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Journal of Bacteriology, July 2005, p. 4327-4337, Vol. 187, No. 13
0021-9193/05/$08.00+0     doi:10.1128/JB.187.13.4327-4337.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Calcium-Induced Virulence Factors Associated with the Extracellular Matrix of Mucoid Pseudomonas aeruginosa Biofilms

S. Sarkisova,¹ M. A. Patrauchan,² D. Berglund,¹ D. E. Nivens,³ and M. J. Franklin^1,4*

Department of Microbiology,¹ Center for Biofilm Engineering, Montana State University, Bozeman, Montana 59717,⁴ Department of Microbiology and Immunology, University of British Columbia, Vancouver V6T 1Z3, Canada,² Department of Food Science, Purdue University, West Lafayette, Indiana 47907³

Received 15 October 2004/ Accepted 24 March 2005

Top Abstract Introduction Materials and Methods Results Discussion References

 
Pseudomonas aeruginosa colonizes the pulmonary tissue of patients with cystic fibrosis (CF), leading to biofilm-associated infections. The pulmonary fluid of CF patients usually contains elevated concentrations of cations and may contain the P. aeruginosa redox-active pigment pyocyanin, which is known to disrupt calcium homeostasis of host cells. Since divalent cations are important bridging ions for bacterial polysaccharides and since they may play regulatory roles in bacterial gene expression, we investigated the effect of calcium ions on the extracellular matrix constituents of P. aeruginosa biofilms. For mucoid strain P. aeruginosa FRD1, calcium addition (1.0 and 10 mM as CaCl₂) resulted in biofilms that were at least 10-fold thicker than biofilms without added calcium. Scanning confocal laser microscopy showed increased spacing between cells for the thick biofilms, and Fourier transform infrared spectroscopy revealed that the material between cells is primarily alginate. An algD transcriptional reporter demonstrated that calcium addition caused an eightfold increase in alg gene expression in FRD1 biofilms. Calcium addition also resulted in increased amounts of three extracellular proteases (AprA, LasB, and PrpL). Immunoblots of the biofilm extracellular material established that AprA was harbored within the biofilm extracellular matrix. An aprA deletion mutation and a mutation in gene for a putative P. aeruginosa calmodulin-like protein did not significantly affect calcium-induced biofilm structure. Two-dimensional gel electrophoresis showed increased amounts of phenazine biosynthetic proteins in FRD1 biofilms and in calcium-amended planktonic cultures. Spectrochemical analyses showed that the calcium addition causes a three- to fivefold increase in pyocyanin production. These results demonstrate that calcium addition affects the structure and extracellular matrix composition of mucoid P. aeruginosa biofilms, through increased expression and stability of bacterial extracellular products. The calcium-induced extracellular matrix of mucoid P. aeruginosa consists primarily of the virulence factor alginate and also harbors extracellular proteases and perhaps pyocyanin, a biomolecule that may further disrupt cellular calcium levels.

Top Abstract Introduction Materials and Methods Results Discussion References

 
Patients with cystic fibrosis (CF) are highly susceptible to bacterial pulmonary infections, particularly chronic infections with Pseudomonas aeruginosa (reviewed in reference 38). P. aeruginosa pulmonary infections are considered biofilm-associated diseases, where the bacteria colonize the surface of pulmonary tissue (36), are often encapsulated in extracellular polysaccharide matrix material (25, 36, 48), secrete quorum-sensing signaling compounds (58), and have increased resistance to antibiotics (reviewed in reference 59) and to host defenses (2, 30, 45). Mutations in the cystic fibrosis transmembrane regulator of CF patients lead to physiological alteration of pulmonary fluid, with the most characteristic manifestation being the increased concentrations of thick pulmonary mucus that includes DNA and actin from lysed neutrophils (38). Disruption of the CF transmembrane regulator also results in secretions with elevated concentrations of sodium and other cations. In addition to these cellular manifestations, extracellular products from infectious bacteria may contribute to the pulmonary abnormalities. The extracellular redox cycling compound produced by P. aeruginosa, pyocyanin, has been shown to disrupt cytosolic calcium concentrations and calcium homeostasis of epithelial cells (8). Pyocyanin has been detected in the pulmonary fluid of patients infected with P. aeruginosa (66). Therefore, this disruption may occur in vivo.

Acute P. aeruginosa infections are usually caused by nonmucoid strains, which do not produce the capsular polysaccharide alginate. Mucoid P. aeruginosa strains typically produce alginate, a high-molecular-weight polymer of O-acetylated D-mannuronate linked by ß 1-4 glycosidic bonds to its C₅ epimer, L-guluronate (14, 20). Once P. aeruginosa strains begin to produce this polymer, pulmonary infections may become chronic and patient prognosis declines. The switch from the nonmucoid to the mucoid phenotype is complex, involving a hierarchy of regulatory proteins (71), including the alternative sigma factor ^e (11, 39, 74), whose activity is repressed by the antisigma factors MucA and MucB (21, 56). Mutations in mucA are often responsible for the switch to the mucoid phenotype in clinical isolates (5). Antibiotics as well as components of host defensive processes may contribute to mucA mutations and to the accompanying phenotypic switch from non-alginate-producing strains and acute infections to alginate-producing strains and chronic infections (42, 53).

Extracellular polymeric substances form the structural material that holds the bacteria within the three-dimensional matrices of biofilms. There are seemingly conflicting reports over the composition of the bacterial extracellular matrix material for P. aeruginosa biofilms. These reports may reflect the differences in strains used in different studies. With mucoid P. aeruginosa FRD1 strains, alginate appears to be the primary constituent of the biofilm extracellular matrix material (48). Studies with this CF isolate and its mutant derivatives showed that alginate affects the three-dimensional architecture of P. aeruginosa FRD1 biofilms. Fourier transform infrared spectroscopy (FTIR) demonstrated that alginate was associated with biofilms of this mucoid strain. Similar results were obtained using a mutant derivative of the nonmucoid strain P. aeruginosa PAO1 engineered to overproduce alginate (25, 60). On the other hand, results using wild-type P. aeruginosa PAO1 and PA14 showed that alginate was not associated with biofilms (72) and that a second polysaccharide likely encoded by a separate polysaccharide biosynthetic gene cluster may provide the extracellular matrix material for those cells (18, 19, 29). In another report, using P. aeruginosa PAO1, DNA was suggested to be the extracellular matrix material, since the addition of DNase to biofilms dispersed the bacteria (64). Many bacterial extracellular polysaccharides, including alginate, contain negatively charged uronic acid residues. These sugar subunits bind calcium ions by ionic interactions, allowing cross-bridging and gelling of the extracellular polysaccharides (28). In the case of alginate produced by algae and the bacterium Azotobacter vinelandii, blocks of L-guluronate residues bind calcium to alginate (12). Although P. aeruginosa does not produce L-guluronate blocks, calcium apparently binds the uronic acid residues and affects the polymer's physical properties (59).

