Evidence map›Paper›PMID 29859294›Full record

ArticleMicrobial pathogenesis2018

BVDV Npro protein mediates the BVDV induced immunosuppression through interaction with cellular S100A9 protein.

Mahmoud F Darweesh, Mrigendra K S Rajput, Lyle J Braun, Jai S Rohila, Christopher C L Chase

Open access · greenAbstract read
In one paragraph

Article in Microbial pathogenesis, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

20 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. DecreasedPeerJ · 2023
    Article
  7. Immune evasion strategies of bovine viral diarrhea virus.Frontiers in cellular and infection microbiology · 2023
    Review
  8. Review
  9. Pestiviruses infection: Interferon-virus mutual regulation.Frontiers in cellular and infection microbiology · 2023
    Review
  10. Review
  11. Article
  12. Article
  13. Innate Inhibiting Proteins Enhance Expression and Immunogenicity of Self-Amplifying RNA.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
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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

5 authors at 1 institution in 1 country.

Mahmoud F DarweeshDepartment of Veterinary and Biomedical Sciences, South Dakota State University, Brookings, SD, USA. Electronic address: mahmoud_f_darweesh@yahoo.com.
Mrigendra K S RajputDepartment of Veterinary and Biomedical Sciences, South Dakota State University, Brookings, SD, USA.
Lyle J BraunDepartment of Veterinary and Biomedical Sciences, South Dakota State University, Brookings, SD, USA.
Jai S RohilaDepartment of Biology-Microbiology, South Dakota State University, Brookings, SD, USA. Electronic address: jai.rohila@ars.usda.gov.
Christopher C L ChaseDepartment of Veterinary and Biomedical Sciences, South Dakota State University, Brookings, SD, USA. Electronic address: christopher.chase@sdstate.edu.
South Dakota State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The innate immune response is a vital part of the body's antiviral defense system. The innate immune response is initiated by various receptor interactions, including danger associated molecular patterns (DAMPs). The S100A9 is a member of the DAMPs protein family and, is released by activated phagocytic cells such as neutrophils, monocytes, macrophages or endothelial cells, and S100A9 induces its effect through TLR4/MyD88 pathway. Bovine viral diarrhea virus (BVDV) is one of the major devastating disease in the cattle industry worldwide. It shows its effect through immunosuppression and develops persistent infection in calves born from infected cows. The current study revealed that BVDV potentially induced immunosuppression by the interaction of BVDV Npro protein with cellular S100A9 protein. The Inhibition of S100A9 protein expression by small interfering RNA (siRNA) enhanced the virus replication in infected cells. Overexpression of bovine S100A9 enhanced the ncpBVDV2a 1373 mediated Type-I interferon production. A co-immunoprecipitation experiment demonstrated a strong interaction between ncp BVDV2a 1373 Npro protein and cellular S100A9 protein. This suggested that BVDV Npro reduced the S100A9 protein availability/activity in infected cells, resulting in reduced Type-I interferon production. A further study of S100A9-BVDV interaction will be need for better understanding of BVDV pathophysiology.

Indexed as

Immunosuppression TherapyAnimalsBovine Virus Diarrhea-Mucosal DiseaseCalgranulin BCattleCattle DiseasesCell LineDiarrhea Viruses, Bovine ViralImmunity, InnateInterferon Type IMyeloid Differentiation Factor 88RNA, Small InterferingToll-Like Receptor 4Viral ProteinsVirus ReplicationCalgranulin BInterferon Type IMyeloid Differentiation Factor 88Npro protein, bovine viral diarrhea virusRNA, Small InterferingToll-Like Receptor 4Viral ProteinsBVDV NproCo-immunoprecipitationImmunosuppressionProtein-protein interactionS100A9 protein

Identifiers

PMID29859294
PMCPMC7127600
OpenAlexW2805558892

What OpenQuestion holds

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Registered trials

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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.