Evidence map›Paper›PMID 30192975›Full record

ArticleThe Journal of infectious diseases2018

Natural History and Pathogenesis of Wild-Type Marburg Virus Infection in STAT2 Knockout Hamsters.

Colm Atkins, Jinxin Miao, Birte Kalveram, Terry Juelich, Jennifer K Smith, David Perez, Lihong Zhang, Jonna L B Westover, Arnaud J Van Wettere, Brian B Gowen and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2018. 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
1.0field-weighted citation impact, top 25% 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, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Generation and characterization of anDisease models & mechanisms · 2020
    Article
  15. Review
  16. Article
  17. Review
  18. Review
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

12 authors at 3 institutions in 2 countries.

Colm AtkinsDepartment of Pathology, University of Texas Medical Branch, Galveston.
Jinxin MiaoDepartment of Animal, Dairy, and Veterinary Sciences, Utah State University, Logan.
Birte KalveramDepartment of Pathology, University of Texas Medical Branch, Galveston.
Terry JuelichDepartment of Pathology, University of Texas Medical Branch, Galveston.
Jennifer K SmithDepartment of Pathology, University of Texas Medical Branch, Galveston.
David PerezDepartment of Pathology, University of Texas Medical Branch, Galveston.
Lihong ZhangDepartment of Pathology, University of Texas Medical Branch, Galveston.
Jonna L B WestoverDepartment of Animal, Dairy, and Veterinary Sciences, Utah State University, Logan.
Arnaud J Van WettereDepartment of Animal, Dairy, and Veterinary Sciences, Utah State University, Logan.
Brian B GowenDepartment of Animal, Dairy, and Veterinary Sciences, Utah State University, Logan.
Zhongde WangDepartment of Animal, Dairy, and Veterinary Sciences, Utah State University, Logan.
Alexander N FreibergDepartment of Pathology, University of Texas Medical Branch, Galveston.
The University of Texas Medical Branch at Galveston · USUtah State University · USZhengzhou University · CN

Funding

Development of a STAT2 knock-out hamster model for wild-type filovirus infectionsR41OD021979 · OD · AURATUS BIO, LLC · PI ROBL, JAMES M, WANG, ZHONGDE · 2016 to 2016
$221k
NIH HHS R41 OD021979
6 · The paper itself

Abstract

Marburg virus (MARV; family Filoviridae) causes sporadic outbreaks of Marburg hemorrhagic fever in sub-Saharan Africa with case fatality rates reaching 90%. Wild-type filoviruses, including MARV and the closely related Ebola virus, are unable to suppress the type I interferon response in rodents, and therefore require adaptation of the viruses to cause disease in immunocompetent animals. In the current study, we demonstrate that STAT2 knockout Syrian hamsters are susceptible to infection with different wild-type MARV variants. MARV Musoke causes a robust and systemic infection resulting in lethal disease. Histopathological findings share features similar to those observed in human patients and other animal models of filovirus infection. Reverse-transcription polymerase chain reaction analysis of host transcripts shows a dysregulation of the innate immune response. Our results demonstrate that the STAT2 knockout hamster represents a novel small animal model of severe MARV infection and disease without the requirement for virus adaptation.

Indexed as

AnimalsCricetinaeCytokinesDisease Models, AnimalDisease SusceptibilityFemaleMaleMarburg Virus DiseaseSTAT2 Transcription FactorCytokinesSTAT2 Transcription Factor

Identifiers

PMID30192975
PMCPMC6249581
OpenAlexW2891936243

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.