Bacterial peptidoglycan serves as a critical modulator of the gut-immune-brain axis in Drosophila

Brain Behav Immun. 2024 Jul:119:878-897. doi: 10.1016/j.bbi.2024.05.009. Epub 2024 May 6.

Abstract

Metabolites and compounds derived from gut-associated bacteria can modulate numerous physiological processes in the host, including immunity and behavior. Using a model of oral bacterial infection, we previously demonstrated that gut-derived peptidoglycan (PGN), an essential constituent of the bacterial cell envelope, influences female fruit fly egg-laying behavior by activating the NF-κB cascade in a subset of brain neurons. These findings underscore PGN as a potential mediator of communication between gut bacteria and the brain in Drosophila, prompting further investigation into its impact on all brain cells. Through high-resolution mass spectrometry, we now show that PGN fragments produced by gut bacteria can rapidly reach the central nervous system. In Addition, by employing a combination of whole-genome transcriptome analyses, comprehensive genetic assays, and reporter gene systems, we reveal that gut bacterial infection triggers a PGN dose-dependent NF-κB immune response in perineurial glia, forming the continuous outer cell layer of the blood-brain barrier. Furthermore, we demonstrate that persistent PGN-dependent NF-κB activation in perineurial glial cells correlates with a reduction in lifespan and early neurological decline. Overall, our findings establish gut-derived PGN as a critical mediator of the gut-immune-brain axis in Drosophila.

Keywords: Drosophila; Gut-brain axis; NF-κB; Peptidoglycan.

MeSH terms

  • Animals
  • Blood-Brain Barrier / immunology
  • Blood-Brain Barrier / metabolism
  • Brain* / immunology
  • Brain* / metabolism
  • Brain-Gut Axis* / physiology
  • Drosophila
  • Drosophila Proteins / metabolism
  • Drosophila melanogaster / metabolism
  • Female
  • Gastrointestinal Microbiome* / physiology
  • NF-kappa B* / metabolism
  • Neuroglia / immunology
  • Neuroglia / metabolism
  • Neurons / metabolism
  • Peptidoglycan* / metabolism

Substances

  • Peptidoglycan
  • NF-kappa B
  • Drosophila Proteins