MyMedR

Occurrence of gastrointestinal nematodes in captive nonhuman primates at Matang Wildlife Centre, Sarawak

Teo SZ, Tuen AA, Madinah A, Aban S, Chong YL

Trop Biomed, 2019 Sep 01;36(3):594-603.

Gastrointestinal nematodes can cause assorted health problems to human and other primates. The status of gastrointestinal nematodes in non-human primates remained less documented in Malaysia. This study aimed to determine the occurrence of gastrointestinal nematodes recovered from the fecal samples of captive non-human primates at the Matang Wildlife Centre (MWC), Sarawak. Fresh fecal samples were collected from 60 non-human primates of six species (i.e. Orangutan, Bornean gibbon, Silvered Leaf monkey, Slow loris, Pig-tailed macaque, and Long-tailed macaque) and processed using simple fecal floatation method and fecal sedimentation method. This study shows high prevalence of nematode infection (>=50%) and co-infection (22 from 45 infected individuals) in all species of captive non-human primates found in MWC, except one individual of young Silvered Leaf monkey was negative for nematode. From these, eight genera of 11 species and one unknown nematode larvae were recovered and among them Oesophagostomum sp., Ascaris sp., and Strongyloides sp. were the most common nematodes infecting the non-human primates. All the Bornean gibbon (n=7) were found to be infected with nematodes. Moreover, Long-tailed macaques at the centre were heavily infected by Ascaris sp. (number of total count, nt = 2132; total mean abundance, MA=113.70). This is the first report of high prevalence nematode infection on multiple species of captive non-human primates in a wildlife centre located in Sarawak. Some of the nematodes are of zoonotic potential. This information is important for health care management, both in-situ and ex-situ conservations of captive and free-ranging nonhuman primates.

Matched MeSH terms: Monkey Diseases/epidemiology; Monkey Diseases/parasitology*

Serological evidence of infection with Tana and Yaba pox viruses among several species of monkey

Downie AW

J Hyg (Lond), 1974 Apr;72(2):245-50.

PMID: 4362411

Sera from cynomolgus monkeys from Malaysia, from Indian rhesus monkeys, from various species of monkeys from Africa and from South America have been examined for neutralizing antibody to Tanapox and Yaba viruses. No antibody was found to either virus in the sera of rhesus monkeys or South American monkeys. A certain proportion of sera from cynomolgus monkeys and various species of African monkey showed antibody to one or other of the viruses, but few of the positive sera showed antibody to both. The results would seem to suggest that infection with the two viruses is endemic in African and Malaysian monkeys but does not occur or is very rare in Indian rhesus and New World monkeys.

Matched MeSH terms: Monkey Diseases/immunology; Monkey Diseases/epidemiology*

Gastrointestinal parasites of zoonotic importance observed in the wild, urban, and captive populations of non-human primates in Malaysia

Adrus M, Zainudin R, Ahamad M, Jayasilan MA, Abdullah MT

J Med Primatol, 2019 02;48(1):22-31.

PMID: 30370934 DOI: 10.1111/jmp.12389

BACKGROUND: A study was undertaken to determine gastrointestinal (GI) parasites commonly found in Malaysia's non-human primates (NHP) living in three different types of populations (wild, urban, and captive) and the basis of major GI parasites of zoonotic importance.

METHODS: A total of 308 samples was collected and microscopically screened from the NHP in the wild (n = 163), urban (n = 76), and captive (n = 69) populations. The samples were taken from 12 species of local NHPs.

RESULTS: At least, 44 species of GI parasites comprising of protozoans (seven species), nematodes (26 species), cestodes (five species), trematodes (five species), and pentastomida (one species) were detected. There were no significant differences for the overall prevalence and no great differences in GI parasite species among the wild, urban, and captive NHP populations.

CONCLUSION: The most common GI parasite was Ascaris spp. (49.7%), followed by Oesophagostomum spp. (26.9%), and 31 species discovered in this study are of known public health importance.

Matched MeSH terms: Monkey Diseases/epidemiology*; Monkey Diseases/parasitology

Microfilarial granulomas in the spleens of wild-caught cynomolgus monkeys (Macaca fascicularis)

Narama I, Miura K, Tsuruta M, Tsuchitani M

Vet Pathol, 1985 Jul;22(4):355-62.

