Kim Hyoung Jun
OIE Reference Laboratory for Viral Hemorrhagic Septicemia (VHS), National Fishery Products Quality Management Services, Busan, 49111 Korea.
Indian J Microbiol. 2019 Jun;59(2):234-236. doi: 10.1007/s12088-019-00791-4. Epub 2019 Mar 5.
Viral hemorrhagic septicemia virus (VHSV), causing severe diseases in farmed fish, is detected and genotyped using conventional reverse-transcription PCR (cRT-PCR) targeting the nucleoprotein gene with corresponding VN F (forward) and VN R (reverse) primers. However, these primers have low sensitivity to VHSV subtype IVa; I investigated the cause for the poor cRT-PCR performance using various primer combinations. The results demonstrated that a 3'-end mismatch in the VN F primer reduced sensitivity and plays a critical role in VHSV detection by cRT-PCR.
病毒性出血性败血症病毒(VHSV)可在养殖鱼类中引发严重疾病,利用靶向核蛋白基因的常规逆转录聚合酶链反应(cRT-PCR)以及相应的VN F(正向)和VN R(反向)引物对其进行检测和基因分型。然而,这些引物对VHSV IVa亚型的敏感性较低;我使用各种引物组合研究了cRT-PCR性能不佳的原因。结果表明,VN F引物的3'端错配降低了敏感性,并且在通过cRT-PCR检测VHSV中起着关键作用。