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Microarray Analysis of <i>Pseudomonas aeruginosa</i> Quorum-Sensing Regulons: Effects of Growth Phase and Environment

Journal of Bacteriology · 2003 · Vol. 185(7) · pp. 2080–2095
Victoria WagnerDaniel BushnellLuciano PassadorAndrew I. BrooksBarbara H. Iglewski

Abstract

Bacterial communication via quorum sensing (QS) has been reported to be important in the production of virulence factors, antibiotic sensitivity, and biofilm development. Two QS systems, known as the las and rhl systems, have been identified previously in the opportunistic pathogen Pseudomonas aeruginosa. High-density oligonucleotide microarrays for the P. aeruginosa PAO1 genome were used to investigate global gene expression patterns modulated by QS regulons. In the initial experiments we focused on identifying las and/or rhl QS-regulated genes using a QS signal generation-deficient mutant (PAO-JP2) that was cultured with and without added exogenous autoinducers [N-(3-oxododecanoyl) homoserine lactone and N-butyryl homoserine lactone]. Conservatively, 616 genes showed statistically significant differential expression (P </= 0.05) in response to the exogenous autoinducers and were classified as QS regulated. A total of 244 genes were identified as being QS regulated at the mid-logarithmic phase, and 450 genes were identified as being QS regulated at the early stationary phase. Most of the previously reported QS-promoted genes were confirmed, and a large number of additional QS-promoted genes were identified. Importantly, 222 genes were identified as being QS repressed. Environmental factors, such as medium composition and oxygen availability, eliminated detection of transcripts of many genes that were identified as being QS regulated.

Bacterial biofilms and quorum sensingBacterial Genetics and BiotechnologyAntimicrobial Peptides and ActivitiesQuorum sensingRegulonBiologyAutoinducerHomoserinePseudomonas aeruginosaGeneBiofilmVirulenceMicrobiology

MeSH terms

Amino Acid SequenceBacterial ProteinsCell DivisionCulture MediaHomoserineMolecular Sequence DataMutationPseudomonas aeruginosa4-ButyrolactoneReproducibility of ResultsGene Expression Regulation, BacterialRegulonHomeodomain ProteinsReverse Transcriptase Polymerase Chain ReactionOligonucleotide Array Sequence Analysis

Funding

  • Cystic Fibrosis Foundation Therapeutics
  • National Institute for Health and Care Research
  • National Institutes of Health
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