CRISPR-based assays for rapid detection of SARS-CoV-2.


Journal

Methods (San Diego, Calif.)
ISSN: 1095-9130
Titre abrégé: Methods
Pays: United States
ID NLM: 9426302

Informations de publication

Date de publication:
07 2022
Historique:
received: 28 07 2020
revised: 16 09 2020
accepted: 06 10 2020
pubmed: 13 10 2020
medline: 22 6 2022
entrez: 12 10 2020
Statut: ppublish

Résumé

COVID-19 pandemic posed an unprecedented threat to global public health and economies. There is no effective treatment of the disease, hence, scaling up testing for rapid diagnosis of SARS-CoV-2 infected patients and quarantine them from healthy individuals is one the best strategies to curb the pandemic. Establishing globally accepted easy-to-access diagnostic tests is extremely important to understanding the epidemiology of the present pandemic. While nucleic acid based tests are considered to be more sensitive with respect to serological tests but present gold standard qRT-PCR-based assays possess limitations such as low sample throughput, requirement for sophisticated reagents and instrumentation. To overcome these shortcomings, recent efforts of incorporating LAMP-based isothermal detection, and minimizing the number of reagents required are on rise. CRISPR based novel techniques, when merge with isothermal and allied technologies, promises to provide sensitive and rapid detection of SARS-CoV-2 nucleic acids. Here, we discuss and present compilation of state-of-the-art detection techniques for COVID-19 using CRISPR technology which has tremendous potential to transform diagnostics and epidemiology.

Identifiants

pubmed: 33045362
pii: S1046-2023(20)30217-6
doi: 10.1016/j.ymeth.2020.10.003
pmc: PMC7546951
pii:
doi:

Substances chimiques

RNA, Viral 0

Types de publication

Journal Article Review Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

594-603

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

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Auteurs

Vivek S Javalkote (VS)

Reliance Industries Ltd, R&D-Synthetic Biology Group, Reliance Corporate Park, Navi Mumbai, India.

Nagesh Kancharla (N)

Reliance Industries Ltd, R&D-Synthetic Biology Group, Reliance Corporate Park, Navi Mumbai, India.

Bhaskar Bhadra (B)

Reliance Industries Ltd, R&D-Synthetic Biology Group, Reliance Corporate Park, Navi Mumbai, India.

Manish Shukla (M)

Reliance Industries Ltd, R&D-Synthetic Biology Group, Reliance Corporate Park, Navi Mumbai, India.

Badrish Soni (B)

Reliance Industries Ltd, R&D-Synthetic Biology Group, Reliance Corporate Park, Navi Mumbai, India.

Ajit Sapre (A)

Reliance Industries Ltd, R&D-Synthetic Biology Group, Reliance Corporate Park, Navi Mumbai, India.

Michael Goodin (M)

Department of Plant Pathology, University of Kentucky, Lexington, KY 40546, USA. Electronic address: mgoodin@uky.edu.

Anindya Bandyopadhyay (A)

Reliance Industries Ltd, R&D-Synthetic Biology Group, Reliance Corporate Park, Navi Mumbai, India. Electronic address: Anindya.b@ril.com.

Santanu Dasgupta (S)

Reliance Industries Ltd, R&D-Synthetic Biology Group, Reliance Corporate Park, Navi Mumbai, India. Electronic address: Santanu.dasgupta@ril.com.

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