Evidence map›Paper›PMID 35098996›Full record

ArticleJournal of cell science2022

Novel stress granule-like structures are induced via a paracrine mechanism during viral infection.

Valentina Iadevaia, James M Burke, Lucy Eke, Carla Moller-Levet, Roy Parker, Nicolas Locker

Abstract read
In one paragraph

Article in Journal of cell science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. AβScientific reports · 2025
    Article
  7. Article
  8. Article
  9. A closer look at mammalian antiviral condensates.Biochemical Society transactions · 2024
    Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. 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

6 authors.

Valentina IadevaiaFaculty of Health and Medical Sciences, School of Biosciences and Medicine, University of Surrey, Guildford GU2 7HX, UK.
James M BurkeDepartment of Biochemistry, University of Colorado, Boulder, CO 80303, USA.
Lucy EkeFaculty of Health and Medical Sciences, School of Biosciences and Medicine, University of Surrey, Guildford GU2 7HX, UK.
Carla Moller-LevetFaculty of Health and Medical Sciences, School of Biosciences and Medicine, University of Surrey, Guildford GU2 7HX, UK.
Roy ParkerDepartment of Biochemistry, University of Colorado, Boulder, CO 80303, USA.
Nicolas LockerFaculty of Health and Medical Sciences, School of Biosciences and Medicine, University of Surrey, Guildford GU2 7HX, UK.ORCID 0000-0002-0053-2897

Funding

Biotechnology and Biological Sciences Research Council BB/N000943/1Biotechnology and Biological Sciences Research Council BB/P068018/1
6 · The paper itself

Abstract

To rapidly adapt to stresses such as infections, cells have evolved several mechanisms, which include the activation of stress response pathways and the innate immune response. These stress responses result in the rapid inhibition of translation and condensation of stalled mRNAs with RNA-binding proteins and signalling components into cytoplasmic biocondensates called stress granules (SGs). Increasing evidence suggests that SGs contribute to antiviral defence, and thus viruses need to evade these responses to propagate. We previously showed that feline calicivirus (FCV) impairs SG assembly by cleaving the scaffolding protein G3BP1. We also observed that uninfected bystander cells assembled G3BP1-positive granules, suggesting a paracrine response triggered by infection. We now present evidence that virus-free supernatant generated from infected cells can induce the formation of SG-like foci, which we name paracrine granules. They are linked to antiviral activity and exhibit specific kinetics of assembly-disassembly, and protein and RNA composition that are different from canonical SGs. We propose that this paracrine induction reflects a novel cellular defence mechanism to limit viral propagation and promote stress responses in bystander cells.

Indexed as

Caliciviridae InfectionsStress GranulesAnimalsCalicivirus, FelineCatsPoly-ADP-Ribose Binding ProteinsRNA Recognition Motif ProteinsVirus ReplicationPoly-ADP-Ribose Binding ProteinsRNA Recognition Motif ProteinsG3BP1Stress granuleVirus

Identifiers

PMID35098996
PMCPMC8976915

What OpenQuestion holds

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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.