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A Novel SARS-CoV-2 Variant of Concern, B.1.526, Identified in New York
Medini K Annavajhala; Hiroshi Mohri; Pengfei Wang; Manoj S Nair; Jason E Zucker; Zizhang Sheng; Angela Gomez-Simmonds; Anne L Kelley; Maya Tagliavia; Yaoxing Huang; Trevor Bedford; David D Ho; Anne-Catrin Uhlemann.
Afiliação
  • Medini K Annavajhala; Columbia University Irving Medical Center, Medicine - Infectious Diseases
  • Hiroshi Mohri; Columbia University Irving Medical Center, Aaron Diamond AIDS Research Center
  • Pengfei Wang; Columbia University Irving Medical Center, Aaron Diamond AIDS Research Center
  • Manoj S Nair; Columbia University Irving Medical Center, Aaron Diamond AIDS Research Center
  • Jason E Zucker; Columbia University Irving Medical Center
  • Zizhang Sheng; Columbia University Irving Medical Center, Medicine - Infectious Diseases
  • Angela Gomez-Simmonds; Columbia University Irving Medical Center, Medicine - Infectious Diseases
  • Anne L Kelley; Columbia University Irving Medical Center, Medicine - Infectious Diseases
  • Maya Tagliavia; Columbia University Irving Medical Center, Medicine - Infectious Diseases
  • Yaoxing Huang; Columbia University Irving Medical Center, Aaron Diamond AIDS Research Center
  • Trevor Bedford; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center
  • David D Ho; Columbia University Irving Medical Center, Aaron Diamond AIDS Research Center
  • Anne-Catrin Uhlemann; Columbia University Irving Medical Center, Medicine - Infectious Diseases
Preprint em Inglês | medRxiv | ID: ppmedrxiv-21252259
ABSTRACT
Recent months have seen surges of SARS-CoV-2 infection across the globe with considerable viral evolution1-3. Extensive mutations in the spike protein may threaten efficacy of vaccines and therapeutic monoclonal antibodies4. Two signature mutations of concern are E484K, which plays a crucial role in the loss of neutralizing activity of antibodies, and N501Y, a driver of rapid worldwide transmission of the B.1.1.7 lineage. Here, we report the emergence of variant lineage B.1.526 that contains E484K and its alarming rise to dominance in New York City in early 2021. This variant is partially or completely resistant to two therapeutic monoclonal antibodies in clinical use and less susceptible to neutralization by convalescent plasma or vaccinee sera, posing a modest antigenic challenge. The B.1.526 lineage has now been reported from all 50 states in the US and numerous other countries. B.1.526 rapidly replaced earlier lineages in New York upon its emergence, with an estimated transmission advantage of 35%. Such transmission dynamics, together with the relative antibody resistance of its E484K sub-lineage, likely contributed to the sharp rise and rapid spread of B.1.526. Although SARS-CoV-2 B.1.526 initially outpaced B.1.1.7 in the region, its growth subsequently slowed concurrent with the rise of B.1.1.7 and ensuing variants.
Licença
cc_by_nc_nd
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Estudo prognóstico Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Estudo prognóstico Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
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