Evidence map›Paper›PMID 34767812›Full record

ArticleThe American journal of pathology2022

Progression and Resolution of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection in Golden Syrian Hamsters.

Kathleen R Mulka, Sarah E Beck, Clarisse V Solis, Andrew L Johanson, Suzanne E Queen, Megan E McCarron, Morgan R Richardson, Ruifeng Zhou, Paula Marinho, Anne Jedlicka and 18 more

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.8field-weighted citation impact, top 12% 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

23 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Animal models of Long Covid: A hit-and-run disease.Science translational medicine · 2024
    Review
  6. Review
  7. Crucial role played by CK8Virologica Sinica · 2024
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Animal models for COVID-19: advances, gaps and perspectives.Signal transduction and targeted therapy · 2022
    Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

28 authors at 1 institution in 1 country.

Kathleen R MulkaDepartment of Molecular and Comparative Pathobiology, The Johns Hopkins School of Medicine, Baltimore, Maryland.
Sarah E BeckDepartment of Molecular and Comparative Pathobiology, The Johns Hopkins School of Medicine, Baltimore, Maryland; Department of Pathology, The Johns Hopkins School of Medicine, Baltimore, Maryland.
Clarisse V SolisDepartment of Molecular and Comparative Pathobiology, The Johns Hopkins School of Medicine, Baltimore, Maryland.
Andrew L JohansonDepartment of Molecular and Comparative Pathobiology, The Johns Hopkins School of Medicine, Baltimore, Maryland.
Suzanne E QueenDepartment of Molecular and Comparative Pathobiology, The Johns Hopkins School of Medicine, Baltimore, Maryland.
Megan E McCarronDepartment of Molecular and Comparative Pathobiology, The Johns Hopkins School of Medicine, Baltimore, Maryland.
Morgan R RichardsonDepartment of Molecular and Comparative Pathobiology, The Johns Hopkins School of Medicine, Baltimore, Maryland.
Ruifeng ZhouW. Harry Feinstone Department of Molecular Microbiology and Immunology, The Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
Paula MarinhoW. Harry Feinstone Department of Molecular Microbiology and Immunology, The Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
Anne JedlickaW. Harry Feinstone Department of Molecular Microbiology and Immunology, The Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
Selena Guerrero-MartinDepartment of Molecular and Comparative Pathobiology, The Johns Hopkins School of Medicine, Baltimore, Maryland.
Erin N ShirkDepartment of Molecular and Comparative Pathobiology, The Johns Hopkins School of Medicine, Baltimore, Maryland.
Alicia M BraxtonDepartment of Molecular and Comparative Pathobiology, The Johns Hopkins School of Medicine, Baltimore, Maryland.
Jacqueline BrockhurstDepartment of Molecular and Comparative Pathobiology, The Johns Hopkins School of Medicine, Baltimore, Maryland.
Patrick S CreisherW. Harry Feinstone Department of Molecular Microbiology and Immunology, The Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
Santosh DhakalW. Harry Feinstone Department of Molecular Microbiology and Immunology, The Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
Cory F BraytonDepartment of Molecular and Comparative Pathobiology, The Johns Hopkins School of Medicine, Baltimore, Maryland.
Rebecca T VeenhuisDepartment of Molecular and Comparative Pathobiology, The Johns Hopkins School of Medicine, Baltimore, Maryland.
Kelly A Metcalf PateDepartment of Molecular and Comparative Pathobiology, The Johns Hopkins School of Medicine, Baltimore, Maryland.
Petros C KarakousisDepartment of Medicine, The Johns Hopkins School of Medicine, Baltimore, Maryland.
Cynthia A ZahnowDepartment of Oncology, The Johns Hopkins School of Medicine, Baltimore, Maryland.
Sabra L KleinW. Harry Feinstone Department of Molecular Microbiology and Immunology, The Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
Sanjay K JainDepartment of Pediatrics, The Johns Hopkins School of Medicine, Baltimore, Maryland.
Patrick M TarwaterDepartment of Epidemiology, The Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
Andrew S PekoszDepartment of Molecular and Comparative Pathobiology, The Johns Hopkins School of Medicine, Baltimore, Maryland; W. Harry Feinstone Department of Molecular Microbiology and Immunology, The Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
Jason S VillanoDepartment of Molecular and Comparative Pathobiology, The Johns Hopkins School of Medicine, Baltimore, Maryland.
Joseph L MankowskiDepartment of Molecular and Comparative Pathobiology, The Johns Hopkins School of Medicine, Baltimore, Maryland; Department of Pathology, The Johns Hopkins School of Medicine, Baltimore, Maryland; Department of Neurology, The Johns Hopkins School of Medicine, Baltimore, Maryland. Electronic address: jmankows@jhmi.edu.
Johns Hopkins COVID-19 Hamster Study Group
Johns Hopkins University · US