PMID: 4035940

Splenic nodules from 38 cynomolgus monkeys (Macaca fascicularis) which were captured in Malaysia and Indonesia were studied histologically. The lesions were characterized by well-circumscribed focal fibrosis, accumulation of eosinophils and histiocytes, hemorrhage or hemosiderosis, and loss of normal splenic architecture. Small arteries in the lesion frequently had intimal thickening and narrowing of the lumen in addition to the presence of microfilariae. Microfilariae were also seen in the extravascular area of the lesion, and were occasionally engulfed by multinucleated giant cells. The splenic lesion was thought to have been initiated by incomplete infarction caused by intimal thickening and microfilarial occupation of the small arteries.

Matched MeSH terms: Monkey Diseases/parasitology; Monkey Diseases/pathology*

Fulltext Phylogeographic Evidence for 2 Genetically Distinct Zoonotic Plasmodium knowlesi Parasites, Malaysia

Yusof R, Ahmed MA, Jelip J, Ngian HU, Mustakim S, Hussin HM, et al.

Emerg Infect Dis, 2016 Aug;22(8):1371-80.

PMID: 27433965 DOI: 10.3201/eid2208.151885

Infections of humans with the zoonotic simian malaria parasite Plasmodium knowlesi occur throughout Southeast Asia, although most cases have occurred in Malaysia, where P. knowlesi is now the dominant malaria species. This apparently skewed distribution prompted an investigation of the phylogeography of this parasite in 2 geographically separated regions of Malaysia, Peninsular Malaysia and Malaysian Borneo. We investigated samples collected from humans and macaques in these regions. Haplotype network analyses of sequences from 2 P. knowlesi genes, type A small subunit ribosomal 18S RNA and cytochrome c oxidase subunit I, showed 2 genetically distinct divergent clusters, 1 from each of the 2 regions of Malaysia. We propose that these parasites represent 2 distinct P. knowlesi types that independently became zoonotic. These types would have evolved after the sea-level rise at the end of the last ice age, which separated Malaysian Borneo from Peninsular Malaysia.

Matched MeSH terms: Monkey Diseases/epidemiology; Monkey Diseases/parasitology*

Fulltext Macacine Herpesvirus 1 in Long-Tailed Macaques, Malaysia, 2009-2011

Lee MH, Rostal MK, Hughes T, Sitam F, Lee CY, Japning J, et al.

Emerg Infect Dis, 2015 Jul;21(7):1107-13.

PMID: 26080081 DOI: 10.3201/eid2107.140162

Macacine herpesvirus 1 (MaHV1; B virus) naturally infects macaques (Macaca spp.) and can cause fatal encephalitis in humans. In Peninsular Malaysia, wild macaques are abundant, and translocation is used to mitigate human-macaque conflict. Most adult macaques are infected with MaHV1, although the risk for transmission to persons who handle them during capture and translocation is unknown. We investigated MaHV1 shedding among 392 long-tailed macaques (M. fascicularis) after capture and translocation by the Department of Wildlife and National Parks in Peninsular Malaysia, during 2009-2011. For detection of MaHV1 DNA, PCR was performed on urogenital and oropharyngeal swab samples. Overall, 39% of macaques were shedding MaHV1 DNA; rates of DNA detection did not differ between sample types. This study demonstrates that MaHV1 was shed by a substantial proportion of macaques after capture and transport and suggests that persons handling macaques under these circumstances might be at risk for exposure to MaHV1.

Matched MeSH terms: Monkey Diseases/epidemiology; Monkey Diseases/virology*

Fulltext Admixture in Humans of Two Divergent Plasmodium knowlesi Populations Associated with Different Macaque Host Species

Divis PC, Singh B, Anderios F, Hisam S, Matusop A, Kocken CH, et al.

PLoS Pathog, 2015 May;11(5):e1004888.

