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首页> 外文期刊>Virus Genes >A duplex real-time RT-PCR assay for the simultaneous genogroup-specific detection of noroviruses in both clinical and environmental specimens.
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A duplex real-time RT-PCR assay for the simultaneous genogroup-specific detection of noroviruses in both clinical and environmental specimens.

机译:用于临床和环境标本中诺如病毒同时基因组特异性检测的双重实时RT-PCR分析。

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摘要

Norovirus (NoV) is the major etiological agent causing foodborne and waterborne outbreaks worldwide. We developed a novel duplex real-time quantitative RT-PCR assay designed for the simultaneous detection of and discrimination between NoV genogroups GI and GII, by targeting the short junction region between ORF1 and ORF2, with sensitivity and efficiency comparable to those of each simplex RT-PCR assay. This new duplex assay was evaluated against clinical stool (n = 82) and environmental (groundwater or surface water, n = 60) specimens from South Korea, and the results were compared with those of conventional RT-PCR (cRT-PCR) assays. The duplex assay detected more positive samples than did the cRT-PCR for both clinical (74 vs. 71) and, more strikingly, environmental (24 vs. 10) specimens. No cross-reactivity against specimens containing other enteric viruses such as rotavirus, adenovirus, and poliovirus were observed. These results suggest that this newly developed duplex real-time RT-PCR assay can be used for the sensitive and simultaneous genogroup-specific detection of NoV in both clinical and environmental specimens.
机译:诺如病毒(NoV)是引起全球食源性和水源性暴发的主要病原体。我们开发了一种新颖的双工实时定量RT-PCR检测试剂盒,设计用于同时检测和区分NoV基因组GI和GII,通过靶向ORF1和ORF2之间的短连接区,其灵敏度和效率可与每个单工RT媲美。 -PCR测定。针对韩国的临床粪便(n = 82)和环境(地下水或地表水,n = 60)标本对这种新的双链体分析进行了评估,并将结果与​​常规RT-PCR(cRT-PCR)进行了比较。在临床(74比71)和环境(24 vs. 10)样本中,双重分析检测到的阳性样本均比cRT-PCR多。没有观察到与含有其他肠病毒如轮状病毒,腺病毒和脊髓灰质炎病毒的标本的交叉反应。这些结果表明,这种新近开发的双工实时RT-PCR分析可用于临床和环境标本中NoV的灵敏和同时基因组特异性检测。

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