primer principio de la neurociencia contemporánea

    OpenAIRE

    Lopera-Chaves, Marta

    2011-01-01

    El presente artículo es una reflexión derivada de la investigación “Aportaciones de Santiago Ramón y Cajal a las bases biológicas de los procesos cognitivos. Fase II: leyes y principios del funcionamiento nervioso”, financiada por el Conadi (Comité Nacional de Investigación) de la Universidad Cooperativa de Colombia, orientada a distinguir las aportaciones de Santiago Ramón y Cajal a las bases biológicas de los procesos cognitivos. La determinación del carácter individual de la neurona, su es...

  12. Caracterización del polimorfismo en el promotor del gen SLC6A4 (5HTTLPR) en una muestra de población colombiana con trastorno depresivo mayor: estudio piloto

    OpenAIRE

    Riveros Barrera, Irene

    2015-01-01

    Estudios han reportado que uno de los factores de riesgo genético para el desarrollo de depresión mayor es la presencia del alelo corto (s) del polimorfismo 5HTTLPR ubicado en el promotor del gen SLC6A4, que produce una menor actividad transcripcional y por lo tanto menor transporte de serotonina de una neurona a otra. Por esta razón procedimos a determinar el genotipo del polimorfismo en el promotor del gen SLC6A4 (5HTTLPR) en una muestra de población colombiana con trastorno depresivo mayor...

  13. Efecto de la pérdida de la inervación dopaminérgica del núcleo subtalámico sobre la conducta motora de ratas

    Directory of Open Access Journals (Sweden)

    Nancy Pavón-Fuentes

    2010-01-01

    Full Text Available Actualmente la enfermedad de Parkinson es considerada como un trastorno del sistema nervioso central que afecta a los ganglios basales. Las características anatomopatológicas más prominentes de esta enfermedad son: degeneración de las células dopaminérgicas de la substantia nigra pars compacta (SNc, la existencia de gliosis y la presencia de cuerpos eosinófilos de inclusión. La relevancia fisiológica de la modulación directa de las neuronas del núcleo subtalámico (NST por neuronas dopaminérgicas de la SNc deviene en un tema polémico. El objetivo de este trabajo fue evaluar el efecto de la lesión selectiva de las neuronas dopaminérgicas que inervan al NST sobre la conducta motora de ratas sanas. Se trabajó con tres grupos experimentales: I: con lesión de la SNc por 6-hidroxidopamina (6-OHDA (n = 20; II: con pérdida de la inervación dopaminérgica del núcleo subtalámico por inyección de 6-OHDA en dicho núcleo (n = 30 y III: control (n = 20. Un mes después de haber inyectado la neurotoxina, fue evaluada la actividad rotatoria inducida por D-anfetamina y apomorfina y las habilidades motoras de extremidades anteriores. Los estudios conductuales y morfológicos evidenciaron que la inyección de 6-OHDA en el NST, induce una pérdida parcial de neuronas en la SNc, en el hemisferio lesionado. La pérdida de la inervación dopaminérgica del NST provoca una asimetría en la conducta motora de los animales que se traduce en un peor desempeño en las habilidades de la extremidad anterior y una conducta motora rotacional intensa, ipsilateral al hemisferio lesionado como consecuencia de la administración de D-anfetamina.

  14. Efecto de fracciones orgánicas de agave angustifolia haw sobre deterioro cognitivo e inmunomodulación.

    OpenAIRE

    Alegría Herrera, Elian Yuritzi

    2016-01-01

    Las especies del género Agave poseen importantes propiedades farmacológicas, una de sus especies más representativas es Agave angustifolia Haw que tiene reportes de uso medicinal para trastornos con un índole inflamatorio; experimentalmente se ha demostrado que la planta posee efecto anti-oxidante, anti-inflamatorio e inmunomodulador. La inflamación periférica desencadena una respuesta neuroinflamatoria en donde participan la barrera hemato-encefálica, células de la glía y neuronas. La neu...

  15. Psicología y construcción de conocimiento en la época

    OpenAIRE

    Frenquelli, Roberto C.