A recent study characterizing biofilms of the marine bacterium Vibrio cholerae implicated calcium ions in O-antigen polysaccharide binding and biofilm maintenance (32). When this bacterium undergoes a switch from higher calcium ion concentrations, such as those found in seawater, to a lower concentration, the biofilms disperse, suggesting that the loss of a calcium ion from an O-antigen polysaccharide may result in disruption of the biofilms and release of individual cells. This destabilizing effect may be specific for calcium, since it was not observed with the addition of magnesium. In addition to their role in biofilm matrix stability, calcium ions may affect bacterial gene expression. In eukaryotic cells, calcium is an important signaling molecule, and it may play a regulatory role in bacteria (27, 49). Many bacteria contain genes for calmodulin-like proteins with characteristic EF-hand motifs (46), including P. aeruginosa PA4107 and possibly plcR (6), which has been shown to bind calcium (61). In P. aeruginosa, secretion and/or stability of certain extracellular proteins is affected by calcium ions. Toxins secreted by the type III secretion system are repressed by calcium (75). The amounts of extracellular elastase (LasB) and LasA, secreted by the type II secretory pathway, increase in the presence of added calcium (52).

Since the calcium ion is known to affect biofilm architecture, we investigated its role in the structure and extracellular matrix constituents of P. aeruginosa biofilms. Surprisingly, we found that added calcium resulted in biofilms of mucoid P. aeruginosa FRD1 that were 10- to 20-fold thicker than biofilms without added calcium. We used this phenomenon to characterize alginate amounts and expression of alg biosynthetic genes within these biofilms and to characterize proteins within the extracellular matrix material. Amounts of extracellular proteases increased in Ca²⁺-amended biofilms, and the proteases were found to be harbored within the Ca²⁺-augmented alginate matrix. Amounts of biosynthetic proteins for the extracellular virulence factor pyocyanin also increased with added calcium. The results indicate that, in mucoid strains of P. aeruginosa, alginate is the primary extracellular matrix material of the biofilms and that this matrix material can act as a reservoir for other extracellular virulence factors.

Top Abstract Introduction Materials and Methods Results Discussion References

 
Bacterial strains, plasmids, and media. Pseudomonas aeruginosa FRD1 and PAO1 were used in this study. P. aeruginosa FRD1 is an alginate-overproducing (mucoid) CF pulmonary isolate (51), and P. aeruginosa PAO1 is a nonmucoid non-CF isolate. The PA4107 and PA1249 genes were deleted from the chromosomes of both FRD1 and PAO1, by using allelic exchange, resulting in replacement of each gene with a gentamicin omega fragment. PA4107 encodes a putative calmodulin-like protein containing predicted Ca²⁺ binding EF-hand motifs, and the strains produced by this deletion were labeled P. aeruginosa PAO1043 calA::aacCI and FRD1043 calA::aacCIW. PA1249 (aprA) encodes alkaline metalloprotease, and its deletions were labeled PAO1252 aprA::aacCI and FRD1252 aprA::aacCI. P. aeruginosa FRD875 algD>xylE (69) was generously provided by Daniel Wozniak (Wake Forest University). For scanning confocal laser microscopy (SCLM) the strains expressed the gfpmut2 from a constitutive promoter from plasmid pMF230 (48).

Escherichia coli and P. aeruginosa were routinely cultured in L broth (10 g tryptone, 5 g yeast extract, 5 g NaCl, per liter). Pseudomonas isolation agar (Difco) was used to select for P. aeruginosa following matings with E. coli. Antibiotics when used were at the indicated concentrations (per milliliter): ampicillin at 100 µg, carbenicillin at 300 µg, and gentamicin at 15 µg for E. coli and 100 µg for P. aeruginosa. General DNA manipulations were performed as described previously (1). Restriction endonucleases were purchased from New England Biolabs. Oligonucleotide primers were synthesized by IDTDNA Corp.

Biofilm minimal medium (BMM) contained (per liter) 9.0 mM sodium glutamate, 50 mM glycerol, 0.02 mM MgSO₄, 0.15 mM NaH₂PO₄, 0.34 mM K₂HPO₄, 145 mM NaCl, 20 µl trace metal solution, and 1 ml vitamin solution. Trace metal solution (per liter of 0.83 M HCl) contained 5.0 g CuSO₄ · 5H₂O, 5.0 g ZnSO₄ · 7H₂O, 5.0 g FeSO₄ · 7H₂O, and 2.0 g MnCl₂ · 4H₂O. Vitamin solution (per liter) contained 0.5 g thiamine and 1 mg biotin. The pH of the medium was adjusted to 7.0. MgSO₄, CaCl₂ · 2H₂O, trace minerals, and vitamins were added to the medium after autoclaving. When used, CaCl₂ · 2H₂O was added to final concentrations from 0.5 to 10.0 mM. Since BMM is at neutral pH and the free phosphate concentration is less than 50 mg/liter, addition of CaCl₂ · 2H₂O does not cause the removal of phosphate as a calcium phosphate precipitate (7, 63). However, to ensure that the observed results were due to Ca²⁺ addition, rather than to phosphate starvation from insoluble calcium phosphate precipitation, experiments were performed with various concentrations of CaCl₂ · 2H₂O (0 to 10 mM) and phosphate (0.05, 0.49, 4.9, and 49 mM). The free phosphate in the culture supernatant was measured by using the vanadomolybdophosphoric acid method (23) following cell growth and centrifugation to remove cells and any possible precipitate. Calcium phosphate precipitates were observed when the phosphate concentration was raised to 49 mM, and when phosphate was 4.9 mM phosphate and calcium was 10 mM. No precipitate was observed in other media (including in BMM), and free phosphate was available after cell growth. Biofilms were cultivated in the absence of carbenicillin, since plasmid pMF230 is stable in these cells over the time course of these experiments without antibiotic selection and since antibiotics may influence biofilm structure.

