Evaluation of an isogenic hemolysin-deficient mutant in the human model of Haemophilus ducreyi infection

J Infect Dis. 1998 Jul;178(1):191-9. doi: 10.1086/515617.

Abstract

Haemophilus ducreyi causes the genital ulcerative disease chancroid. One putative virulence factor of H. ducreyi is a pore-forming hemolysin that displays toxicity against human fibroblasts and keratinocytes. In order to test the role of the hemolysin in pathogenesis, an isogenic hemolysin-deficient mutant was constructed, designated 35000HP-RSM1. The lipooligosaccharide, outer membrane protein patterns, and growth attributes of 35000HP-RSM1 were identical to its parent, 35000HP. Human subjects were challenged on the upper arm with the isogenic isolates in a double-blinded, randomized, escalating dose-response study. Pustules developed at a similar rate at sites inoculated with the mutant or parent. The cellular infiltrate and bacterial load in lesions were also similar. These results indicate the hemolysin does not play a role in pustule formation. Due to the limitations of this model, the role of the hemolysin at later stages of infection could not be determined.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Chancroid / microbiology*
  • Chancroid / pathology
  • Double-Blind Method
  • Female
  • Haemophilus ducreyi / classification
  • Haemophilus ducreyi / genetics
  • Haemophilus ducreyi / pathogenicity*
  • Hemolysin Proteins / genetics
  • Hemolysin Proteins / physiology*
  • Humans
  • Male
  • Mutagenesis
  • Phenotype
  • Virulence

Substances

  • Hemolysin Proteins