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Appl Environ Microbiol. Aug 2007; 73(15): 5034–5040.
Published online Jun 15, 2007. doi:  10.1128/AEM.00366-07
PMCID: PMC1951048

A Cyclic AMP Receptor Protein-Regulated Cell-Cell Communication System Mediates Expression of a FecA Homologue in Stenotrophomonas maltophilia[down-pointing small open triangle]

Abstract

Stenotrophomonas maltophilia WR-C possesses an rpf/diffusible signal factor (DSF) cell-cell communication system. It produces cis-Δ2-11-methyl-dodecenoic acid, a DSF, and seven structural derivatives, which require rpfF and rpfB for synthesis. Acquisition of iron from the environment is important for bacterial growth as well as the expression of virulence genes. We identified a gene homologous to fecA, which encodes a ferric citrate receptor that transports exogenous siderophore ferric citrate from the environment into the bacterial periplasm. Western blot analysis with anti-FecA-His6 antibody showed that the FecA homologue was induced in the iron-depleted medium supplemented with a low concentration of ferric citrate. Deletion of rpfF or rpfB resulted in reduced FecA expression compared to the wild type. Synthetic DSF restored FecA expression by the ΔrpfF mutant to the wild-type level. Reverse transcription-PCR showed that the fecA transcript was decreased in the ΔrpfF mutant compared to the wild type. These data suggest that DSF affected the level of fecA mRNA. Transposon inactivation of crp, which encodes cyclic AMP (cAMP) receptor protein (CRP) resulted in reduced FecA expression and rpfF transcript level. Putative CRP binding sites were located upstream of the rpfF promoter, indicating that the effect of CRP on FecA is through the rpf/DSF pathway and by directly controlling rpfF. We propose that CRP may serve as a checkpoint for iron uptake, protease activity, and hemolysis in response to environmental changes such as changes in concentrations of glucose, cAMP, iron, or DSF.

Stenotrophomonas maltophilia is found in a wide variety of environments such as soil, sewage, foods, plant rhizospheres, and hospital disinfectant solutions (5, 16, 17). It was previously identified as Pseudomonas maltophilia and then renamed Xanthomonas maltophilia before being reclassified in a new genus, Stenotrophomonas (35, 42). S. maltophilia is recognized as an emerging human pathogen and is associated with endocarditis, bacteremia, cystic fibrosis, and infections of the respiratory and urinary tracts, central nervous system, eyes, skin, and soft tissue (16).

Bacteria use small molecules in response to cell density to coordinate physiological processes, a process termed quorum sensing. A cell-cell communication system mediated by a diffusible signal factor (DSF), cis-Δ2-11-methyl-dodecenoic acid, was first identified in Xanthomonas campestris pv. campestris (13, 22, 48). This system is encoded by genes within an rpf (regulation of pathogenicity factors) cluster. RpfB, a putative long-chain fatty acyl coenzyme A (CoA) ligase, and RpfF, a putative enoyl CoA hydratase, are required for DSF biosynthesis (4). In X. campestris pv. campestris, RpfC and RpfG, a two-component system, regulate DSF production and interact with RpfF (2, 29). The rpf/DSF system in X. campestris pv. campestris is involved in the regulation of various biological functions and processes such as extracellular enzyme and exopolysaccharide production, biofilm formation, flagellum synthesis, resistance to toxins and oxidative stress, aerobic respiration, cross-kingdom communication, and virulence (13, 21, 30, 51). We previously isolated S. maltophilia strain WR-C from the clogged infiltrative area of a septic system used for wastewater disposal (45) and showed that it possesses a DSF cell-cell communication system (33). In addition to DSF, S. maltophilia strain WR-C produces seven structural derivatives that are not shared by X. campestris pv. campestris. These eight compounds have signaling functions and also act as wetting agents for flagellum-independent translocation (33). Other physiological processes regulated by the DSF system in S. maltophilia have not been determined.

