Characterization of a Vibrio cholerae virulence factor homologous to the family of TonB-dependent proteins

Mol Microbiol. 1992 Aug;6(16):2407-18. doi: 10.1111/j.1365-2958.1992.tb01415.x.


IrgA is an iron-regulated virulence factor for infection in an animal model with classical Vibrio cholerae strain 0395. We detected gene sequences hybridizing to irgA at high stringency in clinical isolates in addition to 0395, including another classical strain of V. cholerae, three V. cholerae strains of the El Tor biotype, three non-O1 isolates of V. cholerae, and individual isolates of Vibrio parahaemolyticus, Vibrio fluvialis, and Vibrio alginolyticus. No hybridization to irgA was seen with chromosomal DNA from Vibrio vulnificus or Aeromonas hydrophila. To verify that irgA is the structural gene for the major iron-regulated outer membrane protein of V. cholerae, we determined the amino-terminal sequence of this protein recovered after gel electrophoresis and demonstrated that it corresponds to the amino acid sequence of IrgA deduced from the nucleotide sequence. Gel electrophoresis showed that two El Tor strains of V. cholerae had a major iron-regulated outer membrane protein identical in size and appearance to IrgA in strain 0395, consistent with the findings of DNA hybridization. We have previously suggested that IrgA might be the outer membrane receptor for the V. cholerae siderophore, vibriobactin. Biological data presented here, however, show that a mutation in irgA had no effect on the transport of vibriobactin and produced no defect in the utilization of iron from ferrichrome, ferric citrate, haemin or haemoglobin. The complete deduced amino acid sequence of IrgA demonstrated homology to the entire class of Escherichia coli TonB-dependent proteins, particularly Cir. Unlike the situation with Cir, however, we were unable to demonstrate a role for IrgA as a receptor for catechol-substituted cephalosporins. The role of IrgA in the pathogenesis of V. cholerae infection, its function as an outer membrane receptor, and its potential interaction with a TonB-like protein in V. cholerae remain to be determined.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Bacterial Proteins / genetics*
  • Base Sequence
  • Biological Transport
  • Catechols / metabolism
  • Chickens
  • DNA, Bacterial
  • Escherichia coli Proteins*
  • Ferrichrome / metabolism
  • Hemagglutination
  • Hemolysis
  • Iron / metabolism
  • Membrane Proteins / genetics*
  • Molecular Sequence Data
  • Mutation
  • Oxazoles*
  • Receptors, Cell Surface*
  • Restriction Mapping
  • Sequence Homology
  • Species Specificity
  • Vibrio cholerae / genetics*
  • Vibrio cholerae / growth & development
  • Vibrio cholerae / pathogenicity


  • Bacterial Proteins
  • Catechols
  • DNA, Bacterial
  • Escherichia coli Proteins
  • Membrane Proteins
  • Oxazoles
  • Receptors, Cell Surface
  • irgA protein, Vibrio cholerae
  • tonB protein, Bacteria
  • tonB protein, E coli
  • Ferrichrome
  • vibriobactin
  • Iron

Associated data

  • GENBANK/M63192