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Autophagy ; 13(2): 371-385, 2017 Feb.
Article in English | MEDLINE | ID: mdl-27875098

ABSTRACT

Autophagy is an evolutionarily conserved intracellular system that maintains cellular homeostasis by degrading and recycling damaged cellular components. The transcription factor HLH-30/TFEB-mediated autophagy has been reported to regulate tolerance to bacterial infection, but less is known about the bona fide bacterial effector that activates HLH-30 and autophagy. Here, we reveal that bacterial membrane pore-forming toxin (PFT) induces autophagy in an HLH-30-dependent manner in Caenorhabditis elegans. Moreover, autophagy controls the susceptibility of animals to PFT toxicity through xenophagic degradation of PFT and repair of membrane-pore cell-autonomously in the PFT-targeted intestinal cells in C. elegans. These results demonstrate that autophagic pathways and autophagy are induced partly at the transcriptional level through HLH-30 activation and are required to protect metazoan upon PFT intoxication. Together, our data show a new and powerful connection between HLH-30-mediated autophagy and epithelium intrinsic cellular defense against the single most common mode of bacterial attack in vivo.


Subject(s)
Autophagy , Bacterial Proteins/toxicity , Basic Helix-Loop-Helix Transcription Factors/metabolism , Caenorhabditis elegans Proteins/metabolism , Caenorhabditis elegans/cytology , Caenorhabditis elegans/microbiology , Endotoxins/toxicity , Epithelium/metabolism , Hemolysin Proteins/toxicity , Animals , Autophagy/drug effects , Autophagy-Related Proteins/genetics , Autophagy-Related Proteins/metabolism , Bacillus thuringiensis Toxins , Base Sequence , Caenorhabditis elegans/drug effects , Caenorhabditis elegans/metabolism , Epithelium/drug effects , Epithelium/ultrastructure , Gene Expression Regulation/drug effects , Intestines/microbiology , Intestines/pathology , Models, Biological , Transcription, Genetic/drug effects
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