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Molecular diagnosis of strongyloidiasis in tropical areas: a comparisonof conventional and real-time polymerase chain reaction with parasitologicalmethods

机译:热带地区强线虫病的分子诊断:比较寄生虫学的常规实时聚合酶链反应的研究方法

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摘要

This study aimed to evaluate the use of conventional polymerase chain reaction (cPCR) and real-time quantitative PCR (qPCR) in the diagnosis of human strongyloidiasis from stool samples in tropical areas. Stool samples were collected from individuals and were determined to be positive for Strongyloides stercoralis (group I), negative for S. stercoralis (group II) and positive for other enteroparasite species (group III). DNA specific to S. stercoralis was found in 76.7% of group I samples by cPCR and in 90% of group I samples by qPCR. The results show that molecular methods can be used as alternative tools for detecting S. stercoralis in human stool samples in tropical areas.
机译:这项研究旨在评估常规聚合酶链反应(cPCR)和实时定量PCR(qPCR)在热带地区粪便样本中诊断人类圆线虫病的应用。从个体收集粪便样品,并确定它们对固结线虫(Strongyloides stercoralis)呈阳性(I组),对固醇链球菌(S. stercoralis)呈阴性(II组),对其他肠寄生虫物种呈阳性(III组)。通过cPCR在I组样本中有76.7%发现了对葡萄球菌特异的DNA,通过qPCR在I组样本中有90%发现了对S. stercoralis特异的DNA。结果表明,分子方法可作为检测热带地区人粪便样本中固醇链球菌的替代工具。

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