PMID: 26020959 DOI: 10.1371/journal.ppat.1004888

Human malaria parasite species were originally acquired from other primate hosts and subsequently became endemic, then spread throughout large parts of the world. A major zoonosis is now occurring with Plasmodium knowlesi from macaques in Southeast Asia, with a recent acceleration in numbers of reported cases particularly in Malaysia. To investigate the parasite population genetics, we developed sensitive and species-specific microsatellite genotyping protocols and applied these to analysis of samples from 10 sites covering a range of >1,600 km within which most cases have occurred. Genotypic analyses of 599 P. knowlesi infections (552 in humans and 47 in wild macaques) at 10 highly polymorphic loci provide radical new insights on the emergence. Parasites from sympatric long-tailed macaques (Macaca fascicularis) and pig-tailed macaques (M. nemestrina) were very highly differentiated (FST = 0.22, and K-means clustering confirmed two host-associated subpopulations). Approximately two thirds of human P. knowlesi infections were of the long-tailed macaque type (Cluster 1), and one third were of the pig-tailed-macaque type (Cluster 2), with relative proportions varying across the different sites. Among the samples from humans, there was significant indication of genetic isolation by geographical distance overall and within Cluster 1 alone. Across the different sites, the level of multi-locus linkage disequilibrium correlated with the degree of local admixture of the two different clusters. The widespread occurrence of both types of P. knowlesi in humans enhances the potential for parasite adaptation in this zoonotic system.

Matched MeSH terms: Monkey Diseases/epidemiology*; Monkey Diseases/parasitology; Monkey Diseases/transmission

Malaysian primate trypanosomes: intra-cytoplasmic pigment

Weinman D

Southeast Asian J. Trop. Med. Public Health, 1971 Mar;2(1):87.

PMID: 5000126

Matched MeSH terms: Monkey Diseases

Biology of the simian malarias of southeast Asia. II. The susceptibility of some Malaysian mosquitoes to infection with five strains of Plasmodium cynomolgi

Bennett GF, Warren M, Cheong WH

J Parasitol, 1966 Aug;52(4):625-31.

PMID: 5969101

Matched MeSH terms: Monkey Diseases

[Incidence of diarrhea and antibiotic therapy in cynomolgus monkeys imported for medical use (author's transl)]

Takasaka M, Morota S, Kasono T, Abe M, Honjo S

Jikken Dobutsu, 1973 Jul;22(3):227-36.

PMID: 4204642

Matched MeSH terms: Monkey Diseases/drug therapy; Monkey Diseases/microbiology; Monkey Diseases/epidemiology*

Some aspects of the nonhuman primates of West Malaysia: captivity to the laboratory

Retnasabapathy A

Jikken Dobutsu, 1973;22 Suppl(0):343-50.

PMID: 4213539

Matched MeSH terms: Monkey Diseases

Fulltext Blood meal analysis of Anopheles vectors of simian malaria based on laboratory and field studies

Jeyaprakasam NK, Low VL, Liew JWK, Pramasivan S, Wan-Sulaiman WY, Saeung A, et al.

Sci Rep, 2022 01 10;12(1):354.

PMID: 35013403 DOI: 10.1038/s41598-021-04106-w

Blood feeding and host-seeking behaviors of a mosquito play an imperative role in determining its vectorial capacity in transmitting pathogens. Unfortunately, limited information is available regarding blood feeding behavior of Anopheles species in Malaysia. Collection of resting Anopheles mosquitoes for blood meal analysis poses a great challenge especially for forest dwelling mosquitoes. Therefore, a laboratory-based study was conducted to evaluate the potential use of mosquitoes caught using human landing catch (HLC) for blood meal analysis, and subsequently to document blood feeding behavior of local Anopheles mosquitoes in Peninsular Malaysia. The laboratory-based experiment from this study revealed that mosquitoes caught using HLC had the potential to be used for blood meal analysis. Besides HLC, mosquitoes were also collected using manual aspirator and Mosquito Magnet. Overall, 47.4% of 321 field-caught Anopheles mosquitoes belonging to six species were positive for vertebrate host DNA in their blood meal. The most frequent blood meal source was human (45.9%) followed by wild boar (27.4%), dog (15.3%) and monkey (7.5%). Interestingly, only Anopheles cracens and Anopheles introlatus (Leucosphyrus Group) fed on monkey. This study further confirmed that members of the Leucosphyrus Group are the predominant vectors for knowlesi malaria transmission in Peninsular Malaysia mainly due to their simio-anthropophagic feeding behavior.

