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Structural basis for mouse receptor recognition by bat SARS2-like coronaviruses.


ABSTRACT: The animal origin of SARS-CoV-2 remains elusive, lacking a plausible evolutionary narrative that may account for its emergence. Its spike protein resembles certain segments of BANAL-236 and RaTG13, two bat coronaviruses considered possible progenitors of SARS-CoV-2. Additionally, its spike contains a furin motif, a common feature of rodent coronaviruses. To explore the possible involvement of rodents in the emergence of SARS-CoV-2 spike, we examined the crystal structures of the spike receptor-binding domains (RBDs) of BANAL-236 and RaTG13 each complexed with mouse receptor ACE2. Both RBDs have residues at positions 493 and 498 that align well with two virus-binding hotspots on mouse ACE2. Our biochemical evidence supports that both BANAL-236 and RaTG13 spikes can use mouse ACE2 as their entry receptor. These findings point to a scenario in which these bat coronaviruses may have coinfected rodents, leading to a recombination of their spike genes and a subsequent acquisition of a furin motif in rodents, culminating in the emergence of SARS-CoV-2.

SUBMITTER: Zhang W 

PROVIDER: S-EPMC11317568 | biostudies-literature | 2024 Aug

REPOSITORIES: biostudies-literature

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Structural basis for mouse receptor recognition by bat SARS2-like coronaviruses.

Zhang Wei W   Shi Ke K   Hsueh Fu-Chun FC   Mendoza Alise A   Ye Gang G   Huang Linfen L   Perlman Stanley S   Aihara Hideki H   Li Fang F  

Proceedings of the National Academy of Sciences of the United States of America 20240731 32


The animal origin of SARS-CoV-2 remains elusive, lacking a plausible evolutionary narrative that may account for its emergence. Its spike protein resembles certain segments of BANAL-236 and RaTG13, two bat coronaviruses considered possible progenitors of SARS-CoV-2. Additionally, its spike contains a furin motif, a common feature of rodent coronaviruses. To explore the possible involvement of rodents in the emergence of SARS-CoV-2 spike, we examined the crystal structures of the spike receptor-b  ...[more]

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