Biofilm growth. The flow cell system for the SCLM experiments was similar to that described previously (48). Briefly, the system consisted of a once-flowthrough flow cell with a medium reservoir, pump, silicone tubing, and a waste container. The flow cell was composed of a polycarbonate support with inlet and outlet ports and a glass coverslip, for SCLM observation of the biofilms, sealed onto the polycarbonate support with a Viton gasket. The SCLM flow cells were maintained in an incubator at 37 ± 1°C during biofilm formation. Prior to inoculation into the flow cells, each strain was incubated in BMM for 16 to 20 h at 37°C. When the cell density reached approximately 1 x 10⁷ cells/ml, as determined by absorption/scattering (optical density at 600 nm [OD₆₀₀]), the cultures were diluted with an appropriate volume of sterile 0.85% NaCl solution to make a 1 x 10⁶-cell/ml inoculum. Approximately 2 ml of this culture was used to inoculate the flow cells under quiescent conditions for 20 min. Flow of sterile BMM was then initiated at a rate of 1.2 ml/min.

For FTIR, algD expression, and proteomic studies, P. aeruginosa biofilms were cultivated on the walls of silicone tubing (0.6-m length, size 18 tubing with interior volume of 40 ml), similarly to the experiments described by Sauer et al. (55). The flow system and inoculation procedure were similar to those described for the SCLM experiments. Following inoculation, sterile BMM was pumped through the tubing at a rate of 2 ml/min for 72 h. Attached cells were removed from the interior surface of the tubing by using the plunger of a 3-ml syringe. Biofilm cells were resuspended in saline solution during harvesting (approximately 150 ml).

FTIR of biofilms. Biofilms were removed from the silicone tubing and spotted onto cards with infrared transparent films (Spectrotech). Prior to spotting, the biofilms were diluted from 2- to 10-fold in saline, to optimize absorbance intensity for each biofilm. The biofilms were dried onto the cards in a laminar flow hood and stored under desiccation prior to analysis. The spectra were collected and processed as described previously (48).

Spectrometric analyses of biofilms. The concentrations of alginate were determined by using the modified carbazole method of Knutson and Jeanes (17, 33). Total protein concentration was determined by a modified version of the method of Lowry et al. (37) using reagents from Sigma Chemical Corp. (catalog no. 690-A).

SDS-PAGE analysis of extracellular proteins. For analysis of extracellular proteins from planktonic cultures, P. aeruginosa PAO1 and FRD1 were incubated overnight in BMM and then diluted 1/100 in fresh BMM and incubated with shaking at 37°C until mid-exponential phase (OD₆₀₀ of 0.4). Cells were removed by two centrifugations (12,000 x g, 30 min each). Cell pellets were used for two-dimensional gel electrophoresis analysis (described below). Trichloroacetic acid (TCA) (final concentration, 20%) was added to the supernatants, and the mixture was incubated on ice for 60 min to precipitate extracellular proteins. The mixture was centrifuged (15,000 x g, 40 min), and the protein pellets were washed five or six times with ice-cold acetone to remove residual TCA. Proteins were solubilized in denaturing protein sample buffer using a water bath sonicator. Proteins (10 µg) were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) using 4% stacking gels and 12% resolving gels (35) and analyzed by Coomassie blue staining. For analysis of extracellular proteins in biofilms, the biofilms were cultivated on silicone tubing as described above. The biofilms were harvested by adding saline to the tubing and removing biofilms with the plunger of a 3-µl syringe. The final cell solution (approximately 150 ml) was centrifuged twice to remove cells, and the cell pellets were analyzed by two-dimensional gel electrophoresis. Extracellular proteins were precipitated from the supernatants using TCA as described for the planktonic cells. N-terminal sequence analysis of proteins was performed by David McCourt (Midwest Scientific) using the Edman degradation method. Matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) mass spectrometry of proteins was performed by Anthony Haag (Mass Spectrometry Lab, University of Texas Medical Branch, Galveston, TX).

Immunoblot analysis. Extracellular extracts (5 µg protein per sample) from planktonic culture and from biofilms were separated by SDS-PAGE and then electroblotted onto nitrocellulose membranes (1). The membranes were probed with AprA antibodies (generously provided by Jeffrey Hobden, Wayne State University). Goat anti-rabbit immunoglobulin G, conjugated to horseradish peroxidase, was used as the secondary antibody. Antibody binding was detected by chemiluminescent analysis (1).

