Dynein Engages and Disassembles Cytosol-Localized Simian Virus 40 To Promote Infection

Madhu Sudhan Ravindran1, Chelsey C Spriggs2, Kristen J Verhey2

  • 1Department of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, Michigan, USA madhusudhan12@gmail.com btsai@umich.edu.

Journal of Virology
|March 30, 2018
PubMed

Insights

Simian virus 40 (SV40) hijacks the cytoplasmic dynein motor in the cytosol. This interaction disassembles the virus, enabling nuclear entry and infection.

Area of Science:

  • Virology
  • Cell Biology
  • Molecular Biology

Background:

  • Nonenveloped viruses, like polyomavirus (PyV), face challenges in trafficking from the cell surface to the nucleus for infection.
  • The precise mechanism of PyV nuclear import from the cytosol remains largely unknown.
  • Understanding viral transport is crucial for developing antiviral strategies.

Purpose of the Study:

  • To elucidate the molecular mechanism of polyomavirus nuclear import from the cytosol.
  • To investigate the role of cellular motors in SV40 (simian virus 40) infection.
  • To identify host factors essential for viral nuclear translocation.

Main Methods:

  • Utilized cell culture models to study SV40 entry and intracellular transport.
  • Employed techniques to visualize viral particles and host motor proteins within infected cells.
  • Investigated the interaction between SV40 and cytoplasmic dynein.

Main Results:

  • SV40 recruits the cytoplasmic dynein motor upon reaching the cytosol.
  • Cytoplasmic dynein mediates the disassembly of the SV40 virion.
  • This disassembly is essential for the virus to enter the nucleus and initiate infection.

Conclusions:

  • The study reveals that SV40 hijacks the cytoplasmic dynein motor for nuclear import.
  • Viral disassembly by a host motor protein is a critical step for infection.
  • This finding provides new insights into nonenveloped virus-host interactions and nuclear entry mechanisms.

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