| Literature DB >> 31726113 |
Wenbin Qiu1, Kai Meng2, Yanyan Liu3, Yuyu Zhang3, Zhao Wang4, Zhi Chen3, Jie Yang3, Wenbo Sun3, Lihui Guo3, Sufang Ren3, Lei Chen5, Guiwen Yang5, Fan Zhang5, Jianli Shi3, Jun Li3, Yijun Du3, Jiang Yu6, Jiaqiang Wu7.
Abstract
Porcine Reproductive and Respiratory Syndrome (PRRS), an acute infectious disease caused by the porcine reproductive and respiratory syndrome virus (PRRSV), is one of the most devastating diseases affecting the global swine industry. In order to establish a multiplex real-time PCR method for the simultaneous detection of the classical PRRSV (C-PRRSV) strain, the highly pathogenic PRRSV (HP-PRRSV) strain and NADC30-like PRRSV (NL-PRRSV) strain, we designed specific primers and TaqMan fluorescent probes based on the Nsp2 target gene sequence of these three different PRRSV strains, and designed American-type PRRSV (PRRSV-U) special primers and probes based on the relatively conserved target gene sequence of ORF7. The method established in this study can quickly and accurately detect and differentiate three types of strains of clinical tissue samples, respectively. This method plays a key role in the rapid diagnosis and determination of PRRSV.Entities:
Keywords: Classical PRRSV; Highly pathogenic PRRSV; NADC30-like PRRSV; Probe real-time PCR; TaqMan
Year: 2019 PMID: 31726113 DOI: 10.1016/j.jviromet.2019.113774
Source DB: PubMed Journal: J Virol Methods ISSN: 0166-0934 Impact factor: 2.014