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RAB1A promotes Vaccinia virus replication by facilitating the production of intracellular enveloped virions

  • Tali Pechenick Jowers
  • , Rebecca J. Featherstone
  • , Danielle K. Reynolds
  • , Helen K. Brown
  • , John James
  • , Alan Prescott
  • , Ismar R. Haga
  • , Philippa M. Beard (Lead / Corresponding author)

    Research output: Contribution to journal › Article › peer-review

    Abstract

    Vaccinia virus (VACV) is a large double-stranded DNA virus with a complex cytoplasmic replication cycle that exploits numerous cellular proteins. This work characterises the role of a proviral cellular protein, the small GTPase RAB1A, in VACV replication. Using siRNA, we identified RAB1A as required for the production of extracellular enveloped virions (EEVs), but not intracellular mature virions (IMVs). Immunofluorescence and electron microscopy further refined the role of RAB1A as facilitating the wrapping of IMVs to become intracellular enveloped virions (IEVs). This is consistent with the known function of RAB1A in maintenance of ER to Golgi transport. VACV can therefore be added to the growing list of viruses which require RAB1A for optimal replication, highlighting this protein as a broadly proviral host factor.

    Original languageEnglish
    Pages (from-to)66-73
    Number of pages8
    JournalVirology
    Volume475
    DOIs
    Publication statusPublished - 15 Jan 2015

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

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