Evidence map›Paper›PMID 19680534›Full record

ArticlePLoS pathogens2009

Essential role of cyclophilin A for hepatitis C virus replication and virus production and possible link to polyprotein cleavage kinetics.

Artur Kaul, Sarah Stauffer, Carola Berger, Thomas Pertel, Jennifer Schmitt, Stephanie Kallis, Margarita Zayas, Margarita Zayas Lopez, Volker Lohmann, Jeremy Luban and 1 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 155 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
155citing papers in PubMed, 2 pooled it
12.6field-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

155 citing papers in PubMed, 2 syntheses or guidelines pooled it, 261 citations in OpenAlex.

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  17. Measuring the subcellular compartmentalization of viral infections by protein complementation assay.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
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95 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
    Lopez, Margarita Zayas [corrected to Zayas, Margarita]
5 · Who and what money

Authors and funding

11 authors at 2 institutions in 2 countries.

Artur KaulDepartment of Molecular Virology, University of Heidelberg, Heidelberg, Germany.
Sarah Stauffer
Carola Berger
Thomas Pertel
Jennifer Schmitt
Stephanie Kallis
Margarita Zayas
Margarita Zayas Lopez
Volker Lohmann
Jeremy Luban
Ralf Bartenschlager
Heidelberg University · DEUniversity of Geneva · CH

Funding

Gag and Cyclophillin in HIV-1 ReplicationR01AI036199 · NIAID · UNIVERSITY OF GENEVA · PI LUBAN, JEREMY · 1994 to 2008
$2.9M
NIAID NIH HHS R01 AI036199NIAID NIH HHS R01AI36199
6 · The paper itself

Abstract

Viruses are obligate intracellular parasites and therefore their replication completely depends on host cell factors. In case of the hepatitis C virus (HCV), a positive-strand RNA virus that in the majority of infections establishes persistence, cyclophilins are considered to play an important role in RNA replication. Subsequent to the observation that cyclosporines, known to sequester cyclophilins by direct binding, profoundly block HCV replication in cultured human hepatoma cells, conflicting results were obtained as to the particular cyclophilin (Cyp) required for viral RNA replication and the underlying possible mode of action. By using a set of cell lines with stable knock-down of CypA or CypB, we demonstrate in the present work that replication of subgenomic HCV replicons of different genotypes is reduced by CypA depletion up to 1,000-fold whereas knock-down of CypB had no effect. Inhibition of replication was rescued by over-expression of wild type CypA, but not by a mutant lacking isomerase activity. Replication of JFH1-derived full length genomes was even more sensitive to CypA depletion as compared to subgenomic replicons and virus production was completely blocked. These results argue that CypA may target an additional viral factor outside of the minimal replicase contributing to RNA amplification and assembly, presumably nonstructural protein 2. By selecting for resistance against the cyclosporine analogue DEBIO-025 that targets CypA in a dose-dependent manner, we identified two mutations (V2440A and V2440L) close to the cleavage site between nonstructural protein 5A and the RNA-dependent RNA polymerase in nonstructural protein 5B that slow down cleavage kinetics at this site and reduce CypA dependence of viral replication. Further amino acid substitutions at the same cleavage site accelerating processing increase CypA dependence. Our results thus identify an unexpected correlation between HCV polyprotein processing and CypA dependence of HCV replication.

Indexed as

Cell Line, TumorCyclophilin AGene SilencingHepacivirusHost-Pathogen InteractionsHumansMutationPolyproteinsRNA, ViralViral Nonstructural ProteinsVirus ReplicationCyclophilin APolyproteinsRNA, ViralViral Nonstructural Proteins

Identifiers

PMID19680534
PMCPMC2718831
OpenAlexW2002980277

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.