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Visual detection of porcine epidemic diarrhea virus using a novel reverse transcription polymerase spiral reaction method

机译:使用新型逆转录聚合酶螺旋反应方法目视检测猪流行性腹泻病毒

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摘要

Porcine epidemic diarrhea virus (PEDV) is a major etiological agent of porcine epidemic diarrhea around the world. Point-of-care testing in the field is lacking owing to the requirement for a simple, robust field applicable test that does not require professional laboratory equipment. The aim of this study was to establish a novel reverse transcription polymerase spiral reaction (RT-PSR) assay for the rapid detection of porcine epidemic diarrhea virus (PEDV). For the assay, a specific RT-PSR primer pair was designed against a conserved region in PEDV ORF3. The RT-PSR was optimized, and PEDV could be detected after a 50?min incubation at 62?°C, in addition to the 15?min required for reverse transcription. No cross-reaction with other porcine infectious viruses was observed. This new method for PEDV detection was 10 times more sensitive than the conventional reverse transcription-polymerase chain reaction (RT-PCR) assay. The positive rates for 65 clinical samples using the new RT-PSR assay and the conventional RT-PCR assay were 58.46% (38/65) and 53.84% (35/65), respectively. In the RT-PSR assay, the addition of a mixture of dyes allowed a positive reaction to be directly observed by the naked eye. These results indicate that this RT-PSR assay is capable of accurately detecting PEDV, and has the advantages of high specificity and sensitivity for the detection of PEDV.
机译:猪流行性腹泻病毒(PEDV)是世界各地猪流行性腹泻的主要原因。由于对不需要专业实验室设备的简单,坚固的现场适用测试的要求,缺乏该领域的护理测试。本研究的目的是建立一种新型逆转录聚合酶螺旋反应(RT-PSR)测定,用于快速检测猪疫情腹泻病毒(PEDV)。对于测定,特定的RT-PSR引物对被设计在PEDV ORF3中的保守区域。优化RT-PSR,除了在62℃下孵育50Ω·℃后,可以检测PEDV,除了逆转录所需的15Ω分钟。观察到与其他猪传染性病毒没有交叉反应。这种用于PedV检测的新方法比传统的逆转录聚合酶链反应(RT-PCR)测定敏感的10倍。使用新的RT-PSR测定和常规RT-PCR测定的65个临床样品的阳性率分别为58.46%(38/65)和53.84%(35/65)。在RT-PSR测定中,添加染料的混合物允许通过肉眼直接观察阳性反应。这些结果表明该RT-PSR测定能够精确地检测PEDV,并且具有对PEDV检测的特异性和灵敏度具有高的优点。

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