ABSTRACT
Pathogenic members of the family Neisseriaceae produce specific receptors to acquire iron from their host’s lactoferrin and transferrin. Recently, putative Moraxella catarrhalislactoferrin receptor genes and a third open reading frame (lbpB, lbpA, and orf3) were cloned and sequenced. We describe the preliminary characterization of isogenic mutants deficient in LbpB, LbpA, or Orf3 protein.
The concentration of free iron in the mammalian host is below levels which permit proliferation of invading microbes. To acquire this essential element, the strict human pathogens Moraxella (Branhamella)catarrhalis, Moraxella lacunata, Neisseria meningitidis, and Neisseria gonorrhoeae and the strict bovine pathogen Moraxella bovis produce host-specific transferrin (Tf) and lactoferrin (Lf) receptors to circumvent the host’s iron sequestration (see reference 15 for a review).
This receptor-mediated mechanism has at least two outer membrane components, designated (Tf binding protein [Tbp] or Lf binding protein [Lbp]) A and B, to facilitate iron capture from host Tf or Lf. The essential TonB-dependent A component spans the outer membrane and contains amphipathic beta sheets that are proposed to ultimately form the channel across the outer membrane (19). The predominately hydrophilic B constituent is attached to the outer membrane via a lipid tail. Naturally occurring B− mutants have not been reported, and genetically engineered B−mutants are either impaired (2, 6, 14) or are unable (16) to utilize the parent iron source in vitro, implying that B provides a selective advantage in vivo. A significant humoral immune response to B occurs during a natural infection, (8, 9), and antibodies to the B component are bactericidal, (10, 11, 18), suggesting B may be a useful vaccine target.
A unique feature of the iron acquisition process in M. catarrhalis is that inactivation of the gene encoding the CopB outer membrane protein abrogates iron acquisition from both human Tf (hTf) and human lactoferrin (hLf) (1, 8). This phenotype is similar to that of insertional mutants in the periplasmic iron binding protein (17) or TonB protein (5) inNeisseria species and infers a role for CopB in the iron acquisition process. Although CopB displays some binding activity toward hLf (7, 8), it may not be related to the iron acquisition process. Insertional inactivation of the CopB homolog, FrpB, in pathogenic Neisseria spp. does not alter iron acquisition from Tf and Lf (4, 20), and there does not appear to be a CopB homolog in other species with a Tf receptor-mediated iron acquisition pathway, such as Haemophilus influenzae (13). This suggests either that the iron acquisition pathway in M. catarrhalis is unique or that the phenotype of the copB mutants is due to indirect effects on the iron acquisition pathway.
The genes encoding the Tf and Lf receptor proteins are normally found in an operon consisting of the gene encoding the B component immediately preceding the A structural gene (6, 15). The arrangement of the receptor genes differs in M. catarrhalis. The tbpA gene precedes the tbpB gene and is separated by an intervening open reading frame (ORF) (18). Although the order of the Lf receptor genes conforms to the standard arrangement, there is a third unique ORF immediately downstream oflbpA with putative independent promoters preceding thelbpA and orf3 genes (11).
To examine the role of the M. catarrhalis LbpB, LbpA, and Orf3 proteins in iron acquisition from Lf and whether the genes coding for these proteins are in an operon, we created defined mutants in which the native coding sequences had been replaced with insertionally inactivated derivatives. The individual lbpB,lbpA, and orf3 genes were PCR amplified (see Table 1 for primers) from M. catarrhalis and subcloned into pT7-7 (22). The ORFs were interrupted with the kan cassette from pUC4K (Fig.1), and the linearized plasmid DNA was used for natural transformation of M. catarrhalis N141 (8), selecting for Kanr isolates. ThelbpB gene was also inactivated by insertion of akanΩ cassette from pHP45 (12) and then replacement of the pHP45 Kanr marker with thekan cassette from pUC4K, since the original kanmarker does not appear to be functional in M. catarrhalis. Southern hybridization and PCR analysis were performed to confirm gene replacement with the insertionally inactivated derivatives (data not shown).
