INTRODUCTION

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Mammalian hosts use iron-binding proteins and iron-sequestering compounds to maintain free iron at a level that is too low for the growth of invading bacterial pathogens (52). Several pathogenic organisms have developed specific mechanisms for iron acquisition which are induced under conditions of iron limitation. The genital mucosal pathogen Neisseria gonorrhoeae is known to use iron from lactoferrin and transferrin for growth (37, 38). The ability to use lactoferrin and transferrin is due to specific receptors (reviewed in reference 11). Gonococci also are able to utilize heme and certain heme-containing proteins as iron sources (15, 38). Two heme-binding proteins (99 and 44 kDa) have been isolated from the total membranes of gonococcal clinical isolates grown under iron-limited conditions (26, 29). Nevertheless, the mechanism of iron uptake from heme-containing proteins is unclear.

Mickelsen and Sparling (38) showed that 18 of 29 gonococcal strains studied were capable of using hemoglobin for growth. Lee and Hill (28) detected hemoglobin binding activity from Neisseria meningitidis grown under iron-limited conditions. More recently, two different meningococcal hemoglobin receptors have been described at the molecular level. Stojiljkovic et al. (49, 50) cloned a gene encoding an iron-regulated outer membrane protein, HmbR, which has amino acid similarity with the family of TonB-dependent membrane receptors. Lewis and Dyer (30) and Lewis et al. (31) described hpuAB, the hemoglobin-haptoglobin utilization operon of N. meningitidis, and suggested that HpuA and HpuB constitute a two-component receptor analogous to the bipartite transferrin receptor TbpB-TbpA (formerly named Tbp2-Tbp1) (reviewed in reference 11). Predicted amino acid sequences of N. meningitidis HpuA and HpuB indicate that, like TbpB and TbpA, HpuB belongs to the TonB-dependent family of high-affinity transport proteins and HpuA is probably a lipoprotein (31).

We previously reported that all tested gonococcal strains can use hemoglobin as a sole source of iron for growth by switching from a non-hemoglobin-utilizing phenotype (Hgb) to a hemoglobin-utilizing phenotype (Hgb⁺) in vitro. In order to distinguish these two phenotypes of the same strain, we classified gonococci able to grow on hemoglobin-Desferal plates as Hgb⁺ variants and those unable to grow on hemoglobin-Desferal plates as Hgb variants (8). The ability to use hemoglobin for growth appears to be a phase-varying phenomenon, because Hgb⁺ variants arise from Hgb parents at a frequency of about 1 × 10⁴ to 2 × 10³ (8). In this communication, we describe the mechanism underlying the phase variation of hemoglobin utilization and the characteristics of a 42-kDa HpuA protein encoded by the gonococcal hpuA gene. We also previously reported that insertional mutants that no longer expressed the 89-kDa HpuB protein cannot utilize hemoglobin to support growth but still grow on heme (8). Now we report on the requirement for HpuA in the utilization of hemoglobin for growth by N. gonorrhoeae.

	MATERIALS AND METHODS

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Bacterial strains and growth conditions. N. gonorrhoeae strains used are listed in Table 1. Both Hgb⁺ and Hgb variants of FA1090 and FA19 were used. Growth conditions were the same as those described by Chen et al. (8), with the exception that the iron chelator Desferal (deferoxamine mesylate; CIBA Pharmaceutical Co.) was used at a 100 µM final concentration for FA1090 and insertional mutants of FA1090. The abilities of FA1090 Hgb and Hgb⁺ variants and their hpuA and/or hpuB insertional mutants to grow on heme were tested on modified gonococcal medium base (GCB) agar plates (8) containing bovine hemin chloride (Sigma) at 5 mg/liter and Desferal at 100 µM. Antibiotic selection in gonococci employed erythromycin at 1 mg/liter for mini-Tn3erm insertions (30), spectinomycin at 100 mg/liter for the  interposon insertions (44), and kanamycin at 60 mg/liter for the aphA-3 cassette insertions (35).

