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Updated: Mar 16, 2026

High Throughput, Real-time, Dual-readout Testing of Intracellular Antimicrobial Activity and Eukaryotic Cell Cytotoxicity
Published on: November 16, 2016
Unhealthy Sugars in Bacterial Cytotoxicity
D Isui Aguilar-Salvador1, Guy Tran Van Nhieu1
1Equipe Communication Intercellulaire et Infections Microbiennes, Centre de Recherche Interdisciplinaire en Biologie (CIRB), Collège de France, 75005 Paris, France; Institut National de la Santé et de la Recherche Médicale (Inserm) U1050, 75654 Paris Cedex 13, France; Centre National de la Recherche Scientifique (CNRS) UMR7241, 75794 Paris Cedex 16, France; MEMOLIFE Laboratory of excellence and Paris Sciences et Lettres, 75005 Paris, France.
Bacterial type three secretion systems (T3SSs) are key to virulence. A new study reveals that cell surface sulfation and fucosylation are critical for activating T3SS-mediated cytotoxicity in Vibrio parahaemolyticus.
Area of Science:
- Microbiology
- Molecular Biology
- Cell Biology
Background:
- Bacterial type three secretion systems (T3SSs) are essential virulence factors.
- The precise mechanisms triggering T3SS activation remain largely unknown.
- Understanding T3SS activation is crucial for developing anti-virulence strategies.
Purpose of the Study:
- To identify host factors involved in the activation of bacterial T3SSs.
- To investigate the role of cell surface modifications in T3SS-mediated cytotoxicity.
Main Methods:
- Genome-wide screening using CRISPR/Cas technology.
- Utilized Vibrio parahaemolyticus as a model pathogen.
- Assessed bacterial cytotoxicity.
Main Results:
- Identified cell surface sulfation as a key process in T3SS activation.
- Demonstrated the importance of cell surface fucosylation in T3SS-mediated cytotoxicity.
- Highlighted a novel link between host cell surface chemistry and bacterial virulence.
Conclusions:
- Cell surface sulfation and fucosylation are critical regulators of bacterial T3SS function.
- These findings provide new insights into the host-pathogen interactions governing T3SS activation.
- Targeting these host cell surface modifications could represent a novel therapeutic approach.

