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Structural and functional characteristics of SARS-CoV-2 Omicron subvariant BA.2 spike
Tang Weichun; Christy Lavine; Haisun Zhu; Krishna Anand; Martina Kosikova; Hyung Joon Kwon; Shaowei Wang; Megan L. Mayer; Michael S. Seaman; Jianming Lu; Hang Xie.
Afiliação
  • Tang Weichun; United States Food and Drug Administration
  • Christy Lavine; Beth Israel Deaconess Medical Center
  • Haisun Zhu; Institute for Protein Innovation
  • Krishna Anand; Institute for Protein Innovation
  • Martina Kosikova; United States Food and Drug Administration
  • Hyung Joon Kwon; United States Food and Drug Administration
  • Shaowei Wang; Codex BioSolutions, Inc.
  • Megan L. Mayer; The Harvard Cryo-EM Center for Structural Biology
  • Michael S. Seaman; Beth Israel Deaconess Medical Center
  • Jianming Lu; Codex BioSolutions, Inc.
  • Hang Xie; Center for Biologics Evaluation and Research, US Food and Drug Administration
Preprint em Inglês | bioRxiv | ID: ppbiorxiv-489772
ABSTRACT
The Omicron subvariant BA.2 has become the dominant circulating strain of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in many countries. We have characterized structural, functional and antigenic properties of the full-length BA.2 spike (S) protein and compared replication of the authentic virus in cell culture and animal model with previously prevalent variants. BA.2 S can fuse membranes more efficiently than Omicron BA.1, mainly due to lack of a BA.1-specific mutation that may retard the receptor engagement, but still less efficiently than other variants. Both BA.1 and BA.2 viruses replicated substantially faster in animal lungs than the early G614 (B.1) strain in the absence of pre-existing immunity, possibly explaining the increased transmissibility despite their functionally compromised spikes. As in BA.1, mutations in the BA.2 S remodel its antigenic surfaces leading to strong resistance to neutralizing antibodies. These results suggest that both immune evasion and replicative advantage may contribute to the heightened transmissibility for the Omicron subvariants.
Licença
cc_no
Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Idioma: Inglês Ano de publicação: 2022 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Idioma: Inglês Ano de publicação: 2022 Tipo de documento: Preprint
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