Literature detail

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.
PMID 34010360 2021 PLoS Pathog eng epublish
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Article

Publication summary

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.

Animals Brain COVID-19 Disease Models, Animal Disease Reservoirs Disease Susceptibility Female Male Peromyscus Spike Glycoprotein, Coronavirus Virus Replication spike protein, SARS-CoV-2

Structured evidence records

Evidence records

3 total
1 records
Extraction confidence 0.85
Key finding

SARS-CoV-2 underwent a 4–amino acid insertion in the spike N-terminal domain that became fixed after passage in deer mice, showing selection-driven genomic evolution.

Virus
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 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.

Genes or proteins
spike protein; N-terminal domain
1 records
Extraction confidence 0.98
Key finding

Experimental infection demonstrated that SARS-CoV-2 replicates efficiently in the respiratory and intestinal tissues of deer mice.

Virus
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.

Method
experimental infection; virus replication assay; challenge study
Sample type
upper respiratory tract; lungs; intestines; oral swabs
Experimental system
in vivo animal experiment
1 records
Extraction confidence 0.95
Key finding

A four–amino-acid insertion in the spike protein N-terminal domain of SARS-CoV-2 became fixed during deer mouse passage, indicating host-driven molecular adaptation.

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 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.

Genes or proteins
spike
Mutations
four–amino-acid insertion in N-terminal domain of spike
Mechanism types
polymerase_activity; replication_efficiency; host_adaptation