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

Mei-Qin Liu1,2, Hao-Feng Lin1,2, Jing Li3

  • 1CAS Key Laboratory of Special Pathogens, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, Hubei, People's Republic of China.

Journal of Virology
|January 23, 2023
PubMed

Insights

A novel pangolin coronavirus (MpCoV-GX) can infect various animal cells and mouse models by utilizing angiotensin-converting enzyme 2 (ACE2). While showing cross-species infection potential, MpCoV-GX exhibits mild pathogenicity in mice, necessitating further wildlife surveillance.

Area of Science:

  • Virology
  • Infectious Diseases
  • Zoonotic Research

Background:

  • Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes COVID-19, a significant global health threat originating from wildlife.
  • SARS-CoV-2-related coronaviruses (SARSr-CoV-2) found in bats and pangolins raise concerns about potential zoonotic spillover.
  • The pathogenicity and transmission potential of pangolin-derived SARSr-CoV-2 strains remain largely uncharacterized.

Purpose of the Study:

  • To investigate the biological characteristics of a pangolin-derived SARSr-CoV-2 strain, MpCoV-GX.
  • To assess MpCoV-GX's receptor usage, cell tropism, and pathogenicity in relevant animal models.
  • To evaluate the cross-species transmission potential and zoonotic risk posed by MpCoV-GX.

Main Methods:

  • Isolation and characterization of the MpCoV-GX strain from a Malayan pangolin.
  • Analysis of MpCoV-GX's ability to utilize angiotensin-converting enzyme 2 (ACE2) from various species for cell entry.
  • Infection studies in cell lines and mouse models (wild-type BALB/c, human ACE2-transgenic, and human ACE2 knock-in mice) to determine pathogenicity.

Main Results:

  • MpCoV-GX successfully utilized ACE2 from humans, pangolins, civets, bats, pigs, and mice, enabling cell entry.
  • The virus infected cell lines derived from humans, monkeys, bats, minks, and pigs.
  • MpCoV-GX infected three different mouse models but exhibited limited pathogenicity, causing only mild lung inflammation.

Conclusions:

  • The pangolin-derived SARSr-CoV-2 strain MpCoV-GX demonstrates broad ACE2 receptor usage and potential for interspecies infection.
  • Despite its infectivity across species, MpCoV-GX shows mild pathogenicity in studied mouse models.
  • Continued surveillance of SARSr-CoV-2 in wildlife populations is crucial for identifying variants with increased pathogenicity and spillover risk.