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Guanghui Wu,2, Nicola J. Gilberthorpe,2 Robert K. Poole,2 and Simon F. Park1*
School of Biomedical and Molecular Sciences, University of Surrey, Guildford GU2 7XH,1 Department of Molecular Biology and Biotechnology, University of Sheffield, Sheffield S10 2TN, United Kingdom2
Received 9 March 2004/ Accepted 17 May 2004
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ABSTRACT |
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INTRODUCTION |
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NO and its reaction products, peroxynitrite in particular, have strong bactericidal activities and during infection campylobacters are likely to encounter these agents from a variety of sources. Invasion of the epithelial mucosa is considered to play an important role during Campylobacter infection (14, 33), and NO and/or its redox products form a key component of the inducible defense of intestinal cells against microbial infection (52). As a result of this antimicrobial mechanism, NO synthesis is markedly increased in patients with infective gastroenteritis (15) and, accordingly, during infection campylobacters are likely to be exposed to significant amounts of NO in the gut. Campylobacters may be exposed to NO in the stomach since the chemical generation of NO in this organ can occur as a consequence of microbial nitrite production in the mouth (10, 29). It has even been suggested that generation of NO in the stomach represents a separate and yet powerful defense against gut pathogens (10, 11). Consequently, although nothing is known of the interaction of campylobacters with NO, resistance to this agent and it redox products are likely to be critical during colonization and infection.
The most fully understood mechanisms for detoxification of NO involve the inducible bacterial flavohemoglobin (Hmp) of Escherichia coli (44) and flavorubredoxin (19). In the presence of oxygen, Hmp detoxifies NO by acting as an NO dioxygenase (20, 23, 54, 55) and affords protection of respiration (47). Under anaerobic conditions, in the absence of Hmp activity, the flavorubredoxin serves as an oxygen-independent NO reductase (19). Hmp may also function to repair NO-damaged lipid membranes, since the purified protein has recently been shown to possess both alkyl hydroperoxide reductase activity and lipid-binding properties (3, 4). However, whether these activities are physiologically relevant has not yet been confirmed by in vivo studies.
The N-terminal domain of Hmp is homologous to the globin family (reviewed in references 43, 54, and 55), having a single protoheme and highly conserved heme pocket, whereas the C-terminal domain has binding sites for FAD and NAD(P)H. Many other microorganisms possess proteins having clear homology to Hmp. These bacterial hemoglobins may be classified into three broad groups (54, 55): the small single-domain globins such as Vgb (49), the flavohemoglobins exemplified by Hmp, and the truncated globins that are 20 to 40 amino acids shorter than vertebrate hemoglobins (40, 51). The functions of the single-domain globins are not clear. Vgb, the archetypal single-domain globin from Vitreoscilla stercoraria has been implicated in oxygen storage, delivery, or reduction based upon its induced expression at low-oxygen tensions (9), the absence of an induced response to nitrosative stress (17), the ability to enhance microaerobic growth when expressed in E. coli (2), and its binding to cytochrome bo' (36). However, Vgb may also have an alternative functional role since a recombinant chimeric version of this globin, which carries a flavoreductase domain, can alleviate nitrosative stress in E. coli (27). We provide here the first conclusive evidence for a single-domain globin that performs an NO scavenging and detoxification function in the organism from which it originated, namely, Campylobacter. We also demonstrate that the globin is uniquely and specifically induced by nitrosative stress and not by oxygen limitation, or superoxide stress as is the case for other globins.
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MATERIALS AND METHODS |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
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was obtained from Life Technologies. Campylobacters were grown at 37 or 42°C when indicated in Mueller-Hinton (MH) broth (Oxoid)or on MH agar containing kanamycin (50 µg ml–1), tetracycline (10 µg ml–1), or chloramphenicol (10 µg ml–1) when necessary. Microaerophilic conditions were generated by using the CampyGen (Oxoid) gas generating kit or a MACS-VA500 microaerophilic work station (10% O2, 10% CO2, and 80% N2) from Don Whitley Scientific, Ltd. For cloning experiments, E. coli DH5 was grown at 37°C in Luria-Bertani (LB) broth or agar containing ampicillin (100 µg ml–1), kanamycin (50 µg ml–1), or tetracycline (10 µg ml–1) as required.
