Full Text Available Among the species of the order Primates exist a huge variety of forms and habitats. This heterogeneity has encouraged the evolution and development of a great number of locomotor adaptations to different environments. Thus, nowadays there are both arboreal and terrestrial groups within the order. The subfamily Cercopithecinae present taxa with both kinds of locomotor behaviours, although the most of them are adapted to a ground life-style. This group probably has an arboreal ancestor and its radiation is relatively recent. Consequently, species belonged to this group present mixed features or sometimes not too much derived ones. Likewise, it is important the fact that the evolutionary history and phylogeny of the group could influence in some characteristics. Both the calcaneum and the talus are two of the largest bones of the foot and are good for inferring the kind of locomotion. For this reason, it has been used these two tarsal bones to study the morphology of eight species of cercopithecines and then deduce functional implications of the kind of locomotion.
Dentro del orden Primates existe una gran variedad de especies distribuidas a lo largo de hábitats muy diversos. Dicha heterogeneidad ha fomentado la evolución y desarrollo de un gran número de adaptaciones locomotoras a los diferentes ambientes en los que habitan. Así, existen en la actualidad tanto grupos arborícolas como terrestres. La subfamilia Cercopithecinae agrupa una serie de taxones que representan ambos comportamientos locomotores, aunque la mayoría de las especies están adaptadas a una vida en el suelo. Se supone que este grupo desciende de un ancestro arborícola y que su radiación es relativamente reciente. En consecuencia, las especies de este grupo presentan características mixtas o poco derivadas en algunas ocasiones. Asimismo, es importante tener en cuenta la influencia que la herencia filogenética puede tener sobre alguno de estos rasgos. El calcáneo y el astrágalo son dos de los huesos más grandes del pie y ambos son buenos indicadores del tipo de locomoción. Por este motivo, se han utilizado estos dos tarsales para llevar a cabo el estudio de la morfología de ocho especies de cercopitecoideos, de tal manera que luego se ha podido hacer una serie de inferencias funcionales en cuanto al tipo de locomocón de las mismas.
Alba, David M; Carlos Calero, Juan Abel; Mancheño, Miguel Ángel; Montoya, Plini; Morales, Jorge; Rook, Lorenzo
The macaque material from the Early Pleistocene site of Quibas (Albanilla, Murcia, Spain), including dentognathic remains, isolated teeth and some postcranial bone fragments, is described. Both metrically and morphologically, this sample must be attributed to Macaca sylvanus (the Barbary macaque). This species is currently distributed through North Africa and Gibraltar, but was much more widely distributed during the Plio-Pleistocene, being represented by several European fossil subspecies. Metrical comparisons of dental size and proportions between extant M. s. sylvanus and fossil Macaca sylvanus florentina from the type locality and other Italian sites are undertaken, in order to classify the remains from Quibas at the subspecies level. The results show that the Quibas sample not only fits the range of variation of M. s. florentina from the type locality, but also differs from the extant Barbary macaque condition in several regards. This permits us to formally attribute the material from Quibas to M. s. florentina. The material described in this paper therefore significantly improves the knowledge of this fossil taxon, particularly regarding the upper dentition, and further confirms the taxonomic distinctiveness of this extinct taxon at the subspecies rank. Taken as a whole, M. s. florentina largely overlaps in dental dimensions with M. s. sylvanus, but differs from the latter by displaying (on average): (1) absolutely longer upper molars (especially M(1) and M(3)); (2) relatively wider upper molars (especially M(1) and M(2)); (3) longer M(3) as compared with the M(2); (4) absolutely longer M(1) and M(3); and (5) relatively narrower M(3). PMID:22014683
Full Text Available The Lion-tailed Macaque (Macaca silenus is a threatened species inhabiting the rainforests of the Western Ghats mountain range in southern India. Once assessed to be less than a thousand individuals remaining in the wild habitats, the population is now estimated to be between 3000 and 3500 individuals. However, the rainforest habitats of the species are highly fragmented. During the past three decades or less, the population of this species has severely declined due to habitat degradation and illegal hunting in several areas of its occurrence. In situ conservation programs included notification of certain areas as Lion-tailed Macaque conservation regions. Several captive breeding programs have been initiated in order to have a viable captive population of the species. However, the analysis reveals that both in situ and ex situ conservation programs have not achieved the desired success and the species is even more endangered than it was a few decades ago. In this article, we discuss these conservation programs and suggest further measures for effective conservation of Lion-tailed Macaques.
