Neural Immune Communication in the Control of Host-Bacterial Pathogen Interactions in the Gastrointestinal Tract

Infect Immun. 2020 Aug 19;88(9):e00928-19. doi: 10.1128/IAI.00928-19. Print 2020 Aug 19.

Abstract

The orchestration of host immune responses to enteric bacterial pathogens is a complex process involving the integration of numerous signals, including from the nervous system. Despite the recent progress in understanding the contribution of neuroimmune interactions in the regulation of inflammation, the mechanisms and effects of this communication during enteric bacterial infection are only beginning to be characterized. As part of this neuroimmune communication, neurons specialized to detect painful or otherwise noxious stimuli can respond to bacterial pathogens. Highlighting the complexity of these systems, the immunological consequences of sensory neuron activation can be either host adaptive or maladaptive, depending on the pathogen and organ system. These are but one of many types of neuroimmune circuits, with the vagus nerve and sympathetic innervation of numerous organs now known to modulate immune cell function and therefore dictate immunological outcomes during health and disease. Here, we review the evidence for neuroimmune communication in response to bacterial pathogens, and then discuss the consequences to host morbidity and mortality during infection of the gastrointestinal tract.

Keywords: Citrobacter; cholinergic anti-inflammatory pathway; enteric bacterial pathogens; enteric nervous system; enteric pathogens; gastrointestinal infection; gastrointestinal inflammation; host defense; neuroimmunology; sensory neurons; vagus nerve.

Publication types

  • Review

MeSH terms

  • Animals
  • Calcitonin Gene-Related Peptide / genetics
  • Calcitonin Gene-Related Peptide / immunology
  • Citrobacter / growth & development
  • Citrobacter / immunology
  • Enteric Nervous System / immunology*
  • Enteric Nervous System / microbiology
  • Enterobacteriaceae Infections / genetics
  • Enterobacteriaceae Infections / immunology*
  • Enterobacteriaceae Infections / microbiology
  • Enterobacteriaceae Infections / pathology
  • Gastrointestinal Microbiome / immunology*
  • Gastrointestinal Tract / immunology*
  • Gastrointestinal Tract / innervation
  • Gastrointestinal Tract / microbiology
  • Gene Expression Regulation / immunology
  • Host-Pathogen Interactions / genetics
  • Host-Pathogen Interactions / immunology
  • Humans
  • Neuroimmunomodulation / genetics*
  • Pathogen-Associated Molecular Pattern Molecules / immunology
  • Pathogen-Associated Molecular Pattern Molecules / metabolism
  • Sensory Receptor Cells / immunology*
  • Sensory Receptor Cells / microbiology
  • TRPA1 Cation Channel / genetics
  • TRPA1 Cation Channel / immunology
  • TRPV Cation Channels / genetics
  • TRPV Cation Channels / immunology
  • Toll-Like Receptors / genetics
  • Toll-Like Receptors / immunology

Substances

  • Pathogen-Associated Molecular Pattern Molecules
  • TRPA1 Cation Channel
  • TRPA1 protein, human
  • TRPV Cation Channels
  • TRPV1 protein, human
  • Toll-Like Receptors
  • Calcitonin Gene-Related Peptide