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

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作者
Lili Wu
Qian Chen
Kefang Liu
Jia Wang
Pengcheng Han
Yanfang Zhang
Yu Hu
Yumin Meng
Xiaoqian Pan
Chengpeng Qiao
Siyu Tian
Pei Du
Hao Song
Weifeng Shi
Jianxun Qi
Hong-Wei Wang
Jinghua Yan
George Fu Gao
Qihui Wang
机构
[1] Chinese Academy of Sciences,CAS Key Laboratory of Microbial Physiological and Metabolic Engineering, Institute of Microbiology
[2] University of Chinese Academy of Sciences,Institute of Physical Science and Information
[3] Anhui University,CAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology
[4] Chinese Academy of Sciences,Faculty of Health Sciences
[5] University of Macau,Ministry of Education Key Laboratory of Protein Sciences, Tsinghua
[6] Tsinghua University,Peking Joint Center for Life Sciences, Beijing Advanced Innovation Center for Structural Biology, Beijing Frontier Research Center of Biological Structures, School of Life Sciences
[7] Emory University,Department of biomedical engineering
[8] Chinese Academy of Sciences,Laboratory of Protein Engineering and Vaccines,Tianjin Institute of Industrial Biotechnology
[9] University of Science and Technology of China,School of Life Sciences
[10] Chinese Academy of Sciences,Research Network of Immunity and Health (RNIH), Beijing Institute of Life Science
[11] Shandong First Medical University & Shandong Academy of Medical Sciences,Key Laboratory of Etiology and Epidemiology of Emerging Infectious Diseases in Universities of Shandong
[12] University of Chinese Academy of Sciences,Savaid Medical School
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摘要
Severe 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.
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