| Literature DB >> 35838953 |
Chongwei Bi1,2, Gerardo Ramos-Mandujano1, Mo Li3.
Abstract
Detection and mutation surveillance of SARS-CoV-2 are crucial for combating the COVID-19 pandemic. Here we describe a lab-based method for multiplex isothermal amplification-based sequencing and real-time analysis of multiple viral genomes. It can simultaneously detect SARS-CoV-2, influenza A, human adenovirus, and human coronavirus and monitor mutations for up to 96 samples in real time. The method proved to be rapid and sensitive (limit of detection: 29 viral RNA copies/μL of extracted nucleic acid) in detecting SARS-CoV-2 in clinical samples. We expect it to offer a promising solution for rapid field-deployable detection and mutational surveillance of pandemic viruses.Entities:
Keywords: Multiplexing; Mutation surveillance; RPA; SARS-CoV-2; Virus detection
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Year: 2022 PMID: 35838953 DOI: 10.1007/978-1-0716-2395-4_6
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745