Nanopore Targeted Sequencing for the Accurate and Comprehensive Detection of SARS‐CoV‐2 and Other Respiratory Viruses

Ming Wang, Aisi Fu, Ben Hu, Y. Tong, Ran Liu, Zhen Liu, Jiashuang Gu, Bin Xiang, Jianghao Liu, Wen Jiang, Gaigai Shen, Wanxu Zhao, Dong Men, Z. Deng, Lilei Yu, Wu Wei, Yan Li, Tiangang Liu
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引用次数: 85

Abstract

The ongoing novel coronavirus pneumonia COVID-19 outbreak in Wuhan, China, has engendered numerous cases of infection and death. COVID-19 diagnosis relies upon nucleic acid detection; however, current recommended methods exhibit high false-negative rates, low sensitivity, and cannot identify other respiratory virus infections, thereby resulting patient misdiagnosis and impeding epidemic containment. Combining the advantages of target amplification and long-read, real-time nanopore sequencing, we developed nanopore target sequencing (NTS) to detect SARS-CoV-2 and other respiratory viruses simultaneously within 6-10 h. Parallel testing with approved qPCR kits of SARS-CoV-2 and NTS using 61 nucleic acid samples from suspected COVID-19 cases confirmed that NTS identified more infected patients as positive, and could also monitor for mutated nucleic acid sequence or other respiratory virus infection in the test sample. NTS is thus suitable for contemporary COVID-19 diagnosis; moreover, this platform can be further extended for diagnosing other viruses or pathogens.
纳米孔靶向测序用于准确和全面检测SARS - CoV - 2和其他呼吸道病毒
正在中国武汉持续爆发的新型冠状病毒肺炎COVID-19已造成大量感染和死亡病例。COVID-19诊断依赖于核酸检测;然而,目前推荐的方法假阴性率高,灵敏度低,不能识别其他呼吸道病毒感染,从而导致患者误诊,阻碍疫情控制。结合目标扩增和长读长实时纳米孔测序的优势,我们开发了纳米孔靶测序(NTS),可在6-10 h内同时检测SARS-CoV-2和其他呼吸道病毒。利用61份疑似病例的核酸样本,与已批准的SARS-CoV-2和NTS qPCR试剂盒平行检测,NTS检测出更多的感染者呈阳性。并可监测检测样本中核酸序列突变或其他呼吸道病毒感染情况。因此,NTS适用于当代COVID-19诊断;此外,该平台还可以进一步扩展,用于诊断其他病毒或病原体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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