INTRODUCTION

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Haemophilus ducreyi causes chancroid, which facilitates transmission of the human immunodeficiency virus (HIV) (16, 31, 40). Usually, chancroid outbreaks occur sporadically in industrialized countries (24, 25, 39). Although now rare in the United States (12), chancroid remains a common public health problem in many developing countries (9, 10, 13, 26, 30, 37).

Recently, Elkins et al. described a 30-kDa outer membrane protein called Ducreyi serum resistance A (DsrA) (14). DsrA is expressed by all naturally occurring strains of H. ducreyi tested, except for three serum-sensitive strains that were avirulent in animal models (14). The dsrA gene was identified and sequenced (14), and the predicted amino acid sequence of DsrA was noted to be similar to the UspA2 protein of Moraxella catarrhalis and YadA of Yersinia spp. (14). Both UspA2 and YadA mediate serum resistance (1, 29). An isogenic dsrA mutant, FX517, of H. ducreyi 35000 was constructed by insertion of a chloramphenicol acetyltransferase (cat) cassette into the dsrA open reading frame and allele exchange. FX517 no longer expressed DsrA and was at least 10-fold more serum susceptible than its parent. FX517 and the three naturally occurring serum-susceptible strains that lacked DsrA were complemented in trans with a plasmid containing dsrA, and all four strains were converted to a serum-resistant phenotype.

The role of DsrA in the pathogenesis of chancroid is currently unknown. Utilizing a human challenge model, we examined whether dsrA was transcribed during experimental infection with H. ducreyi. We also compared the ability of 35000 and FX517 to cause infection in human volunteers.

	MATERIALS AND METHODS

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Bacteria. H. ducreyi 35000 and FX517 were described previously (14). 35000HP is a human-passaged variant of 35000 (4, 5, 34).

Detection of dsrA transcripts in vivo. Biopsies of pustules and normal skin were obtained from five infected and two uninfected volunteers as described in detail elsewhere (36a). RNA was isolated, and cDNA was synthesized from the biopsies, from uninfected skin, and from uninfected skin homogenized with 10⁶ CFU of 35000HP using Ultraspec RNA (Biotecx Laboratories, Inc., Houston, Tex.) and Advantage RT-for-PCR Kit (Clontech Laboratories, Palo Alto, Calif.) as described elsewhere (36a). RNA that was not subjected to reverse transcription (RT) was included to control for DNA contamination. Amplification of target cDNA was performed with the dsrA-9 and dsrA-11 primers (14) using the PCR Core Kit Plus (Roche Molecular Biochemicals, Indianapolis, Ind.). PCR-positive and -negative control templates included genomic DNA from 35000HP and H₂O, respectively. Amplicons were analyzed by electrophoresis of 10 µl of each PCR reaction on 1.2% agarose gels stained with ethidium bromide.

Human challenge protocol. Healthy adult male and female volunteers over 18 years of age were recruited for the study. Informed consent was obtained from the subjects for participation and for HIV serology, in accordance with the human experimentation guidelines of the U.S. Department of Health and Human Services and the Institutional Review Board of Indiana University-Purdue University Indianapolis. The experimental challenge protocol, preparation and inoculation of the bacteria, calculation of the estimated delivered dose (EDD), and clinical observations were done exactly as described previously (3-5, 34, 35). When a papule was present, the area of erythema was calculated by measuring the greatest dimension vertically and horizontally in millimeters and then multiplying the two measurements. Subjects were observed until they reached a clinical endpoint, defined as either 14 days after inoculation, development of a painful pustule, or resolution of infection at all sites. When a clinical endpoint was achieved, the code was broken and up to two sites with active disease (one inoculated with the parent and one inoculated with the mutant), if present, were biopsied with a punch forceps. The subjects were then treated with two doses of oral ciprofloxacin as described previously.

Biopsies. Specimens were cut into portions. One portion was fixed in formalin, and immunohistological studies were done as previously described (28, 34, 35). One portion was homogenized in 1 ml of freezing medium (3% [wt/vol] tryptic soy broth, 10% glycerol, 10% heat-inactivated fetal calf serum) for 2 min on ice and cultured semi-quantitatively as described previously (34, 35).

