| Literature DB >> 33673107 |
Mark J Osborn1, Akshay Bhardwaj1, Samuel P Bingea1, Friederike Knipping1, Colby J Feser1, Christopher J Lees1, Daniel P Collins2, Clifford J Steer3,4, Bruce R Blazar1, Jakub Tolar1.
Abstract
Clustered regularly interspaced short palindromic repeat (CRISPR/Cas) proteins can be designed to bind specified DNA and RNA sequences and hold great promise for the accurate detection of nucleic acids for diagnostics. We integrated commercially available reagents into a CRISPR/Cas9-based lateral flow assay that can detect severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) sequences with single-base specificity. This approach requires minimal equipment and represents a simplified platform for field-based deployment. We also developed a rapid, multiplex fluorescence CRISPR/Cas9 nuclease cleavage assay capable of detecting and differentiating SARS-CoV-2, influenza A and B, and respiratory syncytial virus in a single reaction. Our findings provide proof-of-principle for CRISPR/Cas9 point-of-care diagnosis as well as a scalable fluorescent platform for identifying respiratory viral pathogens with overlapping symptomology.Entities:
Keywords: CRISPR/Cas9; SARS-Co-V2; lateral flow assay
Year: 2021 PMID: 33673107 PMCID: PMC7918862 DOI: 10.3390/bioengineering8020023
Source DB: PubMed Journal: Bioengineering (Basel) ISSN: 2306-5354