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The cgb gene was mutated by using the inverse PCR protocol described by Wren et al. (53), which deleted 2 bp of the open reading frame and introduced a unique BglII restriction site. Oligonucleotide primers HMP7 (5'-gcaacaAGATCTAAGCTTTTGGTTGTTCTCCTGAAATT-3') and HMP8 (5'-gcaacaAGATCTGCAATGGCGATTTTAATGGCGGCT-3') containing unique restriction sites for BglII (underlined) and clamp sequences and not complementary to C. jejuni DNA (lowercase) were used. The PCR fragment, generated by using a two-stage cycling program (12), was digested with BglII and self-ligated. The resulting plasmid was digested with BglII, and a kanamycin resistance (Kanr) cassette with BamHI ends from pJMK30 (J. Ketley, University of Leicester) was inserted. This step generated the suicide plasmid pKE18, which was introduced into C. jejuni NCTC 11168 by electroporation (12) and into C. coli UA585 by natural transformation (50).
The gene encoding AhpC (Cj0334) was disrupted by insertional mutagenesis with a chloramphenicol gene by using plasmid pAV103 as described previously (1). The insertion was confirmed by PCR, and the single ahpC and double cgb ahpC mutants were designated CJA01 and CJAC01, respectively.
Sequencing of the C. coli UA585 cgb gene. The cgb gene from C. coli UA585 was amplified by PCR with primers HMP1 and HMP3 (5'-GGATCCTGTTGATGATACGCTTATAGATGA-3') and cloned into the pCR2.1-TOPO TA cloning vector (Invitrogen). Nucleotide sequence analysis was carried out by the dideoxy chain termination method by using a CEQ dye terminator cycle sequencing quick start kit on a CEQ 2000 sequencer (Beckman Coulter).
Reverse transcriptase PCR. RNA was extracted from NCTC 11168 and CJCGB01 by using Qiagen RNeasy and RNAprotect as described by the manufacturer. Briefly, for each extraction, 2 ml of culture was transferred into 4 ml of RNA protect reagent, followed by incubation at room temperature for 5 min. The samples were next centrifuged at 6,000 x g for 10 min, the supernatant was discarded, and the cells were lysed after the addition of 100 µl of Tris-EDTA buffer containing 1 mg of lysozyme (Sigma) ml–1. The RNA was purified by using the RNeasy kit (Qiagen). To remove contaminating DNA, 1 µg of total RNA was treated with DNA-free kit (Ambion) according to the manufacturer's instructions.
First-strand cDNA synthesis was performed with 100 ng of total RNA with random hexamers (250 ng; Invitrogen) and Superscript III RT (Invitrogen). PCR amplification consisted of 35 cycles of 45 s of denaturation at 94°C, 30 s of annealing at 55°C, and 1 min of extension at 72°C. The oligonucleotides used to amplify Cj1585c were the forward primer RED6 (5'-TACCGTTGAACCTGCCTTTC-3') and the reverse primer RED5 (5'-CGGAATGTGCTGTGGAACTA-3'), and for Cj1587c we used the forward primer ABC1 (5'-ATCTGCAACACTTGCCCATT-3') and the reverse primer ABC2 (5'-AATGCAAAGGCGCGTAGTA-3'). The PCR products were analyzed by gel electrophoresis on 0.8% agarose.
Oxidative and nitrosative stress tolerance assays. S-Nitrosoglutathione (GSNO) was obtained from Sigma or synthesized according to the method of Hart (22) and kindly donated by M. N. Hughes. Concentrations of GSNO in stock solutions were determined from absorbance at 334 nm by using a molar absorption coefficient of 900 M–1 cm–1 (35). Cumene hydroperoxide, methyl viologen, and sodium nitroprusside (SNP) were also obtained from Sigma. The NO-releasing agent spermine NONOate (Calbiochem) was also used.
