PqsR-dependent and PqsR-independent regulation of motility and biofilm formation by PQS in Pseudomonas aeruginosa PAO1

J Basic Microbiol. 2014 Jul;54(7):633-43. doi: 10.1002/jobm.201300091. Epub 2013 Aug 29.

Abstract

Pseudomonas aeruginosa is an opportunistic pathogen capable of group behaviors including swarming motility and biofilm formation. Swarming motility plays an important role in the bacterium's spread to new environments, attachment to surfaces, and biofilm formation. Bacterial biofilm is associated with many persistent infections and increased resistance to antibiotics. In this study, we tested the effect of a 2-alkyl-4(1H)-quinolone (AHQ) signal, the Pseudomonas quinolone signal (PQS) on P. aeruginosa swarming and biofilm formation. Our results show that PQS repressed the swarming motility of P. aeruginosa PAO1. Such repression was independent of its cognate receptor PqsR and was not related to changes in the flagellae, type IV pili or the production of the surface-wetting agent rhamnolipid surfactant. While PQS did not affect twitching motility in PAO1, a pqsR deletion abolished twitching motility, indicating that pqsR is required for twitching motility. Our results also indicate that the enhancement of biofilm formation by PQS is at least partially dependent on the GacAS-Rsm regulatory pathway but does not involve the las or rhl QS systems.

Keywords: Biofilm; Pseudomonas Quinolone Signal; Pseudomonas aeruginosa; Swarming.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / genetics*
  • Bacterial Proteins / metabolism
  • Biofilms / drug effects*
  • Biofilms / growth & development
  • Fimbriae, Bacterial / physiology
  • Flagella / drug effects
  • Flagella / physiology
  • Gene Deletion
  • Gene Expression Regulation, Bacterial*
  • Glycolipids / biosynthesis
  • Movement / drug effects
  • Movement / physiology
  • Pseudomonas aeruginosa / drug effects*
  • Pseudomonas aeruginosa / genetics
  • Pseudomonas aeruginosa / metabolism
  • Quinolones / metabolism
  • Quinolones / pharmacology*
  • Quorum Sensing
  • Receptors, Cell Surface / genetics*
  • Receptors, Cell Surface / metabolism
  • Signal Transduction

Substances

  • 2-heptyl-3-hydroxy-4-quinolone
  • Bacterial Proteins
  • Glycolipids
  • Quinolones
  • Receptors, Cell Surface
  • rhamnolipid