An Isogenic Hemoglobin Receptor–Deficient Mutant ofHaemophilus ducreyiIs Attenuated in the Human Model of Experimental Infection
Author(s) -
Jaffar A. AlTawfiq,
Kate R. Fortney,
Barry P. Katz,
Antoinette F. Hood,
Christopher A. Elkins,
Stanley M. Spinola
Publication year - 2000
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/315309
Subject(s) - haemophilus ducreyi , mutant , hemoglobin , microbiology and biotechnology , biology , heme , pasteurellaceae , inoculation , haemophilus , gene , immunology , bacteria , genetics , biochemistry , haemophilus influenzae , enzyme , antibiotics
Haemophilus ducreyi expresses a conserved hemoglobin-binding outer-membrane protein (HgbA). To test the role of HgbA in pathogenesis, we infected 9 adults with isolate 35000 and its isogenic hgbA-inactivated mutant (FX504) on their upper arms in a double-blinded, escalating dose-response study. Papules developed at similar rates at sites inoculated with the mutant or parent. The pustule-formation rate was 55% (95% confidence interval [CI], 30. 8%-78.5%) at parent sites and 0 (95% CI, 0-10.5%) at mutant sites (P<.0001). The recovery rate of H. ducreyi from surface cultures was 16% (n=142) from parent sites and 0 (n=213) from mutant sites (P<. 0001). H. ducreyi was recovered at biopsy from 6 of 7 parent sites and from 0 of 3 mutant sites. The results indicate that hemoglobin may be a critical source of heme or iron for the establishment of H. ducreyi infection in humans.
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