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首页> 外文期刊>Virology Journal >Establishing a TaqMan-Based Real-Time PCR Assay for the rapid detection and quantification of the newly emerged duck tembusu virus
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Establishing a TaqMan-Based Real-Time PCR Assay for the rapid detection and quantification of the newly emerged duck tembusu virus

机译:建立基于TaqMan的实时PCR分析法,用于快速检测和定量新出现的鸭tembusu病毒

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To establish an accurate, rapid, and a quantifiable method for the detection of the newly emerged duck Tembusu virus (DTMUV) that recently caused a widespread infectious disease in ducks in China, we developed a TaqMan-based real-time PCR assay by using E gene-specific primers and a TaqMan probe. This real-time PCR assay was 100 times more sensitive than the conventional PCR. The reproducibility and specificity of the real-time PCR assay were confirmed using plasmids containing E genes or RNAs and DNAs extracted from well-known viruses causing duck diseases. The reliability of this real-time PCR assay was confirmed in 19 of the 24 swab samples, 22 of the 24 tissue samples collected from experimentally infected ducks, as well as 15 of the 21 clinical samples collected from sick ducks since they were verified as DTMUV-positive. The results reveal that the newly established real-time PCR assay might be a useful diagnostic method for epidemiologically investigating and closely observing the newly emerged DTMUV.
机译:为了建立一种准确,快速,可量化的方法来检测最近在中国鸭中引起广泛传染病的新出现的鸭Tembusu病毒(DTMUV),我们使用E开发了基于TaqMan的实时PCR检测试剂盒。基因特异性引物和TaqMan探针。这种实时PCR分析的灵敏度是常规PCR的100倍。使用含有E基因的质粒或从知名的引起鸭病的病毒中提取的RNA和DNA证实了实时PCR分析的可重复性和特异性。由于已被验证为DTMUV,因此在24个拭子样品中的19个,从实验感染的鸭子中采集的24个组织样品中的22个以及从病鸭中采集的21个临床样品中的15个中,证实了这种实时PCR测定的可靠性。 -正。结果表明,新建立的实时荧光定量PCR方法可能是一种流行病学调查和密切观察新出现的DTMUV的有用的诊断方法。

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