利用新型多重实时 RT-PCR 法同时超快检测泛 SARS 冠状病毒和甲型/乙型流感病毒。

IF 2.5 4区 医学 Q3 VIROLOGY
Changping Xu , Zhengyang Wang , Beibei Yu , Zhenhuang Pan , Jun Ni , Yan Feng , Shiwang Huang , Maomao Wu , Jiancang Zhou , Lei Fang , Zhiwei Wu
{"title":"利用新型多重实时 RT-PCR 法同时超快检测泛 SARS 冠状病毒和甲型/乙型流感病毒。","authors":"Changping Xu ,&nbsp;Zhengyang Wang ,&nbsp;Beibei Yu ,&nbsp;Zhenhuang Pan ,&nbsp;Jun Ni ,&nbsp;Yan Feng ,&nbsp;Shiwang Huang ,&nbsp;Maomao Wu ,&nbsp;Jiancang Zhou ,&nbsp;Lei Fang ,&nbsp;Zhiwei Wu","doi":"10.1016/j.virusres.2024.199410","DOIUrl":null,"url":null,"abstract":"<div><p>Here we report an ultrafast quadruplex RT-qPCR assay with robust diagnostic ability to detect and distinguish pan-SARS-CoVs and influenza A/B viruses within 35 min. This quadruplex RT-qPCR assay comprised of one novel RNA-based internal control targeting human β2-microglobulin (<em>B2M</em>) for process accuracy and three newly-designed primers-probe sets targeting the envelope protein (<em>E</em>) of pan-SARS-CoV, matrix protein (<em>MP</em>) of influenza A virus and non-structural (<em>NS</em>) region of influenza B virus. This quadruplex assay exhibited a sensitivity comparable to its singleplex counterparts and a slightly higher to that of the Centers for Disease Control and Prevention-recommended SARS-CoV-2 and influenza A/B assays. The novel assay showed no false-positive amplifications with other common respiratory viruses, and its 95 % limits of detection for pan-SARS-CoV and influenza A/B virus was 4.26–4.52 copies/reaction. Moreover, the assay was reproducible with less than 1 % coefficient of variation and adaptable testing different clinical and environmental samples. Our ultrafast quadruplex RT-qPCR assay can serve as an attractive tool for effective differentiation of influenza A/B virus and SARS-CoV-2, but more importantly prognose the reemergence/emergence of SARS and novel coronaviruses or influenza viruses from animal spillover.</p></div>","PeriodicalId":23483,"journal":{"name":"Virus research","volume":null,"pages":null},"PeriodicalIF":2.5000,"publicationDate":"2024-05-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0168170224001035/pdfft?md5=d09a3c3ddb5d508366021282c790ad4e&pid=1-s2.0-S0168170224001035-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Simultaneous and ultrafast detection of pan-SARS-coronaviruses and influenza A/B viruses by a novel multiplex real-time RT-PCR assay\",\"authors\":\"Changping Xu ,&nbsp;Zhengyang Wang ,&nbsp;Beibei Yu ,&nbsp;Zhenhuang Pan ,&nbsp;Jun Ni ,&nbsp;Yan Feng ,&nbsp;Shiwang Huang ,&nbsp;Maomao Wu ,&nbsp;Jiancang Zhou ,&nbsp;Lei Fang ,&nbsp;Zhiwei Wu\",\"doi\":\"10.1016/j.virusres.2024.199410\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Here we report an ultrafast quadruplex RT-qPCR assay with robust diagnostic ability to detect and distinguish pan-SARS-CoVs and influenza A/B viruses within 35 min. This quadruplex RT-qPCR assay comprised of one novel RNA-based internal control targeting human β2-microglobulin (<em>B2M</em>) for process accuracy and three newly-designed primers-probe sets targeting the envelope protein (<em>E</em>) of pan-SARS-CoV, matrix protein (<em>MP</em>) of influenza A virus and non-structural (<em>NS</em>) region of influenza B virus. This quadruplex assay exhibited a sensitivity comparable to its singleplex counterparts and a slightly higher to that of the Centers for Disease Control and Prevention-recommended SARS-CoV-2 and influenza A/B assays. The novel assay showed no false-positive amplifications with other common respiratory viruses, and its 95 % limits of detection for pan-SARS-CoV and influenza A/B virus was 4.26–4.52 copies/reaction. Moreover, the assay was reproducible with less than 1 % coefficient of variation and adaptable testing different clinical and environmental samples. Our ultrafast quadruplex RT-qPCR assay can serve as an attractive tool for effective differentiation of influenza A/B virus and SARS-CoV-2, but more importantly prognose the reemergence/emergence of SARS and novel coronaviruses or influenza viruses from animal spillover.</p></div>\",\"PeriodicalId\":23483,\"journal\":{\"name\":\"Virus research\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2024-05-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S0168170224001035/pdfft?md5=d09a3c3ddb5d508366021282c790ad4e&pid=1-s2.0-S0168170224001035-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Virus research\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0168170224001035\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"VIROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Virus research","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0168170224001035","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"VIROLOGY","Score":null,"Total":0}
引用次数: 0

