SARS-CoV-2 immune evasion by the B.1.427/B.1.429 variant of concern

Matthew McCallum(University of Washington), Jessica Bassi(Vir Biotechnology (Switzerland)), Anna De Marco(Vir Biotechnology (Switzerland)), Alex Chen(VIR Biotechnology (United States)), Alexandra C. Walls(University of Washington), Julia di Iulio(VIR Biotechnology (United States)), M. Alejandra Tortorici(University of Washington), Mary-Jane Navarro(University of Washington), Chiara Silacci-Fregni(Vir Biotechnology (Switzerland)), Christian Saliba(Vir Biotechnology (Switzerland)), Kaitlin R. Sprouse(University of Washington), Maria L. Agostini(VIR Biotechnology (United States)), Dora Pinto(Vir Biotechnology (Switzerland)), Katja Culap(Vir Biotechnology (Switzerland)), Siro Bianchi(Vir Biotechnology (Switzerland)), Stefano Jaconi(Vir Biotechnology (Switzerland)), Elisabetta Cameroni(Vir Biotechnology (Switzerland)), John E. Bowen(University of Washington), Sasha W. Tilles(University of Washington), Matteo Samuele Pizzuto(Vir Biotechnology (Switzerland)), Sonja Bernasconi Guastalla, Giovanni Bona(Clinica Luganese Moncucco), Alessandra Franzetti-Pellanda(Clinica Luganese Moncucco), Christian Garzoni(Clinica Luganese Moncucco), Wesley C. Van Voorhis(University of Washington), Laura E. Rosen(VIR Biotechnology (United States)), Gyorgy Snell(VIR Biotechnology (United States)), Amalio Telenti(VIR Biotechnology (United States)), Herbert W. Virgin(VIR Biotechnology (United States)), Luca Piccoli(Vir Biotechnology (Switzerland)), Davide Corti(Vir Biotechnology (Switzerland)), David Veesler(University of Washington)
Science
July 1, 2021
Cited by 462Open Access
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Abstract

A novel variant of concern (VOC) named CAL.20C (B.1.427/B.1.429), which was originally detected in California, carries spike glycoprotein mutations S13I in the signal peptide, W152C in the N-terminal domain (NTD), and L452R in the receptor-binding domain (RBD). Plasma from individuals vaccinated with a Wuhan-1 isolate-based messenger RNA vaccine or from convalescent individuals exhibited neutralizing titers that were reduced 2- to 3.5-fold against the B.1.427/B.1.429 variant relative to wild-type pseudoviruses. The L452R mutation reduced neutralizing activity in 14 of 34 RBD-specific monoclonal antibodies (mAbs). The S13I and W152C mutations resulted in total loss of neutralization for 10 of 10 NTD-specific mAbs because the NTD antigenic supersite was remodeled by a shift of the signal peptide cleavage site and the formation of a new disulfide bond, as revealed by mass spectrometry and structural studies.


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