Iron is relatively abundant on earth, but it is biologically unavailable in its oxidized form (ferric oxyhydroxide) and when sequestered by iron storage proteins (43). Acquisition of iron from the environment is important for bacterial growth as well as expression of some virulence genes (39, 43). Ferric citrate is one of the heterologous siderophores that serves as an iron source for Escherichia coli and other gram-negative bacteria (28, 41, 49). Many bacteria possess fecIRA homologues, but the ferric citrate transport system and fecIRA-induced regulation have been studied only in Escherichia coli strain K-12 (8, 28). Ferric citrate is transported into E. coli through outer membrane receptor FecA, which also mediates the transcription of fecABCDE transport genes. Located upstream are the regulatory genes fecIR (25, 37). In the periplasm, the C-terminal region of FecR interacts with the N-terminal region of FecA and transfers the signal across the cytoplasmic membrane into the cytoplasm, where the N-terminal portion of FecR interacts with the sigma factor FecI. FecI binds to RNA polymerase and initiates the transcription of fecABCDE (37). Iron transport systems in S. maltophilia have not been identified.

The cyclic AMP (cAMP) receptor protein (CRP) is a transcriptional regulator present in bacteria that responds to environmental conditions (6). CRP controls gene expression by binding cAMP and interacts at the promoters of targeted genes (14). It is well known as a regulator for genes involved in carbohydrate catabolism. The reduced levels of intracellular CRP and cAMP caused by glucose result in catabolite repression (36). CRP is reported to directly or indirectly regulate a variety of genes such as those for fatty acid utilization, iron uptake, and acyl homoserine lactone (AHL)- or autoinducer 2 (AI-2)-mediated quorum-sensing regulation or synthesis (1, 10, 20, 23, 44).

In this study, we investigated other targeted genes or biological processes controlled by the rpf/DSF system in S. maltophilia. The rpf/DSF system regulated the expression of a FecA homologue, which has not been shown to be regulated by any other known quorum sensing system. The rpf/DSF system was shown to be regulated by RpfC through protein-protein interaction with RpfF in Xanthomonas spp. (2, 29), but no transcriptional regulator has yet been identified. Here, an activator that is homologous to CRP was identified and shown to positively regulate rpfF, possibly by binding to an rpfF upstream region. In addition, CRP indirectly controlled FecA expression. It also controlled protease and hemolytic activity independently of the rpfF/DSF system.

MATERIALS AND METHODS

Bacterial strains and growth conditions.

All bacterial strains and plasmids used in this study are shown in Table Table1.1. S. maltophilia WR-C and its mutant derivatives were routinely grown in Trypticase soy (TS) broth (Becton Dickinson, Sparks, MD) at 30°C unless otherwise stated. S. maltophilia wild type (WT) and mutants harbored the vector pBBR1MCS5 unless specified otherwise. All E. coli strains were grown in Luria-Bertani (LB) broth (Becton Dickinson) at 37°C. For FecA expression and reverse transcription-PCR (RT-PCR) analysis, strains were grown in fecA medium (1 g NH4Cl, 3 g KH2PO4, 6 g Na2HPO4·7H2O, 4 g glucose, and 0.02% l-methionine per liter, supplemented with 0.1 mM 2,2′-dipyridyl and 0.5 mM ferric citrate). When required, antibiotics were added to the medium at the following concentrations: ampicillin (Ap), 100 μg ml−1; carbenicillin, 50 μg ml−1; chloramphenicol, 5 μg ml−1; gentamicin (Gm), 50 μg ml−1; kanamycin (Km), 50 μg ml−1.

TABLE 1.
Strains and plasmids used in this study

Generation of transposon mutants.

S. maltophilia WR-C transposon mutants were generated using EZ::TN <R6Kγori/KAN-2> Tnp Transposome (Epicentre, Madison, WI) as described by Huang et al. (34). The transposon flanking regions were rescued by “rescue cloning,” as described by the manufacturer, and sequenced using primers KAN-2 FP-1 and R6KAN-2 RP-1. Additional primers were used to sequence the full genes and flanking regions. Twenty microliters of overnight cultures in TS broth was spot inoculated on skim milk or blood agar plates to screen for defects in hemolysis and protease activity. For protease assays, TS agar plates containing 2% skim milk were incubated at 30°C for 1 day. The appearance of a clear zone around the inoculum indicates protease activity. Hemolytic activity was tested with blood agar plates that contained 5% defibrinated rabbit red blood cells in Tris-buffered saline (50 mM Tris-HCl, 150 mM NaCl, pH 7.4) and 1.5% Bacto agar and that were incubated at 30°C for 2 days. The appearance of a greenish zone around the inoculum indicates alpha-hemolysis.

Construction of plasmids and strains.