Ehlers, Bernhard; Spiess, Katja; Leendertz, Fabian;
lymphocryptoviruses (LCVs) are now known, with hosts from six primate families (Hominidae, Hylobatidae, Cercopithecidae, Atelidae, Cebidae and Pitheciidae). Further work extended genomic sequences for 25 LCVs to 3.4-7.4 kbp. Phylogenetic trees were constructed, based on alignments of protein sequences inferred from...... proposed that major elements of the LCV tree represented synchronous evolution with host lineages, with the earliest node in both trees being the separation of Old and New World lines, but that some virus lineages originated by interspecies transfer. From comparisons of branch lengths, it was inferred that...
Soledad Gómez, M; Gracenea, M; Montoliu, I; Feliu, C; Monleon, A; Fernandez, J; Enseñat, C
The faunistic results regarding intestinal parasitism by protozoa and helminths in 21 primate species (three Cebidae, thirteen Cercopithecidae, one Hylobatidae, one Lemuridae, three Pongidae) are reported. The primate species were housed in four separate galleries. Six faecal samples of each host species were subjected to coprological analysis. Fifteen parasite species were detected: 11 protozoa (Entamoeba coli, E. chattoni, E. hartmanni, Iodamoeba bütschlii, Endolimax nana, Giardia intestinalis, Chilomastix mesnilii, Enteromonas hominis, Trichomonas intestinalis, Balantidium coli, and Blastocystis hominis) and 4 helminths (Ancylostoma sp., Strongyloides fuelleborni, Strongyloides sp., and Trichuris trichiura). The results reveal certain parasitic similarities between host species housed in the same gallery; however, these primate species do not always carry identical parasite species. PMID:9210027
Infection with hepatitis B virus (HBV) has been detected in human populations throughout the world, as well as in a number of ape species (Pan troglodytes, Gorilla gorilla, gibbons [Nomascus and Hylobates species] and Pongo pygmaeus). To investigate the distribution of naturally occurring HBV infection in these species and other African Old World monkey species (Cercopithecidae), we screened 137 plasma samples from mainly wild caught animals by polymerase chain reaction (PCR) using several of highly conserved primers from the HB surface (HBs) gene, and for HBs antigen (HBsAg) by ELISA. None of the 93 Cercopithecidae screened (6 species) showed PCR or serology evidence for HBV infection; in contrast 2 from 8 chimpanzees and 5 from 22 gibbons were PCR-positive with each set of primers. Complete genome sequences from each of the positive apes were obtained and compared with all previously published complete and surface gene sequences. This extended phylogenetic analysis indicated that HBV variants from orangutans were interspersed by with HBV variants from southerly distributed gibbon species (H. agilis and H. moloch) occupying overlapping or adjacent habitat ranges with orangutans; in contrast, HBV variants from gibbon species in mainland Asia were phylogenetically distinct. A geographical rather than (sub)species association of HBV would account for the distribution of HBV variants in different subspecies of chimpanzees in Africa, and explain the inlier position of the previously described lowland gorilla sequence in the chimpanzee clade. These new findings have a number of implication for understanding the origins and epidemiology of HBV infection in non-human primates
Md Robiul Karim
Full Text Available To appreciate the genetic diversity and zoonotic implications of Enterocytozoon bieneusi in nonhuman primates (NHPs in zoos, we genotyped E. bieneusi in captive NHPs in seven zoos located at six major cities in China, using ribosomal internal transcribed spacer (ITS-based PCR and sequence analyses. A total of 496 fecal specimens from 36 NHP species under nine families were analyzed and E. bieneusi was detected in 148 (29.8% specimens of 25 NHP species from six families, including Cercopithecidae (28.7%, Cebidae (38.0%, Aotidae (75.0%, Lemuridae (26.0%, Hylobatidae (50.0% and Hominidae (16.2% (P = 0.0605. The infection rates were 29.0%, 15.2%, 18.2%, 37.3%, 29.2%, 37.7% and 44.8% in Shijiazhuang Zoo, Wuhan Zoo, Taiyuan Zoo, Changsha Wild Animal Zoo, Beijing Zoo, Shanghai Zoo and Shanghai Wild Animal Park, respectively (P = 0.0146. A total of 25 ITS genotypes were found: 14 known (D, O, EbpC, EbpA, Type IV, Henan-IV, BEB6, BEB4, Peru8, PigEBITS5, EbpD, CM1, CM4 and CS-1 and 11 new (CM8 to CM18. Genotype D was the most prevalent one (40/148, followed by CM4 (20/148, CM1 (15/148, O (13/148, CM16 (13/148, EbpC (11/148. Of them, genotypes D, EbpC, CM4 and O were widely distributed in NHPs (seen in 9 to 12 species whereas genotypes CM1 and CM16 were restricted to one to three NHP species. In phylogenetic analysis, 20 genotypes (121/148, 81.8%, excluding genotypes BEB4, BEB6, CM9, CM4 and CM18, belonged to group 1 with zoonotic potential. New genotype CM9 clustered in group 2 with BEB4 and BEB6. The remaining two genotypes CM4 and CM18 formed new cluster (group 9 in between two other genotypic clusters found in primates. The findings of high diversity in E. bieneusi genotypes and their zoonotic potentiality concluded the importance of captive NHPs as reservoir hosts for human microsporidiosis.
