Utility of in vivo transcription profiling for identifying Pseudomonas aeruginosa genes needed for gastrointestinal colonization and dissemination

Research output: Contribution to journalJournal articlepeer-review

  • Andrew Y Koh
  • Per J Mikkelsen
  • Roger S Smith
  • Kathleen T Coggshall
  • Akinobu Kamei
  • Givskov, Michael
  • Stephen Lory
  • Gerald B Pier
Microarray analysis of Pseudomonas aeruginosa mRNA transcripts expressed in vivo during animal infection has not been previously used to investigate potential virulence factors needed in this setting. We compared mRNA expression in bacterial cells recovered from the gastrointestinal (GI) tracts of P. aeruginosa-colonized mice to that of P. aeruginosa in the drinking water used to colonize the mice. Genes associated with biofilm formation and type III secretion (T3SS) had markedly increased expression in the GI tract. A non-redundant transposon library in P. aeruginosa strain PA14 was used to test mutants in genes identified as having increased transcription during in vivo colonization. All of the Tn-library mutants in biofilm-associated genes had an attenuated ability to form biofilms in vitro, but there were no significant differences in GI colonization and dissemination between these mutants and WT P. aeruginosa PA14. To evaluate T3SS factors, we tested GI colonization and neutropenia-induced dissemination of both deletional (PAO1 and PAK) and insertional (PA14) mutants in four genes in the P. aeruginosa T3SS, exoS or exoU, exoT, and popB. There were no significant differences in GI colonization among these mutant strains and their WT counterparts, whereas rates of survival following dissemination were significantly decreased in mice infected by the T3SS mutant strains. However, there was a variable, strain-dependent effect on overall survival between parental and T3SS mutants. Thus, increased transcription of genes during in vivo murine GI colonization is not predictive of an essential role for the gene product in either colonization or overall survival following induction of neutropenia.
Original languageEnglish
JournalP L o S One
Volume5
Issue number12
Pages (from-to)e15131
ISSN1932-6203
DOIs
Publication statusPublished - 1 Dec 2010

    Research areas

  • Animals, Antibodies, Monoclonal, Biofilms, Gastrointestinal Tract, Gene Expression Profiling, Mice, Mice, Inbred C3H, Mutation, Neutropenia, Nucleic Acid Hybridization, Polymerase Chain Reaction, Pseudomonas Infections, Pseudomonas aeruginosa, Transcription, Genetic, Virulence Factors

ID: 33952278