The sensitivity of strains to a range of oxidative and nitrosative stress-inducing factors was initially assayed in a plate diffusion assay using the method described by Baillon et al. (1). For viability assays, C. jejuni strains were grown microaerobically overnight at 37°C to form a lawn on MH agar. The lawns were harvested in MH broth and adjusted to an optical density at 600 nm (OD600) of 0.35. A total of 100 µl of the cell suspension was inoculated into 50 ml of MH broth, and 180 µl of this diluted cell suspension was dispensed into 96-well microtiter plates. The plates were incubated microaerobically and shaken horizontally (175 rpm) at 37°C for 1 h. After 1 h, 20 µl of GSNO or SNP solutions were added to the wells in duplicate to give final concentrations of 0.2, 0.4, 0.8, 1.6, and 2 mM. Spermine NONOate was also used but at lower concentrations. In addition, 20-µl aliquots of MH broth were added to other wells as controls. Viable counts were carried out after a further 1 h of incubation under the conditions described above. All assays were repeated three times.
Growth of C. jejuni in the presence of GSNO. Wild-type NCTC 11186 and the cgb mutant CJCGB01 were grown in MH liquid medium with vancomycin (10 µg ml–1) in the microaerophilic work station at 40°C overnight before they were inoculated at 1% to 10 ml of MH broth (without vancomycin) in 50-ml flasks containing different concentrations of GSNO. The cultures were shaken (100 rpm), and growth was monitored by measuring the ODs of samples at various time points.
Measuring gene expression by using cgb-astA and sodB-astA reporter gene fusions. The promoter regions of cgb and sodB (45) were amplified from C. coli UA585 by using PCR and oligonucleotide primer pairs CGB3 (5'-GGTACCCACTACAAGTACTCCATCACAAGA-3')-CGB4 (5'-CCCGGGCTGCCATTAAAATTGCCATAGCTAAGG-3') and SOD3 (5'-GGTACCGCTACAATATTTTGTCAAACTACT-3')-SOD4 (5'-CCCGGGATCTTCAGTGATAGGTGTAGCTGC-3'). The restriction sites for KpnI and SmaI, incorporated into the primers to facilitate subcloning, are indicated by underlining. PCR, under conditions described previously (12), was used to generate 627- and 521-bp fragments derived from cgb and sodB, respectively, that were cloned into pCR2.1. Inserts were isolated as SmaI and KpnI fragments and cloned into the integrational Campylobacter vector pSP105 (8) that had been digested with the same restriction enzymes. This generated the vectors pKE54 and pKE55 containing the promoter regions of the cgb and sodB genes, respectively. A promoterless arylsulfatase gene (56) including the Shine-Dalgarno sequence was amplified from genomic DNA derived from C. jejuni NCTC 11828 by using PCR and the oligonucleotide primers AST1 (5'-CCCGGGTTAAAGGATTGATCATGAGACTTAG-3') and AST2 (5'-CTGCAGAGAAAATGCTTCTATTACACTATT-3') with restriction sites for SmaI and PstI (underlined). The PCR cycling conditions used are described previously (12). The 2,094-bp DNA fragment generated in this manner was cloned into pCR2.1 and then excised by using SmaI and PstI. This was then ligated into the site created by digestion of the vectors pKE54 and 55 with SmaI and then PstI to generate the integrational vectors pKE56 (cgb-astA transcriptional fusion) and pKE58 (sodB-astA). These were transformed into the naturally competent strain C. coli UA585 as described previously (50). Transformants were recovered after incubation under microaerophilic conditions at 37°C on MH agar plates containing tetracycline (10 µg ml–1).
Overnight cultures of the C. coli strains containing astA transcriptional fusions were grown microaerobically at 37°C in 10 ml of MH broth or 10 ml of MH broth containing tetracycline (10 µg ml–1), respectively. These cultures were adjusted to OD600 of 0.3, and each strain was inoculated (100 µl) into flasks containing 100 ml of MH broth and incubated microaerobically at 37°C for 16 h with shaking (125 rpm). Samples were taken to record viable counts, the OD, and arylsulfatase activity (see below), after which GSNO was added to flasks to give final concentrations of 0.05, 0.1, and 0.25 mM. Arylsulfatase activity was also measured after addition of 0.005, 0.01, and 0.05 mM SNP and 1, 5, and 10 µM methyl viologen. Samples were taken at regular intervals.
