Apolipoprotein E interacts with hepatitis C virus nonstructural protein 5A and determines assembly of infectious particles

Authors

  • Wagane J. A. Benga,

    1. Institut National de la Santé et de la Recherche Médicale (INSERM) Unite 748, Strasbourg, France
    2. Institut de Virologie, Université de Strasbourg, Strasbourg, France
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    • These authors contributed equally to this work.

  • Sophie E. Krieger,

    1. Institut National de la Santé et de la Recherche Médicale (INSERM) Unite 748, Strasbourg, France
    2. Institut de Virologie, Université de Strasbourg, Strasbourg, France
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    • These authors contributed equally to this work.

  • Maria Dimitrova,

    1. Institut National de la Santé et de la Recherche Médicale (INSERM) Unite 748, Strasbourg, France
    2. Institut de Virologie, Université de Strasbourg, Strasbourg, France
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    • These authors contributed equally to this work.

  • Mirjam B. Zeisel,

    1. Institut National de la Santé et de la Recherche Médicale (INSERM) Unite 748, Strasbourg, France
    2. Institut de Virologie, Université de Strasbourg, Strasbourg, France
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  • Marie Parnot,

    1. Institut National de la Santé et de la Recherche Médicale (INSERM) Unite 748, Strasbourg, France
    2. Institut de Virologie, Université de Strasbourg, Strasbourg, France
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  • Joachim Lupberger,

    1. Institut National de la Santé et de la Recherche Médicale (INSERM) Unite 748, Strasbourg, France
    2. Institut de Virologie, Université de Strasbourg, Strasbourg, France
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  • Eberhard Hildt,

    1. Institut für Infektionsmedizin, Molekulare Medizinische Virologie, Kiel, Germany
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  • Guangxiang Luo,

    1. Department of Microbiology, Immunology and Molecular Genetics, University of Kentucky College of Medicine, Lexington, KY
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  • John McLauchlan,

    1. MRC Virology Unit, Glasgow, UK
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  • Thomas F. Baumert,

    Corresponding author
    1. Institut National de la Santé et de la Recherche Médicale (INSERM) Unite 748, Strasbourg, France
    2. Institut de Virologie, Université de Strasbourg, Strasbourg, France
    3. Pôle Hépato-digestif, Nouvel Hôpital Civil, Hôpitaux Universitaires de Strasbourg, Strasbourg, France
    • Inserm U748, 3 rue Koeberlé, F-67000 Strasbourg, France
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    • fax: (33)-3-68-85-37-50.

  • Catherine Schuster

    Corresponding author
    1. Institut National de la Santé et de la Recherche Médicale (INSERM) Unite 748, Strasbourg, France
    2. Institut de Virologie, Université de Strasbourg, Strasbourg, France
    • Inserm U748, 3 rue Koeberlé, F-67000 Strasbourg, France
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    • fax: (33)-3-68-85-37-24.


  • Potential conflict of interest: Nothing to report.

Abstract

Chronic hepatitis C virus (HCV) infection is a major cause of liver disease worldwide. Restriction of HCV infection to human hepatocytes suggests that liver-specific host factors play a role in the viral life cycle. Using a yeast-two-hybrid system, we identified apolipoprotein E (apoE) as a liver-derived host factor specifically interacting with HCV nonstructural protein 5A (NS5A) but not with other viral proteins. The relevance of apoE–NS5A interaction for viral infection was confirmed by co-immunoprecipitation and co-localization studies of apoE and NS5A in an infectious HCV cell culture model system. Silencing apoE expression resulted in marked inhibition of infectious particle production without affecting viral entry and replication. Analysis of particle production in liver-derived cells with silenced apoE expression showed impairment of infectious particle assembly and release. The functional relevance of the apoE–NS5A interaction for production of viral particles was supported by loss or decrease of apoE–NS5A binding in assembly-defective viral mutants. Conclusion: These results suggest that recruitment of apoE by NS5A is important for viral assembly and release of infectious viral particles. These findings have important implications for understanding the HCV life cycle and the development of novel antiviral strategies targeting HCV–lipoprotein interaction. (HEPATOLOGY 2010)

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