Although both SARS-CoV-1 and SARS-CoV-2 utilize ACE2 to mediate infection, the distinctive infectivity and pathogenicity displayed by SARS-CoV-2 is likely to be associated with the acquisition of a polybasic furin-cleavage site in the spike protein, which, together with enhanced binding affinity of the SARS-CoV-2 RBD for ACE2, would significantly broaden the tissue tropism of this virus17,32. This evidence concerns the gene CHMP5 and infection.