Chen Hao-tai, Zhang Jie, Sun De-hui, Ma Li-na, Liu Xiang-tao, Quan Kai, Liu Yong-sheng
Key Laboratory of Animal Virology of Ministry of Agriculture, State Key Laboratory of Veterinary Etiological Biology, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou 730046, China.
J Virol Methods. 2008 Nov;153(2):266-8. doi: 10.1016/j.jviromet.2008.07.006. Epub 2008 Sep 2.
A reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay targeting the open reading frames 1a of highly pathogenic porcine reproductive and respiratory syndrome virus genome was developed. The 10 reference strains, 1 clinical isolation strain and 122 positive samples were tested. Positive reactions were confirmed for all strains and specimens by reverse transcription loop-mediated isothermal amplification and nested reverse transcription polymerase chain reaction (RT-PCR). The results showed this detection technique is more reliable and convenient for rapid and sensitive diagnosis of highly pathogenic porcine reproductive and respiratory syndrome virus infection.
建立了一种针对高致病性猪繁殖与呼吸综合征病毒基因组开放阅读框1a的逆转录环介导等温扩增(RT-LAMP)检测方法。对10株参考毒株、1株临床分离毒株和122份阳性样本进行了检测。通过逆转录环介导等温扩增和巢式逆转录聚合酶链反应(RT-PCR)对所有毒株和样本进行了阳性反应确认。结果表明,该检测技术对于高致病性猪繁殖与呼吸综合征病毒感染的快速、灵敏诊断更加可靠和便捷。