Arylsulfatase enzyme assay. Arylsulfatase activity in whole cells was measured by a modification of the methods described by Henderson and Milazzo (24) and by Delisle and Milazzo (7). Routinely, 10 ml of culture was centrifuged at 3,500 rpm for 15 min, and cells resuspended in 1 ml of 0.1 M Tris-HCl buffer (pH 7.0) and kept on ice for 10 min. One milliliter of 20 mM p-nitrophenyl sulfate (Sigma) in 0.1 M Tris-HCl (pH 7.0) was added to the cells, followed by incubation at 37°C for 1 h. The reaction was terminated by centrifugation at 13,000 rpm for 5 min. The amount of liberated free p-nitrophenol was determined spectrophotometrically at 410 nm from 1 ml of the supernatant by using a Helios Alpha spectrophotometer (Unicam) with a 1-cm path length. The results are expressed as a ratio of micrograms of p-nitrophenol (determined by applying the Beer Lambert Law) to OD600/hour.
Purification of Cgb, preparation of antibodies, and immunoblotting.
The purification of the Cgb protein will be described in detail elsewhere. In brief, Cgb was overexpressed in the pET16b vector (from Novagen) and purified with DEAE-Sepharose, butyl-Toyopearl 650s hydrophobic, and Superdex 200 gel filtration columns. Antibody to Cgb was raised essentially as described before for the E. coli hemoglobin (47), except that test bleeds were performed after the third and fourth injections. The animals were bled out after a fifth injection. In preparation for immunoblotting, C. jejuni cultures were grown in MH medium at 42°C with shaking at 110 rpm in the microaerophilic work station. After 10 h, 6 ml of culture was supplemented with 4 ml of fresh MH medium in 20 ml of Sterilin tubes and grown for a further 1 h. GSNO was added to final concentrations of 0.05, 0.1, or 0.25 mM; cells were harvested at different time points after the addition of chloramphenicol (100 µg ml–1), washed with Tris-buffered saline buffer without phenol red (46), and stored at –70°C overnight. Cells were then resuspended in Tris-buffered saline (75 µl), and an equal volume of acid-washed glass beads (25 µl, 106 µm and finer, G-4649; Sigma) was added. The samples were vigorously vortexed for four periods of 1 min, with chilling on ice during the intervals. The disrupted cell suspension was centrifuged at 13,800 x g and assayed for protein with the Bio-Rad protein assay kit and bovine serum albumin as the standard. Then, 10 µg of each sample was subjected to sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The anti-Cgb antibody was diluted 2,000-fold for use with a 2,000-fold dilution of peroxidase-conjugated monoclonal anti-rabbit immunoglobulin G (
-chain specific, clone RG-96, A-1949; Sigma) as the secondary antibody. Western blots and detection by using enhanced chemiluminescence (Amersham Biosciences) were done as described previously (47). Blot intensities were quantified by scanning the film with a Syngene Gene Genius gel documentation and analysis system.
To study the regulation of Cgb by aeration, cells were grown overnight in MH broth with vancomycin (10 µg ml–1) before being subcultured (3%) into 5, 10, 25, 35, or 45 ml of MH broth in 50-ml flasks and grown in the microaerophilic work station at 40°C with shaking at 110 rpm. After 5 h of growth, chloramphenicol (100 µg ml–1) was added to stop further protein synthesis. Cells were harvested after a further 10 min of incubation. Western blotting was performed as described above, except that more protein (45 µg) was loaded to each lane.
