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Rapid detection of SARS-CoV-2 with CRISPR-Cas12a

The recent outbreak of betacoronavirus Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), which is responsible for the Coronavirus Disease 2019 (COVID-19) global pandemic, has created great challenges in viral diagnosis. The existing methods for nucleic acid detection are of high sensitiv...

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Detalles Bibliográficos
Autores principales: Xiong, Dan, Dai, Wenjun, Gong, Jiaojiao, Li, Guande, Liu, Nansong, Wu, Wei, Pan, Jiaqiang, Chen, Chen, Jiao, Yingzhen, Deng, Huina, Ye, Junwei, Zhang, Xuanxuan, Huang, Huiling, Li, Qianyun, Xue, Liang, Zhang, Xiuming, Tang, Guanghui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7737895/
https://www.ncbi.nlm.nih.gov/pubmed/33320883
http://dx.doi.org/10.1371/journal.pbio.3000978
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author Xiong, Dan
Dai, Wenjun
Gong, Jiaojiao
Li, Guande
Liu, Nansong
Wu, Wei
Pan, Jiaqiang
Chen, Chen
Jiao, Yingzhen
Deng, Huina
Ye, Junwei
Zhang, Xuanxuan
Huang, Huiling
Li, Qianyun
Xue, Liang
Zhang, Xiuming
Tang, Guanghui
author_facet Xiong, Dan
Dai, Wenjun
Gong, Jiaojiao
Li, Guande
Liu, Nansong
Wu, Wei
Pan, Jiaqiang
Chen, Chen
Jiao, Yingzhen
Deng, Huina
Ye, Junwei
Zhang, Xuanxuan
Huang, Huiling
Li, Qianyun
Xue, Liang
Zhang, Xiuming
Tang, Guanghui
author_sort Xiong, Dan
collection PubMed
description The recent outbreak of betacoronavirus Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), which is responsible for the Coronavirus Disease 2019 (COVID-19) global pandemic, has created great challenges in viral diagnosis. The existing methods for nucleic acid detection are of high sensitivity and specificity, but the need for complex sample manipulation and expensive machinery slow down the disease detection. Thus, there is an urgent demand to develop a rapid, inexpensive, and sensitive diagnostic test to aid point-of-care viral detection for disease monitoring. In this study, we developed a clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR associated proteins (Cas) 12a-based diagnostic method that allows the results to be visualized by the naked eye. We also introduced a rapid sample processing method, and when combined with recombinase polymerase amplification (RPA), the sample to result can be achieved in 50 minutes with high sensitivity (1–10 copies per reaction). This accurate and portable detection method holds a great potential for COVID-19 control, especially in areas where specialized equipment is not available.
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spelling pubmed-77378952021-01-08 Rapid detection of SARS-CoV-2 with CRISPR-Cas12a Xiong, Dan Dai, Wenjun Gong, Jiaojiao Li, Guande Liu, Nansong Wu, Wei Pan, Jiaqiang Chen, Chen Jiao, Yingzhen Deng, Huina Ye, Junwei Zhang, Xuanxuan Huang, Huiling Li, Qianyun Xue, Liang Zhang, Xiuming Tang, Guanghui PLoS Biol Methods and Resources The recent outbreak of betacoronavirus Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), which is responsible for the Coronavirus Disease 2019 (COVID-19) global pandemic, has created great challenges in viral diagnosis. The existing methods for nucleic acid detection are of high sensitivity and specificity, but the need for complex sample manipulation and expensive machinery slow down the disease detection. Thus, there is an urgent demand to develop a rapid, inexpensive, and sensitive diagnostic test to aid point-of-care viral detection for disease monitoring. In this study, we developed a clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR associated proteins (Cas) 12a-based diagnostic method that allows the results to be visualized by the naked eye. We also introduced a rapid sample processing method, and when combined with recombinase polymerase amplification (RPA), the sample to result can be achieved in 50 minutes with high sensitivity (1–10 copies per reaction). This accurate and portable detection method holds a great potential for COVID-19 control, especially in areas where specialized equipment is not available. Public Library of Science 2020-12-15 /pmc/articles/PMC7737895/ /pubmed/33320883 http://dx.doi.org/10.1371/journal.pbio.3000978 Text en © 2020 Xiong et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Methods and Resources
Xiong, Dan
Dai, Wenjun
Gong, Jiaojiao
Li, Guande
Liu, Nansong
Wu, Wei
Pan, Jiaqiang
Chen, Chen
Jiao, Yingzhen
Deng, Huina
Ye, Junwei
Zhang, Xuanxuan
Huang, Huiling
Li, Qianyun
Xue, Liang
Zhang, Xiuming
Tang, Guanghui
Rapid detection of SARS-CoV-2 with CRISPR-Cas12a
title Rapid detection of SARS-CoV-2 with CRISPR-Cas12a
title_full Rapid detection of SARS-CoV-2 with CRISPR-Cas12a
title_fullStr Rapid detection of SARS-CoV-2 with CRISPR-Cas12a
title_full_unstemmed Rapid detection of SARS-CoV-2 with CRISPR-Cas12a
title_short Rapid detection of SARS-CoV-2 with CRISPR-Cas12a
title_sort rapid detection of sars-cov-2 with crispr-cas12a
topic Methods and Resources
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7737895/
https://www.ncbi.nlm.nih.gov/pubmed/33320883
http://dx.doi.org/10.1371/journal.pbio.3000978
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