Matched MeSH terms: Monkey Diseases/blood; Monkey Diseases/parasitology; Monkey Diseases/transmission*

Fulltext Characterizing the genetic diversity of the monkey malaria parasite Plasmodium cynomolgi

Sutton PL, Luo Z, Divis PCS, Friedrich VK, Conway DJ, Singh B, et al.

Infect Genet Evol, 2016 06;40:243-252.

PMID: 26980604 DOI: 10.1016/j.meegid.2016.03.009

Plasmodium cynomolgi is a malaria parasite that typically infects Asian macaque monkeys, and humans on rare occasions. P. cynomolgi serves as a model system for the human malaria parasite Plasmodium vivax, with which it shares such important biological characteristics as formation of a dormant liver stage and a preference to invade reticulocytes. While genomes of three P. cynomolgi strains have been sequenced, genetic diversity of P. cynomolgi has not been widely investigated. To address this we developed the first panel of P. cynomolgi microsatellite markers to genotype eleven P. cynomolgi laboratory strains and 18 field isolates from Sarawak, Malaysian Borneo. We found diverse genotypes among most of the laboratory strains, though two nominally different strains were found to be genetically identical. We also investigated sequence polymorphism in two erythrocyte invasion gene families, the reticulocyte binding protein and Duffy binding protein genes, in these strains. We also observed copy number variation in rbp genes.

Matched MeSH terms: Monkey Diseases/parasitology*

Hepatitis A virus in primates outside captivity

Lancet, 1981 Oct 24;2(8252):928-9.

PMID: 6117705

Matched MeSH terms: Monkey Diseases/microbiology*

Dipetalonema digitatum (Chandler 1929) infection in the leaf monkey, Presbytis obscura (Reid)

Mak JW, Inder-Singh, Yen PK, Yap LF

Southeast Asian J. Trop. Med. Public Health, 1980 Mar;11(1):141.

PMID: 6773151

Matched MeSH terms: Monkey Diseases/parasitology*

Group A rotavirus infection in animals from an animal house and in wild-caught monkeys

Awang A, Yap K

J Diarrhoeal Dis Res, 1990 Sep;8(3):82-6.

PMID: 2122998

Randomly selected samples from different animal colonies from two laboratory animal houses and from the wild-caught monkeys were tested for the presence of anti-rotavirus antibodies to estimate the rates of infection with group A rotavirus. Antibodies to the common group A rotaviral antigen were detected by a competitive enzyme-linked immunosorbent assay (ELISA) using reagents of WHO ELISA rotavirus detection kit. The results of the study showed that white mice, albino rats, and guinea pigs from long-established breeding colonies and resident house rats and house shrews from the animal house had no serological evidence of rotaviral infection. In contrast, one mousedeer from a colony of 19 animals and most of the rabbits from two separate breeding colonies at the same animal house were serologically positive for the infection. Also a significant number of the same species of monkey kept in captivity were found to acquire the infection. Leaf monkeys had no serological evidence of rotaviral infection. The infection rate in wild cynomolgus monkeys did not seem to be influenced by the different ecological environments of their respective habitats. The rate of infection in adults and juveniles was similar.

Matched MeSH terms: Monkey Diseases/epidemiology*

Natural virus infections in cynomolgus monkeys

Suzuki M

Jpn. J. Med. Sci. Biol., 1981 Aug;34(4):261-3.

PMID: 7321300

Matched MeSH terms: Monkey Diseases/epidemiology*

Serologic survey with the sera of monkeys in regard to their natural infection with measles virus

Yamanouchi K, Fukuda A, Kobune F, Hikita M, Shishido A

Jpn. J. Med. Sci. Biol., 1969 Apr;22(2):117-21.

PMID: 4981321

Matched MeSH terms: Monkey Diseases/immunology*

Simian malarias in man: facts, implications, and predictions