Evidence map›Paper›PMID 23935497›Full record

ArticlePLoS pathogens2013

Rab18 binds to hepatitis C virus NS5A and promotes interaction between sites of viral replication and lipid droplets.

Shadi Salloum, Hongliang Wang, Charles Ferguson, Robert G Parton, Andrew W Tai

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed
7.7field-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

87 citing papers in PubMed, 153 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Molecular therapy. Nucleic acids · 2024
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  9. Review
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  11. Article
  12. Emerging role of lipophagy in liver disorders.Molecular and cellular biochemistry · 2024
    Review
  13. Review
  14. Article
  15. Review
  16. Molecular therapy. Nucleic acids · 2022
    Article
  17. Review
  18. Article
  19. Article
  20. Review

27 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.

Shadi SalloumDivision of Gastroenterology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, United States of America.
Hongliang Wang
Charles Ferguson
Robert G Parton
Andrew W Tai
Michigan United · USUniversity of Queensland · AUUniversity of Michigan–Ann Arbor · US

Funding

University of Michigan Center for Gastrointestinal ResearchP30DK034933 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI OWYANG, CHUNG · 1986 to 2021
$22.5M
Subversion of hepatocyte phosphoinositide metabolism by hepatitis C virusR01DK097374 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TAI, ANDREW W. · 2013 to 2017
$1.7M
Characterization of a host hepatocyte factor that regulates HCV replicationK08AI083785 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TAI, ANDREW W. · 2010 to 2012
$397k
NIAID NIH HHS AI083785NIAID NIH HHS K08 AI083785NIDDK NIH HHS 5P30DK034933NIDDK NIH HHS DK097374NIDDK NIH HHS P30 DK034933NIDDK NIH HHS R01 DK097374
6 · The paper itself

Abstract

Hepatitis C virus (HCV) is a single-stranded RNA virus that replicates on endoplasmic reticulum-derived membranes. HCV particle assembly is dependent on the association of core protein with cellular lipid droplets (LDs). However, it remains uncertain whether HCV assembly occurs at the LD membrane itself or at closely associated ER membranes. Furthermore, it is not known how the HCV replication complex and progeny genomes physically associate with the presumed sites of virion assembly at or near LDs. Using an unbiased proteomic strategy, we have found that Rab18 interacts with the HCV nonstructural protein NS5A. Rab18 associates with LDs and is believed to promote physical interaction between LDs and ER membranes. Active (GTP-bound) forms of Rab18 bind more strongly to NS5A than a constitutively GDP-bound mutant. NS5A colocalizes with Rab18-positive LDs in HCV-infected cells, and Rab18 appears to promote the physical association of NS5A and other replicase components with LDs. Modulation of Rab18 affects genome replication and possibly also the production of infectious virions. Our results support a model in which specific interactions between viral and cellular proteins may promote the physical interaction between membranous HCV replication foci and lipid droplets.

Indexed as

Cell Line, TumorHepacivirusHepatitis CHumansIntracellular MembranesMembrane LipidsProteomicsrab GTP-Binding ProteinsRNA-Dependent RNA PolymeraseViral Nonstructural ProteinsVirus ReplicationMembrane LipidsNS-5 protein, hepatitis C virusRAB18 protein, humanrab GTP-Binding ProteinsRNA-Dependent RNA PolymeraseViral Nonstructural Proteins

Identifiers

PMID23935497
PMCPMC3731246
OpenAlexW1987689660

What OpenQuestion holds

Textmetadata
LicenceCC0
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.