The assembly of the EPS matrix in 3D

We examined over time the morphogenesis of mixed-species biofilms on saliva-coated apatitic (sHA) discs. We focused on the development of the architecture in three-dimensions (3D), which is associated with the early accumulation of EPS on the sHA surface and the subsequent construction of an EPS-rich matrix. The formation and the sequence of assembly of the EPS matrix are heavily influenced by the type of sugars included in the test system (Figure 1A). Following the introduction of 1% sucrose, a heterogeneous layer of EPS is formed on the sHA surface, and localized accumulations of microorganisms are observed on the EPS surface after 43 h (Figure 1Ag; see arrows). After 67 h of development (Figure 1Ah), the cells are densely packed with EPS, forming a 3D bacterial structure (termed EPS-microcolony complex; highlighted in Figure 1Ah). After 115 h, the size of these bacterial structures had increased in several dimensions; they became more enmeshed in, and surrounded by, the EPS-matrix as time elapsed (Figure 1Ai). Two distinct locations of EPS-microcolony complexes were observed: those attached to the EPS layer formed on the sHA (Figure 1Ah), and those tethered to the body of the matrix, near the fluid interface (highlighted in Figure 1Ai). These observations, made when sucrose is abundant (1%) in the test system, are in marked contrast from those made when sucrose was limited (0.1%) or was replaced completely by glucose. A thin EPS layer on the sHA surface, and a few small EPS-attached microcolonies (at later stages) were detected in biofilms formed with 0.1% sucrose (Figure 1Ad–f). When 1% glucose was present, neither an EPS layer nor 3D bacterial islets were assembled. Rather, a thin and mostly homogenous accumulation of bacterial cells adherent to the sHA surface was observed (Figure 1Aa–c). The close-up images reveal that the structural organization of the accumulated cells lacking an EPS matrix is based primarily on cell to cell binding (co-aggregation).

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Figure 1. Dynamics of the morphogenesis, 3D architecture development and microbial population shifts of mixed-species biofilms.

(A) Representative 3D rendering images of mixed-species biofilms at distinct time points. Images (a–c) represent biofilms formed after the introduction of 1% (w/v) glucose. Images (d–f) represent biofilms formed in the presence of 0.1% (w/v) sucrose. Images (g–i) represent biofilms formed after the introduction of 1% (w/v) sucrose. The EPS channel is depicted in red, while the cells are depicted in green. At the upper left of each panel, the two channels are displayed separately, while the merged image is displayed at the bottom right. Lateral (side) views of each biofilm are displayed at the bottom left, while a magnified (close-up) view of each small box depicted in the merged image is positioned in the upper right corner of each panel. (B) The data are mean values ± s.d. (n = 30). The asterisks (*) indicate that the each of the values (EPS and bacterial biomass) in the 1% sucrose group are significantly different from others (P<0.05, Tukey-Krammer HSD). (C) Bacterial species [S. mutans (10² CFU/ml), A. naeslundii (10⁶ CFU/ml), and S. oralis (10⁷ CFU/ml)] were inoculated in the culture medium supplemented with 0.1% (w/v) sucrose until 29 h for establishment of the initial biofilm community [S. oralis (5.6±3.5×10⁶ CFU), A. naeslundii (9.4±6.5×10⁴ CFU) and S. mutans (8.8±2.5×10³ CFU)]. The biofilms were then challenged with an environmental change by introducing 1% (w/v) sucrose (B-2) or 1% (w/v) glucose (B-3). Viable populations of S. mutans, S. oralis, and A. naeslundii recovered from the biofilms were counted (number of CFU recovered per biofilm) over time, and the proportion of each strain at each time point was calculated based on CFU data. Microbial population at 115 h in: 1% sucrose (1.1±0.2×10¹¹ CFU of S. mutans; 2.1±2.9×10⁹ CFU of S. oralis; 1.7±0.4×10⁷ CFU of A. naeslundii), 0.1% sucrose (6.7±0.8×10⁹ CFU of S. mutans; 1.4±1.9×10¹⁰ CFU of S. oralis; 9.3±1.3×10⁹ CFU of A. naeslundii), and 1% glucose (2.6±1.9×10⁹ CFU of S. mutans; 3.2±0.4×10¹⁰ CFU of S. oralis). The data are mean values ± s.d. (n = 12). The asterisks (*) indicate that the values from each strain are significantly different from each other (P<0.05).

https://doi.org/10.1371/journal.ppat.1002623.g001

The presence of 1% sucrose also increased the biomass of the biofilms as a consequence of the assembly of an EPS-rich matrix and the development of the architecture in 3D. Sucrose-grown biofilms resulted in thicker biofilms containing up to 10-fold more EPS (and also more bacterial biomass) than those formed with 1% glucose at 115 h (Figure 1B; P<0.05). The essential role S. mutans and/or its products played in the development of the 3D architecture was revealed by the failure to assemble any matrix or EPS-enmeshed microcolonies when S. oralis and A. naeslundii were cultured together in the absence of S. mutans [22].

The availability of specific carbohydrates also influences the proportion of the bacterial species during mixed-species biofilm development. At the baseline, before introduction of 1% sucrose, bacterial cells on the sHA surface were comprised mainly of S. oralis and few A. naeslundii cells, with S. mutans as the least abundant species (P<0.05; Figure 1C). However, the introduction of 1% sucrose (at 29 h) had a dramatic effect. The proportion of S. mutans rapidly increased, as it became the dominant species within 115 h-old biofilms (Figure 1B-2; P<0.05; CFU values in the figure legend). In contrast, under carbohydrate-limited conditions (0.1% sucrose), the proportions and the number of the bacterial species on the sHA surface were equally distributed (115 h end-point, Figure 1B-1; P>0.05). Introduction of 1% glucose (in the absence of sucrose) resulted in a population dominated by S. oralis throughout the biofilm development period (Figure 1B-3; P<0.05).

As might be expected, the pH in the culture medium surrounding the biofilm also changes over time. The pH values in the culture medium after the introduction of 1% sucrose or 1% glucose were not significantly different from each other (final pH 4.2 to 4.7), but were lower than those in the medium containing 0.1% sucrose (sugar-limiting condition, pH 6.1 to 6.2; P<0.05) (see Table S1).

The introduction of 1% sucrose and its subsequent metabolism by S. mutans induces the transition from a non-virulent microbial community (high levels of S. oralis and small numbers of S. mutans; [11], [30]) to a highly acidogenic and aciduric population. The data reveal the importance of EPS production on surfaces, which provides a continuum of adhesion sites for glucan-binding pathogens (e.g. S. mutans), while simultaneously generating a matrix with complex 3D architectures that can create uniquely structured low pH environments.

