Loading…

A CRISPR-based approach using dead Cas9-sgRNA to detect SARS-CoV-2

Rapid, highly specific, and robust diagnostic kits to detect viruses and pathogens are needed to control disease spread and transmission globally. Of the many different methods proposed to diagnose COVID-19 infection, CRISPR-based detection of nucleic acids tests are among the most prominent. Here,...

Full description

Saved in:
Bibliographic Details
Published in:Frontiers in molecular biosciences 2023-06, Vol.10, p.1201347-1201347
Main Authors: Aouida, Mustapha, Saifaldeen, Maryam, Al-Ansari, Dana E, Taleb, Sara, Hssain, Ali Ait, Ramotar, Dindial
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Rapid, highly specific, and robust diagnostic kits to detect viruses and pathogens are needed to control disease spread and transmission globally. Of the many different methods proposed to diagnose COVID-19 infection, CRISPR-based detection of nucleic acids tests are among the most prominent. Here, we describe a new way of using CRISPR/Cas systems as a rapid and highly specific tool to detect the SARS-CoV-2 virus using the dCas9-sgRNA-based technique. As a proof of concept, we used a synthetic DNA of the M gene, one of the SARS-CoV-2 virus genes, and demonstrated that we can specifically inactivate unique restriction enzyme sites on this gene using CRISPR/Cas multiplexing of dCas9-sgRNA- and dCas9-sgRNA- . These complexes recognize and bind to the target sequence spanning the and restriction enzyme sites, respectively, and protect the M gene from digestion by and/or . We further demonstrated that this approach can be used to detect the M gene when expressed in human cells and from individuals infected with SARS-CoV-2. We refer to this approach as dead Cas9 Protects Restriction Enzyme Sites, and believe that it has the potential to be applied as a diagnostic tool for many DNA/RNA pathogens.
ISSN:2296-889X
2296-889X
DOI:10.3389/fmolb.2023.1201347