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A novel diagnostic test to screen SARS-CoV-2 variants containing E484K and N501Y mutations.
Zhao, Yanan; Lee, Annie; Composto, Kaelea; Cunningham, Marcus H; Mediavilla, Jose R; Fennessey, Samantha; Corvelo, André; Chow, Kar Fai; Zody, Michael; Chen, Liang; Kreiswirth, Barry N; Perlin, David S.
  • Zhao Y; Center for Discovery and Innovation, Hackensack Meridian Health, Nutley, NJ, USA.
  • Lee A; Hackensack Meridian School of Medicine, Nutley, NJ, USA.
  • Composto K; Center for Discovery and Innovation, Hackensack Meridian Health, Nutley, NJ, USA.
  • Cunningham MH; Center for Discovery and Innovation, Hackensack Meridian Health, Nutley, NJ, USA.
  • Mediavilla JR; Center for Discovery and Innovation, Hackensack Meridian Health, Nutley, NJ, USA.
  • Fennessey S; Center for Discovery and Innovation, Hackensack Meridian Health, Nutley, NJ, USA.
  • Corvelo A; New York Genome Center, New York, NY, USA.
  • Chow KF; New York Genome Center, New York, NY, USA.
  • Zody M; Core Laboratory, Department of Pathology, Hackensack University Medical Center, Hackensack, NJ, USA.
  • Chen L; New York Genome Center, New York, NY, USA.
  • Kreiswirth BN; Center for Discovery and Innovation, Hackensack Meridian Health, Nutley, NJ, USA.
  • Perlin DS; Hackensack Meridian School of Medicine, Nutley, NJ, USA.
Emerg Microbes Infect ; 10(1): 994-997, 2021 Dec.
Article in English | MEDLINE | ID: covidwho-1225582
Preprint
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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.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Spike Glycoprotein, Coronavirus / SARS-CoV-2 / COVID-19 / Mutation Type of study: Diagnostic study / Observational study / Prognostic study Topics: Variants Limits: Humans Country/Region as subject: North America Language: English Journal: Emerg Microbes Infect Year: 2021 Document Type: Article Affiliation country: 22221751.2021.1929504

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Spike Glycoprotein, Coronavirus / SARS-CoV-2 / COVID-19 / Mutation Type of study: Diagnostic study / Observational study / Prognostic study Topics: Variants Limits: Humans Country/Region as subject: North America Language: English Journal: Emerg Microbes Infect Year: 2021 Document Type: Article Affiliation country: 22221751.2021.1929504