Dynamics of expression of S. mutans EPS-associated genes and proteins

The EPS biogenesis machinery of S. mutans (triggered by sucrose) can be affected over time by changes in the environmental conditions and by the presence of other members of the biofilm community [4], [11], [15]. We explored how the introduction of 1% (w/v) sucrose influences the expression of EPS-related genes and proteins in S. mutans during mixed-species biofilm formation and maturation. S. mutans produces three glucosyltransferases (encoded by gtfB, gtfC and gtfD) and an endodextranase (dexA) that participate in the synthesis and degradation of glucans [31], [32]. In addition, a fructosyltransferase and a fructan hydrolase (ftf and fruA, respectively) [33] catalyze the synthesis and breakdown of fructans composed predominantly of β-2,1 linkages [34].

The expression profiles of the S. mutans gtfBCD, dexA, ftf, and fruA genes and their products are shown in Figure 2. The data reveal that the expression of gtfB, gtfC, and dexA was significantly induced between 43 and 67 h (during the transition from initial cell accumulation to EPS-microcolony development on the sHA surface) compared to the level of expression at other time points (e.g. 91 and 115 h) (Figure 2A). MudPIT analyses indicated that the abundance (i.e. spectral counts) of GtfB and GtfC were elevated within the biofilms at 67 h (Figure 2C), showing that greater amounts of these proteins were proportionally present compared to the later time point (115 h). The induction of these exoenzymes at earlier stages of biofilm development is highly relevant for the assembly of the EPS-rich matrix. The secreted Gtfs bind to sHA and bacterial surfaces, displaying enhanced enzymatic activity when bound [4], [17]. The surface-adsorbed GtfB and GtfC enzymes produce large amounts of glucans in situ, wherein S. mutans binds in high numbers [19]. As a result, it promotes local accumulation of both EPS and bacterial cells.

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Figure 2. Expression of Streptococcus mutans EPS-associated genes and proteins during mixed-species biofilm development.

(A) This panel shows RT-qPCR analysis of gtfB, gtfC, gtfD, fruA, ftf and dexA gene expression by S. mutans in mixed-species biofilms at specific time points after introduction of 1% (w/v) sucrose. The data shown are mean values ± s.d. (n = 12). The asterisks (*) indicate that the expression level of gtfB, gtfC (at 67 h) is significantly different from other time points (P<0.05, Tukey-Krammer HSD). (B) This panel displays RT-qPCR analysis of gtfB, gtfC, and dexA gene expression by S. mutans in single- or mixed-species biofilm at 67 h, after introduction of 1% (w/v) sucrose. The data shown are mean values ± s.d. (n = 12). The expression level of the specific S. mutans genes is significantly different between single- and mixed-species biofilms (P<0.05). (C) This panel contains MudPIT analysis of expression of EPS-related proteins by S. mutans in mixed-species biofilms at specific time points after introduction of 1% (w/v) sucrose (n = 2). Spectral counts were used for quantification of proteins in each of the time points tested; standard deviations for protein data are not shown in the table. (D) This panel depicts MudPIT analysis of the abundance of GtfB, GtfC, and DexA by S. mutans in single- or mixed-species biofilms at 67 h after introduction of 1% (w/v) sucrose (n = 2). Spectral counts were used for quantification of proteins in each of the time points tested; standard deviations for protein data are not shown in the table.

https://doi.org/10.1371/journal.ppat.1002623.g002

Biofilms found in nature, such as dental plaque, are usually composed of mixed-species. The influence that one species within a biofilm has on the gene expression of another species within the same biofilm has not been fully explored. We investigated the expression of gtfB, gtfC and dexA in S. mutans cells grown in single-species compared to those grown in mixed-species biofilms (after introduction of 1% sucrose). Expression of S. mutans gtfB and gtfC, and to a lesser extent dexA, were elevated in mixed-species biofilms compared to that observed in single-species biofilms (P<0.05; Figures 2B and 2D), which resulted in elevated amounts of the respective proteins in the milieu. It is likely that gtfB and gtfC were induced in the presence of the other oral species by autoinducer molecules, such as Al-2 [35]. The interspecies signaling mediated by the LuxS system (associated with Al-2 synthesis) has been shown to modulate S. mutans biofilm formation [36] by enhancing the expression of gtfB and gtfC but not the gtfD gene [37]. This observation is congruent with our gene/protein expression data. Deficient biofilm formation in an S. mutans luxS mutant can be complemented by the Al-2 produced by several bacteria in vitro, although not by S. oralis ATCC 10557 [37] (a different strain, not ATCC 35037, which we used in this study). The exact mechanisms of how Al-2 based signaling up-regulates Gtfs in S. mutans within mixed-species biofilms have not been fully elucidated. Whether additional signaling molecules are released by these co-habitants that might suppress gtfs expression in S. mutans remain to be determined.

Noticeably, the magnitude of the gtfBC transcript response was greater than the expected increase in the abundance of the respective proteins. This apparent discrepancy is likely due to differences in the sensitivity of protein (spectral counts by MudPIT) and mRNA transcript (RT-qPCR) detection technologies. In addition, it is possible that post-transcriptional controls can alter protein levels via gene-specific control of translation, or can affect the balance between mRNA stability and degradation [38].

The molecular mechanisms involved with the assembly of the matrix are poorly understood because the basic knowledge about the regulation and temporal production of EPS within mixed-species biofilms are still lacking [5]. We show that the expression of gtfB and gtfC is enhanced during the early stages of biofilm development and in the presence of other organisms. The synthesis of EPS by these exoenzymes may have direct implications with the sequential construction and the architecture of the matrix.

The role of GtfB and GtfC in the assembly of structured 3D matrix

The influences of the concerted actions of GtfB and GtfC in the formation and structural organization of biofilm matrix were further explored by means of gene deletion studies. Deletion of both gtfB and gtfC markedly impaired the ability of the mutant strain to assemble an EPS layer on the sHA surface or further synthesize a 3D EPS-rich matrix. The mutant strain was also unable to form EPS-microcolony complexes on sHA surfaces (vs. mixed-species biofilms formed in the presence of the parental strain S. mutans UA159; Figure 3A). Close-up images reveal mostly cell to cell co-aggregation (similar to that observed in 1% glucose group). COMSTAT and DUOSTAT analyses confirmed the absence of any detectable microcolony structures, a reduction in the overall biofilm biomass, and a virtual lack of EPS (data not shown).

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Figure 3. Mixed-species biofilms formed with S. mutans ΔgtfBC::kan or with parental strain UA159 treated with mutanase.

The biofilms were formed in the presence of the gtfBC null mutant (A) or parental strain UA159 (B) with 1% (w/v) sucrose. Selected areas in (A) and (B) show detailed views of separated and merged confocal images of bacterial cells (green) and EPS (red). The biomass values of EPS and bacterial cells in the biofilms were calculated using COMSTAT. The data shown are mean values ± s.d. (n = 15).

https://doi.org/10.1371/journal.ppat.1002623.g003

The deletion of each of these genes individually resulted in distinctive patterns of EPS and bacterial accumulation on apatitic surfaces (Figure S1). When the gtfB null mutant was used to form biofilms, the initial EPS layer was detected, but the assembly of EPS-microcolony complexes was completely abolished (Figure S1). In contrast, when the gtfC null mutant was used in the system, the initial EPS-layer formation was greatly impaired while a few small microcolonies (vs. biofilm with UA159) were detected on the sHA surface (possibly associated with still functional gtfB).

