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A CRISPR-based and post-amplification coupled SARS-CoV-2 detection with a portable evanescent wave biosensor
The continuing pandemic of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, which causes coronavirus disease 2019 (COVID-19), has spread globally and its reliable diagnosis is one of the foremost priorities for protecting public health. Herein a rapid (<1 h), easy-to-implem...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8182983/ https://www.ncbi.nlm.nih.gov/pubmed/34119838 http://dx.doi.org/10.1016/j.bios.2021.113418 |
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author | Yang, Yihan Liu, Jinchuan Zhou, Xiaohong |
author_facet | Yang, Yihan Liu, Jinchuan Zhou, Xiaohong |
author_sort | Yang, Yihan |
collection | PubMed |
description | The continuing pandemic of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, which causes coronavirus disease 2019 (COVID-19), has spread globally and its reliable diagnosis is one of the foremost priorities for protecting public health. Herein a rapid (<1 h), easy-to-implement, and accurate CRISPR-based evanescent wave fluorescence biosensing platform for detection of SARS-CoV-2 is reported. The collateral effect of Cas13a is combined with a universal autonomous enzyme-free hybridization chain reaction (HCR) by designing a cleavage hairpin reporter, which is cleaved upon target recognition, and hence releasing the initiator sequence to trigger the downstream HCR circuits. Detection of HCR assemblies is accomplished by first adsorbing to the desthiobiotin-modified optical fiber, followed by fluorescence emission induced by an evanescent field. Three Cas13a crRNAs targeting the genes of S, N and Orf1ab of SARS-CoV-2 are programmed to specifically target SARS-CoV-2 or broadly detect related coronavirus strains, such as MERS-CoV and SARS-CoV. The HCR amplification coupled Cas13a-based biosensing platform is capable of rapid detection of SARS-CoV-2 with attomolar sensitivity. This method is further validated by adding target RNA of SARS-CoV-2 in negative oropharyngeal swabs. The good discrimination capability of this technique demonstrates its promising potential for point-of-care diagnosis of COVID-19. |
format | Online Article Text |
id | pubmed-8182983 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81829832021-06-07 A CRISPR-based and post-amplification coupled SARS-CoV-2 detection with a portable evanescent wave biosensor Yang, Yihan Liu, Jinchuan Zhou, Xiaohong Biosens Bioelectron Article The continuing pandemic of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, which causes coronavirus disease 2019 (COVID-19), has spread globally and its reliable diagnosis is one of the foremost priorities for protecting public health. Herein a rapid (<1 h), easy-to-implement, and accurate CRISPR-based evanescent wave fluorescence biosensing platform for detection of SARS-CoV-2 is reported. The collateral effect of Cas13a is combined with a universal autonomous enzyme-free hybridization chain reaction (HCR) by designing a cleavage hairpin reporter, which is cleaved upon target recognition, and hence releasing the initiator sequence to trigger the downstream HCR circuits. Detection of HCR assemblies is accomplished by first adsorbing to the desthiobiotin-modified optical fiber, followed by fluorescence emission induced by an evanescent field. Three Cas13a crRNAs targeting the genes of S, N and Orf1ab of SARS-CoV-2 are programmed to specifically target SARS-CoV-2 or broadly detect related coronavirus strains, such as MERS-CoV and SARS-CoV. The HCR amplification coupled Cas13a-based biosensing platform is capable of rapid detection of SARS-CoV-2 with attomolar sensitivity. This method is further validated by adding target RNA of SARS-CoV-2 in negative oropharyngeal swabs. The good discrimination capability of this technique demonstrates its promising potential for point-of-care diagnosis of COVID-19. Elsevier B.V. 2021-10-15 2021-06-07 /pmc/articles/PMC8182983/ /pubmed/34119838 http://dx.doi.org/10.1016/j.bios.2021.113418 Text en © 2021 Elsevier B.V. All rights reserved. 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 Yang, Yihan Liu, Jinchuan Zhou, Xiaohong A CRISPR-based and post-amplification coupled SARS-CoV-2 detection with a portable evanescent wave biosensor |
title | A CRISPR-based and post-amplification coupled SARS-CoV-2 detection with a portable evanescent wave biosensor |
title_full | A CRISPR-based and post-amplification coupled SARS-CoV-2 detection with a portable evanescent wave biosensor |
title_fullStr | A CRISPR-based and post-amplification coupled SARS-CoV-2 detection with a portable evanescent wave biosensor |
title_full_unstemmed | A CRISPR-based and post-amplification coupled SARS-CoV-2 detection with a portable evanescent wave biosensor |
title_short | A CRISPR-based and post-amplification coupled SARS-CoV-2 detection with a portable evanescent wave biosensor |
title_sort | crispr-based and post-amplification coupled sars-cov-2 detection with a portable evanescent wave biosensor |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8182983/ https://www.ncbi.nlm.nih.gov/pubmed/34119838 http://dx.doi.org/10.1016/j.bios.2021.113418 |
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