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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...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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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. |
format | Online Article Text |
id | pubmed-7737895 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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