The surface-formed glucans produced by GtfB (in particular) and GtfC are rich in α-1,3-linked glucose [39], conferring a highly insoluble and structurally rigid polymer that may be critical for the construction of a 3D matrix architecture. We investigated whether digestion of α-1,3 glucosyl-linkages would impact the structural integrity of the EPS-matrix and EPS-microcolony complexes. Introduction of mutanase (α-1,3 glucanase; EC 3.2.1.59), after biofilm formation, essentially caused the collapse of the matrix architecture (Figure 3B). The absence or removal of the insoluble glucans dismantled the framework of the matrix on which cell-associated glucan binding proteins can bind in situ. Thus, a lack of insoluble glucan eliminated any structural cell to matrix bridging, causing the disassembly of the EPS-microcolony (see selected area in Figure 3B). COMSTAT analysis also confirmed that there was a substantial reduction in the biomass of both the cellular and EPS components of the biofilms following mutanase treatment (Figure 3B). The data clearly demonstrate that α-1,3-linked glucans (only present in GtfB and to lesser extent in GtfC-derived glucans) are critical for the structural integrity of a 3D matrix and microcolonies; this observation is in agreement with the results derived from the genetic studies.

The location of GtfB- and GtfC-derived polysaccharides may modulate the sequential assembly of the matrix. Each of the secreted Gtfs binds to a particular surface in an enzymatically active form. GtfC has the greatest affinity for the pellicle, whereas GtfB binds preferentially to microbial surfaces [4]. The glucans synthesized by GtfC assemble the initial EPS layers on the sHA surface, which provide enhanced binding sites for S. mutans [18], [19], [40]. The highly insoluble, branched, and structurally rigid glucans (rich in α-1,3 linkages) formed by GtfB embed the cells, contributing to the scaffolding of the EPS matrix. In addition, the Gtfs can bind to self-produced glucans, influencing the further growth of the matrix in situ [4]. The local accumulation of EPS and bacterial cells mediate the construction of 3D EPS-microcolony complexes through cell-matrix adhesions within mixed-species biofilms. Thus, the enhanced expression of both gtfB and gtfC by S. mutans in the presence of A. naeslundii and S. oralis (Figure 2B–D) could explain why the size of the microcolonies formed in mixed-species biofilms is larger than those in single-species biofilms (Figure S2).

The mutants lacking the gtfB and/or gtfC genes are essentially non-virulent in vivo, as determined using a well-established rodent model of dental caries [41]. Furthermore, treatment with an egg-derived antibody raised against cell-associated GtfB (that inhibits enzymatic activity) markedly reduced the development of carious lesions in rats [42]. These observations demonstrate the importance of EPS synthesis in the expression of biofilm virulence. However, how this phenomenon is associated with the assembly of the 3D EPS matrix and what its spatial arrangement is with bacterial cells remain to be elucidated. Early studies used only simple cell-labeling methods [4].

Spatial arrangement between EPS and bacterial cells during the construction of 3D EPS-microcolony complexes

The formation of densely packed bacterial islets is mediated through cell-matrix interactions over time. Therefore, we examined the spatial arrangement of EPS and bacterial cells at each of the developmental stages during morphogenesis of mixed-species biofilms (Figure 4). The same scale was used to demonstrate the three-dimensional evolution of EPS-mediated bacterial aggregation over time (Figure 4A). The cross-sectional images for each time point are shown in Figure 4Ab–m. EPS is detected (1) between the bacterial cells, (2) surrounding, (3) covering, and (4) filling the spaces between the microcolonies, bridging them together and tethering them to the sHA surface.

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Figure 4. Structural arrangement between EPS and bacterial cells during the assembly of surface-attached EPS-microcolony complex.

(A) This figure gives representative images of 3D renderings of mixed-species biofilms after introduction of 1% (w/v) sucrose. Panel (a) shows the dynamic evolution of surface-attached microcolonies over time. Panels (b–m) show cross sectional images of selected area for close-up views of the structural organization of EPS (red) and bacterial cells (green) during the development of an EPS-microcolony complex. The arrows indicate EPS bridging (i, j) and providing support for aggregation of multiple microcolonies (l, m). (B) The amount of co-localization between bacteria and EPS was calculated using DUOSTAT. The graph shows the percentage of bacteria and EPS colocalized within the biofilm over time (mean values ± s.d; n = 15). The asterisks (*) indicate that the values from each time point are significantly different from each other (P<0.05, Tukey-Krammer HSD).

https://doi.org/10.1371/journal.ppat.1002623.g004

Based on the location of EPS, we speculate that polysaccharide-mediated biofilm construction forms complex 3D bacterial islets through the following sequence: initial adhesion, cell clustering (Figure 4Ab–d), and formation of a core of EPS-enmeshed bacterial cells that provides a supporting framework to facilitate microcolony establishment (Figure 4e–g). The transition from initial cell clustering to microcolony formation bears some similarities to the transition mediated by PsL (an exopolysaccharide) in Pseudomonas aeruginosa biofilms [8]. As the biofilm matures, EPS also surrounds individual microcolonies and appears to bridge them (Figure 4Ah–j), resulting in the formation of multi-microcolony aggregates (Figure 4Ak–m). Results from computational analyses show that >80% of the total cells are co-localized with EPS at 115 h (Figure 4B), as an increasing amount of the bulk of biofilm is composed of polysaccharides (congruent with our confocal images). We suggest that individual microcolonies encased in polysaccharides may serve as architectural units that become connected during biofilm construction, forming compartmentalized networks that confer highly heterogeneous yet cohesive environments within the 3D architecture.

The adhesion between the bacterial cell and the EPS-matrix may be mediated in part through cell-surface glucan-binding protein C (GbpC) and possibly GbpB, both of which are expressed by S. mutans [4], [43]. Secreted (extracellular) GbpA and GbpD may also bind to and provide cross-linking between glucans on the sHA surface and those on bacterial surfaces [4], [43], thus contributing to the maintenance of the 3D architecture. Furthermore, extracellular DNA (eDNA) may have a structural function in the extracellular matrix. eDNA enhances S. mutans adhesion and surface aggregation [44] and could be incorporated during EPS-rich matrix development by binding to bacterial cells and to exopolysaccharides [23], possibly contributing to the formation of microcolonies.

The assembly of EPS-matrix changes the biofilm architecture in 3D while the bacterial populations are dynamically shifted towards dominance of S. mutans, a Gtf-producing, glucan-binding and aciduric/acidogenic pathogen. Concomitantly, EPS-microcolony complexes are formed in specific regions within the biofilms (bound to the sHA surface and tethered to the matrix) via localized cell to matrix adhesions, while other areas are devoid of such structures. This highly heterogeneous architecture and assembly of a variety of bacterial islets, particularly those in close proximity to sHA, may create ecological and environmental niches that are essential for biofilm virulence.