Sequencing the gonococcal hpuA gene. Double-stranded PCR products, purified with a Geneclean II kit (Bio 101, Inc.), were sequenced directly. Chromosomal DNAs of FA1090 Hgb⁺ and FA1090 Hgb were used as templates for PCRs. Initially, the putative open reading frame of FA1090 hpuA was identified from the database of the Gonococcal Genome Sequencing Project (Advanced Center for Genome Technology, University of Oklahoma) by searching for the coding sequence of the N terminus of FA1090 HpuB (8). The 19-mer upstream PCR primer (hpu.01, GCAGGCACGTCCGATTTCC) was designed based on the sequence 108 bp upstream of the ATG codon of the putative hpuA open reading frame (Fig. 1). A 20-mer downstream primer (hpu.14, ACAAAACCCAAAAACTCGGAC) was designed, based on the N-terminal amino acid sequence of HpuB, to generate PCR DNA fragments covering the entire hpuA gene (Fig. 1). Two PCRs were carried out for each variant. One used purified chromosomal DNA, and the other used boiled cells, as the template. PCR products were pooled for sequencing. Both strands of the PCR-generated hpuA DNA were sequenced by using hpu.01, hpu.14, and four additional internal primers.

View larger version (18K): [in this window] [in a new window]   FIG. 1.   Descriptive map of FA1090 hpuA. Numbers indicate positions of first nucleotides. The open reading frames (ORFs) for hpuA and hpuB start at nucleotide positions 01 and 1,110, respectively. Beginning from position 43 is a consensus coding sequence for a type-II signal peptidase cleavage site, LAAC. A run of multiple guanine residues was located in hpuA, starting from position 58. The asterisk indicates a stop codon. A 1,130-bp fragment was isolated between the NarI site in hpuA and an XbaI site in the vector for mutagenesis. The PpuMI site was the insertion site for making various mutants. The primer pair, hpu.01 and hpu.14, was used in PCRs for the cloning of hpuA. The other primer pair, hpu.01 and hpu.02, was used to generate PCR products for enumerating guanine residues in the poly(G) tract.

Cloning of the hpuA gene. Routine molecular cloning techniques as described by Sambrook et al. (47) were used. Plasmid DNAs were isolated by either the Wizard Minipreps DNA purification system (Promega) or the Qiagen DNA purification system. Chromosomal DNA from N. gonorrhoeae was purified by the method of Stern et al. (48). The 1,360-bp PCR DNA made from the FA1090 Hgb template and the 1,361-bp PCR DNA made from the FA1090 Hgb⁺ template were inserted into the pCRII vector by using the TA cloning kit (Invitrogen) to yield pUNCH258 and pUNCH259, respectively.

Insertional mutagenesis of the hpuA gene. (i) Construction of polar hpuA insertional mutants. In order to avoid potential variations in the poly(G) region during experimental manipulation of hpuA, insertional mutagenesis of hpuA was carried out within a NarI-XbaI fragment isolated from pUNCH258 (Fig. 1). The NarI site was located 108 bp downstream of the poly(G) tract, and the XbaI site was present in the polylinker of pCRII. The NarI-XbaI fragment was subcloned into the pBluescript II KS⁺ phagemid (Stratagene) digested with XbaI-AccI to yield pUNCH260. In order to avoid blocking of PpuMI digestion by Dcm methylase activity, pUNCH260 was moved from Escherichia coli DH5MCR (Bethesda Research Laboratories) to GM2163 (New England Biolabs). The 2-kb  interposon fragment isolated from SmaI-cut pHP45 (44) was ligated with pUNCH260, digested with PpuMI, and filled in with the Klenow fragment of DNA polymerase I (Fig. 1) to yield pUNCH268. pUNCH268, containing an  insert in the hpuA fragment, was then transformed into FA1090 Hgb and FA1090 Hgb⁺ to generate FA6981 and FA6982, respectively. Transformant colonies were screened for resistance to spectinomycin at 100 mg/liter and the inability to grow on hemoglobin-Desferal plates.

