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Genetic variation of Enterobius vermicularis among schoolchildren in Thailand

Published online by Cambridge University Press:  29 October 2018

K. Tomanakan
Affiliation:
Department of Parasitology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand Research and Diagnostic Center for Emerging Infectious Diseases, Khon Kaen University, Khon Kaen, Thailand
O. Sanpool
Affiliation:
Department of Parasitology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand Research and Diagnostic Center for Emerging Infectious Diseases, Khon Kaen University, Khon Kaen, Thailand
P. Chamavit
Affiliation:
Department of Parasitology, Faculty of Science and Technology, Huachiew Chalermprakiet University, Samut Prakan, Thailand
V. Lulitanond
Affiliation:
Department of Microbiology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand
P.M. Intapan*
Affiliation:
Department of Parasitology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand Research and Diagnostic Center for Emerging Infectious Diseases, Khon Kaen University, Khon Kaen, Thailand
W. Maleewong
Affiliation:
Department of Parasitology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand Research and Diagnostic Center for Emerging Infectious Diseases, Khon Kaen University, Khon Kaen, Thailand
*
Author for correspondence: P.M. Intapan, E-mail: [email protected]

Abstract

Enterobiasis, caused by the nematode Enterobius vermicularis, is a common health problem among schoolchildren in Thailand. We provide the first molecular identification of this nematode from Thai schoolchildren and document genetic variation among E. vermicularis eggs using sequence analyses of the mitochondrial cytochrome c oxidase subunit 1 (cox1) gene and the nuclear ribosomal DNA second internal transcribed spacer (ITS2). A cross-sectional parasitological survey was conducted in schoolchildren (n = 491) in five regions of Thailand between May 2015 and December 2016. The diagnosis of Enterobius infection was made using the adhesive tape perianal swab technique. Enterobius eggs were recovered from 43 participants (8.75%). DNA was extracted from these eggs and the cox1 gene and partial ITS2 region amplified using the polymerase chain reaction (PCR). Nineteen amplified PCR products of the cox1 gene (441 bp) and 18 of the ITS2 region (623 bp) were subsequently sequenced. All sequences were identified as belonging to E. vermicularis based on database searches. Phylogenetic analysis and a median-joining network of available E. vermicularis cox1 sequences showed 66 haplotypes. We found haploclusters (types A and B) represented among the Thai sequences. Six haplotypes from Thailand fell into type A (of Nakano et al., 2006) (along with sequences from Japan and Korea) and five haplotypes into type B (with sequences from Japan, Iran, Czech Republic, Greece, Denmark and Sudan). The overall haplotype diversity (Hd) was 0.9888. Transmission of worms with type B haplotypes from primates to humans in Asia or from humans in Europe possibly occurs in Thailand.