Relevance of biofilm-matrix architecture in virulence

Acid production alone may not be the key factor in the expression of virulence, but rather how and where acidic microenvironments are formed and maintained within the biofilm. Results from previous studies reveal average pH values in biofilms. In contrast, our data show punctate areas of low pH values that are heterogeneously distributed within complex 3D biofilm architecture.

Creation of localized acidic microenvironment.

The in situ pH mapping of the biofilm shows spatially heterogeneous pH microenvironments throughout the 3D biofilm architecture, despite the presence of buffered neutral pH in the external environment (Figure 5A). The darker areas in the pH profile represent acidic pH values, whereas the brighter areas represent pH values that are close to neutral (indicated by the pH-visualization bar in Figure 5A).

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Figure 5. Three-dimensional pH mapping of intact mixed-species biofilm.

(A) This figure displays representative images of the pH profile throughout the biofilm 3D architecture and the spatial distribution of pH within the selected EPS-microcolony complex in mixed-species biofilms formed after introduction of 1% sucrose. Dark areas are indicative of regions of low pH, while white or light areas are indicative of regions of pH that are close to neutral, as indicated by the scale bar. The EPS channel is depicted in red, while the cells are depicted in green. Arrows indicate various acidic pH regions within the microcolony and at the sHA interface. Red arrows indicate acidic pH regions (i) across the structure and (ii) at the microcolony/sHA interface. Yellow arrows indicate pH close to neutral at the microcolony/fluid phase interface. White arrows indicate the corresponding pH landmarks in the merged panel. (B) This panel shows temporal changes of in situ pH across the EPS-microcolony complex after the biofilm was exposed to sodium phosphate-based buffer (pH 7.0) for a total of 120 min.

https://doi.org/10.1371/journal.ppat.1002623.g005

Environments with low pH values were found only in the interior of the EPS-microcolony complexes within the biofilm (highlighted in Figure 5A). A close-up view of the pH map of these bacterial islets reveals three distinct pH profiles (see arrows; Figure 5A) as follows: (1) regions that display pH values that are close to neutral at the microcolony/fluid phase, (2) a range of acidic “pockets” across the structure (from the sHA surface to the fluid phase interface), and (3) acidic pH at the microcolony/sHA interface. The presence of discrete regions containing low pH (4.5 to 5.5) indicates that the acids accumulated and confined in these particular areas are not rapidly neutralized when incubated in neutral pH (7.0) buffer; more than 120 minutes of exposure are required before neutralization occurs (Figure 5B).

The presence of acidic regions at the microcolony-sHA interface has direct implications for cariogenesis. Acids present at the surface of the biofilm attachment increase local demineralization of the hydroxyapatite mineral, which is the main constituent of the tooth enamel [45]. Therefore, cross-sectional images of the biofilm at the sHA surface and pH mapping in the same field of view were acquired to illustrate the spatial distribution of surface-attached microcolonies and pH values (Figure 6A). It is readily apparent that the presence of surface attached-microcolonies (white line) corresponded with acidic pH on the sHA surface (darker areas highlighted with yellow lines). The pH measurements taken by ratiometric imaging analysis show that the pH at the microcolony/sHA interface was below 5.5 (regarded as the critical pH for rapid dissolution of enamel), and the pH value was significantly more acidic compared to areas without such particular 3D structures (highlighted in orange in the pH map image) (P<0.05; Figure 6B).

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Figure 6. In situ pH mapping at the EPS-microcolony complex and sHA interface.

(A) This figure shows representative cross sectional images (bird's eye view) at the sHA surface. White marks indicate the areas with surface-attached microcolonies (in the bacteria channel; depicted in green) while yellow marks show the corresponding area in the pH channel; the orange mark indicate an area without surface-attached microcolony. Dark areas are indicative of regions of low pH, while white or light areas are indicative of regions of pH that are close to neutral. (B) This table shows the pH values at the sHA interface for areas with and without surface-attached microcolonies after 30 min incubation in sodium phosphate-based buffer (pH 7.0). The data shown are mean values ± s.d. (n = 90). The asterisks (*) indicate that the differences between the two conditions are statistically significant (P<0.05, Tukey-Krammer HSD).

https://doi.org/10.1371/journal.ppat.1002623.g006

The presence of localized and elevated concentrations of acids at the surface of biofilm attachment has clinical relevance, as it could explain the heterogeneous pattern of carious lesions during the onset of this disease in humans. Dental caries is characterized by the temporal and localized/punctate appearance of regions of demineralization on the tooth enamel under plaque, clinically known as “white spots” [46]. These “white spots” eventually coalesce into a broader lesion, rather than a diffuse and homogeneous layer of erosion. Thus, the appearance of the lesions and the level of demineralization may be associated with the size of the surface-attached EPS-microcolony complexes. Correlation analysis showed that there is a linear relationship between low pH on the sHA surface and the diameter or height of these bacterial islets (Figure 7).

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Figure 7. Relationship of in situ pH at sHA surface with size of surface-attached EPS-microcolony complexes.

This figure depicts mixed-species biofilms (67 h) formed after the introduction of 1% (w/v) sucrose, which were processed for measurement of in situ pH at the interface between sHA surface and microcolonies. All the pH values were sorted by (A) the diameter and (B) height (distance from surface to fluid-phase) of the surface-attached microcolonies. The data shown are values from three separate experiments (n = 90). Correlation analysis showed that there is a linear relationship between pH and microcolony diameter (Pearson's test, P<0.0001, r-square 0.259) and height (P<0.0001, r-square 0.367).

https://doi.org/10.1371/journal.ppat.1002623.g007

Biofilms formed with the gtfB null mutant (lacking a 3D matrix and EPS-microcolony complexes) were readily neutralized after incubation in neutral pH buffer and failed to generate any acidic microenvironments (Figure S3). Interestingly, biofilms formed with the gtfC null mutant contained isolated and small EPS-microcolony complexes, which displayed some acidic pockets, although these were neutralized within 30 minutes (Figure S3). Collectively, the data clearly demonstrate that there is a substantial limitation to diffusion, which is associated with the assembly of EPS-rich matrix and the size of EPS-enmeshed microcolonies. Their presence could trap acid at the sHA surface and/or restrict access of neutralizing buffer (e.g. saliva) to areas of low pH within the biofilm. The data are consistent with Tatevossian's findings [47], which show that the concentration of solutes in human dental plaque fluid differs markedly from those observed in saliva.

The precise mechanisms involved in limiting diffusion are unclear. It is possible that the presence of glucans produced by oral streptococci limit diffusion of charged ions in and out of the plaque-biofilm, whereas uncharged substances, such as sucrose, may diffuse readily [45], [47], [48]. In contrast, others have noted that EPS has little effect on acid diffusion when using artificial plaque and in vitro modeling [49], [50]. However, none of these studies evaluated intact biofilms, as investigated here. Our data show the importance of how the matrix is assembled three-dimensionally and how it is spatially arranged with the bacterial cells to act as a diffusion-limiting physical barrier.

