
pmid: 33476695
pmc: PMC7813513
(Uploaded by Plazi for the Bat Literature Project) Bats carry diverse severe acute respiratory syndrome-related coronaviruses (SARSr-CoVs). The suspected inter species transmission of SARSr-CoVs from bats to humans has caused two severe CoV pandemics, the SARS pandemic in 2003 and the recent COVID-19 pandemic. The receptor utilization of SARSr-CoV plays the key role in determining the host range and the interspecies transmission ability of the virus. Both SARS-CoV and SARSCoV-2 use angiotensin-converting enzyme 2 (ACE2) as their receptor. Previous studies showed that WIV1 strain, the first living coronavirus isolated from bat using ACE2 as its receptor, is the prototype of SARS-CoV. The receptor-binding domain (RBD) in the spike protein (S) of SARS-CoV and WIV1 is responsible for ACE2 binding and medicates the viral entry. Comparing to SARS-CoV, WIV1 has three distinct amino acid residues (442, 472, and 487) in its RBD. This study aimed at exploring whether these three residues could alter the receptor utili zation of SARSr-CoVs. We replaced the three residues in SARS-CoV (BJ01 strain) S with their counterparts in WIV1 S, and then evaluated the change of their utilization of bat, civet, and human ACE2s using a lentivirusbased pseudovirus infection system. To further validate the S-ACE2 interactions, the binding affinity between the RBDs of these S proteins and the three ACE2s were verified by flow cytometry. The results showed that the single amino acid substitution Y442S in the RBD of BJ01 S enhanced its utilization of bat ACE2 and its binding affinity to bat ACE2. On the contrary, the reverse substitution in WIV1 S (S442Y) significantly attenuated the pseudovirus utilization of bat, civet and human ACE2s for cell entry, and reduced its binding affinity with the three ACE2s. These results suggest that the S442 is critical for WIV1 adapting to bats as its natural hosts. These findings will enhance our understanding of host adaptations and cross-species infections of coronaviruses, contributing to the prediction and prevention of coronavirus epidemics.
Cancer Research, bats, bat, Article, Host Specificity, Viverridae, Virology, Chiroptera, Animals, Humans, Animalia, Chordata, Cells, Cultured, Binding Sites, SARS-CoV-2, COVID-19, Biodiversity, Virus Internalization, Infectious Diseases, Spike Glycoprotein, Coronavirus, Mammalia, Angiotensin-Converting Enzyme 2
Cancer Research, bats, bat, Article, Host Specificity, Viverridae, Virology, Chiroptera, Animals, Humans, Animalia, Chordata, Cells, Cultured, Binding Sites, SARS-CoV-2, COVID-19, Biodiversity, Virus Internalization, Infectious Diseases, Spike Glycoprotein, Coronavirus, Mammalia, Angiotensin-Converting Enzyme 2
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