Phenotypes of recovered bacteria. Individual colonies from the inocula, surface cultures, and biopsies were picked, suspended in freezing medium, and frozen in 96-well plates. The colonies were scored for susceptibility to chloramphenicol on chloramphenicol-containing chocolate agar plates. At least 30 individual colonies per specimen, if available, were analyzed. If 30 colonies had the correct phenotype, then we were confident (95% probability) that, at most, only 11% of the colonies could have the incorrect phenotype in a specimen.

	RESULTS

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In vivo expression of dsrA. Transcription of dsrA was examined by RT-PCR of biopsies of five pustules obtained from four volunteers at sites infected with 35000 or 35000HP. RT-PCR was also performed on cDNA prepared from uninfected skin with or without added 35000HP. The expected 385-bp RT-PCR product was obtained from uninfected skin supplemented with bacteria and from the five biopsies of pustules but not from the uninfected control (Fig. 1 and data not shown). The sequence of the 385-bp amplicon generated with genomic DNA from 35000HP was identical to the published sequence of dsrA. Thus, dsrA was transcribed during experimental infection of human volunteers.

View larger version (33K): [in this window] [in a new window]   FIG. 1.   Composite agarose gel stained with ethidium bromide from PCR and RT-PCR products obtained using dsrA primers. Lanes 1 and 2 contain 35000HP genomic DNA and no template, respectively. cDNA (lanes 3, 5, 7, and 9) and RNA that was not reverse transcribed (lanes 4, 6, 8, and 10) were prepared from uninfected skin (lanes 3 and 4), uninfected skin homogenized with H. ducreyi (lanes 5 and 6), a biopsy from volunteer 160 (lanes 7 and 8), and a biopsy from volunteer 142 (lanes 9 and 10).

Human inoculation experiments. Seven healthy adults (four females, three males; age range of 21 to 46 years; mean age ± the standard deviation, 33.9 ± 8.3 years) volunteered for the study. Three subjects (158, 159, and 160) were challenged in the first iteration, and three subjects (155, 165, and 166) were challenged in the second iteration (Table 1). Subject 161 withdrew prior to inoculation.

Bacterial recovery and cellular infiltrate from mutant and parent lesions. From daily surface cultures, H. ducreyi was recovered intermittently from 1 of 12 parent sites, while no bacteria were recovered from the 18 mutant sites or the 6 heat-killed sites. Four subjects had parent sites that contained pustules at endpoint and were biopsied. H. ducreyi were recovered (range, 2.6 × 10⁴ to 4.1 × 10⁶ CFU per g of tissue) from four of four parent biopsies. We also examined the cellular infiltrate in two parent biopsies. Micropustules with polymorphonuclear leukocytes were present in the epidermis (data not shown). The dermis contained a perivascular infiltrate of mononuclear cells and some polymorphonuclear leukocytes, and the venules were lined with reactive endothelial cells. The mononuclear cells stained positively with a CD3 marker verifying their T-cell origin (data not shown). No disease was present at the mutant sites at endpoint, and no mutant sites were biopsied in accordance with our protocols.

Confirmation of the antibiotic susceptibility of the recovered bacteria. To confirm that the inocula were correct and that no cross-contamination of sites had occurred during infection, individual colonies from each of the broth cultures used to prepare the inocula, from surface cultures, and from biopsy specimens were analyzed for chloramphenicol susceptibility (Cm^s). For the two parent and two mutant broth cultures used to prepare the inocula, all 88 parent colonies and 88 mutant colonies tested were phenotypically correct (mutant, Cm^r; parent, Cm^s). All 40 colonies obtained from surface cultures of parent sites were phenotypically correct (Cm^s). A total of 192 parent colonies obtained from biopsies were phenotypically correct (Cm^s). Thus, all colonies tested from the inocula, surface cultures, and biopsies had the expected antibiotic susceptibility.