Oligonucleotide primers used for PCR
Construction of M. catarrhalis N141 isogenic mutants. A kanamycin resistance marker (kan) derived from pUC4K with either flanking EcoRI sites, NcoI sites, or HincII sites was ligated into either the uniqueEcoRI site of the lbpB gene, between theNcoI sites of the lbpA gene (intervening DNA removed), or the unique SspI site of the Lfr orf3gene, respectively. The DNA was linearized with restriction sites that flanked the DNA inserts and then used for natural transformation intoM. catarrhalis N141, and mutants were selected on BHI medium containing 20 μg of kanamycin sulfate per ml.
In order to demonstrate that the insertional inactivation resulted in loss of the appropriate protein, we performed Western blot analysis with the isogenic mutants. Equal wet volumes of pelleted cells (avoids optical density estimation errors due to clumping) grown under iron-limiting conditions were boiled in Laemmli sample buffer, separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), and electroblotted in triplicate. We had previously generated a rabbit polyclonal antiserum against Lbp isolated fromM. catarrhalis (8); this serum was preabsorbed with LbpB-maltose binding protein (Mbp) (see below) and used to develop one blot (Fig. 2A). Compared to the parental strain (Fig. 2A, lane 1), LbpA production was not altered in the orf3::kan mutant (Fig. 2A, lane 5) or thecopB::kan mutant (Fig. 2A, lane 6). In contrast, LbpA production was abolished in both thelbpA::kan (lane 4) andlbpB::kanΩ (lane 3) mutants, and was diminished following insertion of the kan cassette into thelbpB gene (lane 2), suggestive of an operonic organization.
Western blot analysis of M. catarrhalismutants. Equal amounts of M. catarrhalis cells grown under iron-limiting conditions were resuspended and boiled in Laemmli sample buffer prior to SDS-PAGE and Western blotting. The remaining binding sites on the blots were blocked with Tris-buffered saline (pH 7.5) containing 0.5% Bio-Rad nonfat dry milk blocker and incubated with rabbit polyclonal antisera (A) predominantly specific for LbpA (B), Mbp::LbpB, or (C) TbpA and TbpB. The blots were washed in Tris-buffered saline and then incubated with HRP-labeled antirabbit sera and developed.
A duplicate blot was probed with antiserum prepared against purified recombinant LbpB-Mbp fusion protein for detection of LbpB production (Fig. 2B). Compared to the parental strain (Fig. 2B, lane 1), insertional inactivation of the lbpB gene (Fig. 2B, lanes 2 and 3) resulted in the loss of LbpB, whereas LbpB expression was unaffected in the lbpA::kan,orf3::kan, and copB::kanmutants (Fig. 2B, lanes 4, 5, and 6, respectively). We were unable to produce a fusion protein of Orf3 with Mbp, and thus could not prepare antiserum for assessment of Orf3 production. As a control, we probed a replicate blot with antiserum prepared against native Tf receptor complex (Fig. 2C) (7). Neither TbpA expression (solid box) nor TbpB expression (solid circle) was altered by any of thekan insertions.
In order to provide alternate evidence for the operonic arrangement oflbpB and lbpA and to determine whetherorf3 was part of the lbp operon, we initiated reverse transcription-PCR (RT-PCR) experiments. The RT-PCR experiments were performed with SuperScript II RNase H− reverse transcriptase (Gibco BRL) according to the manufacturer’s instructions. Total RNA was isolated with the Qiagen RNeasy mini kit (Qiagen, Inc.) and subjected to amplification-grade DNase I (Gibco BRL) treatment in the presence of RNasin (Promega Corporation). cDNA was generated by using oligonucleotide 728 (Fig. 1) and treated with RNase H (Gibco BRL), prior to being used as a template for subsequent PCR. RT-PCR products were obtained from intergenic regions betweenlbpB::lbpA andlbpA::orf3 (see Fig. 4, lanes 2 and 4, respectively). The same reactions did not yield the corresponding bands when RNA from the lbpB::kanΩ strain was used (data not shown). As a control to exclude the possibility of chromosomal contamination, oligonucleotides specific for the M. catarrhalis tbpA gene were used. The tbpA gene was amplified only from the chromosomal preparation (Fig. 4, lane 5), but not the cDNA preparations (lane 6).