Two-dimensional gel electrophoresis of cellular proteins. Cells from planktonic and biofilm cultures were obtained as described above. Cell pellets were washed twice with saline solution and resuspended in TE buffer (10 mM Tris-HCl, 1 mM EDTA, pH 8.0) containing 0.3 mg/ml of phenylmethylsulfonyl fluoride. Cells were disrupted by sonication (12 times for 10 s, 4 W, 4°C), and the cell debris and unbroken cells were removed by centrifugation (12,000 x g, 60 min, 4°C). The protein concentrations of the supernatants were determined by using the modified Lowry assay, and 200 µg of protein was loaded per gel. Protein samples were stored as aliquots at –80°C. Two-dimensional gel electrophoresis was performed similarly to the protocol described previously (55). Proteins were loaded by in gel rehydration using 18-cm IPG strips with a pH range of 4 to 7 and rehydrated for 20 to 24 h. Solubilization buffer consisted of 9 M urea, 2.14 M thiourea, 4% CHAPS (3-[(3-cholamidopropyl)-dimethylammonio]-1-propanesulfonate), 2% (wt/vol) carrier ampholytes, 0.037 M dithiothreitol, and a trace amount of bromphenol blue. Isoelectric focusing was conducted using a Maltiphor II (Pharmacia) at 20°C. Proteins were focused for a total 28 kV · h. IPG strips were reduced and alkylated for 15 min by 11.3 mM dithiothreitol and 12 mM iodacetamide, in buffer containing 6 M urea, 4% (wt/vol) SDS, 30% (vol/vol) glycerol, 50 mM Tris-HCl, and a trace amount of bromphenol blue, pH 6.8. Strips were embedded on top of SDS-polyacrylamide gels using 0.75% (wt/vol) agarose in electrophoresis buffer. Second-dimension electrophoresis was carried out on 11% polyacrylamide gels (230 by 200 by 1 mm) using a vertical Hoefer Dalt system (Pharmacia) at 10°C using 10 mA/gel for 4 h and then 40 mA/gel for 14 to 16 h. Gels were stained for 72 h with 0.03% (wt/vol) Coomassie brilliant blue G-250 in 16% (wt/vol) ammonium sulfate, 24% (vol/vol) methanol, and 4.8% (vol/vol) orthophosphoric acid.

Catechol-2,3-dioxygenase assays for algD gene expression. The assay of XylE activity was performed as described previously (57, 68). For analysis of planktonic cultures, P. aeruginosa FRD875 algD-xylE was incubated in BMM overnight and then diluted to an OD₅₄₀ of 0.1 in fresh BMM. Cultures were incubated with shaking at 37°C and 250 rpm and sampled hourly. One-ml samples were pelleted at 13,000 x g for 15 min, and the pellets were resuspended in 1 ml of assay buffer (50 mM potassium phosphate buffer, pH 7.5, 10% acetone). Samples were kept on ice until assayed. An aliquot (20 to 50 µl) of each sample was combined with 940 to 970 µl of assay buffer containing 1.0 mM catechol, and the OD₃₇₅ was monitored over time for 10 min, during incubation at 25°C. Catechol-2,3-dioxygenase activity was measured by monitoring the formation of the reaction product 2-hydroxymuconic semialdehyde at 375 nm ( = 4.4 M^–1 cm^–1). Increase in OD₃₇₅ was measured against a 1.0-ml blank containing only assay buffer-catechol solution. The enzyme activity was recorded as the amount of enzyme required to produce 1 nmol of product per minute per µg of protein at 25°C. For analysis of gene expression activity in biofilms, P. aeruginosa FRD858 algD-xylE was cultivated on silicone tubing as described above. Attached cells were removed from the interior surface of tubing using a 3-ml syringe plunger at 24, 48, and 72 h of incubation. The cells were resuspended in BMM to give an optical density of 0.40 to 0.43 (OD₅₄₀). The catechol-2,3-dioxygenase assays were performed as described for the planktonic cells.

Pyocyanin analysis. Pyocyanin production was determined as described previously (13). P. aeruginosa was incubated for 18 h at 37°C in peptone broth (1% peptone, 1% NaCl, 1% glycerol) with 0 to 10 mM CaCl₂ and with 0 to 49 mM added phosphate. Pyocyanin was extracted from 5 ml of culture with 1 ml of chloroform. The chloroform extraction was repeated four times, and the organic fractions were pooled and evaporated. The residue was dissolved in 1 ml of 0.2 N HCl, and the amount of extracted pyocyanin was determined spectrophotometrically at 520 nm, with conversion to µg of pyocyanin per ml of culture by using the coefficient 17.1 (13, 34). Pyocyanin production is reported as µg of pyocyanin per mg of cellular protein.

SCLM analysis of biofilms. The bacteria were observed using a Leica TCS-SP confocal microscope (Leica Microsystems, Heidelberg, Germany) using a 10x or 40x objective. The green fluorescent protein was excited with the 488-nm line of an argon laser, and emission was collected at 500 to 550 nm. Confocal stacks were collected, and images were processed using Imaris 3.0 (Bitplane AG) and Adobe Photoshop. Image analyses were performed using the COMSTAT program, as described by Heydorn et al. (26).

Top Abstract Introduction Materials and Methods Results Discussion References

 
Scanning confocal laser microscopy reveals increased thickness of mucoid P. aeruginosa biofilms with added Ca²⁺. Our previous results using alginate-producing and alginate-impaired mutant strains of P. aeruginosa demonstrated that alginate contributes to the thickness of P. aeruginosa biofilms, allowing them to form microcolonies that extend from the substratum (48). Here, we observed similar results for biofilms of mucoid strain P. aeruginosa FRD1 (Fig. 1A). Using COMSTAT analysis of SCLM images, the mean and standard deviation for the thickness of FRD1 biofilms was 35 ± 10 µm at 24 h and 95 ± 21 µm at 48 h, similar to our previous findings. When biofilms were grown in the presence of added Ca²⁺ (1.0 and 10.0 mM CaCl₂), we observed as much as a 20-fold increase in biofilm thickness at 24 h (Fig. 1B), with the FRD1 biofilms averaging 670 ± 80 µm thick. The maximum thickness of these biofilms extended to both sides of the flow cell (approximately 1 mm). By 48 h the Ca²⁺-amended biofilm completely filled the flow chamber, with only small channels where the back pressure apparently caused disruption of the biofilm and allowed flow to proceed. The COMSTAT results demonstrated an approximately twofold-greater cellular biomass per area in the FRD1 biofilms without added Ca²⁺ than in the Ca²⁺-amended biofilms, suggesting that the Ca²⁺-amended biofilms were thicker but had less cellular material and greater spacing between cells. Viable cell counts, performed at 18 h of biofilm growth, also showed fewer cells in the Ca²⁺-amended biofilms. The average cell density of Ca²⁺-amended biofilms was 2.5 x 10⁷ cells/cm² compared to 1.2 x 10⁸ cells/cm² in the biofilms cultivated without added Ca²⁺.