(ii) Construction of a nonpolar hpuA insertional mutant. A mutagenic cassette designed to be inserted into a gene of an operon without affecting transcription of downstream genes (35) was adopted for our construction of a nonpolar hpuA mutant. The 800-bp aphA-3 insert cassette was isolated from pUC18K by SmaI digestion (35) and was ligated to PpuMI-digested pUNCH260 to generate pUNCH271. pUNCH271 was then transformed into FA1090 Hgb⁺ to create FA6983. Transformant colonies were screened for resistance to kanamycin at 60 mg/liter and the inability to grow on hemoglobin-Desferal plates.

Enumeration of G residues. The cloned hpuA gene in pUNCH258 and pUNCH259 was sequenced with M13 reverse primer (Invitrogen). The guanine residues in hpuA from FA6981, FA6982, and FA6983 were enumerated from PCR products generated by the primer pair hpu.01 and hpu.02 in order to confirm that gonococcal transformants containing the mutagenized fragment of hpuA kept the same number of guanine residues in the poly(G) tract as was present in the parents. Primer hpu.01 was used in sequencing those partial hpuA fragments from mutants.

DNA hybridization. Southern blots were utilized to confirm that allelic exchange occurred as expected. Chromosomal DNAs of FA1090 Hgb, FA1090 Hgb⁺, and hpuA or hpuB insertional mutants of FA1090 Hgb⁺ (FA6982, FA6983, and FA6929) were digested with ClaI and separated on 0.7% agarose gels. Gels were transferred bidirectionally to Magnagraph nylon membranes (Micron Separations). Blots were probed, as described in Results, with random-primed digoxigenin-dUTP-labeled DNA and were developed according to the Genius labeling and detection instructions (Boehringer Mannheim Biochemicals).

Peptide synthesis and immunization. A 20-mer peptide was designed based on the predicted strong antigenicity of the last 17 amino acids of the C terminus of HpuA (CGG-EKKLDDTSQDTNHLTKQ). Another peptide (CGG-ADPAPQSAQTLN) was designed previously based on the N-terminal amino acid sequence of HpuB (8). Peptide synthesis was performed at the University of North Carolina Program in Molecular Biology and Biotechnology MicroProtein Chemistry Facility with a multiple peptide synthesizer (Rainin Symphony). Peptide synthesis and immunization followed the procedures described by Elkins (16) and Chen et al. (8).

Affinity purification of antibodies raised against the N-terminal peptide of HpuB and the C-terminal peptide of HpuA. Postimmune antipeptide sera for HpuB (8) and HpuA were each affinity purified to eliminate reactivity to antigens other than HpuA and HpuB. A modification of a previously published method as reported by Elkins et al. (17) was used for the affinity purification of antipeptide antibodies on immobilized peptide coupled on thiopropyl-agarose columns (Sigma) (42).

Preparations of whole-cell dot blots and outer membranes from gonococci grown under iron-replete and iron-stressed conditions. Gonococci were grown in iron-sufficient and iron-limited media. Gonococcal medium broth containing Kellogg's supplement I was inoculated from overnight plate-grown gonococcal cultures (Hgb on GCB plates and Hgb⁺ on hemoglobin-Desferal plates). After one mass doubling, cultures were split. Desferal was added to a 100 µM concentration to induce iron starvation in one flask, whereas supplement II (ferric nitrate at 12 µM) was added to the other flask. After 4 h of growth with either the chelator or the iron supplement, cells were harvested by centrifugation. The density of harvested cells was adjusted to an optical density of 0.2 at 600 nm (approximately 2 × 10⁸ CFU/ml) with phosphate-buffered saline. Dot blots were prepared from wells loaded with 100 µl of the adjusted cell suspensions. Total membranes and outer membranes were prepared as previously described (16). The protein content was determined by a bicinchoninic acid assay (Pierce).

Purification of hemoglobin-binding proteins from total membranes. Purification of hemoglobin-binding proteins used bovine hemoglobin-agarose (chromatography specialty resin) supplied by Sigma. Purification with solid-phase hemoglobin-agarose followed a procedure described by Elkins (16). Hemoglobin-binding proteins were eluted in Laemmli sample buffer for analytical sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and Western blotting (immunoblotting).

