Publication:
Development of a real-time PCR assay with fluorophore-labelled hybridization probes for detection of Schistosoma mekongi in infected snails and rat feces

dc.contributor.authorO. Sanpoolen_US
dc.contributor.authorP. M. Intapanen_US
dc.contributor.authorT. Thanchomnangen_US
dc.contributor.authorP. Sri-Aroonen_US
dc.contributor.authorV. Lulitanonden_US
dc.contributor.authorL. Sadaowen_US
dc.contributor.authorW. Maleewongen_US
dc.contributor.otherKhon Kaen Universityen_US
dc.contributor.otherMahasarakham Universityen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-06-11T04:29:55Z
dc.date.available2018-06-11T04:29:55Z
dc.date.issued2012-09-01en_US
dc.description.abstractSchistosoma mekongi, a blood-dwelling fluke, is a water-borne parasite that is found in communities along the lower Mekong River basin, i.e. Cambodia and Lao People's Democratic Republic. This study developed a real-time PCR assay combined with melting-curve analysis to detect S. mekongi in laboratory setting conditions, in experimentally infected snails, and in fecal samples of infected rats. The procedure is based on melting-curve analysis of a hybrid between an amplicon from S. mekongi mitochondrion sequence, the 260 bp sequence specific to S. mekongi, and specific fluorophore-labelled probes. This method could detect as little as a single cercaria artificially introduced into a pool of 10 non-infected snails, a single cercaria in filtered paper, and 2 eggs inoculated in 100 mg of non-infected rat feces. All S. mekongi-infected snails and fecal samples from infected rats were positive. Non-infected snails, non-infected rat feces, and genomic DNA of other parasites were negative. The method gave high sensitivity and specificity, and could be applied as a fast and reliable tool for cercarial location in water environments in endemic areas and for epidemiological studies and eradication programmes for intermediate hosts. © 2012 Cambridge University Press.en_US
dc.identifier.citationParasitology. Vol.139, No.10 (2012), 1266-1272en_US
dc.identifier.doi10.1017/S0031182012000649en_US
dc.identifier.issn14698161en_US
dc.identifier.issn00311820en_US
dc.identifier.other2-s2.0-84866082181en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/13410
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84866082181&origin=inwarden_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleDevelopment of a real-time PCR assay with fluorophore-labelled hybridization probes for detection of Schistosoma mekongi in infected snails and rat fecesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84866082181&origin=inwarden_US

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