Early adaptive developments of Pseudomonas aeruginosa after the transition from life in the environment to persistent colonization in the airways of human cystic fibrosis hosts

Environ Microbiol. 2010 Jun;12(6):1643-58. doi: 10.1111/j.1462-2920.2010.02211.x. Epub 2010 Apr 7.

Abstract

Pseudomonas aeruginosa is an opportunistic pathogen ubiquitous to the natural environment but with the capability of moving to the host environment. Long-term infection of the airways of cystic fibrosis patients is associated with extensive genetic adaptation of P. aeruginosa, and we have studied cases of the initial stages of infection in order to characterize the early adaptive processes in the colonizing bacteria. A combination of global gene expression analysis and phenotypic characterization of longitudinal isolates from cystic fibrosis patients revealed well-known characteristics such as conversion to a mucoid phenotype by mucA mutation and increased antibiotic resistance by nfxB mutation. Additionally, upregulation of the atu operon leading to enhanced growth on leucine provides a possible example of metabolic optimization. A detailed investigation of the mucoid phenotype uncovered profound pleiotropic effects on gene expression including reduction of virulence factors and the Rhl quorum sensing system. Accordingly, mucoid isolates displayed a general reduction of virulence in the Caenorhabditis elegans infection model, altogether suggesting that the adaptive success of the mucoid variant extends beyond the benefits of alginate overproduction. In the overall perspective the global phenotype of the adapted variants appears to place them on paths in direction of fully adapted strains residing in long-term chronically infected patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptation, Physiological*
  • Alginates / metabolism
  • Animals
  • Child
  • Cystic Fibrosis / microbiology*
  • Gene Expression Regulation, Bacterial
  • Glucuronic Acid / metabolism
  • Hexuronic Acids / metabolism
  • Humans
  • Microarray Analysis
  • Molecular Sequence Data
  • Mutation
  • Phenotype
  • Pseudomonas Infections / microbiology*
  • Pseudomonas aeruginosa* / genetics
  • Pseudomonas aeruginosa* / pathogenicity
  • Pseudomonas aeruginosa* / physiology
  • Respiratory System / microbiology*
  • Virulence / genetics

Substances

  • Alginates
  • Hexuronic Acids
  • Glucuronic Acid