Cloning and characterization of a novel haemolysin in Vibrio cholerae O1 that does not directly contribute to the virulence of the organism

Microbiology (Reading). 2002 Jul;148(Pt 7):2181-2189. doi: 10.1099/00221287-148-7-2181.

Abstract

A previously undescribed haemolysin, distinct from the major Vibrio cholerae O1 El Tor haemolysin, HlyA, was cloned from the O1 classical biotype strain Z17561. This novel haemolysin showed 71.5% overall similarity to the delta-thermostable direct haemolysin of Vibrio parahaemolyticus, and so it has been termed V. cholerae delta-thermostable haemolysin (Vc-deltaTH, encoded by the dth gene). An ORF found immediately downstream, which appears to be transcriptionally and translationally linked to dth, displayed strong homology to the family of acyl-CoA synthetases. When expressed from an inducible promoter in Escherichia coli, Vc-deltaTH was shown to be a 22.8 kDa protein active on sheep red blood cells. Co-expression of acs with dth had no effect on the haemolytic activity or cytoplasmic localization of Vc-deltaTH. A V. cholerae Z17561 dth::Km(R) mutant showed unaltered behaviour in the infant mouse cholera model.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Animals, Newborn
  • Cholera / microbiology
  • Cholera / physiopathology*
  • Cloning, Molecular*
  • Disease Models, Animal
  • Hemagglutination Tests
  • Hemolysin Proteins / genetics*
  • Hemolysin Proteins / metabolism*
  • Humans
  • Mice
  • Molecular Sequence Data
  • Mutation
  • Sequence Analysis, DNA
  • Subcellular Fractions / metabolism
  • Vibrio cholerae / genetics
  • Vibrio cholerae / metabolism
  • Vibrio cholerae / pathogenicity*
  • Virulence

Substances

  • Hemolysin Proteins

Associated data

  • GENBANK/AJ007495