Whole-cell dot blot hemoglobin binding assay. FA1090 Hgb⁺, FA6929, and hpuA insertional mutants of FA1090 Hgb⁺ (FA6982 and FA6983) were examined for their ability to bind hemoglobin in a whole-cell dot blot assay. Human hemoglobin was biotinylated with N-hydroxysuccinimide-SS-Biotin (21331D; Pierce) according to the manufacturer's instructions at a molar ratio of 23:1 at 4°C for 2 h. The unbound biotin was removed by dialysis overnight in phosphate-buffered saline at 4°C. The binding was detected by a colorimetric procedure using alkaline phosphatase-conjugated streptavidin (Pierce) as the secondary reagent.

Western blot analysis of membrane proteins. SDS-PAGE and Western blotting of total membrane proteins, outer membrane proteins, and hemoglobin-binding proteins purified from total membranes were performed as described by Harlow and Lane (20). One nitrocellulose membrane each was prepared for Western blotting of total membrane, outer membrane, and hemoglobin-binding proteins. These membranes were cut into upper and lower panels along a line drawn between 55 and 60 kDa. The upper panels were probed with affinity-purified serum raised against the N-terminal peptide of HpuB (8), and the lower panels were probed with affinity-purified serum raised against the C-terminal peptide of HpuA.

	RESULTS

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Gonococcal hpuA gene. We obtained the sequence of hpuA from both FA1090 Hgb and FA1090 Hgb⁺ by sequencing PCR products of the primer pair hpu.01 and hpu.14 directly. Data containing DNA sequence of FA1090 hpuA have been released incrementally by the N. gonorrhoeae Genome Sequencing Project. The sequence identical to our FA1090 Hgb hpuA sequence was released as part of the February 1997 update. Since the sequence of the FA1090 hpuAB operon is now readily available from the database of the project (the University of Okalahoma's Advanced Center for Genome Technology at http://www.dna1.chem.uoknor.edu) and from GenBank (accession no. AF031495), the hpuA sequence is not listed in detail in this communication.

PCR clones and insertional mutants of hpuA. Curiously, pUNCH258 and pUNCH259, which were plasmids containing cloned hpuA from FA1090 Hgb and FA1090 Hgb⁺, respectively, both contained 9 G's in the poly(G) tract. It seems that reversion had occurred in the E. coli transformation of pUNCH259 and that the selection was skewed to clones containing 9 G's. Insertional mutagenesis of FA1090 Hgb⁺ resulted in hpuB mutant FA6929 (8) and hpuA mutants FA6982 and FA6983. All three mutants contained 10 G's in the poly(G) tract, whereas the hpuA insertional mutant of FA1090 Hgb, FA6981, contained 9 G's. Thus, gonococcal transformation with a fragment of hpuA containing either the  interposon or the aphA-3 cassette did not alter the poly(G) region. Changes in hemoglobin utilization phenotypes of these transformants reflected changes that resulted from insertional inactivation of the hpuA and/or the hpuB alleles.

Southern blot analysis of hpuA insertional mutants. In order to confirm that each mutant had the appropriate insertion, Southern blotting was performed with three separate DNA probes. One was an 850-bp hpuB fragment of the EcoRI digest of the plasmid pSM85k (30). The other two were the DNA fragments of SmaI-cut  interposon (2,082 bp) and SmaI-cut aphA-3 cassette (787 bp). When chromosomal DNA from either FA1090 Hgb or FA1090 Hgb⁺ was digested with ClaI, the hpuB probe hybridized with a DNA fragment of roughly 8 kb. In FA6929, FA6982, or FA6983, the same probe hybridized with fragments of approximately 9 to 10 kb. Due to the large sizes of ClaI-digested fragments, exact sizes of labeled fragments were hard to estimate; nevertheless, sizes of fragments from the mutants were appropriately larger than the size of the fragment from the parent (Fig. 2, upper panel). The  probe hybridized with FA6982 DNA only (Fig. 2A, lower panel), and the aphA-3 probe hybridized with FA6983 DNA only (Fig. 2B, lower panel), at the appropriate size positions as predicted.