A solid-phase binding assay under low-stringency buffer conditions, which enhance detection of Lf-Lbp interactions (6, 8), was performed to evaluate the ligand-binding properties of the isogenic mutant strains. In comparison to the parental strain, thelbpB::kan and lbpA::kanmutants displayed only weak Lf binding activity (Fig.3). Residual Lf binding activity was detected with the lbpB::kanΩ mutant, possibly due to nonspecific interactions between the cationic portion of Lf (3) with other components present, perhaps CopB (8). In contrast, the Lf binding activity of theorf3::kan and copB::kanmutants was comparable to that of the parental strain. All isolates displayed similar binding activity for horseradish (HRP) peroxidase-conjugated hTf (data not shown).
Analysis of binding of various mutants to HRP-hLf conjugates. Equal amounts of resuspended M. catarrhaliscells grown under iron-limiting conditions were spotted onto the cellulose acetate-nitrocellulose membranes. The blot was placed in blocking solution and then incubated in low-stringency Lf binding buffer (50 mM Tris buffer containing 0.1 M NaCl [pH 6.0]), containing 1:1,000 dilutions of peroxidase-conjugated hLf (HRP-hLf). The blots were repeatedly washed in Tris-buffered saline and then developed with the HRP-substrate mixture.
The defined mutants were then examined for their ability to utilize various iron sources by using a previously described plate growth assay (7). Iron-starved organisms were spread onto brain heart infusion (BHI) medium (Difco, Detroit, Mich.) containing the iron chelator etheylenediaminedi( o -hydroxyphenylacetic) acid (EDDHA [100 μM]) and sterile disks containing the individual iron sources were placed onto the medium to allow localized diffusion. The bovine pathogen M. bovis, which utilizes only bovine Lf and Tf, and an M. catarrhalis N141 copB mutant, which binds hLf and hTf normally, but cannot utilize these iron sources (1, 8), served as controls. Growth of M. boviswas observed only when bovine Lf or Tf, and not hLf or hTf, was provided as the iron source (Table 2). With the exception of the copB mutant, which was unable to utilize either the human or bovine form of Lf or Tf (1, 8), growth on hTf by the various mutants was indistinguishable from that of the parent. When we tested the M. catarrhalis lbpA::kan mutant, no growth surrounding the hLf-impregnated disk was observed (Table 2), affirming that LbpA is essential for utilization of iron bound to Lf. Similarly, no detectable growth was observed by the lbpB::kanΩ mutant when hLf was supplied as the sole iron source, consistent with the lack of LbpA produced in this strain. A small zone of growth surrounding the Lf-impregnated disk (approximately 0.5 mm in diameter) was observed with the lbpB::kan mutant (LbpB−), suggesting this mutant retains the capacity to utilize Lf, provided the iron source was present in a sufficiently high concentration. In contrast, the zones of growth surrounding the Lf-impregnated disks for the M. catarrhalis parental strain andorf3::kan mutant appeared as dispersed areas of growth (approximately 4 to 6 mm in diameter), presumably indicative of the ability to use Lf at lower concentrations.
