| ID | 56068 |
| JaLCDOI | |
| FullText URL | |
| Author |
Darwinata, Agus Eka
Department of Bacteriology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Gotoh, Kazuyoshi
Department of Bacteriology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Mima, Takehiko
Department of Bacteriology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Yamamoto, Yumiko
Department of Bacteriology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Yokota, Kenji
Graduate School of Health Sciences, Okayama University
Matsushita, Osamu
Department of Bacteriology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
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| Abstract | The bacterium Vibrio alginolyticus, an opportunistic pathogen in humans, has a type III secretion system (T3SS) that is responsible for its cytotoxicity toward eukaryotic cells. The effector of T3SS that is responsible for the cytotoxicity had not been identified. Here we demonstrate that VepA, a homolog of the T3SS effector in V. parahaemolyticus, is required for cytotoxicity in V. alginolyticus. VepA induces lysosomal membrane permeabilization, and it allows the leakage of only small molecules into the cytosol. Our findings revealed that VepA induces cathepsin-independent cell death in mammalian cells. The ferrous ion, one of the small molecules in the lysosome contents, appears to be involved in the cell death caused by V. alginolyticus VepA.
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| Keywords | cell death
lysosomal membrane permeability
VepA
Vibrio alginolyticus
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| Amo Type | Original Article
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| Publication Title |
Acta Medica Okayama
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| Published Date | 2018-06
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| Volume | volume72
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| Issue | issue3
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| Publisher | Okayama University Medical School
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| Start Page | 231
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| End Page | 239
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| ISSN | 0386-300X
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| NCID | AA00508441
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| Content Type |
Journal Article
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| language |
English
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| Copyright Holders | CopyrightⒸ 2018 by Okayama University Medical School
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| File Version | publisher
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| Refereed |
True
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| PubMed ID |