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Detection of Bovine Viral Diarrhea Virus (BVDV) Using Reverse Transcription Polymerase Chain Reaction Assay

机译:逆转录聚合酶链反应法检测牛病毒性腹泻病毒(BVDV)

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References(18) Cited-By(3) The reverse transcription polymerase chain reaction (RT-PCR) was applied to detect bovine viral diarrhea virus (BVDV) for the rapid diagnosis. The primers were selected from the p80 region of BVDV gene. The RT-PCR assay detected all of the 17 BVDV strains tested including cytopathogenic and non-cytopathogenic strains, while specific amplification was not observed from 17 bovine viruses other than BVDV. Detection limit of the assay was 101.5 TCID 50/ml. Sera and organ samples were collected from four field bovine viral diarrhea-mucosal disease (BVD-MD) cases; mucosal disease, abortion, diarrhea and persistent infection. The RT-PCR assay detected BVDV from those samples more than conventional virus isolation method.
机译:参考文献(18)引用了(3)逆转录聚合酶链反应(RT-PCR)用于检测牛病毒性腹泻病毒(BVDV)以进行快速诊断。引物选自BVDV基因的p80区域。 RT-PCR分析检测到所有17种BVDV菌株,包括致细胞病和非致细胞毒株,而除BVDV之外的17种牛病毒均未观察到特异性扩增。该测定的检出限为101.5 TCID 50 / ml。从四个野牛牛腹泻-粘膜病(BVD-MD)病例中收集血清和器官样本;粘膜疾病,流产,腹泻和持续感染。与常规病毒分离方法相比,RT-PCR分析从这些样品中检测到BVDV的可能性更高。

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