Literature detail

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.
PMID 36688655 2023 J Virol eng ppublish
PubMed DOI Browse context

Article

Publication summary

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. <b>IMPORTANCE</b> 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.

interspecies infection MpCoV-GX pangolin SARS-CoV-2-related coronavirus COVID-19 Host Specificity Pangolins Angiotensin-Converting Enzyme 2 Animals Cell Line China Chiroptera Humans Lung Mice Mice, Transgenic SARS-CoV-2 Swine

Structured evidence records

Evidence records

8 total
6 records
Extraction confidence 1.00
Key finding

MpCoV-GX can use the ACE2 receptor from multiple species, including humans, pangolins, civets, bats, pigs, and mice, to mediate viral cell entry.

Location
Not specified
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.

Method
cell entry assay
Receptors
ACE2
Extraction confidence 1.00
Key finding

MpCoV-GX can use the ACE2 receptor from Malayan pangolin for viral cell entry.

Location
Not specified
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.

Method
cell entry assay
Receptors
ACE2
Extraction confidence 1.00
Key finding

MpCoV-GX can use the ACE2 receptor from civet for viral cell entry.

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 and infect cell lines derived from humans, monkeys, bats, minks, and pigs.

Method
cell entry assay
Receptors
ACE2
Extraction confidence 1.00
Key finding

MpCoV-GX can use the ACE2 receptor from bat for viral cell entry.

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 and infect cell lines derived from humans, monkeys, bats, minks, and pigs.

Method
cell entry assay
Receptors
ACE2
Extraction confidence 1.00
Key finding

MpCoV-GX can use the ACE2 receptor from pig for viral cell entry.

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 and infect cell lines derived from humans, monkeys, bats, minks, and pigs.

Method
cell entry assay
Receptors
ACE2
Extraction confidence 1.00
Key finding

MpCoV-GX can use the ACE2 receptor from mouse for viral cell entry.

Location
Not specified
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.

Method
cell entry assay
Receptors
ACE2
1 records
Extraction confidence 0.95
Key finding

MpCoV-GX, a SARS-CoV-2-related virus from Malayan pangolin, can infect cells from bat, civet, and pig, showing animal-to-animal cross-species transmissibility.

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. These findings suggest the potential of cross-species transmission of MpCoV-GX.

Method
cell culture infection; ACE2 receptor usage assay
Study design
cell infection assay
Transmission direction
animal-to-animal
Geographic raw
Guangxi, China
Country inferred
China
1 records
Extraction confidence 1.00
Key finding

MpCoV-GX from Malayan pangolin can enter cells using ACE2 from multiple mammals, infect various mammalian cell lines, and cause mild lung infection in human ACE2-transgenic mice.

Location
Not specified
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. The virus could infect three mouse models but showed limited pathogenicity, with mild peribronchial and perivascular inflammatory cell infiltration observed in lungs.

Method
experimental infection; cell-entry assay; pathogenicity test
Sample type
lungs
Experimental system
in vivo animal experiment