Role of lipooligosaccharides in experimental dermal lesions caused by Haemophilus ducreyi
- PMID: 1855979
- PMCID: PMC258062
- DOI: 10.1128/iai.59.8.2601-2608.1991
Role of lipooligosaccharides in experimental dermal lesions caused by Haemophilus ducreyi
Abstract
The mouse and rabbit intradermal injection models have been used to define factors that may be important in Haemophilus ducreyi pathogenesis. We used H. ducreyi strains with diverse geographic origins and phenotypic characteristics to evaluate the experimental models. Injection of live and heat-killed bacteria caused skin abscesses in both models. Semiquantitative cultures of skin injected with live bacteria showed that H. ducreyi failed to replicate in animal tissue. These data suggested that the experimental lesions were caused by a heat-stable substance such as lipooligosaccharide (LOS). In mice, injection of H. ducreyi and Haemophilus influenzae LOS and Escherichia coli lipopolysaccharide caused mild to moderate inflammation. In rabbits, injection of H. ducreyi LOS caused intradermal abscesses that were histologically similar to those caused by live and heat-killed bacteria. H. ducreyi and Neisseria gonorrhoeae LOS caused significantly larger lesions than equivalent amounts of H. influenzae LOS and E. coli lipopolysaccharide in the rabbit model. We conclude that the intradermal injection models are not valid models to study the growth of H. ducreyi in vivo. However, these data indicate that H. ducreyi LOS may play an important role in the pathogenesis of chancroid and that the rabbit model should be useful in studying H. ducreyi LOS toxicity at the cellular level.
Similar articles
-
The role of Haemophilus ducreyi bacteria, cytotoxin, endotoxin and antibodies in animal models for study of chancroid.Microb Pathog. 1992 Sep;13(3):203-17. doi: 10.1016/0882-4010(92)90021-f. Microb Pathog. 1992. PMID: 1291843
-
Characterization of skin lesions in mice following intradermal inoculation of Haemophilus ducreyi.J Exp Pathol (Oxford). 1990 Apr;71(2):233-44. J Exp Pathol (Oxford). 1990. PMID: 2331407 Free PMC article.
-
The cytolethal distending toxin of Haemophilus ducreyi aggravates dermal lesions in a rabbit model of chancroid.Microbes Infect. 2005 May;7(5-6):867-74. doi: 10.1016/j.micinf.2005.02.009. Epub 2005 Apr 20. Microbes Infect. 2005. PMID: 15876546
-
Chancroid: from clinical practice to basic science.AIDS Patient Care STDS. 2000 Jan;14(1):19-36. doi: 10.1089/108729100318109. AIDS Patient Care STDS. 2000. PMID: 12240879 Review.
-
Haemophilus ducreyi: pathogenesis and protective immunity.Trends Microbiol. 1995 Mar;3(3):87-92. doi: 10.1016/s0966-842x(00)88888-5. Trends Microbiol. 1995. PMID: 7773593 Review.
Cited by
-
Use of pyocin to select a Haemophilus ducreyi variant defective in lipooligosaccharide biosynthesis.Infect Immun. 1994 Jun;62(6):2379-86. doi: 10.1128/iai.62.6.2379-2386.1994. Infect Immun. 1994. PMID: 8188362 Free PMC article.
-
Inactivation of the Moraxella catarrhalis superoxide dismutase SodA induces constitutive expression of iron-repressible outer membrane proteins.Infect Immun. 2002 Apr;70(4):1889-95. doi: 10.1128/IAI.70.4.1889-1895.2002. Infect Immun. 2002. PMID: 11895952 Free PMC article.
-
A hemoglobin-binding outer membrane protein is involved in virulence expression by Haemophilus ducreyi in an animal model.Infect Immun. 1996 May;64(5):1724-35. doi: 10.1128/iai.64.5.1724-1735.1996. Infect Immun. 1996. PMID: 8613384 Free PMC article.
-
A diffusible cytotoxin of Haemophilus ducreyi.Proc Natl Acad Sci U S A. 1997 Apr 15;94(8):4056-61. doi: 10.1073/pnas.94.8.4056. Proc Natl Acad Sci U S A. 1997. PMID: 9108104 Free PMC article.
-
Characterization of a Haemophilus ducreyi mutant deficient in expression of cytolethal distending toxin.Infect Immun. 1999 Aug;67(8):3900-8. doi: 10.1128/IAI.67.8.3900-3908.1999. Infect Immun. 1999. PMID: 10417154 Free PMC article.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases