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基于多重高分辨率熔解曲线分析开发实时荧光定量PCR检测方法:土壤传播性蠕虫和血吸虫种类检测与鉴别的初步研究

Developing a real-time PCR assay based on multiplex high-resolution melt-curve analysis: a pilot study in detection and discrimination of soil-transmitted helminth and schistosome species.

作者信息

Cunningham Lucas J, Stothard J Russell, Osei-Atweneboana Mike, Armoo Samuel, Verweij Jaco J, Adams Emily R

机构信息

Department of Parasitology,Liverpool School of Tropical Medicine,Liverpool, L3 5QA,UK.

Department of Environmental Biology and Health,Council for Scientific and Industrial Research - Water Research Institute,P.O. Box M 32, Accra 102001,Ghana.

出版信息

Parasitology. 2018 Nov;145(13):1733-1738. doi: 10.1017/S0031182018001361. Epub 2018 Aug 28.

DOI:10.1017/S0031182018001361
PMID:30152296
Abstract

With the push towards control and elimination of soil-transmitted helminthiasis and schistosomiasis in low- and middle-income countries, there is a need to develop alternative diagnostic assays that complement the current in-country resources, preferably at a lower cost. Here, we describe a novel high-resolution melt (HRM) curve assay with six PCR primer pairs, designed to sub-regions of the nuclear ribosomal locus. Used within a single reaction and dye detection channel, they are able to discriminate Ancylostoma duodenale, Necator americanus, Strongyloides stercoralis, Ascaris lumbricoides, Trichuris trichiuria and Schistosoma spp. by HRM curve analysis. Here we describe the primers and the results of a pilot assessment whereby the HRM assay was tested against a selection of archived fecal samples from Ghanaian children as characterized by Kato-Katz and real-time PCR analysis with species-specific TaqMan hydrolysis probes. The resulting sensitivity and specificity of the HRM was 80 and 98.6% respectively. We judge the assay to be appropriate in modestly equipped and resourced laboratories. This method provides a potentially cheaper alternative to the TaqMan method for laboratories in lower resource settings. However, the assay requires a more extensive assessment as the samples used were not representative of all target organisms.

摘要

随着低收入和中等收入国家推动控制和消除土壤传播的蠕虫病和血吸虫病,有必要开发替代诊断检测方法,以补充当前国内资源,最好成本更低。在此,我们描述了一种新型的高分辨率熔解(HRM)曲线检测方法,该方法使用六对PCR引物,针对核糖体基因座的亚区域设计。在单个反应和染料检测通道中使用时,它们能够通过HRM曲线分析区分十二指肠钩虫、美洲板口线虫、粪类圆线虫、蛔虫、鞭虫和血吸虫属。在此我们描述了引物以及初步评估的结果,在该评估中,HRM检测方法针对加纳儿童的一系列存档粪便样本进行了测试,这些样本已通过加藤厚涂片法和使用物种特异性TaqMan水解探针的实时PCR分析进行了特征鉴定。HRM检测方法的灵敏度和特异性分别为80%和98.6%。我们认为该检测方法适用于设备和资源适度的实验室。对于资源较少地区的实验室而言,此方法为TaqMan方法提供了一种潜在的更便宜的替代方案。然而,由于所使用的样本不代表所有目标生物体,该检测方法需要更广泛的评估。

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