Pangolin-derived sarbecoviruses show attenuated pathogenicity and transmissibility than SARS-CoV-2 in human ACE2 transgenic hamsters.

Hao-Feng Lin1 Ren-Di Jiang2,3 Li-Na Ji3,4 Jin-Wei Zhang5 Qian-Chun Gong3 Hao-Rui Si6 Yuan-Sen Shi6 Xin-Hua Lin3 Chen Qiu5 Jian-Min Li5 Mei-Qin Liu1
Affiliations 6 institutions
  1. The First Affiliated Hospital of Guangzhou Medical University, Guangzhou Laboratory Clinical Base, State Key Laboratory of Respiratory Disease, Guangzhou Medical University, Guangzhou, China.
  2. School of Public Health, Nanjing Medical University, Nanjing, China.
  3. State Key Laboratory of Genetic Engineering, Greater Bay Area Institute of Precision Medicine (Guangzhou), School of Life Sciences, Zhongshan Hospital, Fudan University, Shanghai, China.
  4. School of Life Sciences, Inner Mongolia University, Hohhot, China.
  5. State Key Laboratory of Reproductive Medicine and Offspring Health, Jiangsu Animal Experimental Center of Medicine and Pharmacy, Animal Core facility, Key Laboratory of Model Animal, Department of Cell Biology, Collaborative Innovation Center for Cardiovascular Disease Translational Medicine, Nanjing Medical University, Nanjing, China.
  6. State Key Laboratory of Respiratory Disease, Guangzhou Medical University, Guangzhou, China.
Active Last checked 2026-09-26 03:30:24 Source: NCBI PubMed

Abstract

Genetic diversity of sarbecoviruses phylogenetically related to SARS-CoV-2 has been identified in Malayan pangolins. However, their potential pathogenicity and risk of cross-species transmission to humans remain largely unknown. In the present study, we performed comparative characterization of SARS-CoV-2 and two pangolin SARS-CoV-2-related viruses, named MpCoV-GD and MpCoV-GX, respectively, in human cell lines and organoids and human ACE2 (hACE2) transgenic hamsters. The cell-to-cell fusion assay showed that the Spike (S) protein of MpCoV-GD induces a stronger membrane fusion than the MpCoV-GX S protein, though weaker than the SARS-CoV-2 S protein. In human cells and organoids, both MpCoV-GX and MpCoV-GD replicated well but less efficiently than SARS-CoV-2. In K18-hACE2 hamsters, MpCoV-GD induced lung pathology comparable to SARS-CoV-2 by showing extensive damage to the alveolar parenchyma, while MpCoV-GX mainly caused alveolar wall thickening due to mild inflammatory cell infiltration. Similar to SARS-CoV-2, the two pangolin coronaviruses were capable of transmitting through direct contact and aerosol exposure, but their infectivity was largely attenuated during aerosol transmission. This study expands our understanding of the biological and infection features of the pangolin-derived sarbecoviruses. It demonstrates that current SARS-CoV-2-related therapeutics and pre-existing immunity can elicit cross-protection against the pangolin sarbecoviruses. Although their pathogenicity and transmissibility are relatively low, our findings suggest the necessity of continuing sarbecovirus surveillance in pangolins and other wildlife for prevention of future disease emergence.IMPORTANCEPangolin-derived sarbecoviruses capable of infecting human cells underscore the role of wildlife as reservoirs for potential zoonotic emergence. MpCoV-GD induces lung pathology comparable to SARS-CoV-2 in hACE2 hamsters, highlighting the need for proactive assessment of novel coronaviruses. Although aerosol transmission of MpCoV-GD and MpCoV-GX is attenuated, their ability to spread via direct contact and airborne routes indicates a tangible risk of cross-species transmission. Importantly, cross-neutralizing activity or inhibition conferred by existing SARS-CoV-2 immunity and therapeutics suggests that current preparedness strategies may help mitigate their impact. These findings reinforce the necessity of sustained surveillance of sarbecoviruses in pangolins and other wildlife to enable early detection and prevention of future outbreaks with significant public health consequences.

