首页> 外文期刊>The Korean Journal of Parasitology >Molecular Differentiation of Opisthorchis viverrini and Clonorchis sinensis Eggs by Multiplex Real-Time PCR with High Resolution Melting Analysis
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Molecular Differentiation of Opisthorchis viverrini and Clonorchis sinensis Eggs by Multiplex Real-Time PCR with High Resolution Melting Analysis

机译:多重实时荧光定量PCR和高分辨率熔体分析技术鉴定维氏梭鱼和华支睾吸虫卵的分子差异

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Opisthorchis viverrini and Clonorchis sinensis are parasites known to be carcinogenic and causative agents of cholangiocarcinoma in Asia. The standard method for diagnosis for those parasite infections is stool examination to detect parasite eggs. However, the method has low sensitivity, and eggs of O. viverrini and C. sinensis are difficult to distinguish from each other and from those of some other trematodes. Here, we report a multiplex real-time PCR coupled with high resolution melting (HRM) analysis for the differentiation of O. viverrini and C. sinensis eggs in fecal samples. Using 2 pairs of species-specific primers, DNA sequences from a portion of the mitochondrial NADH dehydrogenase subunit 2 (nad 2) gene, were amplified to generate 209 and 165 bp products for O. viverrini and C. sinensis, respectively. The distinct characteristics of HRM patterns were analyzed, and the melting temperatures peaked at 82.4±0.09℃ and 85.9±0.08℃ for O. viverrini and C. sinensis, respectively. This technique was able to detect as few as 1 egg of O. viverrini and 2 eggs of C. sinensis in a 150 mg fecal sample, which is equivalent to 7 and 14 eggs per gram of feces, respectively. The method is species-specific, rapid, simple, and does not require fluorescent probes or post-PCR processing for discrimination of eggs of the 2 species. It offers a new tool for differentiation and detection of Asian liver fluke infections in stool specimens.
机译:Viistruchis viverrini和Clonorchis sinensis是在亚洲被认为是胆管癌致癌和致病因素的寄生虫。诊断这些寄生虫感染的标准方法是粪便检查以检测寄生虫卵。然而,该方法的灵敏度低,并且很难区分O. viverrini和C. sinensis的卵以及与其他一些吸虫的卵。在这里,我们报告多重实时PCR结合高分辨率熔解(HRM)分析,用于粪便样品中的O. viverrini和C. sinensis卵分化。使用两对物种特异性引物,扩增来自线粒体NADH脱氢酶亚基2(nad 2)基因的一部分的DNA序列,分别产生Vi.r. viverrini和C. sinensis的209和165 bp产物。分析了HRM图谱的独特特征,分别对Viverrini和C. sinensis的熔融温度分别达到了82.4±0.09℃和85.9±0.08℃的峰值。在150 mg粪便样本中,该技术能够检测到少至1个卵形产卵形小卵菌和2个中华C形卵,分别相当于每克粪便7个和14个卵。该方法是物种特异性的,快速,简单的,不需要荧光探针或PCR后处理即可区分这2种蛋。它为鉴别和检测粪便标本中的亚洲肝吸虫感染提供了一种新工具。

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