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

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 rea...

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Autores principales: Wu, Tao, Ge, Yiyue, Zhao, Kangchen, Zhu, Xiaojuan, Chen, Yin, Wu, Bin, Zhu, Fengcai, Zhu, Baoli, Cui, Lunbiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7388781/
https://www.ncbi.nlm.nih.gov/pubmed/32758712
http://dx.doi.org/10.1016/j.virol.2020.07.006
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author Wu, Tao
Ge, Yiyue
Zhao, Kangchen
Zhu, Xiaojuan
Chen, Yin
Wu, Bin
Zhu, Fengcai
Zhu, Baoli
Cui, Lunbiao
author_facet Wu, Tao
Ge, Yiyue
Zhao, Kangchen
Zhu, Xiaojuan
Chen, Yin
Wu, Bin
Zhu, Fengcai
Zhu, Baoli
Cui, Lunbiao
author_sort Wu, Tao
collection PubMed
description 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 °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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spelling pubmed-73887812020-07-30 A reverse-transcription recombinase-aided amplification assay for the rapid detection of N gene of severe acute respiratory syndrome coronavirus 2(SARS-CoV-2) Wu, Tao Ge, Yiyue Zhao, Kangchen Zhu, Xiaojuan Chen, Yin Wu, Bin Zhu, Fengcai Zhu, Baoli Cui, Lunbiao Virology Article 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 °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. Published by Elsevier Inc. 2020-10 2020-07-29 /pmc/articles/PMC7388781/ /pubmed/32758712 http://dx.doi.org/10.1016/j.virol.2020.07.006 Text en © 2020 Published by Elsevier Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Wu, Tao
Ge, Yiyue
Zhao, Kangchen
Zhu, Xiaojuan
Chen, Yin
Wu, Bin
Zhu, Fengcai
Zhu, Baoli
Cui, Lunbiao
A reverse-transcription recombinase-aided amplification assay for the rapid detection of N gene of severe acute respiratory syndrome coronavirus 2(SARS-CoV-2)
title A reverse-transcription recombinase-aided amplification assay for the rapid detection of N gene of severe acute respiratory syndrome coronavirus 2(SARS-CoV-2)
title_full A reverse-transcription recombinase-aided amplification assay for the rapid detection of N gene of severe acute respiratory syndrome coronavirus 2(SARS-CoV-2)
title_fullStr A reverse-transcription recombinase-aided amplification assay for the rapid detection of N gene of severe acute respiratory syndrome coronavirus 2(SARS-CoV-2)
title_full_unstemmed A reverse-transcription recombinase-aided amplification assay for the rapid detection of N gene of severe acute respiratory syndrome coronavirus 2(SARS-CoV-2)
title_short A reverse-transcription recombinase-aided amplification assay for the rapid detection of N gene of severe acute respiratory syndrome coronavirus 2(SARS-CoV-2)
title_sort reverse-transcription recombinase-aided amplification assay for the rapid detection of n gene of severe acute respiratory syndrome coronavirus 2(sars-cov-2)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7388781/
https://www.ncbi.nlm.nih.gov/pubmed/32758712
http://dx.doi.org/10.1016/j.virol.2020.07.006
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