Evidence map›Paper›PMID 37491352›Full record

ArticleNature communications2023

Genetically diverse mouse models of SARS-CoV-2 infection reproduce clinical variation in type I interferon and cytokine responses in COVID-19.

Shelly J Robertson, Olivia Bedard, Kristin L McNally, Carl Shaia, Chad S Clancy, Matthew Lewis, Rebecca M Broeckel, Abhilash I Chiramel, Jeffrey G Shannon, Gail L Sturdevant and 19 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.5field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. The Mac1 ADP-ribosylhydrolase is a Therapeutic Target for SARS-CoV-2.bioRxiv : the preprint server for biology · 2025
    Article
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  8. Article
  9. Article
  10. Molecular determinants of cross-species transmission in emerging viral infections.Microbiology and molecular biology reviews : MMBR · 2024
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Nonhuman primate models of pediatric viral diseases.Frontiers in cellular and infection microbiology · 2024
    Review
  17. Animal models for COVID-19 and tuberculosis.Frontiers in immunology · 2023
    Review
  18. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

29 authors at 4 institutions in 2 countries.

Shelly J RobertsonLaboratory of Virology, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, NIH, Hamilton, MT, USA.
Olivia BedardThe Jackson Laboratory, Bar Harbor, ME, USA.
Kristin L McNallyLaboratory of Virology, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, NIH, Hamilton, MT, USA.
Carl ShaiaRocky Mountain Veterinary Branch, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, NIH, Hamilton, MT, USA.ORCID http://orcid.org/0000-0001-8907-8821
Chad S ClancyRocky Mountain Veterinary Branch, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, NIH, Hamilton, MT, USA.ORCID http://orcid.org/0000-0002-5354-9270
Matthew LewisLaboratory of Virology, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, NIH, Hamilton, MT, USA.
Rebecca M BroeckelLaboratory of Virology, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, NIH, Hamilton, MT, USA.
Abhilash I ChiramelLaboratory of Virology, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, NIH, Hamilton, MT, USA.
Jeffrey G ShannonLaboratory of Neurological Infections and Immunity, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, NIH, Hamilton, MT, USA.ORCID http://orcid.org/0000-0003-4211-4308
Gail L SturdevantLaboratory of Virology, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, NIH, Hamilton, MT, USA.
Rebecca RosenkeRocky Mountain Veterinary Branch, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, NIH, Hamilton, MT, USA.
Sarah L AnzickResearch Technologies Branch, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD, USA.
Elvira ForteThe Jackson Laboratory, Bar Harbor, ME, USA.
Christoph PreussThe Jackson Laboratory, Bar Harbor, ME, USA.
Candice N BakerThe Jackson Laboratory, Bar Harbor, ME, USA.ORCID http://orcid.org/0009-0008-7793-3008
Jeffrey M HarderThe Jackson Laboratory, Bar Harbor, ME, USA.
Catherine BruntonThe Jackson Laboratory, Bar Harbor, ME, USA.
Steven MungerThe Jackson Laboratory, Bar Harbor, ME, USA.ORCID http://orcid.org/0000-0002-8458-1871
Daniel P BrunoResearch Technologies Branch, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD, USA.
Justin B LackResearch Technologies Branch, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD, USA.
Jacqueline M LeungResearch Technologies Branch, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD, USA.ORCID http://orcid.org/0000-0001-8040-7422
Amirhossein ShamsaddiniResearch Technologies Branch, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD, USA.
Paul GardinaResearch Technologies Branch, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD, USA.
Daniel E SturdevantResearch Technologies Branch, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD, USA.
Jian SunResearch Technologies Branch, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD, USA.
Craig MartensResearch Technologies Branch, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD, USA.
Steven M HollandDivision of Intramural Research, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD, USA.
Nadia A RosenthalThe Jackson Laboratory, Bar Harbor, ME, USA. Nadia.Rosenthal@jax.com.ORCID http://orcid.org/0000-0002-7599-7365
Sonja M BestLaboratory of Virology, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, NIH, Hamilton, MT, USA. sbest@niaid.nih.gov.ORCID http://orcid.org/0000-0003-0206-297X
National Institute of Allergy and Infectious Diseases · USJackson Laboratory · USLung Institute · USSpringer Nature (United States) · US

Funding

Infectious Diseases Research Technologies Core - BethesdaZICAI001051 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI CHERRY, JAMES · 2009 to 2025
$226.1M
Infectious Diseases Research Technologies Core - RMLZICAI001052 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI CHERRY, JAMES · 2009 to 2025
$133.3M
Virus-Host Interactions: Induction and Evasion of Host Innate ImmunityZIAAI001125 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI BEST, SONJA · 2010 to 2025
$28.1M
Animal Research Support of COVID StudiesZIGAI001330 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI HANLEY, PATRICK · 2023 to 2024
$2.7M
Mechanisms of immunopathology of COVID-19/ARDS, and strategies to mitigate detrimental inflammatory responsesZIAAI001292 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI BEST, SONJA · 2020 to 2025
$2.4M
Genome-wide CRISPRa screen to determine the antiviral repertoire of the cellZIAAI001349 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI BEST, SONJA · 2021 to 2025
$2.1M
Intramural NIH HHS ZIA AI001125
6 · The paper itself

Abstract

Inflammation in response to severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection drives severity of coronavirus disease 2019 (COVID-19) and is influenced by host genetics. To understand mechanisms of inflammation, animal models that reflect genetic diversity and clinical outcomes observed in humans are needed. We report a mouse panel comprising the genetically diverse Collaborative Cross (CC) founder strains crossed to human ACE2 transgenic mice (K18-hACE2) that confers susceptibility to SARS-CoV-2. Infection of CC x K18-hACE2 resulted in a spectrum of survival, viral replication kinetics, and immune profiles. Importantly, in contrast to the K18-hACE2 model, early type I interferon (IFN-I) and regulated proinflammatory responses were required for control of SARS-CoV-2 replication in PWK x K18-hACE2 mice that were highly resistant to disease. Thus, virus dynamics and inflammation observed in COVID-19 can be modeled in diverse mouse strains that provide a genetically tractable platform for understanding anti-coronavirus immunity.

Indexed as

COVID-19Interferon Type IAnimalsCytokinesDisease Models, Animalgamma-GlobulinsHumansInflammationLungMelphalanMiceMice, TransgenicSARS-CoV-2Cytokinesgamma-GlobulinsInterferon Type IK-18 conjugateMelphalan

Identifiers

PMID37491352
PMCPMC10368652
OpenAlexW4385258023

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.