View larger version (53K): [in this window] [in a new window]   FIG. 2.   Southern blot analysis of hpuA and hpuB insertional mutants. Chromosomal DNAs from FA1090 parent and mutant strains were digested with ClaI and transferred bidirectionally to prepare two blots per gel. Hgb was the non-hemoglobin-utilizing variant, while Hgb+ was the hemoglobin-utilizing variant and the recipient for insertional mutation. (A) Blots of DNA fragments from FA6982, a polar insertional hpuA mutant, were probed with an hpuB fragment (upper panel) and an  fragment (lower panel). (B) Blots of DNA fragments from FA6929, an hpuB mutant, and FA6983, a nonpolar hpuA mutant, were probed with an hpuB fragment (upper panel) and an aphA-3 fragment (lower panel).

Localization of the HpuA protein. Expression of both HpuA and HpuB was iron regulated. While HpuB could be detected in stained gels of whole-cell lysates, total membrane proteins, outer membrane proteins, or hemoglobin-binding proteins (8), HpuA was not readily visible in the Coomassie-stained gels, the silver-stained (51) gels, or autoradiographs of iodinated membrane protein gels (data not shown). However, Western blotting with affinity-purified antibody raised against the C-terminal peptide of HpuA revealed an iron stress-induced 42-kDa band in whole cells (data not shown) and membrane preparations. This band appeared along with the 89-kDa HpuB in iron-stressed FA1090 Hgb⁺ (Fig. 3A and B, lanes 2) and FA19 Hgb⁺ (data not shown) but was absent in the hpuA insertional mutants FA6982 and FA6983 (Fig. 3A and B, lanes 6 and 8). The HpuA of hemoglobin-utilizing variants could be affinity purified from total membrane proteins with immobilized hemoglobin (Fig. 3C, lane 2).

View larger version (25K): [in this window] [in a new window]   FIG. 3.   Detection of HpuA and HpuB among the total membrane proteins (A), the outer membrane proteins (B), and the hemoglobin-binding proteins (C) prepared from the hpuA and/or hpuB mutants of FA1090 Hgb+ grown under iron-replete (Fe+) or iron-stressed (Fe) conditions. FA6929 is an hpuB insertional mutant, and FA6982 and FA6983 are polar and nonpolar hpuA insertional mutants, respectively. Western blots of total membrane proteins, outer membrane proteins, and hemoglobin-binding affinity-purified proteins were cut into two panels each, one probed with affinity-purified anti-HpuB serum (upper panels) and the other probed with affinity-purified anti-HpuA serum (lower panels).

Expression of HpuA and HpuB in mutants. Since we were unable to identify any consensus promoter sequence for hpuB, it was expected that insertional mutation of the upstream hpuA with the  interposon would prevent expression of both HpuA and HpuB. On the other hand, since the aphA-3 gene is preceded by translation stop codons in all three reading frames and is followed by a consensus ribosome binding site and a start codon (35), it was expected that successful insertion of the aphA-3 cassette in hpuA would prevent expression of HpuA but not of HpuB.

Hemoglobin binding and utilization of hpuA insertional mutants. Iron-stressed, hemoglobin-utilizing FA1090 Hgb⁺ bound biotinylated human hemoglobin in a whole-cell dot blot assay (Fig. 4). The binding was inhibited by excess unlabeled hemoglobin but not by excess hemin at a molar ratio of 100:1 (data not shown). The hpuB insertional mutant, FA6929, and the polar and nonpolar hpuA insertional mutants, FA6982 and FA6983, all demonstrated impaired binding of biotinylated hemoglobin (Fig. 4). None of the hpuA or hpuB mutants of FA1090 Hgb⁺ (FA6929 [HpuA⁺ HpuB], FA6982 [HpuA HpuB], or FA6983 [HpuA HpuB⁺]) was able to grow on modified GCB plates using human hemoglobin as the sole iron source (Fig. 5). Nevertheless, all three mutants and both FA1090 Hgb and FA1090 Hgb⁺ grew well on modified GCB plates containing hemin (data not shown).

