Post-phagocytosis activation of NLRP3 inflammasome by two novel T6SS effectors

Author:

Cohen Hadar1ORCID,Baram Noam1,Fridman Chaya Mushka1,Edry-Botzer Liat1,Salomon Dor1ORCID,Gerlic Motti1ORCID

Affiliation:

1. Department of Clinical Microbiology and Immunology, Sackler Faculty of Medicine, Tel Aviv University

Abstract

The type VI secretion system (T6SS) is used by bacteria to deliver toxic effectors directly into target cells. Most T6SSs mediate antibacterial activities, whereas the potential anti-eukaryotic role of T6SS remains understudied. Here, we found a Vibrio T6SS that delivers two novel effectors into mammalian host immune cells. We showed that these effectors induce a pyroptotic cell death in a phagocytosis-dependent manner; we identified the NLRP3 inflammasome as being the underlying mechanism leading to the T6SS-induced pyroptosis. Moreover, we identified a compensatory T6SS-induced pathway that is activated upon inhibition of the canonical pyroptosis pathway. Genetic analyses revealed possible horizontal spread of this T6SS and its anti-eukaryotic effectors into emerging pathogens in the marine environment. Our findings reveal novel T6SS effectors that activate the host inflammasome and possibly contribute to virulence and to the emergence of bacterial pathogens.

Funder

Israel Science Foundation

Tel Aviv University Recanati

Clore Israel Foundation

Tel Aviv University

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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