Characterization of Entry Pathways, Species-Specific Angiotensin-Converting Enzyme 2 Residues Determining Entry, and Antibody Neutralization Evasion of Omicron BA.1, BA.1.1, BA.2, and BA.3 Variants

Author:

Neerukonda Sabari Nath1,Wang Richard1,Vassell Russell1,Baha Haseebullah1,Lusvarghi Sabrina1,Liu Shufeng1ORCID,Wang Tony1ORCID,Weiss Carol D.1ORCID,Wang Wei1ORCID

Affiliation:

1. US Food and Drug Administration, Office of Vaccine Research and Review, Center for Biologics Evaluation, Research and Review, Silver Spring, Maryland, USA

Abstract

The ongoing emergence of SARS-CoV-2 Omicron variants with an extensive number of spike mutations poses a significant public health and zoonotic concern due to enhanced transmission fitness and escape from neutralizing antibodies. We studied three Omicron lineage variants (BA.1, BA.2, and BA.3) and found that transmembrane serine protease 2 has less influence on Omicron entry into cells than on D614G, and Omicron exhibits greater sensitivity to endosomal entry inhibition compared to D614G.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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