View larger version (16K): [in this window] [in a new window]   FIG. 4.   Dot blot assay showing binding of biotinylated human hemoglobin to iron-replete (Fe+) and iron-stressed (Fe) whole cells. FA1090 Hgb+ is the parent strain. FA6929 is an hpuB insertional mutant, and FA6982 and FA6983 are polar and nonpolar hpuA insertional mutants, respectively.

View larger version (75K): [in this window] [in a new window]   FIG. 5.   Growth phenotypes on GCB plate (A) and hemoglobin-Desferal plate (B). FA1090 Hgb is the non-hemoglobin-utilizing variant, and FA1090 Hgb+ is the hemoglobin-utilizing variant. FA6929 is an hpuB insertional mutant, and FA6982 and FA6983 are polar and nonpolar hpuA insertional mutants of FA1090 Hgb+, respectively.

	DISCUSSION

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In order to examine the mechanism underlying the phase variation of hemoglobin utilization by N. gonorrhoeae, we studied the expression and function of a 42-kDa outer membrane protein, HpuA, identified in the hemoglobin-utilizing variants of both FA19 and FA1090 grown under iron-stressed conditions. While hpuA was located immediately upstream from hpuB, the gene encoding the previously reported 89-kDa hemoglobin-binding outer membrane protein (8), we were unable to identify any consensus promoter sequence that might direct the transcription of hpuB within the short DNA fragment between the stop codon of hpuA and the start codon of hpuB. Polar insertional mutation of hpuA prevented production of both HpuA and HpuB. Thus, it is most likely that, in N. gonorrhoeae, hpuA and hpuB are comprised in a two-component operon similar to that in N. meningitidis (31).

Variation in the expression of gonococcal HpuA and HpuB was associated with variation in the length of a run of G residues at the 5' end of hpuA, located within the sequence encoding the N-terminal amino acids for mature protein. The hemoglobin-utilizing variants contained 10 G's, whereas the non-hemoglobin-utilizing variants contained 9 G's (Fig. 1). When hpuA had only 9 G's, a stop codon occurred immediately at the end of the poly(G) tract. In Hgb⁺ variants, the 10-G poly(G) tract enabled a change of the translational reading frame and thus the expression of HpuA and HpuB. This apparently explains the high frequency (1 × 10⁴ to 2 × 10³) of spontaneous Hgb-to-Hgb⁺ variation observed in all tested gonococcal strains (8). Other gonococcal phase-varying systems include Pil (19, 36), PilC (25), Opa (33, 48), and lipooligosaccharide (2). The mechanism for phase variation of HpuA and HpuB is similar to that for Opa, PilC, and lipooligosaccharide in that each apparently uses slipped-strand mispairing to alter the length of a short DNA repeat, which affects translational frame and therefore expression (13, 18, 25, 39, 40).

Although we have been unable to develop a protocol to detect the on-phase-to-off-phase switch of hemoglobin utilization, it is likely that the postulated on-to-off switch also occurs at a relatively high frequency. It is unclear what advantage might be gained by phase variation and iron repression of hemoglobin-binding protein expression. We speculate, however, that phase variation of a hemoglobin-binding protein in gonococci would enable efficient utilization of menstrual hemoglobin. Recently, two genes encoding hemoglobin-binding proteins of Haemophilus influenzae (HgpA and HgpB) have been cloned (23, 24, 45). Regions of CCAA nucleotide-repeating units immediately following the putative leader cleavage site were identified in both hgpA and hgpB. It has been postulated that alteration of the reading frame across the CCAA region of hgpA or hgpB by strand slippage would lead to production of either protein (23). Thus, the heme-regulated expression of H. influenzae hemoglobin-binding proteins might very well be another example of phase variation of hemoglobin-binding proteins.

The gonococcal hpuA gene encodes a consensus signal peptidase II cleavage site (21), suggesting that HpuA is lipid modified. The difference between the observed molecular mass (42 kDa) and the calculated molecular mass (36 kDa) is consistent with lipid modification of HpuA. The nonintegral membrane protein characteristics of HpuA were demonstrated in membrane preparations of the HpuA⁺ HpuB mutant FA6929. In the absence of the integral outer membrane protein HpuB, HpuA could not be detected among Sarkosyl-resistant outer membrane proteins (Fig. 3B) or total membrane proteins subjected to hemoglobin-agarose purification (Fig. 3C). On the other hand, the absence of HpuA had no obvious effect on the hemoglobin binding ability of HpuB (Fig. 3C). It is possible that the apparently decreased binding of FA6983 cells to biotinylated hemoglobin (Fig. 4) was due to decreased production of HpuB instead of impaired hemoglobin binding by HpuB (Fig. 3C).

