Zhang Zhujun, Liu Dong, Hu Jiao, Sun Wenqiang, Liu Kaituo, Li Juan, Xu Haixu, Liu Jing, He Lihong, Jiang Daxiu, Gu Min, Hu Shunlin, Wang Xiaoquan, Liu Xiaowen, Liu Xiufan
Animal Infectious Disease Laboratory, School of Veterinary Medicine, Yangzhou University, 48 East Wenhui Road, Yangzhou, Jiangsu, China.
Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonosis, Yangzhou University, Yangzhou, Jiangsu, China.
Arch Virol. 2019 Apr;164(4):1111-1119. doi: 10.1007/s00705-019-04180-6. Epub 2019 Feb 21.
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.
H5禽流感病毒(AIV)和速发型新城疫病毒(v-NDV)是《国际兽疫局陆生动物卫生法典》中列出的病原体,被视为家禽生产中需要根除的关键病原体。为了研究它们的传播特性并指导预防工作,需要用于快速检测H5 AIV和v-NDV的分子技术。使用鸡胚进行传统的病毒分离耗时较长,不能用作快速诊断技术。在本研究中,成功建立了一种针对六种H5 AIV进化枝、三种v-NDV亚型和一种中等毒力NDV亚型的多重实时RT-PCR(RRT-PCR)检测方法。我们的多重NDV和H5 AIV RRT-PCR对每种病原体的检测限为每个反应五拷贝,具有良好的线性和效率(H5 AIV为y = -3.194x + 38.427,NDV为y = -3.32x + 38.042)。多重PCR显示出良好的批内和批间重复性,变异系数(CV)小于1%。此外,使用RRT-PCR方法时,临床样本中H5 AIV和NDV的总体检测率高于使用传统病毒分离方法获得的检测率。因此,我们的方法为活禽市场中各种H5 AIV进化枝以及多种速发型和中等毒力NDV亚型的监测提供了一种有前景的技术。