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FIG. 1. SCLM images of P. aeruginosa biofilms at 24 h of growth. (A) P. aeruginosa FRD1 biofilm cultivated in BMM without added CaCl2, viewed at an angle; magnification, x100. (B) Angle view of FRD1 biofilm cultivated in BMM with 10 mM CaCl2; magnification, x100. (C) Top view and confocal reconstructed transverse sections of P. aeruginosa PAO1 biofilm, cultivated in BMM without added CaCl2; magnification, x400. (D) Top view and transverse reconstructions of PAO1 biofilm, cultivated in BMM with 10 mM CaCl2; magnification, x400. All cells expressed the gfp-mut2 from plasmid pMF230 for visualization with SCLM.

Biofilms of the nonmucoid strain P. aeruginosa PAO1 showed a small increase in thickness with added Ca²⁺ (Fig. 1C), compared to biofilms without added Ca²⁺. At 48 h, the PAO1 biofilms averaged 120 ± 25 µm with Ca²⁺ and 95 ± 20 µm without Ca²⁺. Cell counts showed a slight increase in the PAO1 biofilms with added Ca²⁺. The Ca²⁺-amended biofilms had 9.5 x 10⁸ cells/cm² at 18 h, compared to 6.1 x 10⁸ cells/cm² in biofilms without added Ca²⁺. A difference in the surface roughness of the biofilms was observed by SCLM and by COMSTAT analysis for the PAO1 biofilms with added Ca²⁺, compared to biofilms without added Ca²⁺ (Fig. 1C and D).

The increased thickness of FRD1 biofilms in the presence of Ca²⁺ is due to an increased amount of alginate in the biofilm extracellular matrix. We characterized the biofilms by using FTIR to provide information on the chemical constituents of the biofilm. For these experiments, biofilms were cultivated on silicone tubing and then harvested for FTIR analysis as described in Materials and Methods. Upon visual inspection, the biofilms associated with the silicone tubing showed a noticeable increase in thickness with added Ca²⁺, similar to observations of biofilms on glass substrata. FTIR revealed differences in the relative amounts of biofilm constituents in the presence or absence of added Ca²⁺. In FRD1 biofilms with no added Ca²⁺, the spectra showed dominant absorbance bands at the following (cm^–1): 1,650 (amide I), 1,545 (amide II), 1,405 (due in part to stretching of the carboxylate ion), 1,250 (due to PO stretching, COC stretching, and/or amide III), and 1,080 (PO and COH stretching). These absorbance bands are primarily the result of cellular components including protein and DNA and are found in both alginate- and non-alginate-producing strains (48). In addition to these absorbance bands, the spectra of the FRD1 biofilms had absorbances at 1,730 (CO stretching of esters), 1,615 (asymmetric stretching of the carboxylate ion—seen as a shoulder on the amide I band), 1,250 (COC of the esters), and 1,060 (COH stretching of alcohols). These additional absorbance bands are due to alginate within the biofilm matrix (48) and are identical to the bands observed for purified alginate (Fig. 2C). For FRD1 biofilms cultivated in the presence of added Ca²⁺ in the medium, the relative abundances of the absorbance bands changed, with the alginate-associated bands becoming dominant. In particular, the band at 1,615 (carboxylate ion) increased and partially obscured the amide I (1,650) and amide II (1,545) bands. The bands at 1,060 (COH) and 1,410 (carboxylate) also showed increases relative to the amide I and amide II bands, indicating an increase in the ratio of carbohydrate to cell protein. The bands associated with the ester linkage to the alginate O-acetyl group (1,730 and 1,250) also demonstrated significant increases in biofilms with Ca²⁺ addition. The increased ratio of alginate to protein in FRD1 biofilms cultivated with added Ca²⁺ was verified by using chemical analysis of these components (Fig. 2F). When biofilms were incubated with no added Ca²⁺, they produced from 0.5 to 1.0 µg of alginate per µg of cellular protein. However, when Ca²⁺ was added, the biofilms contained approximately a 10-fold increase in the amount of alginate per cellular protein, with the FRD1 biofilms having 6 µg alginate per µg of protein at 24 h and 10 µg alginate per µg of protein at 48 h.

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FIG. 2. Infrared spectra of P. aeruginosa biofilms originally cultivated on silicone tubing for 72 h. (A) P. aeruginosa FRD1 cultured in BMM with no added CaCl2. Absorbance bands associated with cell biomass include (cm–1) 1,650 (amide I), 1,545 (amide II), 1,405 (stretching of the carboxylate ion), 1,250 (PO stretching, COC stretching, and/or amide III), and 1,080 (PO and COH stretching). Absorbance bands due to alginate include (cm–1) 1,735 (CO stretching of esters), 1,615 (asymmetric stretching of the carboxylate ion), 1,250 (COC of the esters), and 1,060 (COH stretching of alcohols). (B) FTIR spectrum of FRD1 biofilm cultivated in BMM with 10 mM CaCl2, showing shift in ratios of alginate-associated bands relative to bands associated with cellular material. (C) FTIR spectrum of alginate purified from FRD1. (D) FTIR spectrum of P. aeruginosa PAO1 biofilm, cultivated in BMM with no added CaCl2, showing no bands associated with alginate. (E) FTIR spectrum of PAO1 biofilm, cultivated in BMM with 10 mM CaCl2, also showing no alginate-associated bands. (F) Amounts of alginate and protein in FRD1 biofilms, determined by colorimetric assays. Black bars, biofilms in BMM with no added CaCl2. Grey bars, biofilms in BMM with 10 mM added CaCl2.

Previous results from Wozniak et al. indicated that alginate was not a component of P. aeruginosa PAO1 biofilms (72). The FTIR spectra here verify those results. In the PAO1 biofilms without added Ca²⁺, the absorbance bands associated with cell protein were present, but not the alginate-associated bands (Fig. 2D). A similar spectrum of PAO1 biofilms was observed in the presence of added Ca²⁺ (Fig. 2E), indicating that the additional thickness and surface roughness associated with the Ca²⁺-amended PAO1 biofilms, as seen by SCLM, were not due to alginate production by these bacteria. An absorbance band at 1,060 cm^–1 was observed in PAO1 biofilms with added Ca²⁺. However, subtraction spectra of biofilms with and without added Ca²⁺ did not give the spectrum of pure alginate (data not shown), as was the case for the FRD1 biofilms (48), indicating that alginate was not associated with either of these PAO1 biofilms.

