Host range and structural analysis of bat‐origin RshSTT182/200 coronavirus binding to human ACE2 and its animal orthologs. (5th January 2023)

• Record Type: Journal Article
• Authors: Hu, Yu; Liu, Kefang; Han, Pu; Xu, Zepeng; Zheng, Anqi; Pan, Xiaoqian; Jia, Yunfei; Su, Chao; Tang, Lingfeng; Wu, Lili; Bai, Bin; Zhao, Xin; Tian, Di; Chen, Zhihai; Qi, Jianxun; Wang, Qihui; Gao, George F
• Is Part Of: EMBO journal. Volume 42:Number 4(2023)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2023-01-05
• Subjects: ACE2 -- interspecies transmission -- RBD -- RshSTT182/200 -- SARS‐CoV‐2; Molecular biology -- Periodicals; 572.805
• DOI: 10.15252/embj.2022111737
• Languages: English
• ISSNs: 0261-4189

Abstract

Abstract: Bat‐origin RshSTT182 and RshSTT200 coronaviruses (CoV) from Rhinolophus shameli in Southeast Asia (Cambodia) share 92.6% whole‐genome identity with SARS‐CoV‐2 and show identical receptor‐binding domains (RBDs). In this study, we determined the structure of the RshSTT182/200 receptor binding domain (RBD) in complex with human angiotensin‐converting enzyme 2 (hACE2) and identified the key residues that influence receptor binding. The binding of the RshSTT182/200 RBD to ACE2 orthologs from 39 animal species, including 18 bat species, was used to evaluate its host range. The RshSTT182/200 RBD broadly recognized 21 of 39 ACE2 orthologs, although its binding affinities for the orthologs were weaker than those of the RBD of SARS‐CoV‐2. Furthermore, RshSTT182 pseudovirus could utilize human, fox, and Rhinolophus affinis ACE2 receptors for cell entry. Moreover, we found that SARS‐CoV‐2 induces cross‐neutralizing antibodies against RshSTT182 pseudovirus. Taken together, these findings indicate that RshSTT182/200 can potentially infect susceptible animals, but requires further evolution to obtain strong interspecies transmission abilities like SARS‐CoV‐2. Synopsis: Bat‐origin coronaviruses RshSTT182 and RshSTT200 share 92.6% genome identity with SARS‐CoV‐2. The structure of the RshSTT182/200 spike protein RBD in complex with human ACE2 and analysis of its ACE2 receptor‐binding spectra indicate that while RshSTTT182/200 has a broad host range, it is narrower than that of SARS‐CoV‐2. The binding affinity of the RshSTT182/200 RBD to hACE2 was ~3 orders of magnitude lower than that of the SARS‐CoV‐2 RBD. RshSTT182‐pseudotyped viruses are able to enter hACE2‐expressing cells at low levels. The structure of the RshSTT182/200 RBD in complex with hACE2 reveals key residues involved in receptor binding. Bat‐origin RshSTT182/200 display a broad host range but show lower receptor‐binding affinity than SARS‐CoV‐2. SARS‐CoV‐2‐induced antibodies can cross‐neutralize RshSTT182. Abstract : Coronaviruses found in Rhinolophus shameli bats can broadly recognize ACE2 orthologs but require further evolution to support interspecies transmission.