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

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 wit...

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Detalles Bibliográficos
Autores principales: McCallum, Matthew, Bassi, Jessica, De Marco, Anna, Chen, Alex, Walls, Alexandra C., Di Iulio, Julia, Tortorici, M. Alejandra, Navarro, Mary-Jane, Silacci-Fregni, Chiara, Saliba, Christian, Sprouse, Kaitlin R., Agostini, Maria, Pinto, Dora, Culap, Katja, Bianchi, Siro, Jaconi, Stefano, Cameroni, Elisabetta, Bowen, John E., Tilles, Sasha W., Pizzuto, Matteo Samuele, Guastalla, Sonja Bernasconi, Bona, Giovanni, Pellanda, Alessandra Franzetti, Garzoni, Christian, Van Voorhis, Wesley C., Rosen, Laura E., Snell, Gyorgy, Telenti, Amalio, Virgin, Herbert W., Piccoli, Luca, Corti, Davide, Veesler, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9835956/
https://www.ncbi.nlm.nih.gov/pubmed/34210893
http://dx.doi.org/10.1126/science.abi7994
Descripción
Sumario: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.