@article{Furnon_W-2025_193662,
title = {Phenotypic evolution of SARS-CoV-2 spike during the COVID-19 pandemic},
author = {Furnon, W. and Cowton, V. and de Lorenzo, G. and Orton, R. and Herder, V. and Cantoni, D. and Ilia, G. and Correa Mendonca, D. and Kerr, K. and Allan, J. and Upfold, N. and Meehan, G. and Bakshi, S. and Das, U. and Arias, S. and McElwee, M. and Little, S. and Logan, N. and Kwok, K. and Smollett, K. and Willett, B. and da Silva Filipe, A. and Robertson, D. and Grove, J. and Patel, A. and Palmarini, M.},
month = {jan},
year = {2025},
abstract = {SARS-CoV-2 variants are mainly defined by mutations in their spike. It is therefore critical to understand how the evolutionary trajectories of spike affect virus phenotypes. So far, it has been challenging to comprehensively compare the many spikes that emerged during the pandemic in a single experimental platform. Here we generated a panel of recombinant viruses carrying different spike proteins from 27 variants circulating between 2020 and 2024 in the same genomic background. We then assessed several of their phenotypic traits both in vitro and in vivo. We found distinct phenotypic trajectories of spike among and between variants circulating before and after the emergence of Omicron variants. Spike of post-Omicron variants maintained enhanced tropism for the nasal epithelium and large airways but displayed, over time, several phenotypic traits typical of the pre-Omicron variants. Hence, spike with phenotypic features of both pre- and post-Omicron variants may continue to emerge in the future.},
pages = {77-93},
volume = {10},
journal = {Nature Microbiology},
publisher = {Springer Nature},
url = {https://doi.org/10.1038/s41564-024-01878-5},
}
