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Article

Bap-Independent Biofilm Formation in Staphylococcus xylosus

by
Carolin J. Schiffer
1,*,
Miriam Abele
2,
Matthias A. Ehrmann
1 and
Rudi F. Vogel
1
1
Lehrstuhl für Technische Mikrobiologie, Technische Universität München, 85354 Freising, Germany
2
Bayerisches Zentrum für Biomolekulare Massenspektrometrie (BayBioMS), 85354 Freising, Germany
*
Author to whom correspondence should be addressed.
Microorganisms 2021, 9(12), 2610; https://doi.org/10.3390/microorganisms9122610
Submission received: 30 November 2021 / Revised: 14 December 2021 / Accepted: 15 December 2021 / Published: 17 December 2021
(This article belongs to the Section Biofilm)
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Abstract

:
The biofilm associated protein (Bap) is recognised as the essential component for biofilm formation in Staphylococcus aureus V329 and has been predicted as important for other species as well. Although Bap orthologs are also present in most S. xylosus strains, their contribution to biofilm formation has not yet been demonstrated. In this study, different experimental approaches were used to elucidate the effect of Bap on biofilm formation in S. xylosus and the motif structure of two biofilm-forming S. xylosus strains TMW 2.1023 and TMW 2.1523 was compared to Bap of S. aureus V329. We found that despite an identical structural arrangement into four regions, Bap from S. xylosus differs in key factors to Bap of S. aureus, i.e., isoelectric point of aggregation prone Region B, protein homology and type of repeats. Disruption of bap had no effect on aggregation behavior of selected S. xylosus strains and biofilm formation was unaffected (TMW 2.1023) or at best slightly reduced under neutral conditions (TMW 2.1523). Further, we could not observe any typical characteristics of a S. aureus Bap-positive phenotype such as functional impairment by calcium addition and rough colony morphology on congo red agar (CRA). A dominating role of Bap in cell aggregation and biofilm formation as reported mainly for S. aureus V329 was not observed. In contrast, this work demonstrates that functions of S. aureus Bap cannot easily be extrapolated to S. xylosus Bap, which appears as non-essential for biofilm formation in this species. We therefore suggest that biofilm formation in S. xylosus follows different and multifactorial mechanisms.

1. Introduction

Staphylococcus (S.) xylosus is a Gram-positive, coagulase-negative commensal of mammal skin with a biotechnological relevance, as it is commonly used as a starter organism for raw sausage fermentation [1]. For persistence in such environments, surface colonization and the formation of biofilms are anticipated as important traits. Biofilm formation is a common property of many bacteria and describes a state where cells are embedded in an extracellular matrix, mainly consisting of exopolysaccharides, proteins and extracellular DNA [2]. Biofilm matrix composition can vary and is dependent on species-specific mechanisms as well as environmental conditions [3]. If biofilms are of a mainly proteinaceous nature, surface proteins play a prominent role in primary adhesion and biofilm maturation as they can either interact with surface structures on adjacent cells or form amyloid structures that promote cellular aggregation [4]. Known surface proteins influencing proteinaceous biofilm matrix assembly include fibronectin binding proteins (FnBPs), Staphylococcus aureus surface protein G (SasG) and the biofilm associated protein (Bap) [5,6]. Bap is a high molecular weight surface protein, which was first described by Cucarella et al. [7]. Bap and its homologues have been shown to mediate multicellular aggregation as well as biofilm formation in several organisms, such as staphylococci and enterococci [8,9]. In S. aureus, V329 Bap is extensively studied, and it has been demonstrated that its functionality is based on self-assembly of N-terminal peptides of the protein into amyloid fibers under acidic conditions [9]. Furthermore, Bap-mediated biofilm formation is influenced by calcium ions in the environment, as they prevent amyloid assembly of Bap-derived peptides and subsequent intercellular aggregation [10]. Other than in the well-studied S. aureus V329, Bap function has only been molecularly characterized by the construction of knockout mutants in S. epidermidis C533 [11]. Studies addressing bap of biofilm-positive S. xylosus strains have been focusing solely on presence/absence of the gene analysed by PCR/hybridization approaches so far [11,12]. Thus, the actual function of the protein in S. xylosus has not been verified experimentally yet.
In a previous study, we demonstrated a strain-specific behavior in biofilm formation among different S. xylosus strains depending on environmental conditions as well as their individual genomic settings with respect to additional biofilm-related genes [13]. The fact that a strain in which bap is naturally defective displayed a biofilm negative phenotype led us to suggest an essential role of Bap in biofilm formation of S. xylosus. In order to test this hypothesis and to ensure that any impact of other genomic determinants is excluded, we generated isogenic bap knockout mutants of biofilm positive strains. Furthermore, we investigated whether S. xylosus and its bap mutants show typical phenotypic characteristics and differences, as they have been reported in Bap-positive S. aureus strains and its respective bap mutants.