To construct the plasmid for complementation of the crp mutant, the coding region, ribosomal binding site, and native promoter of crp in S. maltophilia WR-C were amplified by PCR with primers crp-F and crp-R (Table (Table2).2). The product was cloned into pGEM-T Easy (Promega, Madison, WI). The fragment containing crp (828 bp) was excised with EcoRI and ligated into pBBR1MCS5 to generate pcrp. For complementation, pcrp was electroporated (12.5 kV/cm, 25 μF, 400 Ω) into the crp mutant. Electroporation, restriction endonuclease digestion, PCR, cloning, DNA extraction, and DNA purification were performed using standard procedures (46).

TABLE 2.
Oligonucleotides used in this study

To construct the plasmid for FecA overexpression, the fecA coding sequence (3,138 bp) and 1 bp upstream of the fecA start codon were PCR amplified with primers HindIII-fecA2 and SacI-fecA2 and cloned into pGEM-T Easy. The product was excised with HindIII and SacI and cloned into pET22b(+) (Novagen, San Diego, CA) to generate pfecA::ET22b(+). The construct was sequenced with T7 promoter and terminator primers (Novagen, Madison, WI) and electroporated into E. coli strain BL21(DE3).

Overexpression of FecA by the pET system for antibody production.

E. coli BL21(DE3) harboring pfecA::ET22b(+) was grown in LB broth containing 50 μg ml−1 carbenicillin at 37°C. Transcription of the fusion gene was induced with 1 mM isopropyl-β-d-thiogalactopyranoside (IPTG) at 37°C and 175 rpm for 2 h. E. coli BL21(DE3) harboring pET22b(+) was used as the control. After induction, cells were harvested and resuspended in lysis buffer (100 mM NaH2PO4, 10 mM Tris-HCl, 6 M urea, pH 8.0). Solubilized proteins were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) using 7.5% polyacrylamide gels, 1× Tris-glycine electrophoresis buffer (25 mM Tris, 250 mM glycine, pH 8.3, and 0.1% SDS, wt/vol), and Mini-PROTEIN II electrophoresis cells (Bio-Rad). The minigels were stained with Coomassie brilliant blue R-250 (0.25%, wt/vol) or were used for protein blotting. The band containing the FecA-His6 fusion protein was excised from the gel and submitted to GeneTel Laboratories (Madison, WI) for immunization of chickens and generation of polyclonal immunoglobulin Y (IgY) antibodies in eggs.

Western blot analysis.

Whole-cell lysates of E. coli BL21(DE3) harboring pET22b(+) and the FecA-His6 fusion protein prepared as described above were separated by SDS-PAGE. The separated proteins were analyzed by immunoblotting with anti-His tag monoclonal antibodies and anti-mouse IgG-alkaline phosphatase (AP) conjugate (Novagen, Madison, WI). The protocol, as described in the manual of the Immuno-Star AP chemiluminescent protein detection systems (Bio-Rad, Hercules, CA), was followed, except that 0.5% casein (Sigma-Aldrich, St. Louis, MO) and CDP-star (Roche Diagnostic Corp., Indianapolis, IN) were used as the blocker and chemiluminescence substrate, respectively.

For FecA expression in S. maltophilia, strains were grown in a low-iron medium (fecA medium) at 30°C and 175 rpm for 3 days. Cells (optical density at 620 nm [OD620] ≈ 0.6) were centrifuged, resuspended in 2× SDS gel loading buffer (100 mM Tris-HCl [pH 6.8], 4% SDS, 0.2% bromophenol blue, 20% glycerol, and 10% β-mercaptoethanol), boiled at 100°C for 10 min, and separated by SDS-PAGE. The separated proteins were analyzed by immunoblotting with anti-FecA-His6 antibody (1:20,000) and rabbit anti-chicken IgY-AP conjugate (1:15,000) (GeneTel Laboratories) according to the manufacturer's instructions, except that 1.5% bovine serum albumin (Sigma-Aldrich, St. Louis, MO) and CDP-star were used as the blocker and chemiluminescence substrate, respectively. The experiment was repeated four times. Data presented are from one representative experiment.

RT-PCR.