	DISCUSSION

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In this study, we amplified dsrA cDNA from RNA of pustules of experimentally infected subjects, suggesting that DsrA was expressed in vivo. We also tested the ability of an isogenic DsrA-deficient mutant (FX517) to infect human volunteers. In our volunteer group, the mutant formed papules at a rate similar to that of the parent strain, but mutant papules were significantly smaller and did not progress to the pustular stage of disease. In previous studies, isogenic hgbA receptor and pal mutants were impaired in their ability to form pustules in humans (3, 17). This is the third demonstration that a putative virulence factor of H. ducreyi facilitates pustule formation in humans.

Our institutional biosafety committee does not permit the testing of mutants complemented with plasmids in human subjects. We cannot exclude the possibility that the decreased virulence of FX517 was due to a secondary mutation or a polar effect of the cat cassette. However, complementation of FX517 in trans restores expression of DsrA and serum resistance to the mutant (14). Thus, it is highly likely that the decreased virulence of FX517 was due to the mutation of dsrA.

The bactericidal activity of human serum is an important component of innate host defenses, and many bacterial pathogens are serum resistant. H. ducreyi 35000 is resistant to normal human serum at concentrations of up to 50% (18). Although initial investigations by Odumeru and colleagues suggested that truncations in the lipooligosaccharide of H. ducreyi mediated serum sensitivity (27), recent studies showed that the loss of serum resistance was due to the loss of DsrA and not to truncations in lipooligosaccharide (14, 18, 36). In natural infection, H. ducreyi is thought to gain access to the skin via wounds that occur during intercourse (25). Puncture wounds are required to initiate experimental infection (35). FX517 may have been less efficient at establishing and maintaining infection in our volunteers because it was killed by serum that leaks into the skin during wound healing and inflammation (20).

DsrA is a member of a growing family of proteins that share homology at their C termini and confer serum resistance and/or the ability to adhere to human cells on their respective organisms (1, 2, 14, 21, 23, 29, 32, 33). This family includes the YadA protein of Yersinia spp., the UspA2 protein of M. catarrhalis and the Eib protein of certain Escherichia coli strains. Each protein appears to have a unique mechanism of diverting complement-mediated antibody killing. For example, YadA binds complement factor H (29), UspA2 binds the complement regulatory protein vitronectin (23), and the Eib proteins bind immunoglobulins via the Fc portion of the molecule (32, 33). The mechanism by which DsrA mediates serum resistance is not known and is currently under investigation.

Attachment of bacteria to host cells is a critical step in the establishment of infection. H. ducreyi attaches to human keratinocytes and fibroblasts in vitro (6, 11, 19, 22, 38). Elkins and colleagues tested the ability of FX517 to attach to a keratinocyte cell line and found that FX517 adhered significantly less efficiently than the parent strain (L. E. Cole, C. Elkins, T. Kawula, Abstr. 100th Gen. Meet. Am. Soc. Microbiol., abstr. B-122, p. 69, 2000). The complemented mutant regained its ability to attach. However, confocal microscopy data failed to show that H. ducreyi binds to keratinocytes throughout the course of experimental infection of human subjects (8; unpublished observations). Thus, the significance of the in vitro observations and their relevance to human disease is not clear.

Throughout the course of experimental infection, H. ducreyi colocalizes with collagen in the upper dermis (unpublished observations). H. ducreyi binds to collagen in vitro (7). YadA mediates binding to collagen through repeated NSVAIG-S motifs in the amino-terminal half of the protein (15). DsrA lacks sequences homologous to the N-terminal half of YadA, and it is unlikely that DsrA mediates collagen binding through a similar motif.

In summary, our data show that dsrA is transcribed in vivo and suggests that expression of DsrA is required for the virulence of H. ducreyi. The homology among DsrA, YadA, UspA2, and the Eib proteins suggests that DsrA may have multiple functions, including serum resistance and cell adherence. Therefore, FX517 may have been attenuated in experimental infection for multiple reasons. Future studies will focus on delineating the mechanisms by which DsrA mediates serum resistance and its possible role in adherence.