| Literature DB >> 28500375 |
Tongjit Thanchomnang1,2, Pewpan M Intapan2,3, Oranuch Sanpool1,2,3, Rutchanee Rodpai2,3, Somjintana Tourtip1, Sujitra Yahom1, Jitsuda Kullawat1, Prayong Radomyos1, Chalida Thammasiri4, Wanchai Maleewong5,6.
Abstract
The parasitic nematodes, Strongyloides stercoralis and Strongyloides fuelleborni, can infect humans and non-human primates. We amplified and sequenced a portion of the 18S ribosomal RNA gene (rRNA) and of the mitochondrial cytochrome c oxidase subunit 1 (cox1) gene of Strongyloides from humans in the study area in Thailand, where people have frequent contact with long-tailed macaques. Fresh stool samples were obtained from 213 people and were examined using the agar plate culture method. The overall prevalence of Strongyloides infection was 8.92% (19/213). From a total of 19 worms (one per infected person), 18 adult males had 18S rRNA sequences identical with that of S. stercoralis and one adult female had a sequence almost identical with that of S. fuelleborni. A median-joining network of cox1 sequences revealed nine new haplotypes from S. stercoralis, and an overall haplotype diversity (Hd) of 0.9309. The single haplotype of S. fuelleborni was also new and contributed to an overall haplotype diversity for that species of 0.9842. This is the first molecular identification of S. stercoralis and S. fuelleborni in a human community having contact with long-tailed macaques in Thailand. It is also the first report of S. fuelleborni infecting a human in Thailand.Entities:
Keywords: Molecular identification; Strongyloides fuelleborni; Strongyloides stercoralis; Strongyloidiasis
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Year: 2017 PMID: 28500375 DOI: 10.1007/s00436-017-5469-z
Source DB: PubMed Journal: Parasitol Res ISSN: 0932-0113 Impact factor: 2.289