For determining fecA and rmlA transcripts, strains were grown at 30°C in fecA medium for 6 (OD620 ≈ 0.01) and 18 h (OD620 ≈ 0.1) unless stated otherwise; for the rpfF transcript, strains were grown in fecA medium without glucose for 2 days (OD620 ≈ 0.1). Total RNA was extracted from 30 ml of culture with Tri Reagent LS (Molecular Research Center, Inc., Cincinnati, OH) and subjected to DNase I treatment with the TURBO DNA-free kit (Ambion, Inc., Austin, TX). RNA concentration was determined by measuring absorbance at 260 nm (A260) with a Synergy HT multidetection microplate reader (Bio-Tek Instrument, Winooski, VT). RT-PCR was performed with the OneStep RT-PCR kit (QIAGEN, Valencia, CA) in a 20-μl reaction mixture containing 20 ng of total RNA, 0.6 μM of each gene-specific primer, 1× QIAGEN OneStep RT-PCR buffer, 400 μM of each deoxynucleoside triphosphate, and 2 units of QIAGEN OneStep RT-PCR enzyme mixture. Primers 20F4-RT and 20R6-RT were used for amplifying fecA (994 bp), primers rmlA-F-RT and rmlA-R-RT were used for amplifying rmlA (613 bp), and primers rpfB-RW3 and rpfF-R were used for amplifying rpfF (845 bp). Primer sequences are listed in Table Table2.2. rmlA was constitutively expressed under the conditions tested in this study and was used as an internal control. RT was performed at 50°C for 30 min, followed by 15 min of reverse transcriptase inactivation at 95°C. The PCR cycling conditions were 94°C for 1 min, 55°C for 30 s, and 72°C for 1 min for a total of 32 cycles and an additional 2-min extension at 72°C. To test for genomic DNA contamination, a negative-control PCR without the RT step was performed by using the PCR Master Mix (Promega, Madison, WI). Ten microliters of RT-PCR mixture was electrophoresed on 1% agarose gels, and the gels were stained with ethidium bromide for visualization under UV. The experiment was repeated four times. Data presented are from one representative experiment.

RESULTS

FecA expression is induced by ferric citrate.

A fecA homologue encoding the ferric citrate receptor FecA was identified in the transposon library of S. maltophilia WR-C. The translated amino acid sequence exhibits 67% identity to the FecA in X. campestris pv. campestris (GenBank accession no. NP_638176). The fecA homologue is flanked upstream by salR, which encodes the sal operon transcriptional repressor and downstream by sapC, which encodes a SapC-related protein (Fig. (Fig.1A).1A). SalR is an LacI family transcriptional regulator; SapC forms part of a paracrystalline surface layer and confers serum resistance in Campylobacter fetus. This gene organization is in part similar to one of the nine X. campestris pv. campestris fecA homologues (GenBank accession no. NP_638176), where sapC is also located downstream. This is in contrast to E. coli, where the binding and transport genes fecBCDE are adjacent to fecA. The full sequences and flanking regions of the S. maltophilia fecA were deposited in the GenBank database (accession number EF011626).

FIG. 1.
Genetic organization and expression of FecA. (A) fecA and flanking genes in Escherichia coli K-12 (E. coli) (7) and S. maltophilia WR-C (GenBank accession no. EF011626). Genes depicted are not proportional to their respective sequence lengths. (B) SDS-PAGE ...

To specifically determine FecA expression in S. maltophilia WR-C by Western blot analysis, full-length fecA (3,135 bp, encoding 1,045 amino acid residues with a molecular mass of 113 kDa) was cloned into the expression vector pET22b(+) containing a C-terminal His6 tag and expressed in E. coli BL21(DE3). The fusion protein was used for antibody production. E. coli BL21(DE3) harboring pfecA::ET22b(+) expressed a 119-kDa FecA-His6 fusion protein under IPTG-induced conditions, which was absent in the control strain harboring pET22b(+) (Fig. (Fig.1B).1B). The FecA-His6 fusion protein was confirmed by Western blot analysis with anti-His tag monoclonal antibody (Fig. (Fig.1C).1C). FecA expression in S. maltophilia WR-C was induced by low concentrations (0.5 and 2.5 mM) of ferric citrate and inhibited when the concentration was increased to 100 mM (Fig. (Fig.1D).1D). This apparent regulation of S. maltophilia FecA expression by ferric citrate implies that FecA may function as a ferric citrate receptor and possibly a transporter. Whether this FecA homologue can be induced by or bind to other types of substrate remains to be determined.

rpfB and rpfF are required for FecA expression.

