Molecular basis of hippopotamus ACE2 binding to SARS-CoV-2.
Ruirui YangPu HanPengcheng HanDedong LiRunchu ZhaoSheng NiuKefang LiuShihua LiWen-Xia TianGeorge Fu GaoPublished in: Journal of virology (2024)
The hippopotami are the first semi-aquatic artiodactyl mammals wherein SARS-CoV-2 infection has been reported. Exploration of the invasion mechanism of SARS-CoV-2 will provide important information for the surveillance of SARS-CoV-2 in hippopotami, as well as other semi-aquatic mammals and cetaceans. Here, we found that hippopotamus ACE2 (hiACE2) could efficiently bind to the RBDs of the SARS-CoV-2 prototype (PT) and variants of concern (VOCs) and facilitate the transduction of SARS-CoV-2 PT and VOCs pseudoviruses into hiACE2-expressing cells. The cryo-EM structure of the SARS-CoV-2 PT S protein complexed with hiACE2 elucidated a few critical residues in the RBD/hiACE2 interface, especially L30 and F83 of hiACE2 which are unique to hiACE2 and contributed to the decreased binding affinity to PT RBD compared to human ACE2. Our work provides insight into cross-species transmission and highlights the necessity for monitoring host jumps and spillover events on SARS-CoV-2 in semi-aquatic/aquatic mammals.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- risk assessment
- endothelial cells
- healthcare
- public health
- angiotensin converting enzyme
- induced apoptosis
- gene expression
- copy number
- oxidative stress
- cell death
- signaling pathway
- cell proliferation
- health information
- cell migration
- genome wide
- induced pluripotent stem cells
- capillary electrophoresis