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Development of a polymerase chain reaction applicable to rapid and sensitive detection of Clonorchis sinensis eggs in human stool samples

机译:聚合酶链反应的开发适用于快速灵敏地检测人粪便样本中的华支睾吸虫卵

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摘要

Microscopic examination of eggs of parasitic helminths in stool samples has been the most widely used classical diagnostic method for infections, but tiny and low numbers of eggs in stool samples often hamper diagnosis of helminthic infections with classical microscopic examination. Moreover, it is also difficult to differentiate parasite eggs by the classical method, if they have similar morphological characteristics. In this study, we developed a rapid and sensitive polymerase chain reaction (PCR)-based molecular diagnostic method for detection of Clonorchis sinensis eggs in stool samples. Nine primers were designed based on the long-terminal repeat (LTR) of C. sinensis retrotransposon1 (CsRn1) gene, and seven PCR primer sets were paired. Polymerase chain reaction with each primer pair produced specific amplicons for C. sinensis, but not for other trematodes including Metagonimus yokogawai and Paragonimus westermani. Particularly, three primer sets were able to detect 10 C. sinensis eggs and were applicable to amplify specific amplicons from DNA samples purified from stool of C. sinensis-infected patients. This PCR method could be useful for diagnosis of C. sinensis infections in human stool samples with a high level of specificity and sensitivity.
机译:粪便样本中寄生虫蠕虫卵的镜检是最常用的感染常规诊断方法,但粪便样本中卵的数量少且数量少,通常会妨碍经典显微检查法对蠕虫感染的诊断。此外,如果寄生虫卵具有相似的形态特征,也很难通过经典方法对其进行区分。在这项研究中,我们开发了一种基于快速灵敏的聚合酶链反应(PCR)的分子诊断方法,用于检测粪便样本中的中华支睾吸虫卵。根据中华C逆转录转座子1(CsRn1)基因的长末端重复序列(LTR)设计了9个引物,并配对了7个PCR引物对。与每个引物对的聚合酶链反应产生了中华C的特异性扩增子,但没有其他横生线虫的扩增子,包括横须角线虫和百日草。特别地,三个引物组能够检测10个中华绒螯蟹卵,并且适用于从纯化自中华绒螯蟹感染患者粪便的DNA样品中扩增特异性扩增子。该PCR方法可用于诊断人类粪便样本中的中华梭状芽胞杆菌感染,具有高度的特异性和敏感性。

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