Mutations that adapt SARS-CoV-2 to mustelid hosts do not increase fitness in the human airway

Author:

Zhou JieORCID,Peacock Thomas P.ORCID,Brown Jonathan C.ORCID,Goldhill Daniel H.ORCID,Elrefaey Ahmed M.E.ORCID,Penrice-Randal RebekahORCID,Cowton Vanessa M.ORCID,Lorenzo Giuditta DeORCID,Furnon WilhelmORCID,Harvey William T.ORCID,Kugathasan RuthiranORCID,Frise RebeccaORCID,Baillon LauryORCID,Lassaunière RiaORCID,Thakur Nazia,Gallo Giulia,Goldswain HannahORCID,Donovan-Banfield I’ahORCID,Dong XiaofengORCID,Randle Nadine P.ORCID,Sweeney Fiachra,Glynn Martha C.,Quantrill Jessica L.ORCID,McKay Paul F.ORCID,Patel Arvind H.ORCID,Palmarini Massimo,Hiscox Julian A.,Bailey DalanORCID,Barclay Wendy S.ORCID

Abstract

AbstractSARS-CoV-2 has a broad mammalian species tropism infecting humans, cats, dogs and farmed mink. Since the start of the 2019 pandemic several reverse zoonotic outbreaks of SARS-CoV-2 have occurred in mink, one of which reinfected humans and caused a cluster of infections in Denmark. Here we investigate the molecular basis of mink and ferret adaptation and demonstrate the spike mutations Y453F, F486L, and N501T all specifically adapt SARS-CoV-2 to use mustelid ACE2. Furthermore, we risk assess these mutations and conclude mink-adapted viruses are unlikely to pose an increased threat to humans, as Y453F attenuates the virus replication in human cells and all 3 mink-adaptations have minimal antigenic impact. Finally, we show that certain SARS-CoV-2 variants emerging from circulation in humans may naturally have a greater propensity to infect mustelid hosts and therefore these species should continue to be surveyed for reverse zoonotic infections.

Publisher

Cold Spring Harbor Laboratory

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