Jin, Zian; Sun, Tao; Xia, Xueshan; Wei, Qiujiang; Song, Yuzhu; Han, Qinqin; Chen, Qiang; Hu, Juan; Zhang, Jinyang
Background Herpes B virus (BV) is a zoonotic disease caused by double-stranded enveloped DNA virus with cercopithecidae as its natural host. The mortality rate of infected people could be up to 70% with fatal encephalitis and encephalomyelitis. Up to now, there are no effective treatments for BV infection. Among the various proteins encoded by monkey B virus, gD, a conserved structural protein, harbors important application value for serological diagnosis of frequent variations of the monkey B virus. Objectives This study aimed to expressed the gD protein of BV in Escherichia coli by a recombinant vector, and prepare specific monoclonal antibodies against gD of BV to pave the way for effective and quick diagnosis reagent research. Materials and Methods The gD gene of BV was optimized by OptimWiz to improve codon usage bias and synthesis, and the recombinant plasmid, pET32a/gD, was constructed and expressed in E. coli Rosetta (DE3). The expressed fusion protein, His-gD, was purified and the BALB/c mice were immunized by this protein. Spleen cells from the immunized mice and SP2/0 myeloma cells were fused together, and the monoclonal cell strains were obtained by indirect enzyme-linked immunosorbent assay (ELISA) screening, followed by preparation of monoclonal antibody ascetic fluid. Results The optimized gD protein was highly expressed in E. coli and successfully purified. Five monoclonal antibodies (mAbs) against BV were obtained and named as 4E3, 3F8, 3E7, 1H3 and 4B6, and with ascetic fluid titers of 2 × 106, 2 × 105, 2 × 105, 2 × 103 and 2 × 102, respectively. The 1H3 and 4E3 belonged to the IgG2b subclass, while 3E7, 3F8 and 4B6 belonged to the IgG1 subclass. Conclusions The cell lines obtained in this work secreted potent, stable and specific anti-BV mAbs, which were suitable for the development of herpes B virus diagnosis reagents.
Retief, J D; Dixon, G H
Protamines P1 and P2 form a family of small basic peptides that represent the major sperm proteins in placental mammals. In human and mouse protamine P2 is one of the most abundant sperm proteins. The protamine P2 gene codes for a P2 precursor, pro-P2 which is later processed by proteolytic cleavages in its N-terminal region to form the mature P2 protamines. We have used polymerase chain amplification to directly sequence the pro-P2 genes of the five major primate families: red howler (Alouatta seniculus) is a New World monkey (Cebidae); the two macaque species, Macaca mulatta and M. nemistrina are Old World monkeys (Cercopithecidae), the gibbon, Hylobates lar, represents one branch of the apes (Hylobatidae); the orangutan, Pongo pygmaeus, gorilla, Gorilla gorilla and two species of chimpanzee Pan paniscus and Pan troglodytes represent a second ape family (Pongidae). These pro-P2 genes are compared with that of human [Domenjoud, L., Nussbaum, G., Adham, I. M., Greeske, G. & Engel, W. (1990) Genomics 8, 127-133]. The overall size and organization of the genes are conserved within the group. The mean length of pro-P2 is 101 residues, with an increase to 102 in M. nemistrina and a decrease to 99 residues in red howler (A. seniculus). In gorilla and red howler one of two 79-bp tandem repeats that occurs 3' of the gene is deleted. Of the 101 deduced amino acids examined, an amino acid change occurs in one or more primates at 45 positions. Considering only the most recently diverged group, the human/gorilla/chimpanzee clade, this represents a very high mutation rate of 0.99 changes/100 sites in 10(6) years. This rapid mutation rate is characteristic of both members of the protamine gene family, P1 and P2. Consideration of the variable nature of the sequences at the multiple sites of proteolysis during the processing of the pro-P2 indicates either that there are several processing enzymes of differing specificities, or more likely that the folded structure of the pro-P2