Fur-dependent MrkHI regulation of type 3 fimbriae in Klebsiella pneumoniae CG43

Microbiology (Reading). 2012 Apr;158(Pt 4):1045-1056. doi: 10.1099/mic.0.053801-0. Epub 2012 Jan 19.

Abstract

Type 3 fimbriae play a crucial role in Klebsiella pneumoniae biofilm formation, but the mechanism of the regulation of the type 3 fimbrial operon is largely unknown. In K. pneumoniae CG43, three regulatory genes, mrkH, mrkI and mrkJ, are located downstream of the type 3 fimbrial genes mrkABCDF. The production of the major pilin MrkA is abolished by the deletion of mrkH or mrkI but slightly increased by the deletion of mrkJ. Additionally, quantitative RT-PCR and a promoter-reporter assay of mrkHI verified that the transcription of mrkHI was activated by MrkI, suggesting autoactivation of mrkHI transcription. In addition, sequence analysis of the mrkH promoter region revealed a putative ferric uptake regulator (Fur) box. Deletion of fur decreased the transcription of mrkH, mrkI and mrkA. The expression of type 3 fimbriae and bacterial biofilm formation were also reduced by the deletion of fur. Moreover, a recombinant Fur was found to be able to bind both promoters, with higher affinity for P(mrkH) than P(mrkA), implying that Fur controls type 3 fimbriae expression via MrkHI. We also proved that iron availability can influence type 3 fimbriae activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adhesins, Bacterial / genetics
  • Adhesins, Bacterial / metabolism*
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Biofilms / growth & development
  • Fimbriae Proteins / genetics
  • Fimbriae Proteins / metabolism*
  • Fimbriae, Bacterial / physiology*
  • Gene Deletion
  • Gene Expression Regulation, Bacterial
  • Genetic Complementation Test
  • Iron / metabolism
  • Klebsiella pneumoniae / genetics*
  • Klebsiella pneumoniae / metabolism
  • Klebsiella pneumoniae / physiology
  • Operon
  • Promoter Regions, Genetic
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism*
  • Transcription, Genetic
  • Transcriptional Activation

Substances

  • Adhesins, Bacterial
  • Bacterial Proteins
  • Klebsiella pneumoniae type 3 fimbrial adhesin
  • Repressor Proteins
  • ferric uptake regulating proteins, bacterial
  • Fimbriae Proteins
  • Iron