| Literature DB >> 33977858 |
Yanan Zhao1,2, Annie Lee1, Kaelea Composto1, Marcus H Cunningham1, Jose R Mediavilla1, Samantha Fennessey3, André Corvelo3, Kar Fai Chow4, Michael Zody3, Liang Chen1,2, Barry N Kreiswirth1,2,5, David S Perlin1,2,5.
Abstract
Spike protein mutations E484K and N501Y carried by SARS-CoV-2 variants have been associated with concerning changes of the virus, including resistance to neutralizing antibodies and increased transmissibility. While the concerning variants are fast spreading in various geographical areas, identification and monitoring of these variants are lagging far behind, due in large part to the slow speed and insufficient capacity of viral sequencing. In response to the unmet need for a fast and efficient screening tool, we developed a single-tube duplex molecular assay for rapid and simultaneous identification of E484K and N501Y mutations from nasopharyngeal swab (NS) samples within 2.5 h from sample preparation to report. Using this tool, we screened a total of 1135 clinical NS samples collected from COVID patients at 8 hospitals within the Hackensack Meridian Health network in New Jersey between late December 2020 and March 2021. Our data revealed dramatic increases in the frequencies of both E484K and N501Y over time, underscoring the need for continuous epidemiological monitoring.Entities:
Keywords: E484K; N501Y; SARS-CoV-2; molecular assay; screening; variants
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Year: 2021 PMID: 33977858 DOI: 10.1080/22221751.2021.1929504
Source DB: PubMed Journal: Emerg Microbes Infect ISSN: 2222-1751 Impact factor: 7.163