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Alteration of epithelial cell lysosomal integrity induced by bacterial cholesterol‐dependent cytolysins
Author(s) -
Malet Julien Karim,
Cossart Pascale,
Ribet David
Publication year - 2017
Publication title -
cellular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.542
H-Index - 138
eISSN - 1462-5822
pISSN - 1462-5814
DOI - 10.1111/cmi.12682
Subject(s) - listeriolysin o , biology , listeria monocytogenes , microbiology and biotechnology , golgi apparatus , organelle , secretion , endoplasmic reticulum , phagolysosome , cytolysin , cytosol , lysosome , cathepsin , endosome , bacteria , phagosome , listeria , biochemistry , phagocytosis , intracellular , genetics , enzyme , virulence , gene
Bacterial pathogens can interfere during infection with host cell organelles, such as mitochondria, the endoplasmic reticulum‐Golgi system or nuclei. As important cellular functions are often compartmentalized in these organelles, their targeting allows pathogens to manipulate key host functions during infection. Here, we identify lysosomes as a new class of organelles targeted by the pathogenic bacterium Listeria monocytogenes . We demonstrate that extracellular Listeria, via secretion of the pore‐forming toxin listeriolysin O, alters lysosomal integrity in epithelial cells but not in macrophages. Listeriolysin O induces lysosomal membrane permeabilization and release of lysosomal content, such as cathepsins proteases, which remain transiently active in the host cytosol. We furthermore show that other bacterial pore‐forming toxins, such as perfringolysin O and pneumolysin, also induce lysosomes alteration. Together, our data unveil a novel activity of bacterial cholesterol‐dependent cytolysins.

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