Pseudomonas aeruginosa as a Model To Study Chemosensory Pathway Signaling

Microbiol Mol Biol Rev. 2021 Jan 13;85(1):e00151-20. doi: 10.1128/MMBR.00151-20. Print 2021 Feb 17.

Abstract

Bacteria have evolved a variety of signal transduction mechanisms that generate different outputs in response to external stimuli. Chemosensory pathways are widespread in bacteria and are among the most complex signaling mechanisms, requiring the participation of at least six proteins. These pathways mediate flagellar chemotaxis, in addition to controlling alternative functions such as second messenger levels or twitching motility. The human pathogen Pseudomonas aeruginosa has four different chemosensory pathways that carry out different functions and are stimulated by signal binding to 26 chemoreceptors. Recent research employing a diverse range of experimental approaches has advanced enormously our knowledge on these four pathways, establishing P. aeruginosa as a primary model organism in this field. In the first part of this article, we review data on the function and physiological relevance of chemosensory pathways as well as their involvement in virulence, whereas the different transcriptional and posttranscriptional regulatory mechanisms that govern pathway function are summarized in the second part. The information presented will be of help to advance the understanding of pathway function in other organisms.

Keywords: Pseudomonas aeruginosa; chemosensory pathway; chemotaxis; signaling.

Publication types

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

MeSH terms

  • Bacterial Proteins / metabolism
  • Chemotaxis / physiology*
  • Gene Expression Regulation, Bacterial / genetics
  • Histidine Kinase / metabolism
  • Methyl-Accepting Chemotaxis Proteins / metabolism
  • Methylation
  • Methyltransferases / metabolism
  • Pseudomonas aeruginosa / metabolism*
  • Signal Transduction / physiology*

Substances

  • Bacterial Proteins
  • Methyl-Accepting Chemotaxis Proteins
  • CheW protein, Bacteria
  • Methyltransferases
  • Histidine Kinase