首页> 外文期刊>The American Journal of Tropical Medicine and Hygiene >Development of multiplex real-time polymerase chain reaction for detection of Entamoeba histolytica, Entamoeba dispar, and Entamoeba moshkovskii in clinical specimens.
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Development of multiplex real-time polymerase chain reaction for detection of Entamoeba histolytica, Entamoeba dispar, and Entamoeba moshkovskii in clinical specimens.

机译:开发用于检测临床标本中的溶血性变形虫,变形虫和变形虫的多重实时聚合酶链反应。

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Multiplex real-time polymerase chain reaction (PCR) was developed for differential detection of Entamoeba histolytica, Entamoeba dispar, and Entamoeba moshkovskii. Specific primers were designed for all three species, and then differentiation of E. histolytica and E. dispar was achieved simultaneously using a hybridization probe and melting curve analysis, whereas E. moshkovskii was detected with a separate probe under the same condition. This assay detected as little as 0.2 pg of E. histolytica DNA and 2 pg each for E. dispar and E. moshkovskii DNA. Thirty-five clinical samples suspected to be E. histolytica infection by microscopy were tested. The results showed 32 positive samples; four samples were E. histolytica and 28 samples were E. dispar. Interestingly, one E. dispar positive sample showed a mixed infection with E. moshkovskii. This is the first report of E. moshkovskii infection from Thailand and this assay is currently the most rapid and sensitive method to differentiate these human amoebas.
机译:开发了多重实时聚合酶链反应(PCR)用于差异检测溶组织性变形虫,变形虫和变形虫。针对所有三个物种设计了特异性引物,然后使用杂交探针和解链曲线分析同时实现了溶组织性大肠杆菌和dispar的分化,而在相同条件下用单独的探针检测到了moshkovskii。该测定法检测到低至0.2 pg的溶组织性大肠杆菌DNA,而每个检测到的E. dispar和E. moshkovskii DNA均为2 pg。通过显微镜检查检查了35例怀疑是溶组织性大肠杆菌感染的临床样品。结果显示32份阳性样品。四个样品是溶组织性大肠杆菌,而28个样品是Dispar。有趣的是,一个Dispar阳性样本显示moshkovskii混合感染。这是来自泰国的E. moshkovskii感染的首次报道,该测定法是目前区分这些人类变形虫最快速,最灵敏的方法。

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