Bacteria-Host Crosstalk: Sensing of the Quorum in the Context of Pseudomonas aeruginosa Infections

J Innate Immun. 2019;11(3):263-279. doi: 10.1159/000494069. Epub 2018 Nov 14.

Abstract

Cell-to-cell signaling via small molecules is an essential process to coordinate behavior in single species within a community, and also across kingdoms. In this review, we discuss the quorum sensing (QS) systems used by the opportunistic pathogen Pseudomonas aeruginosa to sense bacterial population density and fitness, and regulate virulence, biofilm development, metabolite acquisition, and mammalian host defense. We also focus on the role of N-acylhomoserine lactone-dependent QS signaling in the modulation of innate immune responses connected together via calcium signaling, homeostasis, mitochondrial and cytoskeletal dynamics, and governing transcriptional and proteomic responses of host cells. A future perspective emphasizes the need for multidisciplinary efforts to bring current knowledge of QS into a more detailed understanding of the communication between bacteria and host, as well as into strategies to prevent and treat P. aeruginosa infections and reduce the rate of antibiotic resistance.

Keywords: Bacteria; Biofilms; Cell-to-cell signaling; Host-pathogen interactions; Innate immunity; Mucosal surfaces; N-acyl homoserine lactones; Proteogenomics; Pseudomonas aeruginosa; Quorum sensing.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • 4-Butyrolactone / analogs & derivatives
  • 4-Butyrolactone / physiology
  • Bacterial Adhesion
  • Biofilms
  • Calcium Signaling
  • Cell Movement
  • Homoserine / analogs & derivatives
  • Homoserine / physiology
  • Host Microbial Interactions*
  • Humans
  • Iron / metabolism
  • Lipopolysaccharides / physiology
  • Pseudomonas Infections / drug therapy
  • Pseudomonas Infections / etiology*
  • Pseudomonas aeruginosa / pathogenicity
  • Pseudomonas aeruginosa / physiology*
  • Quorum Sensing / physiology*

Substances

  • Lipopolysaccharides
  • N-(3-oxododecanoyl)homoserine lactone
  • Homoserine
  • Iron
  • 4-Butyrolactone