| Literature DB >> 31031439 |
Abstract
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.Entities:
Keywords: 3′-Terminal region of forward primer; Conventional RT-PCR; Low sensitivity; Viral hemorrhagic septicemia virus
Year: 2019 PMID: 31031439 PMCID: PMC6458197 DOI: 10.1007/s12088-019-00791-4
Source DB: PubMed Journal: Indian J Microbiol ISSN: 0046-8991 Impact factor: 2.461