Inhibition of respiration by nitric oxide and consumption of NO by C. jejuni. Next, 4 ml of an overnight culture of Campylobacter in MH broth with vancomycin (10 µg ml–1) was inoculated into 150 ml of MH broth in 250-ml baffled flasks, and the cells were incubated for 5 h in the microaerophilic work station at 40°C with shaking at 110 rpm. GSNO was then added to a final concentration of 0.05 mM. At this point the OD600 was between 0.16 and 0.20. At this concentration of GSNO, the growth of neither the mutant nor the wild type was inhibited, but the expression of Cgb was induced. The cells were further incubated for 1 h before harvesting and washed in 50 mM morpholinepropanesulfonic acid (MOPS) plus 50 mM NaCl (pH 7.0) (MOPS buffer). Cell respiration was measured with an oxygen electrode as described by Stevanin et al. (48). Sodium formate (2 mM) used as respiratory substrate was incubated with MOPS buffer before the cells were added. NO solution was used to inhibit the respiration. Alternatively, NO solution was added before the addition of cells in order to measure NO consumption by cells.
Adherence and invasion of Caco-2 cells and nitrite assay. Caco-2 cells (ECACC) were grown as monolayers in minimal essential Eagle medium (Sigma). After infection of these with campylobacters, adhesion, invasion, and intracellular survival was assessed as described previously (12). As a stable nonvolatile breakdown product of NO, nitrite can be used to measure NO production in human colon epithelial cells (52). Nitrite levels in cell culture bathing medium were measured by the Griess reagent system (Promega). Caco-2 cells were seeded into six-well tissue culture trays (12) and infected with C. jejuni NCTC 11168 and CJCGB01. Wells containing Caco-2 cells without Campylobacter and others containing minimum essential Eagle medium with C. jejuni NCTC 11168 and CJCGB01 alone were used as controls. All were incubated for 3 h at 37°C in 5% CO2, after which 1 ml of cell culture bathing medium was transferred to 1.5-ml microfuge tubes. Tubes were centrifuged at 13,000 rpm for 3 min to precipitate the cells, and nitrite levels were measured according to the manufacturer's instructions by using 50 µl of supernatant. Absorbance was assayed at 540 nm and was compared to a standard curve by using sodium nitrite.
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RESULTS |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
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PCR was used to clone cgb from C. coli and C. jejuni. Sequence analysis of the C. coli cgb gene (GenBank no. AY321511) showed that the corresponding C. coli protein was closely related to Cgb (87% amino acid identity) (Fig. 1a).
Generation of Cgb-deficient mutants of C. jejuni and C. coli. The gene encoding cgb was disrupted in both C. jejuni and C. coli by insertion of a Kanr cassette, at a position 165 bp downstream from the ATG start codon, by using the suicide plasmid pKE18 (see Materials and Methods). Confirmation that the genomic copy of cgb was disrupted was obtained by Southern blot analysis (data not shown) and the corresponding mutants designated CJCGB01 (C. jejuni) and CCCGB01 (C. coli). In C. jejuni, mutants that had the Kanr cassette in opposite orientations behaved identically in all tests (data not shown), suggesting that the phenotype caused by the cgb mutation was not due to polar effects generated by the antibiotic resistance marker. Furthermore, the insertion of the Kanr cassette did not effect expression the genes immediately proximal to cgb (Cj1585c and Cj1587c) as determined by reverse transcriptase PCR (data not shown).
Cgb confers resistance to nitrosative stress but does not provide protection against superoxide or peroxides. The role of the C. jejuni Cgb was investigated by comparison of nitrosative stress resistance in the wild-type and cgb mutant strains. Diffusion assays on solid medium revealed that the cgb mutant of C. jejuni was hypersensitive to GSNO (a nitrosating agent) with a significantly greater zone of killing compared to the wild type (P = 0.002; two-tailed t test assuming equal variance). However, sensitivities to methyl viologen, hydrogen peroxide, and cumene hydroperoxide were equivalent to the wild-type (nonsignificant t test; Table 2).
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Contribution of Cgb to nitrosative stress resistance in C. jejuni and C. coli.