The presence of a high density of acidogenic and aciduric bacteria within these structures can facilitate the conversion of sucrose (and other fermentable carbohydrates) into acids via the glycolytic pathway. Furthermore, degradation of extracellular soluble glucans by S. mutans dextranase (also up-regulated within biofilm) and degradation of intracellular polysaccharides increases the availability of fermentable sugars (e.g. maltose and glucose) [4], [23], [31]. The metabolism of these carbohydrates could also contribute to the acidification of the resultant 3D milieu. The presence of alkali-generating bacteria in biofilms may also influence the local pH [51]. The use of metabolic activity markers could help to elucidate whether acidification is an active process or a secondary consequence of cell numbers (density). It is apparent that the combination of the physical and metabolic factors could, at least in part, explain the spatial distribution of punctate acidic regions in our in vitro biofilms and the low fasting pH values observed in plaque from caries-active individuals.

The formation of a heterogeneous acidic environment is biologically relevant, as pH changes could trigger dynamic shifts in the microbial population according to the ecological plaque model [11]. Niches with low pH values would activate the acid stress adaptive responses of particular organisms clustered in these EPS-sheltered acidic pockets, favoring survival/growth of aciduric and glucan-binding pathogens, such as S. mutans (initially in low-numbers) [24], [25]. Local pH concentrations would also affect the spatial distribution of the bacterial species throughout the 3D biofilm architecture. The positioning of the microorganisms and their stress response mechanisms may correlate with their susceptibility to, or affinity for, low pH environments. In addition, persistent low pH niches may also affect the expression of the gtf genes, as expression of gtfBC is induced in response to acidification and the presence of excess metabolizable carbohydrates [52]. These genes would therefore likely be up-regulated locally, coinciding with areas that are undergoing active matrix remodeling and acidogenesis.

Creation of protective microenvironments.

The microorganisms within biofilms display increased resistance to antimicrobials in comparison to their planktonic counterparts [1], [5], [53]. This phenomenon is generally associated with poor antimicrobial penetration (due to the presence of an extracellular matrix), activation of adaptive stress responses (including production of persister cells and induction of quorum sensing mechanisms), and physiological heterogeneity within the biofilm population [26], [54]. However, the importance of spatially heterogeneous environments and spatially complex cell-matrix arrangements in bacterial antimicrobial resistance within biofilms has received limited attention.

The construction of bacterial islets that are enmeshed and surrounded by an EPS-rich matrix could create localized areas of microbial resistance to antimicrobials within the biofilm. Therefore, we evaluated the viability of two distinct groups of bacterial cells within the same intact biofilm system in response to the immediate local effects of chlorhexidine (CHX) exposure (by time-lapsed measurements). We examined (1) cells within EPS-microcolony complexes, and (2) cells outside (or not forming) such structures (Figure 8). CHX is a broad spectrum antibacterial agent commonly used in mouthwash (at concentrations between 0.12–0.2%) to suppress the levels of mutans streptococci in the oral cavity [55]. The overlay images of live (in green) and dead (in red) cells after exposure to 0.12% CHX are shown in Figure 8A. Clearly, the inside of the EPS-enmeshed microcolony (Figure 8A-1) contains a greater proportion of live cells than those residing outside the structured communities over time (Figure 8A-2).

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Figure 8. Time-lapse imaging of bacterial viability after exposure of the biofilm to 0.12% (v/v) chlorhexidine (CHX).

Panel (A) shows the relative populations of live (SYTO 9-labeled; depicted in green) and dead (propidium iodide-labeled; depicted in red) cells over time in the mixed-species biofilm formed with the parental strain (A-1; cells within EPS-microcolony complex and A-2; cells outside EPS-microcolony complex) and the ΔgtfBC::kan mutant (A-3) after exposure to CHX. Panel (B) shows the survival rate of live cells. The data shown are mean values ± s.d. (n = 6). The asterisks (*) indicate that the differences between the conditions tested (cells within EPS-microcolony complex vs. cells outside EPS-microcolony complex or cells not forming such structures, i.e. biofilm formed with ΔgtfBC::kan) are statistically significant (P<0.05).

https://doi.org/10.1371/journal.ppat.1002623.g008

The survival rate of each group of bacterial cells was also calculated using the confocal images (Figure 8B). The data show that less than 10% of the total cells within the EPS-microcolony complex were killed after 15 min exposure. In contrast, more than 70% of the cells outside the structure were not viable (P<0.05). In the absence of the matrix, cells were highly susceptible to CHX. Mixed-species biofilms formed with the gtfBC null mutant strain were rapidly killed by CHX (Figure 8A-3; Figure 8B). Similarly, bacterial cells that generally do not organize into EPS-microcolony complexes, such as those in biofilms grown in 1% glucose, were also highly susceptible to killing by CHX (60–75% of the cells were dead after 15 min exposure to CHX; data not shown). Chlorhexidine (CHX) is a cationic bisbiguanidine [55]. The presence of negatively charged EPS (possibly due to association with lipoteichoic acids) could retard the diffusion of positively charged CHX molecules into biofilms [48], [53], [56]. However, our data show that antimicrobial resistance is not a general attribute associated with the simple physical presence of EPS, but rather with the way the matrix is assembled with the bacterial cells, which likely restricts access of CHX into EPS-microcolony structures.

Furthermore, the cells clustered within EPS-microcolony complexes may develop direct antimicrobial resistance in response to cell density and/or the presence of acidic microenvironments in these bacterial islets [26], [54]. These observations support the concept that antimicrobial resistance is a site-specific property within the greater biofilm architecture, although we were unable to explore the additional possibilities described above.

Results from a recent study [57] demonstrated the importance of a structured environment (using fabricated interconnected chambers within a microfluidic device) for rapid evolution of bacterial antibiotic resistance via the creation of steep chemical gradients. Our findings agree with the modeling of Zhang et al. [57], recapitulating spatial heterogeneities in our de facto biofilm system. Simply put, the EPS-matrix creates highly compartmentalized, yet interconnected and cohesive microenvironments. As a result, acidic regions and niches of antimicrobial resistance are created locally, demonstrating the importance of the 3D architecture in the evolution of virulent oral biofilms.

Conclusion

In this study, we show that the concerted actions of S. mutans-derived GtfB and GtfC, in the presence of sucrose, form a heterogeneous layer of EPS on the sHA surface. The surface-formed EPS promotes local accumulation of bacteria. The continuous production of EPS in situ coats the organisms and they rapidly aggregate, forming densely packed bacterial islets (termed EPS-microcolony complexes). Over time, these 3D structures become interconnected through surrounding EPS. The sequential accumulation of EPS on sHA and bacterial surfaces assembles an intricate and complex 3D matrix that leads to a highly compartmentalized architecture within an intact mixed-species biofilm.

