Previous Article | Next Article ![]()
Infect. Immun., 05 1995, 1754-1761, Vol 63, No. 5
MJ Alfa, MK Stevens, P DeGagne, J Klesney-Tait, JD Radolf and EJ Hansen
To identify virulence-associated properties of Haemophilus ducreyi, 34
strains of this sexually transmitted pathogen were evaluated for in vitro
phenotypic characteristics of potential relevance to chancroid pathogenesis
and for their ability to produce lesions in the temperature-dependent
animal model for chancroid. Of the 34 strains tested, all but three
produced a cytopathic effect on human foreskin fibroblasts (HFF) and all
but six strains formed large microcolonies on HFF monolayers. A subset of
12 selected strains underwent more extensive analyses and, when evaluated
for both their cytadherence kinetics and growth in the presence of HFF
monolayers, it was found that several of these strains had a very limited
ability to attach to HFF cells. When the same 12 strains were tested in the
temperature- dependent rabbit model, only the seven strains which were
positive in all of these in vitro-based tests readily produced lesions. In
contrast, the five strains that were noted to be deficient in one or more
of the phenotypic characteristics scored in the in vitro systems did not
produce lesions. This association between the traits measured in vitro and
the ability to produce dermal lesions was significant (P = 0.0012). These
results suggest that in vitro behavior may be used to predict the virulence
potential of H. ducreyi strains. Moreover, the phenotypic characteristics
described in this study are appropriate focal points for efforts to
determine the molecular basis of the virulence of this pathogen.
Copyright © 1995, American Society for Microbiology
Use of tissue culture and animal models to identify virulence- associated traits of Haemophilus ducreyi
Department of Medical Microbiology, University of Manitoba, Canada.
This article has been cited by other articles:
| J. Bacteriol. | J. Virol. | Eukaryot. Cell |
|---|
| Microbiol. Mol. Biol. Rev. | Clin. Vaccine Immunol. | All ASM Journals |
|---|