Abstract

The digestive tract is the first organ affected by the ingestion of foodborne bacteria. While commensal bacteria become resident, opportunistic or virulent bacteria are eliminated from the gut by the local innate immune system. Here we characterize a new mechanism of defense, independent of the immune system, in Drosophila melanogaster. We observed strong contractions of longitudinal visceral muscle fibers for the first 2 hours following bacterial ingestion. We showed that these visceral muscle contractions are induced by immune reactive oxygen species (ROS) that accumulate in the lumen and depend on the ROS-sensing TRPA1 receptor. We then demonstrate that both ROS and TRPA1 are required in a subset of anterior enteroendocrine cells for the release of the DH31 neuropeptide which activates its receptor in the neighboring visceral muscles. The resulting contractions of the visceral muscles favors quick expulsion of the bacteria, limiting their presence in the gut. Our results unveil a precocious mechanism of defense against ingested opportunistic bacteria, whether they are Gram-positive like Bacillus thuringiensis or Gram-negative like Erwinia carotovora carotovora. Finally, we found that the human homolog of DH31, CGRP, has a conserved function in Drosophila.

Highlights

  • The intestinal mucosa is endowed with several systems of defense to fight against the bacteria that are swallowed along with food

  • The innate immune system is the main mean mounted by the gut lining in response to ill-causing bacteria to avoid detrimental impact

  • We found that the enteroendocrine cells perceive the presence of chlorine bleach in the lumen thanks to a sensor

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Summary

Introduction

The intestinal mucosa is endowed with several systems of defense to fight against the bacteria that are swallowed along with food. The gut epithelium accelerates its cellular renewal to quickly replace damaged cells [8]. Another mechanism that is poorly understood, despite long-standing empirical evidence of its role in the eviction of pathogens, is visceral contractions or spasms. A denervated small intestine of guinea pig displays enhanced contractility upon infection by the parasitic nematode Trichinella spiralis, suggesting an intrinsic signal that triggers gut contractions. This enhanced motility is necessary for efficient elimination of the worm [9]. The JAK/STAT pathway has been implicated in this hypercontractility, which is triggered by many parasitic nematodes [11, 12]

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