    2009-01-01

    Mi propuesta se centrará en las consideraciones acerca de la Fisiología Humana, en especial la Neurofisiología, como un hilo conductor entre las nociones de Instinto, Apego, Intersubjetividad y Desarrollo del Pensamiento. Semejante recorrido, resultará fácil comprenderlo, sólo es posible encararlo bajo el paraguas de la Complejidad y lo que llamamos la Lógica de lo Viviente. De hecho, el concepto de Neuronas Espejo, acuñado por las investigaciones de Rizzolatti y colaboradores, será el eje so...

  16. Entorno virtual de visualización 3D de la vía óptica y sistema oculomotor, a partir de secciones seriadas de resonancia magnética

    OpenAIRE

    2011-01-01

    [ES] Los millones de neuronas localizadas en el cerebro reciben constantemente información que elaboran y procesan para, en muchos casos, tomar decisiones. Esta fuente de información está constituida principalmente por los sentidos. A su vez, el sistema nervioso central puede tomar la iniciativa y actuar sobre diversos órganos de los sentidos para regular su rendimiento. Una gran parte de la información que recibe el cerebro humano procede del sistema de recepción visual. El sistema de in...

  17. Factores implicados en la regulación del desarrollo de las vías del dolor.

    OpenAIRE

    Valdés Sánchez, Teresa

    2015-01-01

    En el presente trabajo de tesis doctoral hemos querido investigar aspectos de la regulación de las neuronas sensoriales periféricas que participan en la detección del dolor y, para ello, hemos estudiado la contribución de la neurotrofina BDNF y de la metaloproteasa MT-5 al desarrollo y mantenimiento de esta población sensorial de indudable inetrés biomédico. Los aspectos más destacables de los hallazgos pueden resumirse en: 1) hemos identificado por primera vez la dependencia trófica postnata...

  18. Activación de la neurogénesis en médula espinal de ratón adulto por factores embrionarios

    OpenAIRE

    Gómez Vicente, Beatriz

    2016-01-01

    Los procesos que tienen lugar tras la lesión medular incluyen la muerte de neuronas, oligodendrocitos, astrocitos, así como la formación de cavidades que pueden interrumpir las vías axonales ascendentes y descendentes. A su vez, existen señales tras la lesión medular que fomentarán la recuperación espontánea tras la proliferación de nuevos precursores neurales en el canal ependimario (células ependimarias). Sin embargo, la reparación espontánea es incompleta y se requiere inter...

  19. EFECTO DE LA VITAMINA C Y DE FACTORES LIBERADOS POR LAS MENINGES EN LA DIFERENCIACION IN VITRO DE LA GLIA RADIAL.

    OpenAIRE

    SILVA ALVAREZ; CARMEN INES

    2009-01-01

    Durante el desarrollo embrionario, las células troncales neurales dan origen a todas las neuronas del sistema nervioso central (SNC) de mamíferos. Usualmente, se consideran dos criterios para definir a una célula troncal, la auto-renovación, idealmente por un número ilimitado de divisiones celulares y la multi-potencialidad, es decir, la capacidad de originar a distintos tipos de células diferenciadas. Previo a la neurogénesis, la placa neural y el tubo neural se componen por sólo una c...

  20. MODULACION DE LA ACTIVIDAD SINAPTICA GABAERGICA POR COACTIVACION DE RECEPTORES PARA ENDOCANABINODES Y ACETILCOLINA EN EL HIPOCAMPO

    OpenAIRE

    COUVE PEREZ, ALEJANDRO

    2010-01-01

    El balance entre la actividad sináptica excitatoria e inhibitoria es fundamental para la regulación de la excitabilidad neuronal y plasticidad sináptica en el Sistema Nervioso Central (SNC) y periférico. Debido a que el control de la excitabilidad neuronal en el SNC es altamente dependiente del nivel de inhibición establecido por la actividad de interneuronas GABAérgicas, el estudio de los fenómenos que se encuentran regulando la actividad sináptica en este tipo de neuronas res...