Transcriptional reporter demonstrates increased algD gene expression in FRD1 planktonic culture and in biofilms with Ca²⁺ addition. The increase in biofilm thickness and the increased amount of alginate in the P. aeruginosa FRD1 biofilms in the presence of added Ca²⁺ may have been due in part to the cross-bridging of Ca²⁺ to the alginate uronic acid residues, thereby retaining the alginate as a gel within these biofilms. However, it is also possible that Ca²⁺ addition resulted in the increased expression of the alg gene cluster and increased biosynthesis of alginate. To test this hypothesis, we used an FRD1-based algD-xylE transcriptional reporter to assay the relative amounts of algD transcription in the presence and absence of added Ca²⁺. The algD-xylE reporter is a single-copy chromosomally encoded reporter that disrupts the alg operon and blocks alginate production. As a result, cell growth of the reporter strain was similar both with and without Ca²⁺ (Fig. 3A), since carbon was not shuttled from cellular material to alginate. In planktonic culture, algD transcription was approximately threefold greater with the addition of 10 mM CaCl₂ to the medium (Fig. 3A). The increase in algD transcription with added Ca²⁺ appeared to plateau at 0.5 mM CaCl₂, having approximately the same level of transcriptional reporter activity at all added [CaCl₂] (Fig. 3B). In addition, an increased amount of accumulated alginate was detected in the culture supernatants of cells at all of the added [CaCl₂] (Fig. 3C). When the reporter strain was cultivated in biofilms, algD transcription increased in the presence of added Ca²⁺ (Fig. 3D). At 24 and 48 h of growth algD transcription was approximately eightfold greater than without added Ca²⁺. The increase in transcription with added Ca²⁺ continued at 72 h. The results indicate that the alginate increase observed by FTIR was due at least in part to increased transcription of the alg gene cluster with added Ca²⁺ and not solely due to increased cross-bridging of the alginate polymer.

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FIG. 3. Effect of Ca2+ on alg expression measured by using an algD>xylE transcriptional fusion. (A) XylE activity of P. aeruginosa FRD875 algD>xylE cells in planktonic culture showing increased alg expression with added Ca2+. Open triangles, XylE activity of cells in BMM. Closed triangles, XylE activity data in BMM with 10 mM CaCl2. Open circles, cell growth of P. aeruginosa FRD875 algD>xylE in BMM measured as total cellular protein. Closed circles, total protein of cells grown in BMM with 10 mM CaCl2. Error bars represent the standard deviations of four samples using duplicate experiments. (B) Effect of [CaCl2] on alg expression at 18 h of planktonic growth, measured as XylE activity. (C) Effect of [CaCl2] on alginate production of FRD1 in planktonic culture at 18 h. (D) Effect of Ca2+ on alg expression by P. aeruginosa FRD875 algD>xylE, cultivated in biofilms. Black bars, XylE activity of cells cultured in BMM. Grey bars, XylE activity of cells in BMM with 10 mM CaCl2. Error bars represent the standard deviations of three to four replicates. Cells exposed to 0.5 to 10.0 mM CaCl2 exhibited significantly different XylE activity (P < 0.05) and alginate production (P < 0.01) compared to cells cultured in 0 mM CaCl2 HMA, 2-hydroxymuconic semialdehyde.

The alginate matrix in Ca²⁺-induced biofilms harbors other extracellular virulence factors. An inverse regulatory relationship was found to exist between alginate production and the extracellular protease LasA (47). However, Ca²⁺ is known to affect the production and/or stability of certain extracellular proteins of P. aeruginosa (52, 75). To determine if Ca²⁺ addition affects expression and/or stability of extracellular proteins from an alginate-producing strain, we extracted cell supernatants of P. aeruginosa FRD1 cultured in BMM with and without added Ca²⁺. With no added Ca²⁺, strain FRD1 had little extracellular protein, as predicted from the previous studies (47). However, with increased [CaCl₂], strain FRD1 had three dominant bands in culture supernatants. We excised the bands and identified the proteins by N-terminal sequence analysis. The 49-kDa band was identified as alkaline metalloprotease AprA (24), the 33-kDa band was identified as elastase LasB (4, 31), and the 27-kDa band is the PrpL protease (65). To ensure that the increased amounts of proteases were due to Ca²⁺ addition and not due to PO₄^3– limitation (by possible PO₄^3– precipitation as calcium phosphate), experiments were performed with various concentrations of Ca²⁺ and PO₄^3– as described in Materials and Methods. At each PO₄^3– concentration there was an increase in the extracellular proteases with increasing Ca²⁺, including medium with greater concentrations of PO₄^3– to Ca²⁺ (1 mM Ca and 4.9 mM PO₄^3–), indicating that the increased amounts of proteases were due primarily to Ca²⁺ addition, and not to PO₄^3– starvation.

Since Ca²⁺ addition caused an increase in the amounts of both alginate and extracellular proteases, we tested the possibility that AprA (the most dominant band in the culture supernatants) was harbored within the alginate biofilm matrix. The extracellular matrix of biofilms from Ca²⁺-amended cultures and cultures lacking added Ca²⁺ was extracted, and the alginates were degraded by using an alginate lyase to release the extracellular proteins from the biofilm matrix. Immunoblot assays were performed on the extracted matrix material using an AprA antibody. Only a faint band was observed in the matrix of P. aeruginosa FRD biofilms cultivated without added Ca²⁺, and no band was observed in biofilms of the aprA deletion mutant strain, P. aeruginosa FRD1252 aprA::aacCI (Fig. 4B). However, a pronounced AprA band was observed in biofilm extracts of the Ca²⁺-amended biofilms, indicating that this protein was maintained in the matrix of these biofilms.

