Positive regulation of fur gene expression via direct interaction of fur in a pathogenic bacterium, Vibrio vulnificus

J Bacteriol. 2007 Apr;189(7):2629-36. doi: 10.1128/JB.01791-06. Epub 2007 Jan 19.

Abstract

In pathogenic bacteria, the ability to acquire iron, which is mainly regulated by the ferric uptake regulator (Fur), is essential to maintain growth as well as its virulence. In Vibrio vulnificus, a human pathogen causing gastroenteritis and septicemia, fur gene expression is positively regulated by Fur when the iron concentration is limited (H.-J. Lee et al., J. Bacteriol. 185:5891-5896, 2003). Footprinting analysis revealed that an upstream region of the fur gene was protected by the Fur protein from DNase I under iron-depleted conditions. The protected region, from -142 to -106 relative to the transcription start site of the fur gene, contains distinct AT-rich repeats. Mutagenesis of this repeated sequence resulted in abolishment of binding by Fur. To confirm the role of this cis-acting element in Fur-mediated control of its own gene in vivo, fur expression was monitored in V. vulnificus strains using a transcriptional fusion containing the mutagenized Fur-binding site (fur(mt)::luxAB). Expression of fur(mt)::luxAB showed that it was not regulated by Fur and was not influenced by iron concentration. Therefore, this study demonstrates that V. vulnificus Fur acts as a positive regulator under iron-limited conditions by direct interaction with the fur upstream region.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / genetics*
  • Bacterial Proteins / metabolism
  • Base Sequence
  • DNA Footprinting
  • DNA Primers
  • Deoxyribonuclease I / metabolism
  • Gene Deletion
  • Gene Expression Regulation, Bacterial
  • Humans
  • Iron / metabolism
  • Kinetics
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Plasmids
  • Promoter Regions, Genetic
  • Recombinant Proteins / metabolism
  • Repressor Proteins / genetics*
  • Repressor Proteins / metabolism
  • Vibrio vulnificus / genetics*
  • Vibrio vulnificus / pathogenicity

Substances

  • Bacterial Proteins
  • DNA Primers
  • Recombinant Proteins
  • Repressor Proteins
  • ferric uptake regulating proteins, bacterial
  • Iron
  • Deoxyribonuclease I