Type
Research Paper
Copyright
Copyright © Cambridge University Press 2018 

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References

Beaver, PC, Jung, RC and Cupp, EW (1984) Examination of specimens for parasites. In Beaver, PC, Jung, RC and Cupp, EW (eds), Clinical Parasitology, 9th edn. Philadelphia: Lea & Febiger, pp. 733758.Google Scholar
Bethony, J et al. (2006) Soil-transmitted helminth infections: ascariasis, trichuriasis, and hookworm. Lancet 367, 15211532.Google Scholar
Blouin, MS (2002) Molecular prospecting for cryptic species of nematodes: mitochondrial DNA versus internal transcribed spacer. International Journal for Parasitology 32, 527531.Google Scholar
Cerva, L, Schrottenbaum, M and Kliment, V (1991) Intestinal parasites: a study of human appendices. Folia Parasitologica (Praha) 38, 59.Google Scholar
Ferrero, MR et al. (2013) Genetic variation in mitochondrial DNA among Enterobius vermicularis in Denmark. Parasitology 140, 109114.Google Scholar
Hagh, VRH et al. (2014) Genetic classification and differentiation of Enterobius vermicularis based on mitochondrial cytochrome c oxidase (cox1) in northwest of Iran. Journal of Pure and Applied Microbiology 8, 39953999.Google Scholar
Hall, TA (1999) BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symposium Series 41, 9598.Google Scholar
Hasegawa, H, Sato, H and Torii, H (2012) Redescription of Enterobius (Enterobius) macaci Yen, 1973 (Nematoda: Oxyuridae: Enterobiinae) based on material collected from wild Japanese macaque, Macaca fuscata (Primates: Cercopithecidae). Journal of Parasitology 98, 152915.Google Scholar
Iniguez, AM et al. (2006) SL1 RNA gene recovery from Enterobius vermicularis ancient DNA in pre-Columbian human coprolites. International Journal for Parasitology 36, 14191425.Google Scholar
Jongsuksantigul, P, Chaeychomsri, W and Techamontrikul, P (1992) Study on prevalence and intensity of intestinal helminthiasis and opisthorchiasis in Thailand. Journal of Tropical Medicine and Parasitology 15, 8095.Google Scholar
Kaewkes, S et al. (1983) Enterobiasis in young schoolchildren in Khon Kaen. Journal of Tropical Medicine and Parasitology 6, 1924.Google Scholar
Kang, S et al. (2009) The mitochondrial genome sequence of Enterobius vermicularis (Nematoda: Oxyurida) - an idiosyncratic gene order and phylogenetic information for chromadorean nematodes. Gene 429, 8797.Google Scholar
Kim, DH et al. (2013) Environmental factors related to enterobiasis in a southeast region of Korea. Korean Journal of Parasitology 51, 139142.Google Scholar
Kim, DH and Yu, HS (2014) Effect of a one-off educational session about enterobiasis on knowledge, preventative practices, and infection rates among schoolchildren in South Korea. PLoS ONE 9(11), e112149.Google Scholar
Kucik, CJ, Martin, GL and Sortor, BV (2004) Common intestinal parasites. American Family Physician 69, 11611168.Google Scholar
Kubiak, K, Dzika, E and Paukszto, Ł (2017) Enterobiasis epidemiology and molecular characterization of Enterobius vermicularis in healthy children in north-eastern Poland. Helminthologia 54, 284291.Google Scholar
Le, TH, Blair, D and McManus, DP (2000) Mitochondrial genomes of human helminths and their use as markers in population genetics and phylogeny. Acta Tropica 77, 243256.Google Scholar
Librado, P and Rozas, J (2009) DnaSP v5: a software for comprehensive analysis of DNA polymorphism data. Bioinformatics 25, 14511452.Google Scholar
Li, HM et al. (2015) Risk factors for Enterobius vermicularis infection in children in Gaozhou, Guangdong, China. Infectious Diseases of Poverty 4, 28.Google Scholar
Nakano, T et al. (2006) Mitochondrial cytochrome c oxidase subunit 1 gene and nuclear rDNA regions of Enterobius vermicularis parasitic in captive chimpanzees with special reference to its relationship with pinworms in humans. Parasitology Research 100, 5157.Google Scholar
Nei, M and Kumar, S (2000) Molecular Evolution and Phylogenetics. New York, NY: Oxford University Press.Google Scholar
Nithikathkul, C et al. (2001) The prevalence of Enterobius vermicularis among primary school students in Samutprakan Province, Thailand. Southeast Asian Journal of Tropical Medicine and Public Health 32, 133137.Google Scholar
Pampiglione, S and Rivasi, F (2009) Enterobiasis in ectopic locations mimicking tumor-like lesions. International Journal of Microbiology 2009, 642481.Google Scholar
Park, JH et al. (2005) A survey of Enterobius vermicularis infection among children on western and southern coastal islands of the Republic of Korea. Korean Journal of Parasitology 43, 129134.Google Scholar
Piperaki, ET et al. (2011) Characterization of Enterobius vermicularis in a human population, employing a molecular-based method from adhesive tape samples. Molecular and Cellular Probes 25, 121125.Google Scholar
Polseela, P et al. (2004) Parasitic infection among primary schoolchildren in Meuang district, Phitsanulok province, Thailand. Southeast Asian Journal of Tropical Medicine and Public Health 35, 120123.Google Scholar
Saksirisampant, W et al. (2006) Prevalence of intestinal parasitic infections among schoolchildren in the central region of Thailand. Journal of the Medical Association of Thailand 89, 19281933.Google Scholar
Serpytis, M and Seinin, D (2012) Fatal case of ectopic enterobiasis: Enterobius vermicularis in the kidneys. Scandinavian Journal of Urology and Nephrology 46, 7072.Google Scholar
Tamura, K et al. (2013) MEGA6 : molecular evolutionary genetics analysis version 6.0. Molecular Biology and Evolution 30, 27252729.Google Scholar
Thompson, JD, Higgins, DG and Gibson, TJ (1994) CLUSTALW: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Research 22, 46734680.Google Scholar
Zelck, UE, Bialek, R and Weiss, M (2011) Molecular phylogenetic analysis of Enterobius vermicularis and development of an 18S ribosomal DNA-targeted diagnostic PCR. Journal of Clinical Microbiology 49, 16021604.Google Scholar
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