TY - JOUR
AU - Lista, Maria Jose
AU - Winstone, Helena
AU - Wilson, Harry D.
AU - Dyer, Adam
AU - Pickering, Suzanne
AU - Galao, Rui Pedro
AU - De Lorenzo, Giuditta
AU - Cowton, Vanessa M.
AU - Furnon, Wilhelm
AU - Suarez, Nicolas M.
AU - Orton, Richard J.
AU - Palmarini, Massimo
AU - Patel, Arvind H.
AU - Snell, Luke
AU - Nebbia, Gaia
AU - Swanson, Chad
AU - Neil, Stuart J. D.
PY - 2022
DA - November
TI - The P681H mutation in the spike glycoprotein of the alpha variant of SARS-CoV-2 escapes IFITM restriction and is necessary for type I interferon resistance
JO - Journal of Virology
VL - 96
IS - 23
DO - https://doi.org/10.1128/jvi.01250-22
AB - The appearance of new dominant variants of concern (VOC) of severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) threatens the global response to the coronavirus disease 2019 (COVID-19) pandemic. Of these, the alpha variant (also known as B.1.1.7), which appeared initially in the United Kingdom, became the dominant variant in much of Europe and North America in the first half of 2021. The spike (S) glycoprotein of alpha acquired seven mutations and two deletions compared to the ancestral virus, including the P681H mutation adjacent to the polybasic cleavage site, which has been suggested to enhance S cleavage. Here, we show that the alpha spike protein confers a level of resistance to beta interferon (IFN-β) in human lung epithelial cells. This correlates with resistance to an entry restriction mediated by interferon-induced transmembrane protein 2 (IFITM2) and a pronounced infection enhancement by IFITM3. Furthermore, the P681H mutation is essential for resistance to IFN-β and context-dependent resistance to IFITMs in the alpha S. P681H reduces dependence on endosomal cathepsins, consistent with enhanced cell surface entry. However, reversion of H681 does not reduce cleaved spike incorporation into particles, indicating that it exerts its effect on entry and IFN-β downstream of furin cleavage. Overall, we suggest that, in addition to adaptive immune escape, mutations associated with VOC may well also confer a replication and/or transmission advantage through adaptation to resist innate immune mechanisms.
PB - American Society for Microbiology
UR - https://eprints.gla.ac.uk/286493/
KW - Coronavirus (COVID-19)
ER