4.6 Article

Inhibition of the Ubiquitin-Proteasome System Affects Influenza A Virus Infection at a Postfusion Step

Journal

JOURNAL OF VIROLOGY
Volume 84, Issue 18, Pages 9625-9631

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/JVI.01048-10

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Funding

  1. Impulse Veterinary Avian Influenza Research in the Netherlands Economic Structure Enhancing Fund
  2. Center for Research on Influenza Pathogenesis (CRIP)
  3. National Institute for Allergy and Infectious Diseases (NIAID) [HHSN266200700010C, U01AI074539, 1F32AI081428]

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We have demonstrated that influenza A virus (IAV) RNA synthesis depends on the ubiquitin-proteasome system. IAV replication was reduced both by proteasome inhibitors and in E36ts20 cells, which contain the thermolabile ubiquitin-activating enzyme E1. While virus entry was not affected in E36ts20 cells, the proteasome inhibitor MG132 retained viral particles in the cytoplasm. Addition-removal experiments of MG132 in combination with bafilomycin A1, a well-established inhibitor of IAV entry and fusion, showed that MG132 affected IAV infection at a postfusion step. This was confirmed by the lack of inhibition of IAV entry by proteasome inhibitors in a virus-like particle fusion assay.

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