Bruchhof B, Marquardt O, Enzmann P J
Federal Research Centre for Virus Diseases of Animals, Tübingen, Germany.
J Virol Methods. 1995 Sep;55(1):111-9. doi: 10.1016/0166-0934(95)00051-u.
Reverse transcriptase-dependent polymerase chain reaction (RT-PCR) was applied to the detection and differentiation of viral hemorrhagic septicemia virus (VHSV) and infectious hematopoietic necrosis virus (IHNV) using primer pairs designed for the amplification of glycoprotein G-specific gene fragments of the two viruses. The products of 443 bp (VHS) and 548 bp (IHN), respectively, were amplified from the total RNA extracts of RTG-2 cells infected with a total of 9 different strains of either VHS virus or IHN virus. Restriction analysis using FokI, and DNA sequencing of the PCR products demonstrated specificity of the amplification. The RT-PCR amplification of VHSV or IHNV G-genes was found to be a simple, highly specific and sensitive method allowing differential diagnosis of VHS and IHN within 8 h.
采用逆转录酶依赖性聚合酶链反应(RT-PCR),利用为扩增两种病毒糖蛋白G特异性基因片段而设计的引物对,对病毒性出血性败血症病毒(VHSV)和传染性造血器官坏死病毒(IHNV)进行检测和鉴别。分别从感染了总共9种不同株VHS病毒或IHNV病毒的RTG-2细胞的总RNA提取物中扩增出443 bp(VHS)和548 bp(IHN)的产物。使用FokI进行限制性分析以及对PCR产物进行DNA测序,证明了扩增的特异性。发现VHSV或IHNV G基因的RT-PCR扩增是一种简单、高度特异且灵敏的方法,能够在8小时内对VHS和IHN进行鉴别诊断。