The relevance of the matrix 3D architecture in biofilm virulence is revealed by our novel pH mapping approach, which uses a pH marker incorporated directly into the matrix. We illustrate spatially heterogeneous pH microenvironments manifested by “acidic pockets” found in the interior of the EPS-enmeshed bacterial islets only, despite exposure to a neutral buffer. This observation is clinically relevant in the context of the oral cavity in which saliva at neutral pH is abundant. The low pH niches favor acid-tolerant organisms, ensuring continued localized acid production; an EPS-rich environment promotes accumulation of the glucan-binding pathogen S. mutans. The environmental changes, associated with the matrix architecture, shift the microbial balance from a non-virulent to a virulent condition. Moreover, regions of acidic pH (<5.5) were found only in the areas where surface-attached EPS-enmeshed microcolonies were present on the sHA surface. The presence of an elevated concentration of acids at the apatitic surface favors local demineralization (while preventing remineralization), thereby facilitating development of carious lesions at these sites. Furthermore, the bacterial cells residing within EPS-microcolony complexes throughout the biofilm architecture are locally sheltered against a potent antimicrobial agent (CHX).

We demonstrated that S. mutans does not always need to dominate within plaque to influence virulence, because the Gtfs released, even at the time of biofilm initiation, adhere to the pellicle and other organisms, mediating the construction of the EPS-rich matrix. Moreover, the expression of GtfB and GtfC is enhanced in the presence of other oral bacteria. Results from previous studies have linked Gtfs to biofilm formation (using standard genetic and/or simple cell staining assays in mono-species biofilms) and expression of virulence (using rodent models) [4]. Our data illuminate the functional roles of GtfB- and GtfC-derived EPS in the basic biology of biofilms. We show how the assembly of a 3D EPS-matrix architecture helps to create spatial heterogeneities, and facilitates the formation of a variety of structured acidic microenvironments within a mixed-species biofilm. Clearly, the data from our study offer new avenues for further elucidation of how cell to matrix interactions govern the creation of ecological and environmental niches that are essential for expression of virulence by an oral biofilm.

The information generated here may pave the way for designing future studies aiming to develop novel methods that better prevent the formation and/or promote the disruption of virulent dental plaque. Furthermore, we introduce novel approaches to study the dynamics of biofilm construction and heterogeneity within the intact 3D architecture. Our observations have broad applicability beyond the mouth, because the imaging techniques introduced could be adapted for use in other biofilm systems in which polymers are formed during matrix development, and varied microenvironments are created.

Bacterial strains

Streptococcus mutans UA159 serotype c (ATCC 700610), a proven virulent cariogenic dental pathogen selected for genomic sequencing [58], Actinomyces naeslundii ATCC 12104, and Streptococcus oralis ATCC 35037 were used to generate mixed-species biofilms. We selected S. oralis and A. naeslundii in addition to S. mutans because these three organisms are found in the supragingival plaque of humans [59]. S. oralis binds to the pellicle and is one of the most commonly detected pioneer colonizers of the saliva-coated tooth surface [59], [60] in the absence of sucrose; strain ATCC 35037 also produces soluble glucans from sucrose and is acid-tolerant [60]. A. naeslundii is also detected during the early stages of plaque formation and may be associated with development of root caries; strain ATCC 12104 is acidogenic and produces fructans [61].

Furthermore, gtfB, gtfC, and gtfBC null mutants (ΔgtfB::kan, ΔgtfC::kan, and ΔgtfBC::kan, respectively), constructed from the parental S. mutans UA159 strain, were generated by standard allelic replacement with a non-polar kanamycin resistance marker and verified by DNA sequence analysis. These strains were kindly provided by Dr. Robert A. Burne (Department of Oral Biology, University of Florida, Gainesville, Florida) [22]. The strains were checked via PCR before use. The cultures were stored at −80°C in tryptic soy broth containing 20% glycerol.

Mixed-species biofilm model

The biofilm method is based on a batch culture approach using saliva-coated hydroxyapatite (sHA) discs, which was designed to mimic the formation of biofilms according to the “ecological plaque-biofilm” concept [11], as recently described by Koo et al. [22]. S. mutans UA159, A. naeslundii ATCC 12104, and S. oralis ATCC 35037 cells were grown in ultrafiltered (10 kDa molecular-weight cut-off membrane; Prep/Scale, Millipore, MA) buffered tryptone-yeast extract broth (UFTYE; 2.5% tryptone and 1.5% yeast extract, pH 7.0) with 1% glucose at 37°C and 5% CO₂ to mid-exponential phase; the ultrafiltration process removes high-molecular weight mannans and other polysaccharides that could interfere with our analyses. These bacterial suspensions were then mixed to provide an inoculum with a defined microbial population of S. mutans (10² CFU/ml), A. naeslundii (10⁶ CFU/ml), and S. oralis (10⁷ CFU/ml), which are critical for the reproducibility of our model [22]. Biofilms were formed on hydroxyapatite discs (1.25 cm diameter, surface area of 2.7±0.2 cm², Clarkson Chromatography Products, Inc., South Williamsport, PA) coated with filter-sterilized clarified whole saliva [22], which were placed in a vertical position using a custom-made disc holder (Figure S4). The mixed population of S. mutans, A. naeslundii, and S. oralis was inoculated in 2.8 ml of UFTYE with 0.1% (w/v) sucrose, and incubated at 37°C and 5% CO₂. During the first 19 h, the organisms were grown undisturbed to allow initial biofilm formation. At this point (19 h), the culture medium was replaced with fresh medium and the biofilms were grown until 29 h for establishment of the initial biofilm community [22]. At 29 h of biofilm growth, the biofilms were transferred to UFTYE containing 1% (w/v) sucrose or 1% (w/v) glucose to induce environmental changes to simulate a cariogenic challenge, while an additional set of biofilms was grown in UFTYE with 0.1% sucrose. The culture medium was then replaced twice daily (8 am and 6 pm) until the end of the experimental period (115 h). The pH of spent culture medium was measured daily using a standard pH electrode. The biofilms were analyzed at specific time points (29, 43, 67, 91, and/or 115 h) by means of confocal imaging/fluorescence, biochemical, reverse transcription quantitative PCR (RT-qPCR), and multi-dimensional protein identification technology (MudPIT) assays (see experimental design scheme in Figure S4). Furthermore, mixed-species biofilms were also formed in the presence of S. mutans UA159 mutant strains defective in gtfB and/or gtfC because they are critical for insoluble EPS synthesis and expression of virulence in vivo [4], [41], [62]. The gtfD mutant was not included because it did not have significant effect on matrix formation and biofilm architecture. All the gtf mutants used in this study exhibited similar planktonic growth rates (vs. UA159) as monitored (at OD_{600 nm}) using an automated turbidimetric Bioscreen C MBC system (Oy Growth Curves Ab Ltd, Helsinki, Finland).

