Influenza Virus Research Center, National Institute of Infectious Diseases, 4-7-1 Gakuen, Musashimurayama-shi, Tokyo 208-0011, Japan.
Department of Pediatrics, Showa General Hospital, 8-1-1 Hanakoganei, Kodaira-shi, Tokyo 187-0002, Japan.
J Virol Methods. 2019 May;267:53-58. doi: 10.1016/j.jviromet.2019.02.010. Epub 2019 Mar 1.
Influenza virus and respiratory syncytial virus cause acute upper and lower respiratory tract infections, especially in children and the elderly. Early treatment for these infections is thought to be important, so simple and sensitive detection methods are needed for use at clinical sites. Therefore, in this study, real-time reverse transcription loop-mediated isothermal amplification assays with quenching primer for influenza virus and respiratory syncytial virus were developed. Evaluation of a total of 113 clinical specimens compared to real-time RT-PCR assays showed that the novel assays could distinguish between the types and subtypes of influenza virus and respiratory syncytial virus and had 100% diagnostic specificity. The diagnostic sensitivity of each assay exceeded 85.0% and the assays showed sufficient clinical accuracy. Furthermore, positive results could be obtained in around 15 min using the novel assays in cases with high concentrations of virus. The developed assays should be useful for identifying influenza virus and respiratory syncytial virus cases not only in experimental laboratories but also in hospital and quarantine laboratories.
流感病毒和呼吸道合胞病毒引起急性上呼吸道和下呼吸道感染,尤其在儿童和老年人中较为常见。人们认为对这些感染的早期治疗很重要,因此需要在临床场所使用简单而敏感的检测方法。因此,在这项研究中,开发了用于流感病毒和呼吸道合胞病毒的实时逆转录环介导等温扩增检测伴荧光基团探针的检测方法。对总共 113 个临床标本的评估结果与实时 RT-PCR 检测方法的比较表明,新方法可以区分流感病毒和呼吸道合胞病毒的类型和亚型,具有 100%的诊断特异性。每个检测方法的诊断灵敏度均超过 85.0%,且具有足够的临床准确性。此外,在病毒浓度较高的情况下,使用新方法大约 15 分钟即可得到阳性结果。开发的检测方法不仅在实验室内,而且在医院和检疫实验室中用于鉴定流感病毒和呼吸道合胞病毒感染的病例应该是有用的。