
Evolutionary arms race dynamics shape the diversity of viruses and their receptors. Identification of key residues which are involved in interspecies transmission is important to predict potential pathogen spillover from wildlife to humans. Previously, we have identified genetically diverse SARSr-CoVs in Chinese horseshoe bats. Here, we show the highly polymorphic ACE2 in Chinese horseshoe bat populations. These ACE2 variants support SARS-CoV and SARSr-CoV infection but with different binding affinities to different spike proteins. The higher binding affinity of SARSr-CoV spike to human ACE2 suggests that these viruses have the capacity for spillover to humans. The positive selection of residues at the interface between ACE2 and SARSr-CoV spike protein suggests long-term and ongoing coevolutionary dynamics between them. Continued surveillance of this group of viruses in bats is necessary for the prevention of the next SARS-like disease.
Models, Molecular, Immunology, Peptidyl-Dipeptidase A, Microbiology, Biological Coevolution, Evolution, Molecular, Virology, Chiroptera, Animals, Humans, Selection, Genetic, Phylogeny, Binding Sites, Genetic Variation, Genetic Diversity and Evolution, Severe acute respiratory syndrome-related coronavirus, Insect Science, Mutation, Spike Glycoprotein, Coronavirus, Receptors, Virus, Angiotensin-Converting Enzyme 2, Coronavirus Infections, HeLa Cells, Protein Binding
Models, Molecular, Immunology, Peptidyl-Dipeptidase A, Microbiology, Biological Coevolution, Evolution, Molecular, Virology, Chiroptera, Animals, Humans, Selection, Genetic, Phylogeny, Binding Sites, Genetic Variation, Genetic Diversity and Evolution, Severe acute respiratory syndrome-related coronavirus, Insect Science, Mutation, Spike Glycoprotein, Coronavirus, Receptors, Virus, Angiotensin-Converting Enzyme 2, Coronavirus Infections, HeLa Cells, Protein Binding
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