Multiple roles of Pseudomonas aeruginosa TBCF10839 PilY1 in motility, transport and infection

Mol Microbiol. 2009 Feb;71(3):730-47. doi: 10.1111/j.1365-2958.2008.06559.x. Epub 2008 Dec 1.

Abstract

Polymorphonuclear neutrophils are the most important mammalian host defence cells against infections with Pseudomonas aeruginosa. Screening of a signature tagged mutagenesis library of the non-piliated P. aeruginosa strain TBCF10839 uncovered that transposon inactivation of its pilY1 gene rendered the bacterium more resistant against killing by neutrophils than the wild type and any other of the more than 3000 tested mutants. Inactivation of pilY1 led to the loss of twitching motility in twitching-proficient wild-type PA14 and PAO1 strains, predisposed to autolysis and impaired the secretion of quinolones and pyocyanin, but on the other hand promoted growth in stationary phase and bacterial survival in murine airway infection models. The PilY1 population consisted of a major full-length and a minor shorter PilY1* isoform. PilY1* was detectable in small extracellular quinolone-positive aggregates, but not in the pilus. P. aeruginosa PilY1 is not an adhesin on the pilus tip, but assists in pilus biogenesis, twitching motility, secretion of secondary metabolites and in the control of cell density in the bacterial population.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biological Transport
  • DNA Transposable Elements
  • DNA, Bacterial / genetics
  • Female
  • Fimbriae Proteins / genetics
  • Fimbriae Proteins / metabolism*
  • Fimbriae, Bacterial / genetics
  • Fimbriae, Bacterial / physiology*
  • Genes, Bacterial
  • Mice
  • Mice, Inbred C3H
  • Mutagenesis
  • Neutrophils / microbiology
  • Phenazines / metabolism
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • Pseudomonas Infections / microbiology*
  • Pseudomonas aeruginosa / genetics
  • Pseudomonas aeruginosa / growth & development*
  • Pseudomonas aeruginosa / metabolism
  • Quinolines / metabolism
  • Respiratory Tract Infections / microbiology

Substances

  • DNA Transposable Elements
  • DNA, Bacterial
  • Phenazines
  • PilY1 protein, Pseudomonas aeruginosa
  • Protein Isoforms
  • Quinolines
  • Fimbriae Proteins