Evidence map›Paper›PMID 24662051›Full record

ArticleMolecular and cellular biology2014

Activation of stress response pathways promotes formation of antiviral granules and restricts virus replication.

Daniel K Rozelle, Claire Marie Filone, Nancy Kedersha, John H Connor

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.1field-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

33 citing papers in PubMed, 54 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Phase separation in immune signalling.Nature reviews. Immunology · 2022
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. A proposed role for the SARS-CoV-2 nucleocapsid protein in the formation and regulation of biomolecular condensates.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  14. Dietary Gluten and Neurodegeneration: A Case for Preclinical Studies.International journal of molecular sciences · 2020
    Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. Translational control during poxvirus infection.Wiley interdisciplinary reviews. RNA · 2019
    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

4 authors at 2 institutions in 1 country.

Daniel K RozelleDepartment of Microbiology and National Emerging Infectious Diseases Laboratories, Boston University School of Medicine, Boston, Massachusetts, USA.
Claire Marie Filone
Nancy Kedersha
John H Connor
Boston University · USBrigham and Women's Hospital · US

Funding

Boston University Clinical and Translational Science Award (CTSA) Program UL1UL1TR000157 · NCATS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI CENTER, DAVID M. · 2012 to 2013
$7.9M
RESEARCH TRAINING IN IMMUNOLOGYT32AI007309 · NIAID · BOSTON UNIVERSITY MEDICAL CAMPUS · PI GUMMULURU, SURYARAM · 1988 to 2024
$7.4M
Development of Near Real-Time, Multiplexed Diagnostics for Viral Hemorrhagic FeveR01AI096159 · NIAID · BOSTON UNIVERSITY MEDICAL CAMPUS · PI CONNOR, JOHN H · 2011 to 2015
$4.8M
Boston University Inflammatory Disorders Training GrantT32AI089673 · NIAID · BOSTON UNIVERSITY MEDICAL CAMPUS · PI WETZLER, LEE MARK · 2011 to 2015
$1.4M
Angiogenin-Induced RNA Cleavage in CancerR01CA168872 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI ANDERSON, PAUL J. · 2013 to 2015
$1.1M
Control of elF4F complex by Vesicular Stomatitis VirusK22AI064606 · NIAID · BOSTON UNIVERSITY MEDICAL CAMPUS · PI CONNOR, JOHN H · 2006 to 2007
$270k
NCATS NIH HHS UL1 TR000157NCATS NIH HHS UL1-TR000157NCI NIH HHS R01 CA168872NIAID NIH HHS 5T32AI 7309NIAID NIH HHS K22 AI064606NIAID NIH HHS K22AI-064606NIAID NIH HHS R01 AI096159NIAID NIH HHS R01AI1096159-01NIAID NIH HHS T32 AI007309NIAID NIH HHS T32 AI089673NIAID NIH HHS T32 AI89673-3
6 · The paper itself

Abstract

The formation of protein-RNA granules is a part of both natural cellular function (P-bodies and nuclear HNRNPs) and the response to cellular stress (stress granules and ND10 bodies). To better understand the role of stress-induced granules in viral infection, we have studied the ability of cells to restrict poxvirus replication through the formation of antiviral granules (AVGs). Of cells infected with a wild-type poxvirus, a small number spontaneously formed AVGs. In these AVG-positive cells, viral gene expression was inhibited. The addition of compounds that altered RNA helicase activity, induced oxidative stress, or stimulated translation initiation factor phosphorylation significantly increased the number of AVG-positive cells. When AVGs formed, both viral translation and titers were decreased even when host translation persisted. Treatment with the antiviral compound isatin β-thiosemicarbazone (IBT), a compound that was used to treat smallpox infections, induced AVGs, suggesting a role for these structures in the pharmacological inhibition of poxvirus replication. These findings provide evidence that AVGs are an innate host response that can be exogenously stimulated to combat virus infection. Since small molecules are able to stimulate AVG formation, it is a potential target for new antiviral development.

Indexed as

Stress, PhysiologicalVirus ReplicationCarrier ProteinsCell Line, TumorCytoplasmic GranulesDNA HelicasesEukaryotic Initiation FactorsHeLa CellsHumansIsatinOxidative StressPhosphorylationPoly-ADP-Ribose Binding ProteinsProtein BiosynthesisRNA HelicasesRNA, MessengerCarrier ProteinsDNA HelicasesEukaryotic Initiation FactorsG3BP1 protein, humanIsatinisatin beta-thiosemicarbazonePoly-ADP-Ribose Binding ProteinsRNA HelicasesRNA, MessengerRNA Recognition Motif ProteinsRNA, Viral

Identifiers

PMID24662051
PMCPMC4019067
OpenAlexW2153675295

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.