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Rapid detection and tracking of Omicron variant of SARS-CoV-2 using CRISPR-Cas12a-based assay
BACKGROUND: The newly emerged SARS-CoV-2 variant of concern (VOC) Omicron is spreading quickly worldwide, which manifests an urgent need of simple and rapid assay to detect and diagnose Omicron infection and track its spread. METHODS: To design allele-specific CRISPR RNAs (crRNAs) targeting the sign...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8849905/ https://www.ncbi.nlm.nih.gov/pubmed/35189535 http://dx.doi.org/10.1016/j.bios.2022.114098 |
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author | Liang, Yuanhao Lin, Hongqing Zou, Lirong Deng, Xiaoling Tang, Shixing |
author_facet | Liang, Yuanhao Lin, Hongqing Zou, Lirong Deng, Xiaoling Tang, Shixing |
author_sort | Liang, Yuanhao |
collection | PubMed |
description | BACKGROUND: The newly emerged SARS-CoV-2 variant of concern (VOC) Omicron is spreading quickly worldwide, which manifests an urgent need of simple and rapid assay to detect and diagnose Omicron infection and track its spread. METHODS: To design allele-specific CRISPR RNAs (crRNAs) targeting the signature mutations in the spike protein of Omicron variant, and to develop a CRISPR-Cas12a-based assay to specifically detect Omicron variant. RESULTS: Our system showed a low limit of detection of 2 copies per reaction for the plasmid DNA of Omicron variant, and could readily detect Omicron variant in 5 laboratory-confirmed clinical samples and distinguish them from 57 SARS-CoV-2 positive clinical samples (4 virus isolates and 53 oropharyngeal swab specimens) infected with wild-type (N = 8) and the variants of Alpha (N = 17), Beta (N = 17) and Delta (N = 15). The testing results could be measured by fluorescent detector or judged by naked eyes. In addition, no cross-reaction was observed when detecting 16 clinical samples infected with 9 common respiratory pathogens. CONCLUSIONS: The rapid assay could be easily set up in laboratories already conducting SARS-CoV-2 nucleic acid amplification tests and implemented routinely in resource-limited settings to monitor and track the spread of Omicron variant. |
format | Online Article Text |
id | pubmed-8849905 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88499052022-02-18 Rapid detection and tracking of Omicron variant of SARS-CoV-2 using CRISPR-Cas12a-based assay Liang, Yuanhao Lin, Hongqing Zou, Lirong Deng, Xiaoling Tang, Shixing Biosens Bioelectron Article BACKGROUND: The newly emerged SARS-CoV-2 variant of concern (VOC) Omicron is spreading quickly worldwide, which manifests an urgent need of simple and rapid assay to detect and diagnose Omicron infection and track its spread. METHODS: To design allele-specific CRISPR RNAs (crRNAs) targeting the signature mutations in the spike protein of Omicron variant, and to develop a CRISPR-Cas12a-based assay to specifically detect Omicron variant. RESULTS: Our system showed a low limit of detection of 2 copies per reaction for the plasmid DNA of Omicron variant, and could readily detect Omicron variant in 5 laboratory-confirmed clinical samples and distinguish them from 57 SARS-CoV-2 positive clinical samples (4 virus isolates and 53 oropharyngeal swab specimens) infected with wild-type (N = 8) and the variants of Alpha (N = 17), Beta (N = 17) and Delta (N = 15). The testing results could be measured by fluorescent detector or judged by naked eyes. In addition, no cross-reaction was observed when detecting 16 clinical samples infected with 9 common respiratory pathogens. CONCLUSIONS: The rapid assay could be easily set up in laboratories already conducting SARS-CoV-2 nucleic acid amplification tests and implemented routinely in resource-limited settings to monitor and track the spread of Omicron variant. Elsevier B.V. 2022-06-01 2022-02-17 /pmc/articles/PMC8849905/ /pubmed/35189535 http://dx.doi.org/10.1016/j.bios.2022.114098 Text en © 2022 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 Liang, Yuanhao Lin, Hongqing Zou, Lirong Deng, Xiaoling Tang, Shixing Rapid detection and tracking of Omicron variant of SARS-CoV-2 using CRISPR-Cas12a-based assay |
title | Rapid detection and tracking of Omicron variant of SARS-CoV-2 using CRISPR-Cas12a-based assay |
title_full | Rapid detection and tracking of Omicron variant of SARS-CoV-2 using CRISPR-Cas12a-based assay |
title_fullStr | Rapid detection and tracking of Omicron variant of SARS-CoV-2 using CRISPR-Cas12a-based assay |
title_full_unstemmed | Rapid detection and tracking of Omicron variant of SARS-CoV-2 using CRISPR-Cas12a-based assay |
title_short | Rapid detection and tracking of Omicron variant of SARS-CoV-2 using CRISPR-Cas12a-based assay |
title_sort | rapid detection and tracking of omicron variant of sars-cov-2 using crispr-cas12a-based assay |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8849905/ https://www.ncbi.nlm.nih.gov/pubmed/35189535 http://dx.doi.org/10.1016/j.bios.2022.114098 |
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