4.4 Article

A reverse-transcription recombinase-aided amplification assay for the rapid detection of N gene of severe acute respiratory syndrome coronavirus 2(SARS-CoV-2)

期刊

VIROLOGY
卷 549, 期 -, 页码 1-4

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.virol.2020.07.006

关键词

SARS-CoV-2; Nucleocapsid protein; Real-time RT-RAA; Real-time RT-PCR

类别

资金

  1. National Major Science & Technology Projects for Infectious Disease Control and Prevention [2017ZX10103008, 2017ZX10302301]
  2. National Natural Science Foundation of China [81871666, 31700035]
  3. Natural Science Foundation of Jiangsu Province [BK20191489]
  4. Jiangsu Provincial Key Medical Discipline of Epidemiology [ZDXKA2016008]
  5. Key Research and Development Project of Jiangsu Province [BE2019761]

向作者/读者索取更多资源

The current outbreak of coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was reported in China firstly. A rapid, highly sensitive, specific, and simple operational method was needed for the detection of SARS-CoV-2. Here, we established a real-time reverse -transcription recombinase-aided amplification assay (RT-RAA) to detect SARS-CoV-2 rapidly. The primers and probe were designed based on the nucleocapsid protein gene (N gene) sequence of SARS-CoV-2. The detection limit was 10 copies per reaction in this assay, which could be conducted within 15 min at a constant temperature (39 degrees C), without any cross-reactions with other respiratory tract pathogens, such as other coronaviruses. Furthermore, compared with commercial real-time RT-PCR assay, it showed a kappa value of 0.959 (p < 0.001) from 150 clinical specimens. These results indicated that this real-time RT-RAA assay may be a valuable tool for detecting SARS-CoV-2.

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