Laser scanning confocal fluorescence microscopy (LCSFM) imaging of biofilm matrix

The sequential assembly of the matrix was determined by directly incorporating a fluorescent marker during synthesis of the extracellular polysaccharide (EPS)-matrix, allowing examination of the three-dimensional (3D) structure within intact biofilms [63], [64]. Briefly, 1 µM Alexa Fluor 647-labeled dextran conjugate (molecular weight, 10 kDa; absorbance/fluorescence emission maxima of 647/668 nm; Molecular Probes, Invitrogen Corp., Carlsbad, CA) was added to the culture medium from the beginning of and during the development of the biofilms. This technique is based on the observation that (fluorescently-labeled) dextran serves as a primer and acceptor for Gtfs (particularly GtfB), and is incorporated into newly formed glucan by the exoenzyme during synthesis of the EPS-matrix over the course of biofilm development [63]; it does not stain the bacterial cells at the concentration used in this study [63]. All the bacterial species in the biofilms were labeled by means of SYTO 9 green fluorescent nucleic acid stain (485/498 nm; Molecular Probes) using standard protocols [63], [64]. The imaging was performed using an Olympus FV 1000 two photon laser scanning microscope (Olympus, Tokyo, Japan) equipped with a 10× (0.45 numerical aperture) or 25× LPlan N (1.05 numerical aperture) water immersion objective lens. The excitation wavelength was 810 nm, and the emission wavelength filter for SYTO 9 was a 495/540 OlyMPFC1 filter, while the filter for Alexa Fluor 647 was an HQ655/40M-2P filter [22]. Each biofilm was scanned at 5 positions randomly selected at the microscope stage [65], and confocal image series were generated by optical sectioning at each of these positions. Three independent biofilm experiments were performed, and 10 image stacks (512×512 pixel for quantification or 1024×1024 pixel for visualization in tagged image file format) were collected for each experiment.

Computational analyses of the confocal biofilm images

The confocal images were analyzed using software for simultaneous visualization and quantification of EPS and bacterial cells within intact biofilms [64]. Amira 5.0.2 (Mercury Computer Systems Inc., Chelmsford, MS) was used to create 3D renderings of each structural component (EPS and bacteria) of the biofilms for visualization of the morphology and 3D architecture as detailed previously [64], [65]. COMSTAT and newly developed DUOSTAT (both are available as free downloadable software at http://www.imageanalysis.dk) were used for quantitative analysis. COMSTAT and DUOSTAT, written as scripts for MATLAB 5.3 (The Mathworks, Natick, MA, USA) equipped with the Image Processing Toolbox (see details at http://www.imageanalysis.dk), converts pixels from confocal image stacks into numerical values, facilitating quantitative characterization of each structural component within 3D biofilm images [64]. We used COMSTAT to calculate the biomass, number, and size (volume, diameter, and height) of microcolonies, as detailed elsewhere [65]. DUOSTAT was developed to calculate the co-localization of two biofilm components (e.g. EPS and bacterial cells) throughout the 3D biofilm architecture [64]. The software overlays the confocal image data sets (one for total bacteria and another for EPS) from the same biofilm, and calculates the proportion of total bacteria image pixels that are co-localized with EPS [64].

Non-invasive 3D in situ pH measurement and visualization

The ability to characterize microenvironments (e.g. spatial pH distribution) within biofilms without disrupting their architectural integrity is a major technical challenge. We used a fluorescent pH indicator, Lysosensor yellow/blue (Molecular Probes), to determine the in situ pH in our biofilm model. Lysosensor yellow/blue is conjugated with dextran (10 kDa MW), which allows the labeled dextran to be directly incorporated into the EPS-matrix [63], as described previously. Once incorporated into the biofilm matrix, the pH values can be measured based on fluorescence intensity ratios of the dual-wavelength fluorophore [66]. Lysosensor yellow/blue exhibits a dual-emission spectral peak (fluorescence emission maxima 452 nm and 521 nm) that is pH dependent [66]. The pH measurements are based on the principle that protonation of the fluorophore shifts its emission spectra, such that increasing ion concentrations increase fluorescence intensity at one wavelength, while decreasing it at the other [67]. The fluorescence intensity of both emission wavelengths and the ratio of fluorescent intensity (I450/I520) within each biofilm image was measured using Image J 1.44 and its calculation tools (e.g. channel 1 divide by channel 2 as detailed in http://rsbweb.nih.gov/ij/download.html). Titration curves of ratios versus pH (ranging from 3.5 to 7.0) were calculated as described previously [67], and were used to convert Lysosensor yellow/blue emission (fluorescence intensity) ratios to pH values. The intensity ratio of both wavelengths serve as a quantitative measure of pH, and Lysosensor yellow/blue is particularly suitable for acidic environments (low sensitivity maximum; pKa∼4.2), as expected in our biofilm model [66]. The experimental protocol and titration curve of ratios versus pH are provided in the supporting information (Protocol S1 and Figure S5).

The confocal images of Lysosensor-incorporated biofilms were acquired before and after incubation in Na₂HPO_4-citric acid buffer at pH 7.0. The images were acquired after 10, 30, 60, and 120 min of incubation in the neutral buffer to evaluate the spatial distribution of pH throughout the intact 3D biofilm architecture. For pH measurement, the ratio of fluorescence intensity of selected areas within each biofilm image were converted to pH values using the titration curves (as described in Protocol S1 and Figure S5) and Image J software (http://www.uhnresearch.ca/facilities/wcif/PDF/ImageJ_Manual.pdf). For visualization of in situ pH distribution within the 3D biofilm architecture, the fluorescence intensity ratios (corresponding to the pH values between 7.0 and 3.5) of all confocal images were reconstructed using Image J, then Amira. The fluorescence intensity was converted into grayscale using the Amira tool-box to correlate with the pH range from 7.0 (white) to 3.5 (black) (Protocol S1). Unlabeled biofilms were also imaged to check whether the autofluorescence of each biological component of the biofilm (i.e. bacterial cells and glucans) would interfere with pH quantification at the wavelengths and laser intensity used in our study; there was no interference with the measurements based on our image analysis.

Microbiological analysis of the mixed-species bacterial population

The biofilms were removed at specific time points (Figure S4) and homogenized by sonication in sterile 0.89% (w/v) NaCl solution (30 sec pulse at an output of 7W; Branson Sonifier 150, Branson Ultrasonics, Danbury, CT); the sonication procedure does not kill any of the bacterial species used in this study [22]. The homogenized suspension was used to determine the number of viable cells by plating on blood agar using an automated EddyJet Spiral Plater (IUL, SA, Barcelona, Spain) to determine the number of viable cells (total number of colony-forming units per biofilm). The three species were differentiated by observation of colony morphology in conjunction with microscopic examination of cells from selected colonies [68]. In addition, the bacterial populations were also assessed by qPCR using species specific primers for S. mutans [69], A. naeslundii, and S. oralis. The A. naeslundii (5- CCTCTGGCTTAACTGGGG -3 and 5- CATTCCACCGCTACACCA -3) and S. oralis (5- CCGCATAAGAGTAGATGTTG -3 and 5- GCCTTGGTGAGCCGTTAC -3) species-specific primers were designed using Beacon Designer 2.0 software (Premier Biosoft International, Palo Alto, CA, USA). Bacterial cell quantification using standard curves based on the genome size of each organism was performed as described previously [69]. The data was expressed as total numbers, and as proportion of each of the bacterial species within the biofilm.