Growth characteristics of M. catarrhalis mutants
The lbpB, lbpA, and orf3 genes were PCR amplified and subcloned into the pT7-7 expression vector, and expression of the recombinant proteins was induced by the addition of the CE6 bacteriophage encoding the T7 RNA polymerase (21). Substantial expression of recombinant LbpA and LbpB was observed, but there was no detectable expression of Orf3. Due to difficulties encountered in reproducibly demonstrating hLf binding activity in bacterial extracts containing the recombinant Lbps, we prepared fusions with Mbp (see Table 1) so that the recombinant proteins could be obtained in purified preparations by amylose affinity chromatography. The purified LbpB-Mbp fusion protein readily demonstrated Lf binding properties in solid-phase binding assays (6) and after SDS-PAGE (without boiling samples) and Western blotting. In contrast, no binding activity was detectable with the LbpA-Mbp fusion protein. These findings are consistent with data obtained from meningococcal andM. catarrhalis Lbps (6, 8, 11).
In this article, we have demonstrated that lbpB,lbpA, and orf3 have an operonic organization inM. catarrhalis. RT-PCR reveals that all three genes compose a polycistronic message (Fig. 4), and insertional inactivation of lbpB with a kanΩcassette eliminated LbpA expression (Fig. 2 and 3). Althoughorf3 belongs to the same operon as lbpB andlbpA, insertional inactivation of this gene did not alter LbpA or LbpB production (Fig. 2), hLf binding activity (Fig. 3), or acquisition of iron from hLf or hTf (Table 2). Thus, the function of Orf3 remains unknown. The rather novel organization of thetbp genes in M. catarrhalis, with thetbpA gene preceding an intervening ORF which in turn precedes tbpB (18), is certainly unlike the operonic organization in other species and warrants further study.
RT-PCR analysis of the lbp operon. M. catarrhalis N141 was grown under iron-limiting conditions were used in the Qiagen RNeasy mini kit for total RNA isolation. Purified RNA was subjected to amplification-grade DNase I (Gibco BRL) in the presence of RNasin (Promega Corporation). RT was performed with SuperScript II RNase H− reverse transcriptase (Gibco BRL) by using oligonucleotide 728. The resulting cDNA was subjected to RNase H (Gibco BRL) prior to use in subsequent PCR analysis. The negative image of the agarose gel is illustrated with the molecular sizes indicated in kilobases on the left. Lanes 1, 3, and 5, PCR with chromosomal DNA. Lanes 2, 4, and 6, PCR with reverse-transcribed cDNA. Lanes 1 and 2, PCR with oligonucleotides 717 and 727. Lanes 3 and 4, PCR with oligonucleotides 738 and 732. Lanes 5 and 6, PCR with oligonucleotides 224 and 424, which amplify M. catarrhalis tbpA.
Insertional inactivation of the lbpA gene in M. catarrhalis (Fig. 1 and 2) clearly demonstrated that LbpA is essential for iron acquisition from hLf (Table 2), consistent with the proposal that it serves as the transmembrane channel for transport of iron across the outer membrane (6, 11). The marked impairment of iron acquisition from hLf in vitro by the isogenic mutant deficient in LbpB (Table 2) suggests that, similar to TbpB (15), it plays an important facilitory role in the iron acquisition process. Since LbpB is present in all clinical isolates examined to date (8), it may be essential in vivo and may serve as a potential vaccine candidate. The pathway for iron acquisition from hLf in Neisseria requires the involvement of TonB (5) for energization and a periplasmic iron binding protein (17) to mediate transport to the cytoplasmic membrane. The pathway in M. catarrhalis likely also involves these components, although there is currently no direct evidence to support this proposal. The current model for the iron acquisition pathway (15) cannot account for the loss of iron acquisition from Lf and Tf in strains devoid of CopB. This suggests that either the pathway model needs to be modified to incorporate an essential role for CopB or that the loss of function is indirect, perhaps by truncated CopB interfering with one of the other pathway components. Further studies are clearly needed to resolve this issue.
ACKNOWLEDGMENTS
We acknowledge the technical assistance of Ronghua Yu in preparing the LbpB-Mbp fusion protein.
This work was supported by Medical Research Council of Canada grant no. MT10350.
Notes
Editor: P. E. Orndorff
FOOTNOTES
- Received 14 July 1998.
- Returned for modification 11 September 1998.
- Accepted 18 December 1998.
- Copyright © 1999 American Society for Microbiology