2. Materials and Methods

2.1. Bacterial Strains and Culture Conditions

S. xylosus TMW 2.1023 and TMW 2.1523 are both biofilm-positive strains, isolated from raw fermented sausages [13]. Escherichia (E.) coli DC10B is a cytosine methyltransferase-negative derivate, often used in transformation experiments to evade type IV restriction modification systems [14].
E. coli DC10B was cultured in Lysogeny Broth (LB, tryptone 10 g/L, yeast extract 5 g/L, NaCl 5 g/L) 37 °C. Staphylococcal strains were cultured at 28 or 37 °C in Trypticase soy broth (TSB, casein peptone 15 g/L, soy peptone 15 g/L, yeast extract 3 g/L) supplemented with either no glucose (TSBN) or 1% glucose (TSB+), brain heart infusion (BHI) broth, or basic medium (BM, 1% peptone, 0.5% yeast extract, 0.5% NaCl, 0.1% Glucose, 0.1% K2HPO4). For transformation experiments, 20 µg/mL (E. coli) or 10 µg/mL (S. xylosus) of chloramphenicol (CarlRoth, Karlsruhe, Germany) were added when necessary.

2.2. DNA Manipulations and Bacterial Transformation: Mutagenesis of the Chromosomal Bap Gene by Allelic Exchange

For inactivation of bap in S. xylosus, regions up—and downstream of the sequence to be deleted were amplified using primers bap1F (5′-ACTCACTATAGGGCGAATTGGAGCTGTTATCAGCAGCTGCTAAG-3′), bap2R (5′-GTATATTGCGACACAATGTAAAGTATATCAG-3′), bap3F (5′-CTTTACATTGTGTCGCAATATACAGCTAG-3′) and bap4R (5′-GCTTGATATCGAATTCCTGCAGCATCTATAACTTTAGCTG-3′). To be able to use the same primer set for both S. xylosus strains (TMW 2.1023, TMW 2.1523), primers were chosen to map on conserved regions of the gene. PCR products were purified using a Monarch PCR and DNA cleanup kit (New England Biolabs (NEB), Ipswich, United Stated). Shuttle vector pIMAY*, which was kindly provided by A. Gründling (Molecular Microbiology, Imperial College London, UK) was digested with restriction enzymes SacI and PstI and PCR fragments were ligated into the vector using Gibson Assembly (NEB). The construct was transformed into E. coli DC10B by electroporation and successful transformants were selected on chloramphenicol plates. Sequencing, to verify correct assembly of the vector, followed. Plasmid was isolated using the Monarch plasmid DNA miniprep kit (NEB) and transformed into electrocompetent S. xylosus cells as described by Monk et al. [15]. Briefly, S. xylosus was cultured overnight in BHI and diluted to an OD600 of 0.5 in BM the next morning. Cultures were then incubated at 37 °C and 200 rpm for another 40 min, harvested, washed twice with ice-cold water and another two times with 10% glycerol in decelerating volumes (1/10, 1/25). Finally, cells were resuspended in 1/200 volume 10% glycerol + 500 mM sucrose and directly subjected to electroporation. At least 1 µg of plasmid was transformed (0.2 cm, 2.5 kV) and cells were immediately suspended in 1 mL BHI + 200 mM sucrose. After one hour at 28 °C, cells were spread on BHI 20CM and incubated at 28 °C for two days. Colonies were picked and allelic replacement was performed as described by Schuster et al. [16]. Lastly, successful allele replacement of the chromosomal bap sequence as well as plasmid loss were verified by colony PCR using primers bap1F and bap4R.