S. mutans gene expression analysis using multiplex RT-qPCR

We performed RT-qPCR to measure the expression profiles of specific genes directly associated with extracellular polysaccharide matrix development, including gtfB, gtfC, gtfD, fruA, ftf, and dexA. RNA was extracted and purified using protocols optimized for biofilms [70]. The RNA integrity number (RIN) for all of our samples was ≥9.0, as determined by on-chip capillary electrophoresis with the Agilent 2100 Bioanalyzer (Agilent Technologies, Inc., Santa Clara, CA). Briefly, cDNAs were synthesized using 0.5 µg of purified RNA and the BioRad iScript cDNA synthesis kit (Bio-Rad Laboratories, Inc., Hercules, CA). To check for DNA contamination, purified total RNA without reverse transcriptase served as a negative control. The resulting cDNA and negative controls were amplified by a Bio-Rad CFX96 system (Bio-Rad Laboratories, Inc., CA) using specific primers and TaqMan probes (Table S2) and iQ Multiplex Powermix (Bio-Rad Laboratories). A standard curve was plotted for each primer set as detailed elsewhere [71]. The standard curves were used to transform the critical threshold cycle (Ct) values to relative numbers of cDNA molecules. Comparative expression was calculated by normalizing each gene of interest to the 16S rRNA gene, which served as a reference gene [71].

S. mutans protein expression analysis by MudPIT

We also examined whether changes in S. mutans gene expression would reflect the levels of their corresponding protein products in biofilms. The S. mutans protein expression profile in whole biofilms was analyzed by MudPIT and specific database search algorithms described previously [72]–[75]. Briefly, biofilms at 67 and 115 h of growth were homogenized by sonication (30 sec pulse at an output of 7W; Branson Sonifier 150) in the presence of protease cocktail inhibitor (Roche). After homogenization, aliquots were taken for bacteria quantification by qPCR and total protein quantification (by acid digestion followed by ninhydrin assay [76]); the protease cocktail inhibitor did not affect the ninhydrin assay as determined experimentally. Total protein was extracted, precipitated, and digested with trypsin, as detailed elsewhere [73], [74]. MS/MS spectra were searched with the ProLuCID algorithm [75] or the Sequest algorithm [77] against an NCBI-RefSeq S. mutans and S. oralis database (01/01/2010) concatenated to a decoy database in which the sequence for each entry in the original database was reversed [73]. All searches were parallelized and performed on a Beowulf computer cluster consisting of 100 1.2 GHz Athlon CPUs. ProLuCID results were assembled and filtered using the DTASelect (version 2.0) program [78]. The false positive rates are estimated by the program from the number and quality of spectral matches to the decoy database. We focused on proteins encoded by S. mutans UA159, and compared biofilms at 67 h- vs. 115 h-old. The level of protein abundance in mixed-species was calculated by normalizing the spectral count to the relative numbers of S. mutans by multiplying the spectral count values by the ratio of S. mutans CFU to the total CFU in the mixed-species biofilms samples.

Susceptibility of EPS matrix to mutanase

The EPS matrix formed in mixed-species biofilms was examined for susceptibility to mutanase [α-1,3 glucanase; EC 3.2.1.59], produced from Trichoderma harzianum, as detailed elsewhere [39]. The enzyme (Novo Nordisk, Denmark) was kindly provided by Dr. William H. Bowen (Center for Oral Biology, University of Rochester Medical Center). Biofilm was formed on the sHA surface, and the EPS-matrix was labeled with Alexa Fluor 647-labeled dextran conjugate (Molecular Probes) as described in the previous sections. At 91 h of biofilm development, mutanase (2 units of enzyme) were added to the culture media. At 115 h, biofilms were retrieved and the bacteria cells were labeled with SYTO 9 (Molecular Probes). Biofilms were examined using confocal fluorescence imaging, and subjected to AMIRA/COMSTAT analysis.

Cell viability within intact biofilms by time-lapsed killing assay

The effects of chlorhexidine (CHX) on the viability of biofilm cells immediately after introduction of the antimicrobial agent were assessed by time-lapsed measurements. The intact biofilms (formed with parental UA159 strain or gtfBC null mutant) were dip washed twice in 0.89% NaCl, then transferred to a Petri dish (Diameter 3.5 cm) containing 2.5 µM SYTO 9 (for labeling live-cells; Molecular Probes) and 2.5 µM propidium iodide-PI (for labeling dead-cells; Molecular Probes) in 4 ml of 0.89% NaCl, and incubated for 30 min at room temperature using standard protocols described by Hope and Wilson [53]. After labeling, confocal images were acquired using an Olympus FV 1000 two photon laser scanning microscope with an 25× LPlan N (1.05 numerical aperture) water-immersion objective lens (Olympus). The excitation wavelength was set at 780 nm and the emission filter for SYTO 9 was the 495/540 OlyMPFC1 filter, while PI was the HQ655/40M-2P filter. Immediately after completion of the first scan, and while keeping the biofilm in the same position, 48 µl of 10% (v/v) CHX solution was carefully added to the 4 ml cell culture dish and mixed to yield a final concentration of 0.12% CHX (v/v). CHX does not react with the dyes used in this study [53]. For the time-lapse series, images of the same field of view were taken at 15, 30, 45, and 60 minutes after CHX exposure. The total biomass of live and dead bacterial cells in each series of confocal images was quantified using COMSTAT. The ratio of live to the total bacteria at each time point was calculated, and the survival rate of live cells (relative to live cells prior to exposure to CHX) was plotted. The survival rate was calculated based on the amount of viable cells over time. The initial number of viable cells immediately before the introduction of CHX (time point 0 min; t _{0 min.}) was considered to be 100%. The number of viable cells after the introduction of CHX was then determined at each time point and the percent-survival rate was determined by comparing to t _{0 min}. Thus, the influence of the structural organization of the matrix on the killing effects of CHX can be monitored in situ and in real-time.

Statistical analysis

An exploratory data analysis was performed to determine the most appropriate statistical test; the assumptions of equality of variances and normal distribution of errors were also checked. The data were then analyzed using ANOVA, and the F test was used to test any difference between the groups (different experimental conditions and distinct time-points within same experimental condition). When significant differences were detected, a pairwise comparison was made between all the groups using Tukey-Kramer HSD method to adjust for multiple comparisons. Pearson's test was also used to evaluate the linear correlation between pH value and microcolony height (or diameter). Software JMP version 3.1 (SAS Institute, Cary, NC, USA) was used to perform the statistical analyses. The level of significance was set at 5%.