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2.
J Parasitol ; 96(5): 954-60, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20950104

ABSTRACT

In order to obtain basic data on parasitic infections of Bornean orangutans, Pongo pygmaeus morio (Owen, 1837), in Danum Valley, Sabah, Malaysia, fecal examinations were conducted. Based on a total of 73 fecal samples from 25 individuals, cysts of Entamoeba coli, Entamoeba spp., and Chilomastix mesnili, cysts and trophozoites of Balantidium coli, and eggs of Trichuris sp. or spp., unknown strongylid(s), Strongyloides fuelleborni, and an unknown oxyurid, plus a rhabditoid larva of Strongyloides sp., were found. Mature and immature worms of Pongobius hugoti Barus et al., 2007 and Pongobius foitovae n. sp. (Oxyuridae: Enterobiinae) were recovered from fecal debris and described. Pongobius foitovae is readily distinguished from P. hugoti by having a much longer esophageal corpus, a longer and distally hooked spicule in males, and a more posteriorly positioned vulva in female. Presence of plural species of non- Enterobius pinworms is a remarkable feature of the orangutan-pinworm relationship, which may reflect speciation process of the orangutans, host switching, and coevolution by pinworms.


Subject(s)
Ape Diseases/parasitology , Oxyuriasis/veterinary , Oxyuroidea/classification , Parasitic Diseases, Animal/parasitology , Pongo pygmaeus/parasitology , Animals , Ape Diseases/epidemiology , Borneo/epidemiology , Feces/parasitology , Female , Malaysia/epidemiology , Male , Oxyuriasis/epidemiology , Oxyuriasis/parasitology , Oxyuroidea/anatomy & histology , Oxyuroidea/isolation & purification , Parasitic Diseases, Animal/epidemiology
3.
Parasitol Int ; 59(3): 407-13, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20621633

ABSTRACT

In order to identify the causative agent of imported strongyloidiasis found in a Japanese mammalogist, who participated in a field survey in Tanzania, the hyper-variable region IV (HVR-IV) of 18S ribosomal DNA and partial mitochondrial cytochrome c-oxidase subunit 1 gene (cox1) were analyzed and compared with Strongyloides fuelleborni collected from apes and monkeys of Africa and Japan, and S. stercoralis from humans, apes and dogs. The HVR-IV and cox1 of the patient's worms were identical to or only slightly differed from those of worms parasitic in Tanzanian chimpanzees and yellow baboons, demonstrating that the patient acquired the infection during her field survey in Tanzania. Phylogenetic analysis with the maximum-likelihood method largely divided isolates of S. fuelleborni into three groups, which corresponded to geographical localities but not to host species. Meanwhile, isolates of S. stercoralis were grouped by the phylogenetic analysis into dog-parasitic and primate-parasitic clades, and not to geographical regions. It is surmised that subspeciation has occurred in S. fuelleborni during the dispersal of primates in Africa and Asia, while worldwide dispersal of S. stercoralis seems to have occurred more recently by migration and the activities of modern humans.


Subject(s)
Cyclooxygenase 1/genetics , RNA, Ribosomal, 18S/genetics , Strongyloides/classification , Strongyloides/genetics , Strongyloidiasis/parasitology , Amino Acid Sequence , Animals , Ape Diseases/parasitology , DNA, Helminth/analysis , DNA, Mitochondrial/genetics , Dog Diseases/parasitology , Dogs , Female , Host-Parasite Interactions , Humans , Japan , Molecular Sequence Data , Monkey Diseases/parasitology , Sequence Analysis, DNA , Species Specificity , Strongyloides/isolation & purification , Strongyloides/physiology , Strongyloidiasis/veterinary , Tanzania
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