We have identified an rpf system in S. maltophilia WR-C and generated mutants with deletions in rpfB and rpfF (33). rpfF was shown to affect siderophore production in Xanthomonas oryzae pv. oryzae (11). To determine if the rpf/DSF system plays a role in the putative ferric citrate transport system in S. maltophilia strain WR-C, the WT and its Δrpf mutants were assessed for FecA expression. Both ΔrpfB and ΔrpfF mutants had a reduced level of FecA expression compared to the WT (Fig. (Fig.2).2). FecA expression was restored in the rpfB- and rpfF-complemented strains to levels similar to that in the WT. These results suggest both rpfB and rpfF participated in FecA expression.

FIG. 2.
Anti-FecA-His6 Western blot of cell lysates from S. maltophilia WT and ΔrpfB, ΔrpfF, and crp::EZTN mutants and the respective complemented strains. Strains were cultured in fecA medium at 30°C and 175 rpm for 3 days.

DSF is a signal for FecA expression and affects the level of fecA mRNA.

rpfF is involved in the synthesis of DSF as well as seven structurally related fatty acids (33). They are Δ2-tridecenoic acid, 10-methyl-dodecanoic acid, 11-methyl-dodecanoic acid, Δ2-12-methyl-tridecenoic acid, Δ2-tetradecenoic acid, Δ2-12-methyl-tetradecenoic acid, and Δ2-13-methyl-tetradecenoic acid. These eight compounds can activate the promoter of engXCA (encodes endoglucanase), as determined by a DSF bioassay using the DSF reporter strain X. campestris 8523/pL6engGUS (47), suggesting a signaling role for them. In addition, deletion of rpfB or rpfF resulted in reduced levels of FecA expression. We therefore hypothesized that DSF and its seven derivatives might be signals for FecA expression. To test this, a commercially available synthetic cis-Δ2-11-methyl-dodecenoic acid (DSF) was added to cultures of the ΔrpfF mutant, which were then incubated for 3 days. The synthetic DSF (25 or 50 μg ml−1) restored FecA expression by the ΔrpfF mutant to the WT level (Fig. (Fig.3),3), suggesting that it is a signal for FecA expression, possibly through affecting levels of fecA mRNA.

FIG. 3.
Effect of synthetic cis-Δ2-11-methyl-dodecenoic acid (DSF) on FecA expression. Cell lysates from S. maltophilia WR-C WT, the ΔrpfF mutant, and the ΔrpfF mutant harboring prpfFrpfF/prpfF) were analyzed by Western blotting ...

RT-PCR analysis showed that the ΔrpfF mutant had a reduced level of the fecA transcript compared to the WT after 18 h of incubation (OD620 ≈ 0.1) in fecA medium (Fig. (Fig.4),4), while no significant difference was observed between the ΔrpfF mutant and the WT after 6 h (OD620 ≈ 0.01). There are no reports of what genes are constitutively expressed in S. maltophilia. We tested housekeeping gene rmlA and found that it was constitutively expressed in fecA medium, TS broth, and LB broth at 30°C for 6 and 18 h, and thus rmlA was used as the control. Deletion of rpfF did not affect the level of rmlA transcript at both times in fecA medium (Fig. (Fig.4).4). These results suggest that the rpf/DSF system plays a role in affecting the level of fecA mRNA.

FIG. 4.
Steady-state levels of fecA and rmlA mRNA in S. maltophilia WT and the ΔrpfF mutant. RNA was isolated from cultures of S. maltophilia WT and the ΔrpfF mutant in fecA medium after 6 h and 18 h at 30°C and 175 rpm. RT-PCR was performed ...

CRP controls FecA expression.

CRP encoded by crp was reported to regulate the iron uptake regulator Fur in E. coli (15). We hypothesized that a putative iron transport system mediated by FecA in S. maltophilia might be controlled by CRP. We obtained a crp transposon insertion mutant in a separate study to identify virulence-associated genes. The S. maltophilia CRP exhibits 87% sequence identity to Xanthomonas campestris catabolite activation-like protein (Clp; GenBank accession no. NP_65866) and 44% identity to E. coli CRP (GenBank accession no. NPp_417816). FecA expression in the WT and crp mutant was examined. Transposon mutation in crp reduced FecA expression (Fig. (Fig.2),2), suggesting that CRP regulates FecA. The transposon mutants were screened for defects in proteolytic activity and hemolysis, because production of these two virulence factors was shown to correlate with cytotoxicity of clinical S. maltophilia isolates to HeLa and Vero cells (26). A clear zone of proteolysis on skim milk agar and zone of alpha-hemolysis on blood agar were obtained with the WT, while no zones of proteolysis or hemolysis were observed with the crp mutant. Both phenotypes were restored in the complemented strain. The full sequences and flanking regions of crp were deposited in the GenBank database (accession number EF011625).