Supporting text Virus Host Location
cross-species infection and transmission 1 pangolin-derived coronaviruses 1 pathogenicity 61 SARS-CoV-2 556

Evidence records

6 total
Experimental Infection
5 records · 3 evidence types
Evidence type
2 records
OVE12227
Key finding

In K18-hACE2 hamsters, MpCoV-GD caused lung pathology comparable to SARS-CoV-2, with extensive damage to the alveolar parenchyma.

Virus
Host
Experimental system
Location
Not specified
Supporting text

In K18-hACE2 hamsters, MpCoV-GD induced lung pathology comparable to SARS-CoV-2 by showing extensive damage to the alveolar parenchyma

Method
comparative pathogenicity assessment in transgenic hamsters | histopathology of lung tissue
Experimental system
human ACE2 (K18-hACE2) transgenic hamster model
OVE12228
Key finding

In K18-hACE2 hamsters, MpCoV-GX produced milder lung disease characterized mainly by alveolar wall thickening due to mild inflammatory cell infiltration.

Virus
Host
Experimental system
Location
Not specified
Supporting text

In K18-hACE2 hamsters, MpCoV-GX mainly caused alveolar wall thickening due to mild inflammatory cell infiltration.

Method
comparative pathogenicity assessment in transgenic hamsters | histopathology of lung tissue
Experimental system
human ACE2 (K18-hACE2) transgenic hamster model
Evidence type
1 records
OVE12226
Key finding

Pangolin sarbecoviruses MpCoV-GX and MpCoV-GD replicate in human cells and organoids, though less efficiently than SARS-CoV-2.

Virus
Host
Location
Not specified
Supporting text

In human cells and organoids, both MpCoV-GX and MpCoV-GD replicated well but less efficiently than SARS-CoV-2.

Method
virus replication assay
Experimental system
human cell lines and human organoids in vitro
Evidence type
2 records
OVE12229
Key finding

MpCoV-GD transmitted via direct contact and aerosol in hACE2 transgenic hamsters, with infectivity attenuated during aerosol transmission.

Virus
Host
Experimental system
Location
Not specified
Supporting text

In K18-hACE2 hamsters, MpCoV-GD induced lung pathology comparable to SARS-CoV-2 by showing extensive damage to the alveolar parenchyma, while MpCoV-GX mainly caused alveolar wall thickening due to mild inflammatory cell infiltration. Similar to SARS-CoV-2, the two pangolin coronaviruses were capable of transmitting through direct contact and aerosol exposure, but their infectivity was largely attenuated during aerosol transmission.

Method
animal transmission model | direct-contact exposure | aerosol exposure
Experimental system
hACE2 transgenic hamster transmission model with direct-contact and aerosol exposure arms
OVE12230
Key finding

MpCoV-GX transmitted via direct contact and aerosol in hACE2 transgenic hamsters, with infectivity attenuated during aerosol transmission.

Virus
Host
Experimental system
Location
Not specified
Supporting text

In K18-hACE2 hamsters, MpCoV-GD induced lung pathology comparable to SARS-CoV-2 by showing extensive damage to the alveolar parenchyma, while MpCoV-GX mainly caused alveolar wall thickening due to mild inflammatory cell infiltration. Similar to SARS-CoV-2, the two pangolin coronaviruses were capable of transmitting through direct contact and aerosol exposure, but their infectivity was largely attenuated during aerosol transmission.

Method
animal transmission model | direct-contact exposure | aerosol exposure
Experimental system
hACE2 transgenic hamster transmission model with direct-contact and aerosol exposure arms
Functional Mechanism
1 records · 1 evidence types
Evidence type
1 records
OVE12225
Key finding

Spike proteins from pangolin sarbecoviruses mediate cell–cell membrane fusion, with MpCoV-GD fusing more strongly than MpCoV-GX but weaker than SARS-CoV-2.

Virus
Host
Not specified
Location
Not specified
Supporting text

The cell-to-cell fusion assay showed that the Spike (S) protein of MpCoV-GD induces a stronger membrane fusion than the MpCoV-GX S protein, though weaker than the SARS-CoV-2 S protein.

Method
cell-to-cell fusion assay