A SARS-CoV-2-Related Virus from Malayan Pangolin Causes Lung Infection without Severe Disease in Human ACE2-Transgenic Mice.

Mei-Qin Liu1,2 Hao-Feng Lin1,2 Jing Li3 Ying Chen1,2 Yun Luo1,2 Wei Zhang1 Ben Hu1 Feng-Juan Tian3 Yun-Jia Hu3 Yu-Jie Liu3 Ren-Di Jiang4 Qian-Chun Gong4 Ang Li1,2 Zi-Shuo Guo1,2 Bei Li1 Xing-Lou Yang1 Yi-Gang Tong3 Zheng-Li Shi1
Affiliations 4 institutions
  1. CAS Key Laboratory of Special Pathogens, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, Hubei, People's Republic of China.
  2. University of Chinese Academy of Sciences, Beijing, People's Republic of China.
  3. College of Life Science and Technology, Beijing University of Chemical Technology, Beijing, China.
  4. State Key Laboratory of Genetic Engineering, School of Life Sciences, Fudan University, Shanghai, China.

Abstract

Coronavirus disease 2019 (COVID-19), which is caused by the novel coronavirus severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is the most severe emerging infectious disease in the current century. The discovery of SARS-CoV-2-related coronaviruses (SARSr-CoV-2) in bats and pangolins in South Asian countries indicates that SARS-CoV-2 likely originated from wildlife. To date, two SARSr-CoV-2 strains have been isolated from pangolins seized in Guangxi and Guangdong by the customs agency of China, respectively. However, it remains unclear whether these viruses cause disease in animal models and whether they pose a transmission risk to humans. In this study, we investigated the biological features of a SARSr-CoV-2 strain isolated from a smuggled Malayan pangolin (Manis javanica) captured by the Guangxi customs agency, termed MpCoV-GX, in terms of receptor usage, cell tropism, and pathogenicity in wild-type BALB/c mice, human angiotensin-converting enzyme 2 (ACE2)-transgenic mice, and human ACE2 knock-in mice. We found that MpCoV-GX can utilize ACE2 from humans, pangolins, civets, bats, pigs, and mice for cell entry and infect cell lines derived from humans, monkeys, bats, minks, and pigs. The virus could infect three mouse models but showed limited pathogenicity, with mild peribronchial and perivascular inflammatory cell infiltration observed in lungs. Our results suggest that this SARSr-CoV-2 virus from pangolins has the potential for interspecies infection, but its pathogenicity is mild in mice. Future surveillance among these wildlife hosts of SARSr-CoV-2 is needed to monitor variants that may have higher pathogenicity and higher spillover risk. IMPORTANCE SARS-CoV-2, which likely spilled over from wildlife, is the third highly pathogenic human coronavirus. Being highly transmissible, it is perpetuating a pandemic and continuously posing a severe threat to global public health. Several SARS-CoV-2-related coronaviruses (SARSr-CoV-2) in bats and pangolins have been identified since the SARS-CoV-2 outbreak. It is therefore important to assess their potential of crossing species barriers for better understanding of their risk of future emergence. In this work, we investigated the biological features and pathogenicity of a SARSr-CoV-2 strain isolated from a smuggled Malayan pangolin, named MpCoV-GX. We found that MpCoV-GX can utilize ACE2 from 7 species for cell entry and infect cell lines derived from a variety of mammalian species. MpCoV-GX can infect mice expressing human ACE2 without causing severe disease. These findings suggest the potential of cross-species transmission of MpCoV-GX, and highlight the need of further surveillance of SARSr-CoV-2 in pangolins and other potential animal hosts.

Supporting text Virus Host Location
interspecies infection 1 MpCoV-GX 1 pangolin 10 SARS-CoV-2-related coronavirus 3 COVID-19 425 Host Specificity 132 Pangolins 29 Angiotensin-Converting Enzyme 2 177 Animals 1948 Cell Line 158 China 229 Chiroptera 371 Humans 1440 Lung 65 Mice 253 Mice, Transgenic 13 SARS-CoV-2 453 Swine 258

Evidence records

5 total
Zoonotic Surveillance
1 records · 1 evidence types
Evidence type
1 records
OVE6673
Key finding

The SARSr-CoV-2 strain MpCoV-GX was successfully isolated from a smuggled Malayan pangolin (Manis javanica) seized in Guangxi, China.

Virus
Host
Location
Not specified
Supporting text

Two SARSr-CoV-2 strains have been isolated from pangolins seized in Guangxi and Guangdong by the customs agency of China, respectively. In this study, we investigated the biological features of a SARSr-CoV-2 strain isolated from a smuggled Malayan pangolin (Manis javanica) captured by the Guangxi customs agency, termed MpCoV-GX.

Sample type
pangolin tissue or sample seized by customs
Experimental Infection
2 records · 2 evidence types
Evidence type
1 records
OVE6676
Key finding

MpCoV-GX infection caused limited pathogenicity with mild inflammatory infiltration in lungs of multiple mouse models, including human ACE2-transgenic mice, without severe disease.

Virus
Host
Location
Not specified
Supporting text

The virus could infect three mouse models but showed limited pathogenicity, with mild peribronchial and perivascular inflammatory cell infiltration observed in lungs. MpCoV-GX can infect mice expressing human ACE2 without causing severe disease.

Method
experimental infection | histopathological examination of lung tissues
Experimental system
mouse infection models (wild-type and human ACE2 expressing mice)
Evidence type
1 records
OVE6675
Key finding

The pangolin-derived coronavirus MpCoV-GX infected cultured cell lines derived from humans, monkeys, bats, minks, and pigs, showing its ability to infect multiple mammalian hosts.

Virus
Host
Location
Not specified
Supporting text

MpCoV-GX can utilize ACE2 from humans, pangolins, civets, bats, pigs, and mice for cell entry and infect cell lines derived from humans, monkeys, bats, minks, and pigs.

Method
cell-culture infection assay | ACE2 receptor usage assay
Sample type
cell lines
Experimental system
cell-culture host range assay using mammalian cell lines expressing species-specific ACE2 receptors
Functional Mechanism
2 records · 1 evidence types
Evidence type
2 records
OVE6674
Key finding

MpCoV-GX can utilize ACE2 receptors from humans, pangolins, civets, bats, pigs, and mice for cell entry.

Virus
Host
Location
Not specified
Supporting text

We found that MpCoV-GX can utilize ACE2 from humans, pangolins, civets, bats, pigs, and mice for cell entry.

Method
receptor-usage assay | cell-entry experiment
Receptors
ACE2
OVE6677
Key finding

MpCoV-GX from a Malayan pangolin can utilize ACE2 from multiple animal species and infect mouse models, indicating cross-species infection potential.

Virus
Host
Location
Supporting text

We found that MpCoV-GX can utilize ACE2 from humans, pangolins, civets, bats, pigs, and mice for cell entry and infect cell lines derived from humans, monkeys, bats, minks, and pigs. Our results suggest that this SARSr-CoV-2 virus from pangolins has the potential for interspecies infection, but its pathogenicity is mild in mice.

Method
receptor usage assay | cell infection assay | animal infection model
Receptors
ACE2