Broad host range of SARS-CoV-2 and the molecular basis for SARS-CoV-2 binding to cat ACE2

Author:

Wu Lili,Chen Qian,Liu Kefang,Wang JiaORCID,Han Pengcheng,Zhang Yanfang,Hu Yu,Meng Yumin,Pan Xiaoqian,Qiao Chengpeng,Tian Siyu,Du Pei,Song HaoORCID,Shi Weifeng,Qi Jianxun,Wang Hong-WeiORCID,Yan JinghuaORCID,Gao George FuORCID,Wang QihuiORCID

Abstract

AbstractSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of the recent pandemic COVID-19, is reported to have originated from bats, with its intermediate host unknown to date. Here, we screened 26 animal counterparts of the human ACE2 (hACE2), the receptor for SARS-CoV-2 and SARS-CoV, and found that the ACE2s from various species, including pets, domestic animals and multiple wild animals, could bind to SARS-CoV-2 receptor binding domain (RBD) and facilitate the transduction of SARS-CoV-2 pseudovirus. Comparing to SARS-CoV-2, SARS-CoV seems to have a slightly wider range in choosing its receptor. We further resolved the cryo-electron microscopy (cryo-EM) structure of the cat ACE2 (cACE2) in complex with the SARS-CoV-2 RBD at a resolution of 3 Å, revealing similar binding mode as hACE2 to the SARS-CoV-2 RBD. These results shed light on pursuing the intermediate host of SARS-CoV-2 and highlight the necessity of monitoring susceptible hosts to prevent further outbreaks.

Funder

Ministry of Science and Technology of the People’s Republic of China

Youth Innovation Promotion Association of the Chinese Academy of Sciences

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Genetics,Molecular Biology,Biochemistry

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