Evidence map›Paper›PMID 25211074›Full record

ArticleCell host & microbe2014

The interferon signaling antagonist function of yellow fever virus NS5 protein is activated by type I interferon.

Maudry Laurent-Rolle, Juliet Morrison, Ricardo Rajsbaum, Jesica M Levingston Macleod, Giuseppe Pisanelli, Alissa Pham, Juan Ayllon, Lisa Miorin, Carles Martinez, Benjamin R tenOever and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell host & microbe, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 123 papers.

0numbers the graph read from it
0cells of the map it votes in
123citing papers in PubMed
10.0field-weighted citation impact, top 2% 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

123 citing papers in PubMed, 163 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. The mechanisms of Zika virus-induced neuropathogenesis.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2024
    Review
  19. Article
  20. Review

63 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 1 institution in 2 countries.

Maudry Laurent-Rolle *Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029. USA.
Juliet Morrison *Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029. USA.
Ricardo RajsbaumDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029. USA.
Jesica M Levingston MacleodDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029. USA.
Giuseppe PisanelliDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029. USA.
Alissa PhamDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029. USA.
Juan AyllonDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029. USA.
Lisa MiorinDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029. USA.
Carles MartinezDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029. USA.
Benjamin R tenOeverDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029. USA.
Adolfo García-SastreDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029. USA.
Icahn School of Medicine at Mount Sinai · US

Funding

Viral Pathogenesis and TherapeuticsU54AI057158 · NIAID · WADSWORTH CENTER · PI LIPKIN, W. IAN · 2003 to 2014
$100.8M
NIAID NIH HHS U54 AI057158NIAID NIH HHS U54AI057158PHS HHS FAI077333A
6 · The paper itself

Abstract

To successfully establish infection, flaviviruses have to overcome the antiviral state induced by type I interferon (IFN-I). The nonstructural NS5 proteins of several flaviviruses antagonize IFN-I signaling. Here we show that yellow fever virus (YFV) inhibits IFN-I signaling through a unique mechanism that involves binding of YFV NS5 to the IFN-activated transcription factor STAT2 only in cells that have been stimulated with IFN-I. This NS5-STAT2 interaction requires IFN-I-induced tyrosine phosphorylation of STAT1 and the K63-linked polyubiquitination at a lysine in the N-terminal region of YFV NS5. We identified TRIM23 as the E3 ligase that interacts with and polyubiquitinates YFV NS5 to promote its binding to STAT2 and trigger IFN-I signaling inhibition. Our results demonstrate the importance of YFV NS5 in overcoming the antiviral action of IFN-I and offer a unique example of a viral protein that is activated by the same host pathway that it inhibits.

Indexed as

Amino Acid MotifsAnimalsCell LineGTP-Binding ProteinsHost-Pathogen InteractionsHumansInterferon-betaPhosphorylationProtein BindingSignal TransductionSTAT1 Transcription FactorSTAT2 Transcription FactorViral Nonstructural ProteinsYellow FeverYellow fever virusGTP-Binding ProteinsInterferon-betaNS5 protein, flavivirusSTAT1 protein, humanSTAT1 Transcription FactorSTAT2 Transcription FactorTRIM23 protein, humanViral Nonstructural Proteins

Identifiers

PMID25211074
PMCPMC4176702
OpenAlexW2134669110

What OpenQuestion holds

Textmetadata
LicenceTDM
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.