ACE2 receptor usage reveals variation in susceptibility to SARS-CoV and SARS-CoV-2 infection among bat species.

Huan Yan1 Hengwu Jiao2 Qianyun Liu1 Zhen Zhang1 Qing Xiong1 Bing-Jun Wang2 Xin Wang1 Ming Guo1 Lin-Fa Wang3 Ke Lan4,5 Yu Chen6 Huabin Zhao7,8
Affiliations 8 institutions
  1. State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University, Wuhan, China.
  2. Department of Ecology, Tibetan Centre for Ecology and Conservation at WHU-TU, Hubei Key Laboratory of Cell Homeostasis, College of Life Sciences, Wuhan University, Wuhan, China.
  3. Duke-NUS Medical School, Singapore, Singapore.
  4. State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University, Wuhan, China. [email protected].
  5. Frontier Science Center for Immunology and Metabolism, Wuhan University, Wuhan, China. [email protected].
  6. State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University, Wuhan, China. [email protected].
  7. State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University, Wuhan, China. [email protected].
  8. Department of Ecology, Tibetan Centre for Ecology and Conservation at WHU-TU, Hubei Key Laboratory of Cell Homeostasis, College of Life Sciences, Wuhan University, Wuhan, China. [email protected].

Abstract

Bats are the suggested natural hosts for severe acute respiratory syndrome coronavirus (SARS-CoV) and the causal agent of the coronavirus disease 2019 (COVID-19) pandemic, SARS-CoV-2. The interaction of viral spike proteins with their host receptor angiotensin-converting enzyme 2 (ACE2) is a critical determinant of potential hosts and cross-species transmission. Here we use virus-host receptor binding and infection assays to examine 46 ACE2 orthologues from phylogenetically diverse bat species, including those in close and distant contact with humans. We found that 24, 21 and 16 of them failed to support infection by SARS-CoV, SARS-CoV-2 or both viruses, respectively. Furthermore, we confirmed that infection assays in human cells were consistent with those in two bat cell lines. Additionally, we used genetic and functional analyses to identify critical residues in bat ACE2 receptors associated with viral entry restrictions. Our results suggest that many bat species may not be the potential hosts of one or both viruses and that no correlation was identified between proximity to humans and probability of being natural hosts of SARS-CoV or SARS-CoV-2. This study demonstrates dramatic variation in susceptibility to SARS-CoV and SARS-CoV-2 infection among bat species and adds knowledge towards a better understanding of coronavirus-bat interaction.

Supporting text Virus Host Location
Chiroptera 371 COVID-19 425 Angiotensin-Converting Enzyme 2 177 Animals 1948 Humans 1440 Peptidyl-Dipeptidase A 57 Receptors, Virus 204 SARS-CoV-2 453 Spike Glycoprotein, Coronavirus 274

Evidence records

1 total
Experimental Infection
1 records · 1 evidence types
Evidence type
1 records
OVE4561
Key finding

Infection assays of 46 bat ACE2 orthologues showed that many failed to support SARS-CoV infection.

Virus
Host
Location
Not specified
Supporting text

Here we use virus-host receptor binding and infection assays to examine 46 ACE2 orthologues from phylogenetically diverse bat species, including those in close and distant contact with humans. We found that 24, 21 and 16 of them failed to support infection by SARS-CoV, SARS-CoV-2 or both viruses, respectively.

Method
infection assay | receptor binding assay
Experimental system
cell-culture system expressing bat ACE2 receptors