CRP positively regulates rpfF transcripts, possibly by binding upstream regions of the rpfF promoter.

rpfF encodes enoyl CoA hydratase, which is an enzyme reported to be involved in fatty acid metabolism in E. coli (20). Genes involved in fatty acid metabolism and homoserine lactone or AI-2 synthesis or regulation have been shown to be directly or indirectly controlled by CRP (1, 10, 20, 23, 44). RT-PCR analysis was conducted to test whether rpfF in S. maltophilia WR-C is controlled by CRP. Reduced rpfF transcript levels in the crp mutant compared to the WT were observed; WT rpfF transcript levels were restored in the complemented strain (Fig. (Fig.5A).5A). Two potential CRP binding sites are located upstream of the rpfF promoter and exhibit 100% identity with the consensus sequences identified in X. campestris (32) (Fig. (Fig.5B).5B). The 5′TGTGA3′ sequence is conserved among other bacteria and critical for CRP binding (14). These results suggest that CRP is a transcriptional activator of rpfF, possibly by binding upstream regions of the rpfF promoter, which in turn affects the expression of FecA.

FIG. 5.
Levels of rpfF transcript determined by RT-PCR in the WT, crp mutant, and its complemented strain (A) and predicted CRP binding sites upstream of the rpfF promoter (B). rpfF mRNA level was determined by RT-PCR. RNA was isolated from cultures of S. maltophilia ...

DISCUSSION

Iron plays important roles in bacterial growth and pathogenesis (43). In this study, a homologue of the ferric citrate receptor FecA was identified in S. maltophilia WR-C. In contrast to E. coli, Pseudomonas aeruginosa, Klebsiella pneumoniae, and Photorhabdus luminescens fecA homologues, but similar to 8 of the 18 P. aeruginosa fecA homologues, the fecIR regulatory genes are not located upstream of fecA (8, 41, 43, 49). These genes may be located elsewhere, or the ferric citrate transport system in S. maltophilia may be controlled differently. Our results suggest that the FecA homologue is regulated by the rpf/DSF cell-cell communication system.

A link between quorum sensing and iron uptake has been postulated for P. aeruginosa, Vibrio harveyi, and X. campestris, although the molecular mechanisms of the interaction vary (12, 30, 40). Unlike P. aeruginosa and V. harveyi, which use AHL, S. maltophilia WR-C utilizes cis-Δ2-11-methyl-dodecenoic acid and seven other structural derivatives (collectively called DSFs) for cell-cell communication (33). Our results from Western blot and RT-PCR analysis of the WT and Δrpf mutants suggest that DSFs act as signals that positively affect the fecA mRNA level. Interaction between the rpf/DSF system and ferric citrate uptake has not been reported previously, although positive regulation of iron uptake by cell-cell signaling has been observed in a variety of systems. Transcriptome analysis of X. campestris pv. campestris demonstrated that DSF upregulated genes encoding receptors for catecholate (e.g., FepA, CitA, and IroN) (30). The quinolone signal upregulates genes for pyoverdin biosynthesis and the pyochelin receptor FptA in P. aeruginosa (9), while transcriptome and proteome analysis showed that AHL activated iron uptake mediated by the ferripyoverdine receptor FpvA, FptA, and the hemin receptor PhuR (3, 53). The response regulator LuxO of the AI-1 and AI-2 signaling system positively regulates siderophore production in Vibrio harveyi (27, 40). LuxS, which is involved in AI-2 synthesis, positively affects expression of fecBCDE in Actinobacillus actinomycetemcomitans (27, 40). In contrast, iron acquisition is down-regulated by the signal molecule phenazine pyocyanine in P. aeruginosa (18).