We could not detect hemoglobin binding by HpuA alone in cell-free systems, but HpuA must play a critical role in the utilization of hemoglobin for growth. FA6983, the mutant which expressed HpuB but not HpuA, bound hemoglobin in affinity purification (Fig. 3C) but was unable to grow on media where hemoglobin was the sole source of iron (Fig. 5). Thus, HpuA and HpuB, while showing differences in their abilities to bind hemoglobin, were both required for hemoglobin utilization by gonococci.

Lee (26) reported isolation of two hemin-binding proteins (HmBPs) by affinity purification from gonococci grown under iron-limited conditions. These two HmBPs have observed molecular masses of 44 and 97 kDa, very close to the 42 and 89 kDa of HpuA and HpuB. HmBPs bound to hemin-agarose, and the binding was competitively inhibited by hemoglobin. Growth on hemoglobin was inhibited by a monoclonal antibody directed against the 97-kDa HmBP (26, 29). These results suggest that HmBPs might be identical to HpuA and HpuB. However, our results showed that neither HpuA nor HpuB was required for growth on hemin plates, and in whole-cell dot blot assays, hemoglobin binding by FA1090 Hgb⁺ was not affected by excess hemin. These are not the results that would be expected if HpuA and HpuB were identical to the HmBPs. In the current absence of sequence data for the HmBPs, and of specific mutants of the HmBPs, we cannot be certain that HpuA and HpuB are different from the HmBPs.

Gonococci possess multiple specific systems to acquire iron from different sources: transferrin and lactoferrin (4, 5, 11, 34), aerobactin (54), enterobactin (46), hemoglobin (38), and, undoubtedly, heme (14, 15, 27). This presumably reflects the differences in available iron at different body sites and under different physiological conditions (53). Acquisition of iron from transferrin, lactoferrin, and hemoglobin may involve a bipartite receptor system. The operon, tbpBA, encoding the outer membrane lipoprotein, TbpB, and the TonB-dependent outer membrane transferrin receptor, TbpA, has been well studied (1, 10, 11). It is also known that there is a gene for a lipoprotein homologous to tbpB in meningococci immediately upstream of lbpA, which encodes the TonB-dependent lactoferrin receptor LbpA (6, 7, 32, 43). Recently, a similar lipoprotein gene has been found in N. gonorrhoeae, immediately upstream of lbpA (3).

The HpuA-HpuB receptor system for utilization of hemoglobin in N. gonorrhoeae is similar in several respects to that of TbpB-TbpA. Gonococcal TbpB, a lipid-modified protein, binds to transferrin in affinity purification but cannot be affinity purified from a TbpA mutant in the presence of the detergent Sarkosyl (9). HpuA, the lipoprotein analogous to TbpB, was not Sarkosyl resistant and could be affinity purified only in the presence of HpuB, the integral outer membrane protein analogous to TbpA. This could reflect a physical association between HpuA and HpuB, such as has been proposed for TbpB and TbpA (12). In N. gonorrhoeae, a TbpB mutant shows reduced binding of transferrin but exhibits growth on transferrin plates; a TbpA mutant binds less transferrin and does not grow on transferrin plates (1). In these respects, the gonococcal TbpB-TbpA system does not correspond to what we have described for HpuA and HpuB; however, in N. meningitidis, both TbpB and TbpA mutants are unable to grow on transferrin-bound iron (22), analogous to the results for the gonococcal HpuA-HpuB system.

The importance of both HpuA and HpuB in gonococcal hemoglobin utilization has been demonstrated, but many questions remain to be answered concerning the exact function and location of HpuA and HpuB. A better understanding of how they interact to facilitate iron uptake from hemoglobin will be the aim of future work.