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FIG. 4. (A) Coomassie blue-stained gel of extracellular proteins produced by planktonic cultures of P. aeruginosa FRD1. Lane 1, proteins from cells cultured in BMM. Lane 2, proteins from cells cultured in BMM with 10 mM CaCl2, showing increased amounts of AprA, LasB, and PrpL. Proteins were identified by N-terminal sequence analysis. (B) Immunoblot of extracellular matrix material from 72-h P. aeruginosa FRD1 biofilms using AprA antibodies. Lane 1, FRD1 in BMM. Lane 2, FRD1 in BMM with 10 mM CaCl2. Lane 3, FRD1252 aprA::aacCI in BMM. Lane 4, FRD1252 aprA::aacCI in BMM with 10 mM CaCl2.

We tested whether the AprA protein contributes to biofilm three-dimensional structure, by comparing SCLM images of P. aeruginosa FRD1 and P. aeruginosa FRD1252 aprA::aacCI. No significant difference was observed between biofilms of these strains (data not shown), indicating that AprA does not have a substantial effect on the structural integrity of the FRD1 biofilms. We also found no difference between the structure of the FRD1 biofilm and those of biofilms of P. aeruginosa FRD1043 calA::aacCI (data not shown), indicating that the gene PA4107, which encodes a putative calmodulin-like protein, also does not play a significant role in calcium-induced biofilm structure.

Phenazine biosynthetic proteins are affected by calcium and by biofilm growth. In addition to the extracellular proteins, we analyzed cellular proteins by two-dimensional gel electrophoresis to determine if Ca²⁺ addition and biofilm growth affect the presence or amounts of certain cellular proteins. Of the protein differences observed, several of the proteins were gel extracted and analyzed by MALDI-TOF mass spectroscopy. Two of the proteins identified as being induced by Ca²⁺ in planktonic culture were the phenazine biosynthetic proteins PhzB2 and PhzG (Fig. 5). These proteins are involved in the synthesis of the phenazine-based redox cycling compound pyocyanin and are encoded on two separate operons (44, 62). To compare protein amounts of PhzB2 and PhzG, we compared protein spot signal intensities for duplicate gels under the four conditions (planktonic growth versus biofilms at 0 mM versus 10 mM added CaCl₂). The results showed that Ca²⁺ addition resulted in a threefold increase in PhzB2 amount during bacterial growth in planktonic culture (Fig. 5A and B). PhzB2 showed increased amounts in biofilms compared to planktonic culture (Fig. 5C and D), with an approximately eightfold increase in biofilms versus planktonic culture at 0 mM CaCl₂ and a threefold increase in biofilms at 10 mM CaCl₂. In biofilms [CaCl₂] had little effect on PhzB2 amounts, with the protein spot signal intensities being similar at both 0 and 10 mM CaCl₂. The amount of PhzG increased approximately fourfold in planktonic culture with the addition of CaCl₂ to the medium (Fig. 5E and F). In biofilms, this protein was 25- to 30-fold greater than its amount in planktonic cultures (Fig. 5G and H) whether or not Ca²⁺ was added.

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FIG. 5. (A to D) Sections of two-dimensional gels showing the effect of Ca2+ and biofilm growth on pyocyanin biosynthetic protein PhzB2 of P. aeruginosa FRD1 under the following conditions: (A) planktonic culture in BMM, (B) planktonic culture in BMM plus 10 mM CaCl2, (C) biofilm culture in BMM, and (D) biofilm culture in BMM plus 10 mM CaCl2. (E to H) Sections of two-dimensional gels showing effect of Ca2+ and biofilm growth on PhzG of P. aeruginosa FRD1 under the following conditions: (E) planktonic culture in BMM, (F) planktonic culture in BMM plus 10 mM CaCl2, (G) biofilm culture in BMM, and (H) biofilm cultured in BMM plus 10 mM CaCl2.

To determine if Ca²⁺ affects production of the P. aeruginosa phenazine product pyocyanin, we assayed pyocyanin production in planktonic culture with and without added CaCl₂. Over time, pyocyanin production was approximately two- to threefold greater when cultures were incubated with 10 mM CaCl₂ than when no CaCl₂ was added to the medium (Fig. 6). When the [PO₄^3–] was varied over a range of 0.05 to 4.9 mM, an increase in pyocyanin production was observed for cultures with 1 mM added Ca²⁺ compared to cultures with no added Ca²⁺, indicating that the observed increase was due to Ca²⁺ addition and not to PO₄^3– starvation.

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FIG. 6. Effect of Ca2+ on pyocyanin biosynthesis by P. aeruginosa FRD1. Diamonds, pyocyanin production in peptone broth planktonic culture. Squares, pyocyanin production in peptone broth plus 10 mM CaCl2.

Top Abstract Introduction Materials and Methods Results Discussion References

 
The results presented here show that the biofilm extracellular matrix of a mucoid strain of P. aeruginosa in Ca²⁺-amended cultures is composed primarily of alginate. Extracellular proteases are present in the extracellular material with the alginate matrix acting as a reservoir to maintain these proteases in the biofilms. Although present, the protease AprA does not play a significant role in the structural integrity of these biofilms. The biofilm matrix also likely contains pyocyanin, since proteins for pyocyanin biosynthesis show increased amounts in biofilm cultures and in cultures amended with Ca²⁺. The extracellular matrix of a mucoid P. aeruginosa biofilm where little Ca²⁺ is present is composed primarily of alginate, with lesser amounts of extracellular proteins.

These results confirm previous findings of both Nivens et al. and Wozniak et al. that alginate is not required for biofilm formation by nonmucoid strains of P. aeruginosa (48, 72). Nivens et al. demonstrated that nonmucoid variants of P. aeruginosa FRD1 were capable of biofilm formation and that no alginate was associated with those biofilms. Using P. aeruginosa PAO1, which does not produce alginate under known conditions, Wozniak et al. demonstrated that this strain was capable of biofilm formation in the absence of alg gene expression. The FTIR results shown here (Fig. 2) confirm that no alginate is associated with PAO1 biofilms. However, in biofilms of the mucoid CF pulmonary isolate FRD1, alginate constitutes the major component of the extracellular matrix material.

