AI Article Synopsis

  • Haemophilus ducreyi requires heme from human hosts for infection, utilizing TonB-dependent transporters, with HgbA being essential for early infection stages.
  • Active immunization with the HgbA protein provides complete protection in pig models of chancroid, indicating its potential as a vaccine.
  • Passive immunization using anti-nHgbA serum offers some protection against related strains, showing that antibodies can block heme acquisition but do not kill the bacteria directly.

Article Abstract

Haemophilus ducreyi, the etiologic agent of chancroid, has an obligate requirement for heme. Heme is acquired by H. ducreyi from its human host via TonB-dependent transporters expressed at its bacterial surface. Of 3 TonB-dependent transporters encoded in the genome of H. ducreyi, only the hemoglobin receptor, HgbA, is required to establish infection during the early stages of the experimental human model of chancroid. Active immunization with a native preparation of HgbA (nHgbA) confers complete protection in the experimental swine model of chancroid, using either Freund's or monophosphoryl lipid A as adjuvants. To determine if transfer of anti-nHgbA serum is sufficient to confer protection, a passive immunization experiment using pooled nHgbA antiserum was conducted in the experimental swine model of chancroid. Pigs receiving this pooled nHgbA antiserum were protected from a homologous, but not a heterologous, challenge. Passively transferred polyclonal antibodies elicited to nHgbA bound the surface of H. ducreyi and partially blocked hemoglobin binding by nHgbA, but were not bactericidal. Taken together, these data suggest that the humoral immune response to the HgbA vaccine is protective against an H. ducreyi infection, possibly by preventing acquisition of the essential nutrient heme.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3147553PMC
http://dx.doi.org/10.1128/IAI.00017-11DOI Listing

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