2.3. Colony Morphology on CRA

Colony morphology of wildtype and mutant strains on congo red agar (CRA, 10 g/L glucose, 0.8 g/L congo red) was assessed as previously described [17]. As congo red interacts with proteins and proteinaceous structures, strains with rough colony margins were considered as Bap positive, whereas Bap negative strains usually retain smooth colony margins.

2.4. Biofilm Formation Assays

Biofilm formation was quantified in 96-well plates as described by Schiffer et al. [13]. Strains were cultured in different media (TSBN, TSB+ (pH 7.2), Lac+ (TSB+ acidified with lactic acid to pH 6.0) and on different supports (hydrophobic (Sarstedt, Nürmbrecht, Germany), hydrophilic (NunclonTM delta, Thermo scientific, Waltham, MA, USA)). The media chosen, represent the three media found in a previous study to influence biofilm formation of the selected strains the most [13]. Lactic acid was used instead of an inorganic acid, as it is a prevalent acid found in one of the habitats of the species S. xylosus (raw fermented sausages). To determine whether calcium influences biofilm formation, CaCl2 was added to the wells to a final concentration of 20 mM when indicated.

2.5. Bacterial Aggregation Assay

Bacterial aggregation was determined by growing cell suspensions (OD600 at t0: 0.1) in test tubes for 24 h at 37 °C, 200 rpm in either TSBN or TSB+. Aggregation behavior was evaluated macroscopically. To investigate whether calcium has an impact on cellular aggregation behavior, CaCl2 was added to a concentration of 20 mM when indicated.

2.6. Growth and pH Dynamics

pH changes of S. xylosus strains in TSB+ were monitored using the icinac system (AMS Systea, Rome, Italy). Growth curves were recorded by determining the optical density over a period of 33 h in a Microplate Reader (SpectrostarNano, BMG Labtech, Ortenburg, Germany).

2.7. SDS Page of Protein Extracts

Bacteria were grown in TSBN until early stationary phase (37 °C, 200 rpm, 12 h). Then, 5 mL of cell culture were harvested (4 °C, 5000× g), washed twice with ice-cold phosphate-buffered saline (PBS) and resuspended in 150 µL PBS + 30% [wt/vol] raffinose (SigmaAldrich, St. Louis, MI, USA). Afterwards, 7 µL lysostaphin (1 mg/mL, SigmaAldrich, St. Louis, MI, USA) and 3 µL of DNAseI (1 mg/mL, SigmaAldrich, St. Louis, MI, USA) were added and after incubation at 37 °C for 2 h, protoplasts were sedimented at 8000× g for 30 min with slow deceleration. Supernatants were stored at −20 °C until subjection to SDS-PAGE analysis (10% resolving, 4% stacking gel).

