Evidence map›Paper›PMID 30181255›Full record

ArticlemBio2018

Phase Transitions Drive the Formation of Vesicular Stomatitis Virus Replication Compartments.

Bianca S Heinrich, Zoltan Maliga, David A Stein, Anthony A Hyman, Sean P J Whelan

Open access · goldAbstract read
In one paragraph

Article in mBio, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 144 papers.

0numbers the graph read from it
0cells of the map it votes in
144citing papers in PubMed
15.0field-weighted citation impact, top 1% 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

144 citing papers in PubMed, 242 citations in OpenAlex.

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  16. Phosphorylation enables allosteric control of a viral condensate.bioRxiv : the preprint server for biology · 2025
    Article
  17. Article
  18. In Vitro Liquid-Liquid Phase Separation Assay for Viral Proteins.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  19. Review
  20. Article

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

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 3 institutions in 2 countries.

Bianca S Heinrich *Department of Microbiology and Immunobiology, Harvard Medical School, Boston, Massachusetts, USA.
Zoltan Maliga *Max Planck Institute for Cell Biology and Genetics, Dresden, Germany.
David A SteinDepartment of Biomedical Sciences, Oregon State University, Corvallis, Oregon, USA.
Anthony A HymanMax Planck Institute for Cell Biology and Genetics, Dresden, Germany hyman@mpi-cbg.de swhelan@hms.harvard.edu.
Sean P J WhelanDepartment of Microbiology and Immunobiology, Harvard Medical School, Boston, Massachusetts, USA hyman@mpi-cbg.de swhelan@hms.harvard.edu.
Harvard University · USMax Planck Institut für Zellbiologie · DEOregon State University · US

Funding

RNA Processing in Non-Segmented Minus-Strand RNA VirusesR37AI059371 · NIAID · WASHINGTON UNIVERSITY · PI WHELAN, SEAN PJ · 2015 to 2024
$5.4M
NIAID NIH HHS R37 AI059371
6 · The paper itself

Abstract

RNA viruses that replicate in the cell cytoplasm typically concentrate their replication machinery within specialized compartments. This concentration favors enzymatic reactions and shields viral RNA from detection by cytosolic pattern recognition receptors. Nonsegmented negative-strand (NNS) RNA viruses, which include some of the most significant human, animal, and plant pathogens extant, form inclusions that are sites of RNA synthesis and are not circumscribed by a membrane. These inclusions share similarities with cellular protein/RNA structures such as P granules and nucleoli, which are phase-separated liquid compartments. Here we show that replication compartments of vesicular stomatitis virus (VSV) have the properties of liquid-like compartments that form by phase separation. Expression of the individual viral components of the replication machinery in cells demonstrates that the 3 viral proteins required for replication are sufficient to drive cytoplasmic phase separation. Therefore, liquid-liquid phase separation, previously linked to organization of P granules, nucleolus homeostasis, and cell signaling, plays a key role in host-pathogen interactions. This work suggests novel therapeutic approaches to the problem of combating NNS RNA viral infections.

Indexed as

Host Microbial InteractionsVirus ReplicationAnimalsCell CompartmentationCell LineChlorocebus aethiopsCytoplasmic GranulesInclusion Bodies, ViralRNA, ViralVero CellsVesiculovirusViral ProteinsRNA, ViralViral Proteinsnegative-strand RNA virusphase separationrhabdovirusviral replicationviroplasmvirus-host interactions

Identifiers

PMID30181255
PMCPMC6123442
OpenAlexW2891317436

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.