SARS-CoV-2 infection, neuropathogenesis and transmission among deer mice: Implications for spillback to New World rodents.

Anna Fagre1 Juliette Lewis1 Miles Eckley1 Shijun Zhan1 Savannah M Rocha2 Nicole R Sexton1 Bradly Burke1 Brian Geiss1 Olve Peersen3 Todd Bass4 Rebekah Kading1 Joel Rovnak1 Gregory D Ebel1 Ronald B Tjalkens2 Tawfik Aboellail1 Tony Schountz1
Affiliations 4 institutions
  1. Department of Microbiology, Immunology and Pathology, College of Veterinary Medicine, Colorado State University, Fort Collins, Colorado, United States of America.
  2. Department of Environmental and Radiological Health Sciences, College of Veterinary Medicine, Colorado State University, Fort Collins, Colorado, United States of America.
  3. Department of Biochemistry and Molecular Biology, College of Natural Sciences, Colorado State University, Fort Collins, Colorado, United States of America.
  4. Veterinary Diagnostic Laboratory, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins, Colorado, United States of America.

Abstract

Coronavirus disease-19 (COVID-19) emerged in late 2019 in China and rapidly became pandemic. As with other coronaviruses, a preponderance of evidence suggests the virus originated in horseshoe bats (Rhinolophus spp.) and may have infected an intermediate host prior to spillover into humans. A significant concern is that SARS-CoV-2 could become established in secondary reservoir hosts outside of Asia. To assess this potential, we challenged deer mice (Peromyscus maniculatus) with SARS-CoV-2 and found robust virus replication in the upper respiratory tract, lungs and intestines, with detectable viral RNA for up to 21 days in oral swabs and 6 days in lungs. Virus entry into the brain also occurred, likely via gustatory-olfactory-trigeminal pathway with eventual compromise to the blood-brain barrier. Despite this, no conspicuous signs of disease were observed, and no deer mice succumbed to infection. Expression of several innate immune response genes were elevated in the lungs, including IFNα, IFNβ, Cxcl10, Oas2, Tbk1 and Pycard. Elevated CD4 and CD8β expression in the lungs was concomitant with Tbx21, IFNγ and IL-21 expression, suggesting a type I inflammatory immune response. Contact transmission occurred from infected to naive deer mice through two passages, showing sustained natural transmission and localization into the olfactory bulb, recapitulating human neuropathology. In the second deer mouse passage, an insertion of 4 amino acids occurred to fixation in the N-terminal domain of the spike protein that is predicted to form a solvent-accessible loop. Subsequent examination of the source virus from BEI Resources determined the mutation was present at very low levels, demonstrating potent purifying selection for the insert during in vivo passage. Collectively, this work has determined that deer mice are a suitable animal model for the study of SARS-CoV-2 respiratory disease and neuropathogenesis, and that they have the potential to serve as secondary reservoir hosts in North America.

Supporting text Virus Host Location
Animals 1948 Brain 13 COVID-19 425 Disease Models, Animal 77 Disease Reservoirs 149 Disease Susceptibility 21 Female 289 Male 224 Peromyscus 4 Spike Glycoprotein, Coronavirus 274 Virus Replication 191 spike protein, SARS-CoV-2 157

Evidence records

5 total
Zoonotic Surveillance
1 records · 1 evidence types
Evidence type
1 records
OVE4802
Key finding

Deer mice are proposed to have the potential to serve as secondary reservoir hosts for SARS-CoV-2 in North America.

Virus
Host
Location
Supporting text

Collectively, this work has determined that deer mice are a suitable animal model for the study of SARS-CoV-2 respiratory disease and neuropathogenesis, and that they have the potential to serve as secondary reservoir hosts in North America.

Method
experimental infection | contact transmission study
Sample type
oral swabs | lungs | intestines
Geographic raw
North America
Experimental Infection
3 records · 3 evidence types
Evidence type
1 records
OVE4801
Key finding

Experimental SARS-CoV-2 infection in deer mice caused virus replication and neuroinvasion but no conspicuous clinical disease or mortality, indicating limited pathogenicity.

Virus
Host
Location
Not specified
Supporting text

To assess this potential, we challenged deer mice (Peromyscus maniculatus) with SARS-CoV-2 and found robust virus replication in the upper respiratory tract, lungs and intestines, with detectable viral RNA for up to 21 days in oral swabs and 6 days in lungs. Virus entry into the brain also occurred, likely via gustatory-olfactory-trigeminal pathway with eventual compromise to the blood-brain barrier. Despite this, no conspicuous signs of disease were observed, and no deer mice succumbed to infection.

Method
experimental infection | clinical observation for disease signs | viral RNA detection
Experimental system
deer mouse infection model
Evidence type
1 records
OVE4798
Key finding

Deer mice (Peromyscus maniculatus) experimentally infected with SARS-CoV-2 showed robust viral replication in respiratory and intestinal tissues, confirming susceptibility to infection.

Virus
Host
Location
Not specified
Supporting text

We challenged deer mice (Peromyscus maniculatus) with SARS-CoV-2 and found robust virus replication in the upper respiratory tract, lungs and intestines, with detectable viral RNA for up to 21 days in oral swabs and 6 days in lungs.

Method
experimental infection | viral RNA detection
Sample type
oral swabs | lungs | intestines | upper respiratory tract
Experimental system
animal challenge model
Evidence type
1 records
OVE4799
Key finding

SARS-CoV-2 was experimentally transmitted via contact from infected to naive deer mice through two passages, demonstrating sustained transmission under controlled conditions.

Virus
Host
Location
Not specified
Supporting text

Contact transmission occurred from infected to naive deer mice through two passages, showing sustained natural transmission and localization into the olfactory bulb.

Method
animal infection challenge | contact exposure experiment | viral RNA detection in recipient oral swabs and tissues
Experimental system
contact transmission model among deer mice under laboratory conditions
Functional Mechanism
1 records · 1 evidence types
Evidence type
1 records
OVE4800
Key finding

During in vivo passage of SARS-CoV-2 in deer mice, a 4–amino acid insertion in the spike N-terminal domain became fixed, indicating adaptive molecular selection.

Virus
Host
Not specified
Location
Not specified
Supporting text

In the second deer mouse passage, an insertion of 4 amino acids occurred to fixation in the N-terminal domain of the spike protein that is predicted to form a solvent-accessible loop. Subsequent examination ... demonstrated potent purifying selection for the insert during in vivo passage.

Genes or proteins
spike protein | N-terminal domain
Mutations
insertion of 4 amino acids in the N-terminal domain
Mechanism types
host-range expansion | receptor binding