| Literature DB >> 30790106 |
Zhujun Zhang1,2,3, Dong Liu1,2,3, Jiao Hu1,2,3, Wenqiang Sun1,2,3, Kaituo Liu1,2,3, Juan Li1,2,3, Haixu Xu1,2,3, Jing Liu1,2,3, Lihong He1,2,3, Daxiu Jiang1,2,3, Min Gu1,2,3, Shunlin Hu1,2,3, Xiaoquan Wang1,2,3, Xiaowen Liu1,2,3, Xiufan Liu4,5,6.
Abstract
H5 avian influenza virus (AIV) and velogenic Newcastle disease virus (v-NDV) are pathogens listed in the OIE Terrestrial Animal Health Code and are considered key pathogens to be eliminated in poultry production. Molecular techniques for rapid detection of H5 AIV and v-NDV are required to investigate their transmission characteristics and to guide prevention. Traditional virus isolation, using embryonated chicken eggs, is time-consuming and cannot be used as a rapid diagnostic technology. In this study, a multiplex real-time RT-PCR (RRT-PCR) detection method for six H5 AIV clades, three v-NDV subtypes, and one mesogenic NDV subtype was successfully established. The detection limit of our multiplex NDV and H5 AIV RRT-PCR was five copies per reaction for each pathogen, with good linearity and efficiency (y = -3.194x + 38.427 for H5 AIV and y = -3.32x + 38.042 for NDV). Multiplex PCR showed good intra- and inter-assay reproducibility, with coefficient of variance (CV) less than 1%. Furthermore, using the RRT-PCR method, H5 AIV and NDV detection rates in clinical samples were higher overall than those obtained using the traditional virus isolation method. Therefore, our method provides a promising technique for surveillance of various H5 AIV clades and multiple velogenic and mesogenic NDV subtypes in live-poultry markets.Entities:
Mesh:
Year: 2019 PMID: 30790106 DOI: 10.1007/s00705-019-04180-6
Source DB: PubMed Journal: Arch Virol ISSN: 0304-8608 Impact factor: 2.574