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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.
Abstract:
During entry, polyomavirus (PyV) is endocytosed and sorts to the endoplasmic reticulum (ER), where it penetrates the ER membrane to reach the cytosol. From the cytosol, the virus moves to the nucleus to cause infection. How PyV is transported from the cytosol into the nucleus, a crucial infection step, is unclear. We found that upon reaching the cytosol, the archetypal PyV simian virus 40 (SV40) recruits the cytoplasmic dynein motor, which disassembles the viral particle. This reaction enables the resulting disassembled virus to enter the nucleus to promote infection. Our findings reveal how a cytosolic motor can be hijacked to impart conformational changes to a viral particle, a process essential for successful infection.IMPORTANCE How a nonenveloped virus successfully traffics from the cell surface to the nucleus to cause infection remains enigmatic in many instances. In the case of the nonenveloped PyV, the viral particle is sorted from the plasma membrane to the ER and then the cytosol, from which it enters the nucleus to promote infection. The molecular mechanism by which PyV reaches the nucleus from the cytosol is not entirely clear. Here we demonstrate that the prototype PyV SV40 recruits dynein upon reaching the cytosol. Importantly, this cellular motor disassembles the viral particle during cytosol-to-nucleus transport to cause infection.
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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