Ac102 Participates in Nuclear Actin Polymerization by Modulating BV/ODV-C42 Ubiquitination during Autographa

Yongli Zhang1,2, Xue Hu1, Jingfang Mu1

  • 1State Key Laboratory of Virology, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.

Journal of Virology
|April 6, 2018
PubMed

Insights

Autographa californica multiple nucleopolyhedrovirus (AcMNPV) uses viral proteins Ac102 and budded virus/occlusion derived virus (BV/ODV)-C42 (C42) to regulate actin polymerization. This interaction stabilizes the nucleation promoting factor (NPF) P78/83, crucial for viral propagation.

Area of Science:

  • Virology
  • Molecular Biology
  • Cell Biology

Background:

  • Actin polymerization is essential for eukaryotic cell function and is exploited by viruses for propagation.
  • Autographa californica multiple nucleopolyhedrovirus (AcMNPV) utilizes viral protein P78/83 as an actin nucleation promoting factor (NPF).
  • AcMNPV protein BV/ODV-C42 (C42) stabilizes P78/83 by inhibiting its proteasomal degradation.

Purpose of the Study:

  • To identify novel viral regulators of P78/83-induced actin polymerization during AcMNPV infection.
  • To elucidate the mechanism by which Ac102 influences P78/83 activity and actin polymerization.

Main Methods:

  • Characterization of an Ac102 knockout bacmid.
  • Analysis of protein-protein interactions between Ac102 and C42.
  • Investigation of ubiquitination status of C42 and its effect on proteasomal degradation.

Main Results:

  • Ac102 regulates nuclear actin polymerization, capsid morphogenesis, and distribution.
  • Ac102 interacts with C42, suppressing its K48-linked ubiquitination and proteasomal degradation.
  • This interaction stabilizes C42, thereby maintaining P78/83 stability and promoting actin polymerization.

Conclusions:

  • Ac102 and C42 form a regulatory cascade controlling viral NPF activity.
  • AcMNPV employs a sophisticated mechanism involving both ubiquitin-dependent and independent pathways to orchestrate actin polymerization.
  • This study reveals a novel viral strategy for manipulating the host actin cytoskeleton for efficient virus propagation.

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