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Rapid detection and differentiation of Clonorchis sinensis and Opisthorchis viverrini eggs in human fecal samples using a duplex real-time fluorescence resonance energy transfer PCR and melting curve analysis

机译:使用实时荧光共振能量转移PCR和熔解曲线分析技术快速检测和区分人粪便中的华支睾吸虫和维氏梭菌卵

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We developed a single step duplex real-time fluorescence resonance energy transfer (FRET) PCR merged with melting curve analysis for the fast detection and differentiation of Clonorchis sinensis and Opisthorchis viverrini eggs in human fecal samples. Two species of mitochondrial NADH dehydrogenase subunit 2 (nad2) DNA elements, the 165-bp nad2 product of C. sinensis and the 209-bp nad2 product of O. viverrini, were amplified by species-specific primers, and the fluorescence melting curve analyses were generated from hybrid of amplicons and two pairs of species-specific fluorophore-labeled probes. By their different fluorescence channels and melting temperatures, both C. sinensis and O. viverrini eggs in infected human fecal samples were detected and differentiated with high (100%) sensitivity and specificity. Detection limit was as little as a single C. sinensis egg and two O. viverrini eggs in 100 mg of fecal sample. The assay could distinguish the DNA of both parasites from the DNA of negative fecal samples and fecal samples with other parasitosis, as well as from the well-defined genomic DNA of human leukocytes and other parasites. It can reduce labor time of microscopic examination and is not prone to carry over contamination of agarose electrophoresis. Our duplex real-time FRET PCR method would be useful to determine the accurate range of endemic areas and/or to discover the co-endemic areas of two liver flukes, C. sinensis and O. viverrini, in Asia. This method also would be helpful for the differential diagnosis of the suspected cases of liver fluke infections among travelers who had visited the endemic countries of those parasites.
机译:我们开发了一种单步双工实时荧光共振能量转移(FRET)PCR技术,并与熔解曲线分析相结合,用于快速检测和区分人类粪便样品中的中华支睾吸虫和维氏梭菌卵。通过物种特异性引物扩增了两种线粒体NADH脱氢酶亚单位2(nad2)DNA元件,中华C的165 bp nad2产物和维氏弧菌的209 bp nad2产物,并通过荧光熔解曲线分析由扩增子和两对物种特异性荧光团标记的探针的杂交产生。通过它们不同的荧光通道和解链温度,可以检测和区分感染人类粪便样品中的中华绒螯蟹卵和卵形拟南芥卵,并具有很高的(100%)敏感性和特异性。在100 mg的粪便样品中,检出限仅为单个中华C卵和两个卵形中华。卵。该测定法可将两种寄生虫的DNA与阴性粪便样品和具有其他寄生虫病的粪便样品的DNA以及人类白细胞和其他寄生虫的明确基因组DNA区分开。它可以减少显微镜检查的劳动时间,并且不易携带琼脂糖电泳污染。我们的双工实时FRET PCR方法将有助于确定亚洲地区两种肝吸虫(C. sinensis和O. viverrini)的流行区域的准确范围和/或发现共流行区域。这种方法也有助于鉴别那些曾经到过这些寄生虫流行国家的旅行者中疑似肝吸虫感染的病例。

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