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Infection-induced host translational blockage inhibits immune responses and epithelial renewal in the Drosophila gut.
Type of publication
Peer-reviewed
Publikationsform
Original article (peer-reviewed)
Publication date
2012
Author
Chakrabarti S, Liehl P, Buchon N, Lemaitre B,
Project
The Drosophila intestinal epithelium: an immune barrier
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Original article (peer-reviewed)
Journal
Cell host & microbe
Volume (Issue)
12(1)
Page(s)
60 - 70
Title of proceedings
Cell host & microbe
Abstract
Typically, immune responses control the pathogen, while repair and stress pathways limit damage caused by pathogenesis. The relative contribution of damage to the outcome of pathogenesis and the mechanistic links between the immune and repair pathways are poorly understood. Here, we analyze how the entomopathogenic bacterium Pseudomonas entomophila induces irreversible damage to the Drosophila gut. We find that P. entomophila ingestion induces a global translational blockage that impairs both immune and repair programs in the fly gut. P. entomophila-induced translational inhibition is dependent on bacterial pore forming toxins and reactive oxygen species produced by the host in response to infection. Translational arrest is mediated through activation of the GCN2 kinase and inhibition of the TOR pathway as a consequence of host damage. Together, our study draws a model of pathogenesis in which bacterial inhibition of translation by excessive activation of stress responsive pathways inhibits both immune and regenerative epithelial responses.
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