Evidence map›Paper›PMID 19269968›Full record

ArticleThe Journal of biological chemistry2009

Initiation of hepatitis C virus infection requires the dynamic microtubule network: role of the viral nucleocapsid protein.

Farzin Roohvand, Patrick Maillard, Jean-Pierre Lavergne, Steeve Boulant, Marine Walic, Ursula Andréo, Lucie Goueslain, François Helle, Adeline Mallet, John McLauchlan and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 7% 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

44 citing papers in PubMed, 1 synthesis or guideline pooled it, 73 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Unraveling the Dynamic Role of Microtubules in the HBV Life Cycle.Journal of clinical and translational hepatology · 2022
    Article
  5. Review
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  19. Distinct functions of diaphanous-related formins regulate HIV-1 uncoating and transport.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  20. Wsv023 interacted withRoyal Society open science · 2017
    Article
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

11 authors at 5 institutions in 2 countries.

Farzin RoohvandUnité des Hépacivirus et Immunité Innée and Institut Pasteur, 25/28 Rue du Dr. Roux, Paris 75724, France.
Patrick MaillardUnité des Hépacivirus et Immunité Innée and Institut Pasteur, 25/28 Rue du Dr. Roux, Paris 75724, France.
Jean-Pierre LavergneInstitut de Biologie et Chimie de Protéines (IBCP-UMR 5086), CNRS, Université Lyon 1, Lyon 69367, France.
Steeve BoulantMedical Research Council Virology Unit, Glasgow G11 5JR, Scotland, United Kingdom.
Marine WalicUnité des Hépacivirus et Immunité Innée and Institut Pasteur, 25/28 Rue du Dr. Roux, Paris 75724, France.
Ursula AndréoUnité des Hépacivirus et Immunité Innée and Institut Pasteur, 25/28 Rue du Dr. Roux, Paris 75724, France.
Lucie GoueslainInstitut de Biologie de Lille (UMR8161), CNRS, Université de Lille I & II, Institut Pasteur de Lille, Lille 59021, France.
François HelleInstitut de Biologie de Lille (UMR8161), CNRS, Université de Lille I & II, Institut Pasteur de Lille, Lille 59021, France.
Adeline MalletPlate-Forme de Microscopie Ultrastructurale, Institut Pasteur, 25/28 Rue du Dr. Roux, Paris 75724, France.
John McLauchlanMedical Research Council Virology Unit, Glasgow G11 5JR, Scotland, United Kingdom.
Agata BudkowskaUnité des Hépacivirus et Immunité Innée and Institut Pasteur, 25/28 Rue du Dr. Roux, Paris 75724, France. Electronic address: agata.budkowska@pasteur.fr.
Institut Pasteur · FRMedical Research Council · GBCentre National de la Recherche Scientifique · FRUniversité Claude Bernard Lyon 1 · FRUniversité de Lille · FR

Funding

Medical Research Council MC_U130184143Medical Research Council MC_UU_12014/1
6 · The paper itself

Abstract

Early events leading to the establishment of hepatitis C virus (HCV) infection are not completely understood. We show that intact and dynamic microtubules play a key role in the initiation of productive HCV infection. Microtubules were required for virus entry into cells, as evidenced using virus pseudotypes presenting HCV envelope proteins on their surface. Studies carried out using the recent infectious HCV model revealed that microtubules also play an essential role in early, postfusion steps of the virus cycle. Moreover, low concentrations of vinblastin and nocodazol, microtubule-affecting drugs, and paclitaxel, which stabilizes microtubules, inhibited infection, suggesting that microtubule dynamic instability and/or treadmilling mechanisms are involved in HCV internalization and early transport. By protein chip and direct core-dependent pull-down assays, followed by mass spectrometry, we identified beta- and alpha-tubulin as cellular partners of the HCV core protein. Surface plasmon resonance analyses confirmed that core directly binds to tubulin with high affinity via amino acids 2-117. The interaction of core with tubulin in vitro promoted its polymerization and enhanced the formation of microtubules. Immune electron microscopy showed that HCV core associates, at least temporarily, with microtubules polymerized in its presence. Studies by confocal microscopy showed a juxtaposition of core with microtubules in HCV-infected cells. In summary, we report that intact and dynamic microtubules are required for virus entry into cells and for early postfusion steps of infection. HCV may exploit a direct interaction of core with tubulin, enhancing microtubule polymerization, to establish efficient infection and promote virus transport and/or assembly in infected cells.

Indexed as

Cell Line, TumorHepacivirusHepatitis CHumansMicrotubulesNucleocapsid ProteinsTubulinVirus AssemblyNucleocapsid ProteinsTubulin

Identifiers

PMID19269968
PMCPMC2679479
OpenAlexW2019008641

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.