2.8. Full Proteome Analysis

For full proteome analysis of S. xylosus cells, 0.1% of overnight cultures were diluted in fresh Lac+ and incubated in Erlenmeyer flasks under agitation (planktonic, 5 mL) or statically in NunclonTM delta surface (Thermo scientific, Waltham, MA, USA) tissue culture plates (sessile, 2 mL) for 24 h at 37 °C. Cell lysis and in-solution digest were performed with minor changes according to the SPEED protocol [18]. Shortly, 2 mL of planktonic cells were harvested, washed twice with ice-cold PBS and resuspended in 100 µL of absolute Trifluoroacetic acid (TFA). Sessile cells were also washed twice with ice-cold PBS to remove any non-adherent cells as well as to remove as many media proteins as possible, and dissolvement of adherent cells was performed by carefully resuspending the biofilm in 100 µL (TFA). All TFA cell suspensions were neutralized to pH 8.1–8.3 by adding nine volumes of Tris (2 M, pH not adjusted). Incubation in a thermomixer for 5 min at 55 °C and 450 rpm (ThermoMixerC, Eppendorf, Hamburg, Germany) as well as short centrifugation followed. Protein concentrations were determined using Bradford assay (B6916, SigmaAldrich, St. Louis, MI, USA) according to manufacturer’s instructions. Then, 15 µg of total protein amount were reduced, alkylated (10 mM Tris-(2-carboxyethyl)-phosphin, 40 mM 2-Chloroacetamide; 5 min, 95 °C) and afterwards diluted with water (1:1). Trypsin digest was performed in an enzyme to protein ratio of 1:50 overnight at 30 °C with mild agitation (400 rpm) and then stopped with 3% Formic acid (FA). Three discs of Empore C18 (3 M, Saint Paul, Minnesota, United States) material were packed in 200 µL pipette tips. The resulting desalting columns were conditioned (100% acetonitrile, can) and equilibrated (40% ACN/0.1% FA followed by 2% ACN/0.1% FA). Peptides were loaded, washed (2% ACN/0.1% FA) and eluted (40% ACN/0.1% FA). For the determination of expression levels of Bap in sessile versus planktonic cultures, around 250 ng peptides of three biological replicates were subjected to an Ultimate 3000 RSLCnano system coupled to a Q-Exactive HF-X mass spectrometer (Thermo Fisher Scientific, Waltham, MA, USA). All acquisition parameters were the same as described by Kolbeck et al. [19]. Proteomic analysis of the mutant strains was done in single measurements. Around 250 ng of peptides were subjected to an Ultimate 3000 RSLCnano system coupled to a Fusion Lumos Tribrid mass spectrometer (Thermo Fisher Scientific, Waltham, MA, USA). All parameters were set as described by Bechtner et al. [20].
Since TMW 2.1523 is a well biofilm former in TSBN [13], it was chosen that planktonic as well as sessile data was sampled for this particular strain not just in Lac+ but also in TSBN.

2.9. Bioinformatic and Statistical Analysis

Bioinformatic analysis and comparative genomics were performed using CLC Main Workbench 8 software (CLC bio, Aarhus, Denmark). Isoelectric point (pI) and molecular weight (MW) were computed using the respective tool from the Expasy server (available under: https://web.expasy.org/compute_pi/, accessed on 29 November 2021), InterPro (86.0) was used to predict signal peptide, transmembrane regions and cell wall anchor and ProScan (screens against PROSITE database) was used to scan for EF-hand motifs (cut off was set to 80% protein identity). Amyloidogenic regions in protein sequences were analyzed by using the amyloid finder tools FoldAmyloid [21], Aggrescan [22], Waltz-DB 2.0 [23] and Tango [24].
Peptide identification and quantification were performed using MaxQuant (v1.6.3.4) with Andromeda97 [25,26]. MS2 spectra were searched against the NCBI proteome databaste of S. xylosus 2.1023 and 2.1523, respectively; common contaminants were included (built-in option in MaxQuant). Trypsin/P was specified as proteolytic enzyme. Precursor tolerance was set to 4.5 ppm and fragment ion tolerance to 20 ppm. Results were adjusted to 1% false discovery rate (FDR) on peptide spectrum match level and protein level employing a target-decoy approach using reversed protein sequences. Minimal peptide length was defined as 7 amino acids; the “match-between-run” function disabled. Carbamidomethylated cysteine was set as fixed and oxidation of methionine and N-terminal protein acetylation as variable modifications. Perseus version 1.6.15.0 [27] and LFQ-Analyst [28] were used for data analysis. Missing label-free quantitation (LFQ) values were imputed from normal distribution. Significant differences in intensities between the conditions chosen, were calculated by student’s t-test with α set to 0.05 FDR correction (Benjamini Hochberg method) was applied to correct p-values. Data are, if not otherwise indicated, presented as means +/− standard errors of the means. Student’s t-tests were performed using Perseus Version 1.6.15.0.

