Broad and Differential Animal Angiotensin-Converting Enzyme 2 Receptor Usage by SARS-CoV-2

Author:

Zhao Xuesen12,Chen Danying12,Szabla Robert3,Zheng Mei12,Li Guoli12,Du Pengcheng12,Zheng Shuangli12,Li Xinglin12,Song Chuan12,Li Rui12,Guo Ju-Tao4ORCID,Junop Murray3,Zeng Hui12,Lin Hanxin5

Affiliation:

1. Institute of Infectious Disease, Beijing Ditan Hospital, Capital Medical University, Beijing, China

2. Beijing Key Laboratory of Emerging Infectious Disease, Beijing, China

3. Department of Biochemistry, Western University, London, Ontario, Canada

4. Baruch S. Blumberg Institute, Hepatitis B Foundation, Doylestown, Pennsylvania, USA

5. Department of Pathology and Laboratory Medicine, Western University, London, Ontario, Canada

Abstract

SARS-CoV-2 uses human ACE2 as a primary receptor for host cell entry. Viral entry mediated by the interaction of ACE2 with spike protein largely determines host range and is the major constraint to interspecies transmission. We examined the receptor activity of 14 ACE2 orthologs and found that wild-type and mutant SARS-CoV-2 lacking the furin cleavage site in S protein could utilize ACE2 from a broad range of animal species to enter host cells. These results have important implications in the natural hosts, interspecies transmission, animal models, and molecular basis of receptor binding for SARS-CoV-2.

Funder

Gouvernement du Canada | Canadian Institutes of Health Research

National Natural Science Foundation of China

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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