Mutation in crp of S. maltophilia WR-C resulted in reduced levels of rpfF transcript and FecA expression. CRP binding sites are located upstream of the rpfF promoter. These results suggest that CRP directly regulates synthesis of DSFs and in turn indirectly controls FecA through the rpf/DSF cell-cell communication system. Erwinia chrysanthemi CRP was shown to bind expI, which is responsible for the synthesis of N-(3-oxohexanoyl)-homoserine lactone and N-(hexanoyl)-homoserine lactone (44). In contrast to the positive regulation by CRP observed in S. maltophilia, E. chrysanthemi CRP acts as a repressor of expI transcription. CRP was also shown to control AI-1, AHL, and AI-2 and mediated the quorum sensing system by activating expression of luxR in Vibrio fischeri, lasR in P. aeruginosa, expR in Erwinia chrysanthemi, and lsrR in E. coli (1, 10, 24, 44, 50). Unlike the AI-1 and AHL signaling systems, DSF synthesis in X. campestris is controlled by two-component regulatory proteins RpfC, RpfG, and RpfH (47). RpfC and RpfG were shown to interact with RpfF (2, 29). In our study, we showed that an activator of rpfF, CRP, regulates the synthesis of DSFs, possibly by protein-DNA interaction.

We were not able to individually isolate each of the DSFs produced by S. maltophilia WR-C, and six of them are not commercially available. These DSFs may display different levels of activity in controlling physiological processes. A relatively high concentration (25 μg ml−1; ≈118 μM) of synthetic DSF was required to restore FecA expression by the ΔrpfF mutant. Whether lower concentrations of some of the other DSFs may exert the same effect cannot be determined at this time. As demonstrated in X. campestris pv. campestris by Wang and coworkers, the minimum concentrations of cis-Δ2-11-methyl-dodecenoic acid and Δ2-tridecenoic acid required for activating the endoglucanase promoter were 0.5 μM and 30 μM, respectively (51). The DSFs produced by S. maltophilia WR-C varied in acyl chain length, ranging from 12 to 14 carbons. We speculate that RpfB and RpfF may exhibit acyl chain specificity or that other enzymes may modulate the chain length. RpfB is homologous to FadD, which is a long- chain fatty acyl CoA ligase (4). The 25-amino-acid-residue signature motif (residues 431 to 455) of E. coli FadD was shown to promote fatty acid chain specificity (19). Pseudomonas AHL synthases were reported to exhibit acyl chain specificity (52), and the β-ketoacyl acyl carrier protein reductase (FabG) might affect the acyl chain length (31).

We propose a model of CRP and DSFs in the regulation of some physiological processes in S. maltophilia WR-C (Fig. (Fig.6).6). CRP may serve as a checkpoint for controlling bacterial growth or expression of virulence factors in response to extracellular signals such as DSF, ferric citrate, and glucose concentrations and intracellular conditions such as levels of ferrous iron and cAMP. Under unfavorable nutrient conditions (e.g., low iron concentration), rpfF in S. maltophilia is activated to synthesize DSFs. The DSFs act as wetting agents for flagellum-independent translocation (33) and as signals for expression of a FecA homologue, which may mediate ferric citrate uptake and in turn promotes bacterial growth. Notably, the ΔrpfB mutant exhibited a growth defect in fecA medium, but not in TS broth (data not shown). The rpf/DSF system does not play a role in biofilm formation, lipopolysaccharide biosynthesis (data not shown), protease production, and hemolysis of rabbit blood cells. Protease production and hemolytic activity in S. maltophilia are controlled by CRP. S. maltophilia and X. campestris pv. campestris share DSF as a signal molecule, suggesting that they could use it for intergenus communication when present in the same environment such as rhizospheres. The role of the rpf/DSF system in biofilm formation and production of extracellular enzymes is different in these two microorganisms, which may imply that they occupy distinct biological niches.

FIG. 6.
A proposed model for the roles of CRP and DSFs in the regulation of various physiological processes in S. maltophilia WR-C. The organism produces DSFs (triangles), which require rpfF and rpfB for synthesis and are secreted outside the cell. The DSF system ...

Acknowledgments

This research was supported by the Wisconsin Small Scale Waste Management Project and the College of Agricultural and Life Sciences, University of Wisconsin—Madison.

We thank M. Kovach for his generous gift of plasmid pBBR1MCS5.

Footnotes

[down-pointing small open triangle]Published ahead of print on 15 June 2007.

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