The effect of the cgb mutation on nitrosative stress resistance was probed further by exposing cells to a variety of nitrosating agents (GSNO or SNP) and a nitric oxide releaser (spermine NONOate) and assessing viability. The cgb mutant was markedly less resistant to all of these agents compared to the wild type (Fig. 2). The difference in viability varied markedly, however, depending on the nature of the compound and its concentration. For example, when GSNO was used, both the mutant and parental strains showed very little reduction in viability at up to 0.4 mM GSNO. In contrast, exposure to 0.8 mM GSNO reduced the viability of the mutant 
102-fold, while counts of the parental strain were not affected at these concentrations. In the presence of spermine NONOate, the wild type showed no decrease in viability at concentrations of up to 0.2 mM, whereas the cgb mutant began to lose viability at NONOate concentrations lower than 0.05 mM. At 0.2 mM, the difference in viability between the two strains was >104-fold. The C. coli Cgb-deficient mutant also displayed a similar sensitivity to GSNO and SNP (data not shown), suggesting that Cgb is a crucial defense against nitrosative stress in at least two Campylobacter species. To confirm that the sensitivity of the cgb mutant to GSNO and spermine NONOate reflected a difference in nitrosative stress resistance and not a changed tolerance to spermine or glutathione, the sensitivity of the wild-type and mutant to these agents was assessed by using the disk diffusion assay. When 10 µl of 100 mM glutathione or spermine was used in this assay, no zones of inhibition were produced for either the wild type or the mutant (data not shown).
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Construction of cgb-astA and sodB-astA reporter gene fusions in C. coli. A novel Campylobacter reporter gene system, based on arylsulfatase, has recently been described (25). This has the advantage that expression of astA can be detected when the reporter gene is present in single copy and that expression can be readily monitored on agar plates by using chromogenic substrates (56), allowing regulatory mutants to be detected. In strain NCTC 11168, astA is present only as a pseudogene (Cj0866) that is not expressed (37) and, consequently, this strain provides a suitable background for this system. Nevertheless, when a copy of the astA was integrated into cgb, no expression of the reporter gene could be detected (data not shown). Consequently, cgb-astA gene fusions were next introduced into C. coli UA585 to determine whether astA expression could be assessed in this background and to provide information on this closely related species. Integrable vectors capable of generating transcriptional fusions via single crossover recombination events in C. coli have been described previously (8). In the present study, these vectors were modified to include an arylsulfatase reporter gene (see Materials and Methods). The integration of the reporter gene fusions into the chromosome was confirmed by Southern hybridization analysis with three different labeled probes (data not shown). Strains containing sodB (control) and cgb fusions to astA were designated CCSF1 and CCCF1, respectively.
Induction of cgb expression by nitrosative stress. Strains containing the reporter gene fusion were grown for 16 h, after which GSNO, SNP, or methyl viologen was added. The parental strain of C. coli does not possess a copy of astA and, when it was assessed for expression, no AstA activity was detected (data not shown). In contrast, a basal level of astA expression was detected when CCCF1 and CCSF1 were grown in MH broth with no additions. This level remained constant throughout the growth experiment at ca. 20 to 30 U (Fig. 3a).
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Purification of Cgb allowed preparation of a polyclonal antibody for immunoblotting of C. jejuni extracts. In cultures not challenged with GSNO, Cgb was undetectable (Fig. 4). However, even after the addition of only 0.05 mM GSNO, a clear band, corresponding to a protein of molecular mass 16 kDa, was detectable, which increased in intensity over 3 h. A similar pattern of induction was seen after the addition of 0.1 or 0.25 mM GSNO (Fig. 4). No Cgb was detected when the culture was incubated for the same time in the absence of GSNO. The possibility that the expression of Cgb was regulated by oxygen was checked by growing C. jejuni in a microaerobic atmosphere, but at different volumes (5, 10, 25, 35, and 45 ml) of medium in 50-ml conical flasks. Such variation of culture volume has been shown previously to be reflected in the oxygen transfer rate (KLa) from the gas to liquid phase (21). Since Cgb was present at a very low level under noninduced conditions, higher amounts of soluble protein (45 µg) were used for Western blotting. No difference was seen under different aeration conditions (results not shown).
