Journal
VIRUSES-BASEL
Volume 14, Issue 2, Pages -Publisher
MDPI
DOI: 10.3390/v14020431
Keywords
vaccinia virus; cell cycle; kinase; p53; DNA damage response
Categories
Funding
- European Research Council [649101-UbiProPox]
- MRC Laboratory for Molecular Cell Biology PhD program
- NIH [R01AI114653]
- Cancer Research UK
- [MC_UU_00012/7]
- [T32AI125207]
- [MC_EX_G0800785]
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Modulation of the host cell cycle is a common strategy used by viruses to create a pro-replicative environment. Vaccinia virus (VACV) has been reported to alter cell cycle regulation and trigger the host cell DNA damage response. This study investigates the effect of VACV infection on cell proliferation and host cell cycle progression. It identifies the viral effectors responsible for inhibiting cell proliferation and shifting the host cell cycle, and reveals the involvement of viral kinases in activating the DNA damage checkpoint and mediating the degradation of checkpoint effectors.
Modulation of the host cell cycle is a common strategy used by viruses to create a pro-replicative environment. To facilitate viral genome replication, vaccinia virus (VACV) has been reported to alter cell cycle regulation and trigger the host cell DNA damage response. However, the cellular factors and viral effectors that mediate these changes remain unknown. Here, we set out to investigate the effect of VACV infection on cell proliferation and host cell cycle progression. Using a subset of VACV mutants, we characterise the stage of infection required for inhibition of cell proliferation and define the viral effectors required to dysregulate the host cell cycle. Consistent with previous studies, we show that VACV inhibits and subsequently shifts the host cell cycle. We demonstrate that these two phenomena are independent of one another, with viral early genes being responsible for cell cycle inhibition, and post-replicative viral gene(s) responsible for the cell cycle shift. Extending previous findings, we show that the viral kinase F10 is required to activate the DNA damage checkpoint and that the viral B1 kinase and/or B12 pseudokinase mediate degradation of checkpoint effectors p53 and p21 during infection. We conclude that VACV modulates host cell proliferation and host cell cycle progression through temporal expression of multiple VACV effector proteins. (209/200.)
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