Li Pei-Qiong, Zhang Jun, Muller Claude P, Chen Jing-Xian, Yang Zi-Feng, Zhang Ren, Li Juan, He Yun-Shao
Department of Anatomy and DaAn Gene Diagnostic Center, Zhongshan School of Medicine, Sun Yat-Sen University, Guangzhou, Guangdong, PR China.
Diagn Microbiol Infect Dis. 2008 Jun;61(2):192-7. doi: 10.1016/j.diagmicrobio.2008.01.007. Epub 2008 Mar 4.
Avian influenza viruses (AIVs) are endemic in wild birds and, if transmitted to poultry, can cause serious economic losses. The aim of this study was to develop a multiplex real-time reverse transcriptase polymerase chain reaction (RT-PCR) for rapid detection of influenza virus type A, including H5 and H9 subtypes. The selected primers and various labeled TaqMan reporter probes corresponding to matrix, H5, and H9 genes were used in a multiplex real-time RT-PCR to simultaneously detect triple fluorescent signals. The results showed that the multiplex real-time RT-PCR assay can be applied to detect RNA of influenza virus type A including H5 and H9 subtypes with a high specificity and a sensitivity of 10 copies per reaction. As a result of its short turnaround times and a high specificity and sensitivity, the assay is very suitable for large-scale screening during AIV outbreaks.
禽流感病毒(AIVs)在野生鸟类中呈地方流行性,如果传播到家禽中,会造成严重的经济损失。本研究的目的是开发一种多重实时逆转录聚合酶链反应(RT-PCR),用于快速检测A型流感病毒,包括H5和H9亚型。将选定的引物和与基质、H5和H9基因对应的各种标记TaqMan报告探针用于多重实时RT-PCR,以同时检测三重荧光信号。结果表明,该多重实时RT-PCR检测方法可用于检测包括H5和H9亚型在内的A型流感病毒RNA,具有高特异性,灵敏度为每个反应10个拷贝。由于其周转时间短、特异性和灵敏度高,该检测方法非常适合在禽流感病毒爆发期间进行大规模筛查。