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110 µM; respiration rate, 1.6 µM s–1) immediately inhibited respiration by ca. 60 to 70%. However, inhibition was transient and respiration resumed at the initial rate after about 90 s. The period of respiratory inhibition coincided precisely with the time during which NO was detectable in the vessel (Fig. 5a). In contrast, addition of NO to Cgb-deficient cells caused a continuous decline in the rate of respiration until all O2 was exhausted; NO was detectable throughout the experiment (Fig. 5b). The half-lives of NO were typically 58 and 131 s for the wild type and the cgb mutant, respectively. In control experiments without NO addition, the respiration of both wild-type and cgb cells was linear down to very low O2 tensions. When lower NO concentrations were used, cell respiration of the mutant resumed at low O2 tension (not shown). These patterns of O2 and NO consumption were reproducible in three to six experiments done on cells from each of two independent growths.
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Intracellular survival was also assessed 24 h after the infection of Caco-2 cells. Although the number of intracellular bacteria had decreased compared to survival at 3 h, numbers of the wild type (1,100 ± 800) and cgb mutant (2,200 ± 1,300) were not significantly different at this time point.
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DISCUSSION |
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In order to investigate the role of the single-domain globin Cgb in the physiology of campylobacters, cgb-deficient mutants of C. jejuni and C. coli were generated. Cgb-deficient cells had levels of resistance comparable to the levels of resistance to methyl viologen, hydrogen peroxide, and organic peroxides, as did wild-type cells. Thus, it seems unlikely that Cgb plays a major role in the resistance of campylobacters to oxidative stresses. In addition, Cgb does not appear to have a physiological role as an alkyl hydroperoxide reductase in C. jejuni at least, as has been suggested for Hmp (4), since the cgb mutation did not confer sensitivity to organic peroxides even in a strain in which the iron-regulated alkyl hydroperoxide reductase, AhpC, was not present.
An important finding of the present study is that cgb mutants showed increased sensitivity to the NO-releasing compound spermine NONOate, as well as to the nitrosating agents GSNO and SNP. All of these compounds are widely used to generate nitrosative stress. However, with SNP, NO release occurs only after nitrosation, i.e., the transfer of the NO+ group to a nucleophilic receptor (43) and, although GSNO may undergo homolysis to generate the oxidized thiol RS. and NO, it can also act as a transnitrosating agent. In contrast, spermine NONOate directly liberates NO with a specified half-life (230 min; Calbiochem data) and can be used to study the effect of NO per se. Since the cgb mutant was hypersensitive to this agent, it might be concluded that Cgb protects campylobacters directly from NO but, in the presence of O2, the NO liberated might act as a nitrosating agent. Thus, care needs to be exercised in interpreting the results with different nitrosative agents. Since Salmonella strains defective in AhpC are hypersusceptible to reactive nitrogen intermediates (5), C. jejuni CJA01 (AhpC–) was also assessed for sensitivity to GSNO. However, in a disk diffusion assay, the ahpC mutant showed no increased sensitivity to this compound.
It is not possible to complement mutations in these strains of Campylobacter by plasmid-borne copies of cgb, since plasmids containing DNA homologous to the genome are unstable in these host backgrounds. Nevertheless, the nitrosative stress-sensitive phenotype is due solely to the inability of cells to express cgb alone for several reasons. First, the Kanr cassette used contains its own promoter but lacks a transcriptional terminator, and when the resistance cassette is inserted with the same transcriptional polarity as the mutated gene, mutations have been shown to be nonpolar on downstream genes (26). In addition, cgb mutants had the same phenotype irrespective of the orientation of the Kanr cassette. Second, the two neighboring open reading frames, Cj1585c and Cj1587c, which encode a putative oxidoreductase and putative ABC transporter, respectively, are expressed in the opposite direction to cgb and on the complementary strand. Furthermore, the insertion of the Kanr cassette did not affect expression of the genes immediately proximal to cgb, as determined by reverse transcriptase PCR, and polar effects can, therefore, be ruled out.
