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A REAL-TIME PCR-BASED ASSAY FOR DETECTION OF WUCHERERIA BANCROFTI DNA IN BLOOD AND MOSQUITOES

机译:基于实时荧光定量PCR技术的血液和蚊子中武克氏杆菌DNA检测

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摘要

We developed and evaluated real-time polymerase chain reaction (PCR) assays for detecting Wuchereria bancrofti DNA in human blood and in mosquitoes. An assay based on detection of the W. bancrofti “LDR” repeat DNA sequence was more sensitive than an assay for Wolbachia 16S rDNA. The LDR-based assay was sensitive for detecting microfilarial DNA on dried membrane filters or on filter paper. We also compared real-time PCR with conventional PCR (C-PCR) for detecting W. bancrofti DNA in mosquito samples collected in endemic areas in Egypt and Papua New Guinea. Although the two methods had comparable sensitivity for detecting filarial DNA in reference samples, real-time PCR was more sensitive than C-PCR in practice with field samples. Other advantages of real-time PCR include its high-throughput capacity and decreased risk of cross-contamination between test samples. We believe that real-time PCR has great potential as a tool for monitoring progress in large-scale filariasis elimination programs.
机译:我们开发并评估了实时聚合酶链反应(PCR)分析方法,用于检测人血和蚊子中的Wuchereria bancrofti DNA。基于班氏克氏杆菌“ LDR”重复DNA序列检测的检测方法比Wolbachia 16S rDNA检测方法更为灵敏。基于LDR的测定对于检测干膜滤膜或滤纸上的微丝DNA敏感。我们还将实时PCR与常规PCR(C-PCR)进行了比较,以检测埃及和巴布亚新几内亚流行地区收集的蚊子样本中的班氏酵母DNA。尽管这两种方法在检测参考样品中的丝状DNA方面具有可比的灵敏度,但在现场样品中,实时PCR的灵敏度比C-PCR更高。实时PCR的其他优点包括高通量能力和降低测试样品之间交叉污染的风险。我们认为,实时PCR作为监测大型丝虫病消除计划进展的工具具有巨大潜力。

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