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SARS-CoV-2 variant of concern fitness and adaptation in primary human airway epithelia.

Authors :
Meganck RM
Edwards CE
Mallory ML
Lee RE
Dang H
Bailey AB
Wykoff JA
Gallant SC
Zhu DR
Yount BL
Kato T
Shaffer KM
Nakano S
Cawley AM
Sontake V
Wang JR
Hagan RS
Miller MB
Tata PR
Randell SH
Tse LV
Ehre C
Okuda K
Boucher RC
Baric RS
Source :
Cell reports [Cell Rep] 2024 Apr 23; Vol. 43 (4), pp. 114076. Date of Electronic Publication: 2024 Apr 10.
Publication Year :
2024

Abstract

The severe acute respiratory syndrome coronavirus 2 pandemic is characterized by the emergence of novel variants of concern (VOCs) that replace ancestral strains. Here, we dissect the complex selective pressures by evaluating variant fitness and adaptation in human respiratory tissues. We evaluate viral properties and host responses to reconstruct forces behind D614G through Omicron (BA.1) emergence. We observe differential replication in airway epithelia, differences in cellular tropism, and virus-induced cytotoxicity. D614G accumulates the most mutations after infection, supporting zoonosis and adaptation to the human airway. We perform head-to-head competitions and observe the highest fitness for Gamma and Delta. Under these conditions, RNA recombination favors variants encoding the B.1.617.1 lineage 3' end. Based on viral growth kinetics, Alpha, Gamma, and Delta exhibit increased fitness compared to D614G. In contrast, the global success of Omicron likely derives from increased transmission and antigenic variation. Our data provide molecular evidence to support epidemiological observations of VOC emergence.<br />Competing Interests: Declaration of interests R.S.B. is a member of advisory boards for VaxArt, Takeda, and Invivyd; has consulted for Gilead; and has collaborative projects with Gilead, J&J, and Hillevax focused on unrelated projects.<br /> (Copyright © 2024. Published by Elsevier Inc.)

Details

Language :
English
ISSN :
2211-1247
Volume :
43
Issue :
4
Database :
MEDLINE
Journal :
Cell reports
Publication Type :
Academic Journal
Accession number :
38607917
Full Text :
https://doi.org/10.1016/j.celrep.2024.114076