摘要

在此,我们报告了一种超快四重 RT-qPCR 检测方法,它具有强大的诊断能力,可在 35 分钟内检测并区分泛 SARS-CoV 和甲型/乙型流感病毒。这种四重 RT-qPCR 检测方法由一个新型 RNA 内对照(以人 β2-微球蛋白 (B2M) 为目标)和三个新设计的引物(以泛 SARS-CoV 的包膜蛋白 (E)、甲型流感病毒的基质蛋白 (MP) 和乙型流感病毒的非结构 (NS) 区为目标)组成,前者可确保检测过程的准确性。这种四重检测法的灵敏度与单重检测法相当,略高于美国疾病控制和预防中心推荐的 SARS-CoV-2 和甲型/乙型流感检测法。这种新型检测方法对其他常见呼吸道病毒没有假阳性扩增,对泛 SARS-CoV 和甲型/乙型流感病毒的 95% 检测限为 4.26-4.52 拷贝/反应。此外,该检测方法的重现性良好,变异系数小于 1%,可用于检测不同的临床和环境样本。我们的超快速四重 RT-qPCR 分析法可作为一种有吸引力的工具,有效区分甲型/乙型流感病毒和 SARS-CoV-2 病毒,更重要的是可预测 SARS 和新型冠状病毒或动物溢出流感病毒的再次出现或出现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Simultaneous and ultrafast detection of pan-SARS-coronaviruses and influenza A/B viruses by a novel multiplex real-time RT-PCR assay

Here we report an ultrafast quadruplex RT-qPCR assay with robust diagnostic ability to detect and distinguish pan-SARS-CoVs and influenza A/B viruses within 35 min. This quadruplex RT-qPCR assay comprised of one novel RNA-based internal control targeting human β2-microglobulin (B2M) for process accuracy and three newly-designed primers-probe sets targeting the envelope protein (E) of pan-SARS-CoV, matrix protein (MP) of influenza A virus and non-structural (NS) region of influenza B virus. This quadruplex assay exhibited a sensitivity comparable to its singleplex counterparts and a slightly higher to that of the Centers for Disease Control and Prevention-recommended SARS-CoV-2 and influenza A/B assays. The novel assay showed no false-positive amplifications with other common respiratory viruses, and its 95 % limits of detection for pan-SARS-CoV and influenza A/B virus was 4.26–4.52 copies/reaction. Moreover, the assay was reproducible with less than 1 % coefficient of variation and adaptable testing different clinical and environmental samples. Our ultrafast quadruplex RT-qPCR assay can serve as an attractive tool for effective differentiation of influenza A/B virus and SARS-CoV-2, but more importantly prognose the reemergence/emergence of SARS and novel coronaviruses or influenza viruses from animal spillover.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Virus research
Virus research 医学-病毒学
CiteScore
9.50
自引率
2.00%
发文量
239
审稿时长
43 days
期刊介绍: Virus Research provides a means of fast publication for original papers on fundamental research in virology. Contributions on new developments concerning virus structure, replication, pathogenesis and evolution are encouraged. These include reports describing virus morphology, the function and antigenic analysis of virus structural components, virus genome structure and expression, analysis on virus replication processes, virus evolution in connection with antiviral interventions, effects of viruses on their host cells, particularly on the immune system, and the pathogenesis of virus infections, including oncogene activation and transduction.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信