The surprising finding here is that Ca²⁺ addition has a major effect on the extracellular matrix of the mucoid P. aeruginosa biofilms, including the amount of alginate produced. Alginate biosynthesis is regulated by a complex hierarchy of proteins (71), including the stress response sigma factor ^e (11, 15, 41). In nonmucoid strains, isolated from environmental sources other than chronic CF pulmonary infections, this sigma factor is sequestered in the membrane by the antisigma factor MucAB (40, 43). Nonmucoid strains show no evidence of alginate production under any environmental conditions described, including in biofilms (72). Alginate-producing strains isolated from the pulmonary fluid of CF patients often have a mutation in mucA (40), causing release of ^e from membrane sequestration and subsequent expression of the ^e-controlled regulon, including the alginate biosynthetic gene cluster (43). Dehydration and high osmolarity have been shown to play roles in alg gene expression in a mucoid strain (3, 10). The results here show that another environmental parameter, Ca²⁺, also affects the amount of alginate produced by a mucoid strain (Fig. 2 and 3). The addition of Ca²⁺ causes at least a threefold increase in alg gene expression during P. aeruginosa FRD1 growth in planktonic culture and as much as an eightfold increase in alg gene expression during biofilm growth. This increase in alg expression results in biofilms that contained 5 to 10 mg of alginate per mg of protein. Biofilms without added Ca²⁺ had approximately 0.5 to 1.0 mg alginate per mg of protein. The increased amount of alginate in Ca²⁺-amended cultures results in biofilms that are as much as 20-fold thicker than those without added Ca²⁺ (Fig. 1). The mechanism for enhanced alg expression caused by Ca²⁺ addition is not known. However, the results suggest that a Ca²⁺-controlled factor(s) may be involved in alg gene regulation, either through a previously identified regulator, such as one of the two-component sensory systems known to be involved in alg regulation (9, 22, 70), or through another regulatory factor that has not yet been identified. In biofilms, Ca²⁺ may play an additional role in the observed increase in biofilm thickness by ionic cross-linking and gelling of the uronic acid residues, thereby modifying the biofilm architecture.

Another surprising finding is the Ca²⁺-induced production of proteinaceous extracellular material in mucoid P. aeruginosa. Previously, an inverse regulatory relationship between expression of alginate biosynthetic genes and expression of LasA was described (47). When P. aeruginosa establishes chronic infections on the pulmonary tissue of CF patients, it synthesizes the immunoprotective compound alginate and represses other immune stimulatory factors, such as extracellular proteins and flagellin (67). In the absence of added Ca²⁺, this phenomenon is corroborated here, since little to no extracellular proteins were observed in cultures where no Ca²⁺ was added to the medium (Fig. 4). However, when Ca²⁺ was added, intense protein bands of AprA, LasB, and PrpL were observed. These proteins were expressed concomitantly with the alg genes, indicating that, although an inverse relationship between alg expression and protease expression may exist, this relationship is dependent on environmental factors, and particularly on the presence of Ca²⁺. The proteases are maintained in the alginate extracellular material, making them components of the P. aeruginosa biofilm extracellular matrix. Since these data are based on protein amounts, Ca²⁺ may affect gene expression, protein stability, or a combination of those two factors.

Also present in the extracellular matrix of Ca²⁺-induced mucoid P. aeruginosa biofilms is the redox cycling compound pyocyanin. The results show that at least two of the pyocyanin biosynthetic proteins, one on each phenazine biosynthetic operon, are induced by Ca²⁺ addition and are also induced by biofilm-associated growth (Fig. 5). The chemical analysis showed increased production of pyocyanin with Ca²⁺ addition in P. aeruginosa FRD1 (Fig. 6). Pyocyanin has been detected in the pulmonary fluid of CF patients (66), suggesting that these operons may be induced in vivo. In addition, using DNA microarray analyses, Wolfgang et al. have demonstrated that the phenazine biosynthetic genes, including both phzB2 and phzG, are induced by mucopurulent respiratory liquids from CF patients (67). Therefore, it is likely that the in vivo Ca²⁺ concentration in pulmonary fluid of CF patients is sufficient for induction of the phenazine biosynthetic genes. Pyocyanin is a redox cycling compound that has a number of effects on host cells, including an effect on the vacuolar ATPase (54). Among other functions, the vacuolar ATPase is important for maintaining cytosolic Ca²⁺ levels in Saccharomyces cerevisiae (16). Pyocyanin has been shown to disrupt calcium homeostasis of human epithelial cells (8). Therefore, pyocyanin production, induced in biofilms and by Ca²⁺, may contribute to altered calcium levels in pulmonary fluid of CF patients and to further induction of the other Ca²⁺-regulated factors.

The mechanism for calcium regulation in bacteria is not known. Calcium plays a regulatory role for channels and transporters (50). Calmodulin-like proteins have been proposed to have originated in high-G+C gram-positive bacteria and ultimately to have been acquired by eukaryotes (76). A calmodulin-like protein and regulator have been described in Sinorhizobium etli and shown to play a role in development of bacteroids during symbiosis of this bacterium with its leguminous host (73). P. aeruginosa encodes a protein with EF-hand motifs (PA4107) (62) characteristic of calmodulin-like proteins. However, deletions of the gene for this protein did not have a regulatory effect on any of the Ca²⁺-induced factors described here, indicating that this protein does not play a regulatory role in the production of these compounds.

 
We thank David McCourt for providing the N-terminal sequence analyses and Anthony Haag for providing the MALDI-TOF analysis. We thank Daniel Wozniak for providing P. aeruginosa FRD875 algD>xylE and Jeffrey Hobden for providing the AprA antiserum.

This work was supported by Public Health Service grant AI-46588 (M.J.F.) from the National Institute of Allergy and Infectious Diseases.

 
* Corresponding author. Mailing address: Department of Microbiology, 109 Lewis Hall, Montana State University, Bozeman, MT 59717. Phone: (406) 994-2420. Fax: (406) 994-4926. E-mail: umbfm{at}montana.edu.

Top Abstract Introduction Materials and Methods Results Discussion References

 

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Journal of Bacteriology, July 2005, p. 4327-4337, Vol. 187, No. 13
0021-9193/05/$08.00+0     doi:10.1128/JB.187.13.4327-4337.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

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