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RT-RPA-Cas12a-based assay facilitates the discrimination of SARS-CoV-2 variants of concern
Timely and accurate detection of SARS-CoV-2 variants of concern (VOCs) is urgently needed for pandemic surveillance and control. Great efforts have been made from a mass of scientists in increasing the detection sensitivity and operability, and reducing the turn-around time and cost. Here, we report...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Authors. Published by Elsevier B.V.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9884195/ https://www.ncbi.nlm.nih.gov/pubmed/36743821 http://dx.doi.org/10.1016/j.snb.2023.133433 |
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author | Tang, Guiyue Zhang, Zilong Tan, Wei Long, Fei Sun, Jingxian Li, Yingying Zou, Siwei Yang, Yujiao Cai, Kezhu Li, Shenwei Wang, Zhiyi Liu, Jiakun Mao, Guobing Ma, Yingxin Zhao, Guo-Ping Tian, Zhen-Gan Zhao, Wei |
author_facet | Tang, Guiyue Zhang, Zilong Tan, Wei Long, Fei Sun, Jingxian Li, Yingying Zou, Siwei Yang, Yujiao Cai, Kezhu Li, Shenwei Wang, Zhiyi Liu, Jiakun Mao, Guobing Ma, Yingxin Zhao, Guo-Ping Tian, Zhen-Gan Zhao, Wei |
author_sort | Tang, Guiyue |
collection | PubMed |
description | Timely and accurate detection of SARS-CoV-2 variants of concern (VOCs) is urgently needed for pandemic surveillance and control. Great efforts have been made from a mass of scientists in increasing the detection sensitivity and operability, and reducing the turn-around time and cost. Here, we report a nucleic acid testing-based method aiming to detect and discriminate SARS-CoV-2 mutations by combining RT-RPA and CRISPR-Cas12a detecting assays (RRCd). With a detection limit of 10 copies RNA/reaction, RRCd was validated in 194 clinical samples, showing 89% positive predictive agreement and 100% negative predictive agreement, respectively. Critically, using specific crRNAs, representatives of single nucleotide polymorphisms and small deletions in SARS-CoV-2 VOCs including N501Y, T478K and ΔH69-V70 were discriminated by RRCd, demonstrating 100% specificity in clinical samples with C(t) < 33. The method completes within 65 min and could offer visible results without using any electrical devices, which probably facilitate point-of-care testing of SARS-CoV-2 variants and other epidemic viruses. |
format | Online Article Text |
id | pubmed-9884195 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Authors. Published by Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98841952023-01-30 RT-RPA-Cas12a-based assay facilitates the discrimination of SARS-CoV-2 variants of concern Tang, Guiyue Zhang, Zilong Tan, Wei Long, Fei Sun, Jingxian Li, Yingying Zou, Siwei Yang, Yujiao Cai, Kezhu Li, Shenwei Wang, Zhiyi Liu, Jiakun Mao, Guobing Ma, Yingxin Zhao, Guo-Ping Tian, Zhen-Gan Zhao, Wei Sens Actuators B Chem Article Timely and accurate detection of SARS-CoV-2 variants of concern (VOCs) is urgently needed for pandemic surveillance and control. Great efforts have been made from a mass of scientists in increasing the detection sensitivity and operability, and reducing the turn-around time and cost. Here, we report a nucleic acid testing-based method aiming to detect and discriminate SARS-CoV-2 mutations by combining RT-RPA and CRISPR-Cas12a detecting assays (RRCd). With a detection limit of 10 copies RNA/reaction, RRCd was validated in 194 clinical samples, showing 89% positive predictive agreement and 100% negative predictive agreement, respectively. Critically, using specific crRNAs, representatives of single nucleotide polymorphisms and small deletions in SARS-CoV-2 VOCs including N501Y, T478K and ΔH69-V70 were discriminated by RRCd, demonstrating 100% specificity in clinical samples with C(t) < 33. The method completes within 65 min and could offer visible results without using any electrical devices, which probably facilitate point-of-care testing of SARS-CoV-2 variants and other epidemic viruses. The Authors. Published by Elsevier B.V. 2023-04-15 2023-01-26 /pmc/articles/PMC9884195/ /pubmed/36743821 http://dx.doi.org/10.1016/j.snb.2023.133433 Text en © 2023 The Authors 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 Tang, Guiyue Zhang, Zilong Tan, Wei Long, Fei Sun, Jingxian Li, Yingying Zou, Siwei Yang, Yujiao Cai, Kezhu Li, Shenwei Wang, Zhiyi Liu, Jiakun Mao, Guobing Ma, Yingxin Zhao, Guo-Ping Tian, Zhen-Gan Zhao, Wei RT-RPA-Cas12a-based assay facilitates the discrimination of SARS-CoV-2 variants of concern |
title | RT-RPA-Cas12a-based assay facilitates the discrimination of SARS-CoV-2 variants of concern |
title_full | RT-RPA-Cas12a-based assay facilitates the discrimination of SARS-CoV-2 variants of concern |
title_fullStr | RT-RPA-Cas12a-based assay facilitates the discrimination of SARS-CoV-2 variants of concern |
title_full_unstemmed | RT-RPA-Cas12a-based assay facilitates the discrimination of SARS-CoV-2 variants of concern |
title_short | RT-RPA-Cas12a-based assay facilitates the discrimination of SARS-CoV-2 variants of concern |
title_sort | rt-rpa-cas12a-based assay facilitates the discrimination of sars-cov-2 variants of concern |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9884195/ https://www.ncbi.nlm.nih.gov/pubmed/36743821 http://dx.doi.org/10.1016/j.snb.2023.133433 |
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