In other bacteria, the expression of two-domain globins is modulated by a number of environmental conditions. In E. coli, Hmp expression is induced by both NO (44) and oxidative stress (30), whereas in B. subtilis Hmp expression is induced by anaerobiosis and nitrite (28). Less information is available concerning the regulation of the single-domain globins, such as Cgb or the truncated globins, although Vgb is expressed in response to oxygen limitation (9). Recent work did not demonstrate the induction of Vgb by nitrosative stress (17). The present study is the first, to our knowledge, to demonstrate upregulation of a single-domain hemoglobin (i.e., non-flavo-hemoglobin) in response to nitrosative stress. For example, the presence of GSNO and SNP stimulated expression of the cgb-astA reporter gene fusion by 4- to 8-fold, whereas expression from a control sodB-astA fusion was not affected by the presence of either of these compounds. The astA gene fusion vectors could be used only in C. coli. Nevertheless, the expression of Cgb in C. jejuni was clearly induced under similar conditions when Western blotting was used to assess its expression. Given the fact that the intergenic region between cgb and Cj1585c is highly conserved, particularly in the region proximal to Cj1585c (Fig. 1b), this finding is not unexpected. Since Cgb expression is not regulated by aeration, we suggest that Cgb is specifically responsible for dealing with nitrosative stress.
NO reacts with many cellular targets, such as FeS-containing proteins, and inhibits respiratory chains. Using uninduced cells, no difference was seen between the wild type and the cgb mutant in terms of the severity and the degree of respiratory inhibition at various NO concentrations. The half-lives of NO signals were identical in both the mutant and the wild type. These results are not surprising given that Cgb was not expressed significantly without induction. However, when the expression of Cgb was induced, it significantly contributed to the protection of respiration and the consumption of nitric oxide. The fact that Cgb-deficient cells consumed NO at a faster rate than measured for its decay in the buffer control suggests that there may be additional mechanisms of NO detoxification in campylobacters. However, this activity is not due to a flavorubredoxin (19) since genes encoding this function are not present in the genome sequence (37).
In other bacterial pathogens, the ability of the cell to detoxify NO and its congeners, through the action of globins, has been correlated with virulence. For example, Salmonella hmp mutants survive phagocytosis by peripheral monocyte-derived macrophages relatively poorly compared to wild-type cells (48). Consequently, Cgb is likely to play some role during colonization and infection. Here, we have shown that, although cells deficient in Cgb are able to invade and survive intracellularly in Caco-2 cells with the same efficiency as the wild-type cells, the levels of NO produced by epithelial cells are much higher in cells infected with the cgb mutant. Since NO production was not detected in cells of C. jejuni incubated in tissue culture medium alone, this NO must be derived from the eukaryotic cells, suggesting that Cgb is required for the efficient removal of NO. Although this difference in NO detoxification was not manifested in differences in invasion potential, this may be due to the fact that other resistance mechanisms, such as the detoxification of superoxide by superoxide dismutase (41), are also involved in intracellular survival.
In conclusion, the data presented here demonstrate for the first time that (i) the single-domain globin Cgb, unlike Vgb, plays a key role in detoxification of NO and related compounds and that (ii) consumption of and protection from NO is inducible and that this is a consequence of the specific induction of Cgb expression by nitrosative stress. Future studies concerning Cgb and its regulators are likely to confirm the importance of this globin in Campylobacter physiology.
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ACKNOWLEDGMENTS |
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We thank Simon Smith (University of Sheffield Antibody Resource Centre) for preparation of antibody, Martin Hughes (King's College London) for helpful advice on NO chemistry and provision of GSNO, and H. Corker for critical reading of the manuscript.
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FOOTNOTES |
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K.T.E. and G.W. contributed equally to this study.
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54-dependent but not 28-dependent flagellar genes in Campylobacter jejuni is associated with formation of the flagellar secretory apparatus. Mol. Microbiol. 50:687-702.[CrossRef][Medline]
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) and CJCGB01 (
) were challenged with the indicated concentrations of GSNO (a), SNP (b), and spermine NONOate (c) for 1 h and then plated on MH agar. The results are a mean of two independent experiments. Bars indicate one standard error.
), 0.1 mM (
, 
), or 0.25 mM (
) (a); SNP at 0.005 mM (
), 0.01 mM (
