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Article Dans Une Revue Veterinary Microbiology Année : 2015

Hypermutator Salmonella Heidelberg induces an early cell death in epithelial cells

Résumé

We have previously described that a strain of Salmonella Heidelberg with a hypermutator phenotype, B182, adhered strongly to HeLa cells. In this work, we showed that this hypermutator Salmonella strain invaded HeLa epithelial cells and induced cytoskeleton alteration. Those changes lead to HeLa cell death which was characteristic of apoptosis. For the first time, we showed that this hypermutator strain induced apoptosis associated with the activation of caspases 2, 9 and 3. Complementation of B182 strain showed a decrease in cells death induction. In the presence of other Salmonella Heidelberg with a normomutator phenotype, such as WT and SL486, cell death and caspase 3 were undetectable. These results suggested that early apoptosis and caspase 3 activation were specific to B182. Besides, B182 induced LDH release and caspase 3 activation in CaCo-2 and HCT116 cells. Heat-treated B182 and diffusible products failed to induce this phenotype. Epithelial cells treatment with cytochalasin D caused the inhibition of B182 internalisation and caspase 3 activation. These results showed that this cell death required active S. Heidelberg B182 protein synthesis and bacterial internalisation. However sipB and sopB, usually involved in apoptosis induced by Salmonella were not overexpressed in B182, contrary to fimA and fliC. Comparative genome analysis showed numerous mutations as in rpoS which would be more investigated. The role of the hypermutator phenotype might be suspected to be implicated in these specific features. This result expands our knowledge about strong mutators frequently found in bacterial organisms isolated from clinical specimens
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Dates et versions

hal-01187143 , version 1 (01-12-2015)

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Sandrine Le Gall-David, Neila Zenbaa, Damien Bouchard, Marie-Thérèse Lavault, Martine Bonnaure-Mallet, et al.. Hypermutator Salmonella Heidelberg induces an early cell death in epithelial cells. Veterinary Microbiology, 2015, 180 (1-2), pp.65-74. ⟨10.1016/j.vetmic.2015.07.034⟩. ⟨hal-01187143⟩
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