Funding

Virology Resource CoreU54CA260492 · NCI · JOHNS HOPKINS UNIVERSITY · PI COX, ANDREA L · 2020 to 2024
$10.4M
Sex differences in the impact of frailty on vaccine-induced immune responses in community-dwelling older adultsU54AG062333 · NIA · JOHNS HOPKINS UNIVERSITY · PI LENG, SEAN XIAO · 2018 to 2022
$8.9M
Training Veterinarians for Careers in Biomedical ResearchT32OD011089 · OD · JOHNS HOPKINS UNIVERSITY · PI JOSEPH L MANKOWSKI · 2012 to 2026
$6.7M
Measuring Intralesional Drug Exposures in Cavitary TB using Noninvasive In Vivo PET ImagingR01AI153349 · NIAID · JOHNS HOPKINS UNIVERSITY · PI JAIN, SANJAY · 2020 to 2024
$3.8M
ACE2-targeted PET radiotracers for investigating spatiotemporal distribution of SARS-CoV-2 organ injury and therapy response.R01AI161829 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI DESAI, TEJAL A., FLAVELL, ROBERT RICHARD · 2021 to 2023
$2.4M
NCI NIH HHS U54 CA260492NIAID NIH HHS HHSN272201400007CNIAID NIH HHS R01 AI153349NIAID NIH HHS R01 AI161829NIA NIH HHS U54 AG062333NIH HHS T32 OD011089
6 · The paper itself

Abstract

To catalyze severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) research, including development of novel interventive and preventive strategies, the progression of disease was characterized in a robust coronavirus disease 2019 (COVID-19) animal model. In this model, male and female golden Syrian hamsters were inoculated intranasally with SARS-CoV-2 USA-WA1/2020. Groups of inoculated and mock-inoculated uninfected control animals were euthanized at 2, 4, 7, 14, and 28 days after inoculation to track multiple clinical, pathology, virology, and immunology outcomes. SARS-CoV-2-inoculated animals consistently lost body weight during the first week of infection, had higher lung weights at terminal time points, and developed lung consolidation per histopathology and quantitative image analysis measurements. High levels of infectious virus and viral RNA were reliably present in the respiratory tract at days 2 and 4 after inoculation, corresponding with widespread necrosis and inflammation. At day 7, when the presence of infectious virus was rare, interstitial and alveolar macrophage infiltrates and marked reparative epithelial responses (type II hyperplasia) dominated in the lung. These lesions resolved over time, with only residual epithelial repair evident by day 28 after inoculation. The use of quantitative approaches to measure cellular and morphologic alterations in the lung provides valuable outcome measures for developing therapeutic and preventive interventions for COVID-19 using the hamster COVID-19 model.

Indexed as

AnimalsCOVID-19CricetinaeDisease Models, AnimalFemaleLungMaleMesocricetusSARS-CoV-2

Identifiers

PMID34767812
PMCPMC8577872
OpenAlexW3214385036

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.