MassIVE MSV000088966

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Shigella Ubiquitin ligase IpaH7.8 targets gasdermin D for degradation to prevent pyroptosis and enable infection

Description

The pore-forming protein gasdermin D (GSDMD) executes lytic cell death called pyroptosis to eliminate the replicative niche of intracellular pathogens. Evolution favors pathogens that circumvent this host defense mechanism. Here, we show that the Shigella ubiquitin ligase IpaH7.8 functions as an inhibitor of GSDMD. Shigella is an enteroinvasive bacterium that causes hemorrhagic gastroenteritis in primates, but not rodents. IpaH7.8 contributes to species specificity by ubiquitinating human, but not mouse, GSDMD and targeting it for proteasomal degradation. Accordingly, infection of human epithelial cells with IpaH7.8-deficient Shigella flexneri results in increased GSDMD-dependent cell death compared with wild type. Consistent with pyroptosis contributing to murine disease resistance, eliminating GSDMD from NLRC4-deficient mice, which are already sensitized to oral infection with Shigella flexneri, leads to further enhanced bacterial replication and increased disease severity. This work highlights a species-specific pathogen arms race focused on maintenance of host cell viability. [doi:10.25345/C5T727H55] [dataset license: CC0 1.0 Universal (CC0 1.0)]

Keywords: TMT ; Global proteome ; ubiquitylome

Contact

Principal Investigators:
(in alphabetical order)
Christopher Rose, Genentech, United States
Submitting User: mnchoi

Publications

Giovanni Luchetti, Justin L. Roncaioli, Roberto A. Chavez, Alexander F. Schubert, Eric M. Kofoed, Rohit Reja, Tommy K. Cheung, Yuxin Liang, Joshua D. Webster, Isabelle Lehoux, Elizabeth Skippington, Janina Reeder, Benjamin Haley, Man Wah Tan, Christopher M. Rose, Kim Newton, Nobuhiko Kayagaki, Russell E. Vance, Vishva M. Dixit.
Shigella ubiquitin ligase IpaH7.8 targets gasdermin D for degradation to prevent pyroptosis and enable infection.
Cell Host Microbe . 2021 Oct 13;29(10):1521-1530.e10. doi: 10.1016/j.chom.2021.08.010. Epub 2021 Sep 6.

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