3. Results

3.1. Protein Motif Structural Organization of S. xylosus Bap

To allow conclusions on structure-function correlations, the protein structures of S. xylosus and S. aureus Bap were compared. To get an idea of the conservation of the protein along the full sequence length, each region was aligned separately. Hereby, we sticked to the four major regions of the protein which were defined previously [7,13]. Bap of S. xylosus TMW 2.1023 and TMW 2.1523 share high sequence similarities, with 99.4% (Region A), 99.4% (Region B), 79.5% (Region C) and 98.4% (Region D) protein identity, respectively. Strain specific differences of S. xylosus Bap mainly rely on the number of C-Repeats, which have previously been shown to have no impact on the biofilm function of Bap [30]. Therefore, both S. xylosus sequences are referred to as BapXYL in this paragraph and compared to the sequence of the phenotypically well-characterized, Bap-positive strain S. aureus V329 (BapAUR).
BapXYL as well as BapAUR are both high molecular weight proteins fulfilling typical criteria of surface proteins such as a 44 amino acid (aa) long N-terminal signal sequence (YSIRK motif) as well as a C-terminal hydrophobic transmembrane segment and the LPxTG cell wall anchor motif. However, deeper sequence comparison of Bap of these two species revealed some notable differences (Table 1).
While the predicted pI of the full protein sequences is almost identical (~3.9), it is noticeably lower in BapXYL when the aggregation prone Region B (BapBAUR: 4.6, BapBXYL: 4.4) is considered only. Further, repeating sequence patterns differ remarkably between the proteins of both species. While BapAUR carries two large repeating sequences in region A, BapAXYL contains only two short tandem repeats. Similar applies for region D repeats. BapDAUR repeats are rich in serine and aspartate, while BapDXYL repeats are not just shorter but also lacking these amino acids and are rather rich in glycine. Another difference is the type of repeats in the C Region of the protein described for both species. For BapCXYL repeats are predicted to be ig-like domain type 6 repeats, while for BapCAUR repeats are characterized as ig-like domain type 3 repeats. It is also noteworthy that BapXYL carries almost twice as many predicted EF hand binding motifs than BapAUR. However, EF hand motifs EF2 and EF3 displayed by Region B of the protein, which have been shown to have a regulating effect on the activity of the protein [10], are identical in both species.
Several online tools were employed to predict amyloidogenic regions of the three protein sequences. All proteins share a region with high amyloidogenic potential, roughly between amino acid 400 and 900 (Figure 1).
However, while this region seems to be the only one with amyloidogenic potential in S. aureus V329, results are less conclusive for BapXYL, as, especially in TMW 2.1523, regions with amyloidogenic structural characteristics are also predicted in the C-terminal part of the protein. For BapAUR, two peptides (I: 487TVGNIISNAG496, II: 579GIFSYS584) are characterized as displaying significant amyloidogenic potential [9]. S. xylosus harbors similar peptide sequences in its Bap sequence, however, not identical (I: 490TVANILNNAG499, II: 582GVFSYS587). To ensure that the sequences of our selected S. xylosus strains are representative for the species, we compared them to a range of other S. xylosus bap sequences as well (see Figure S1). In this context we also included the sequence of S. epidermidis C533 into the alignments, as Tormo et al. [11] have previously reported a biofilm negative phenotype for this strain upon deletion of bap. Sequence analysis confirmed that S. aureus and S. epidermidis Bap are closely related and share high sequence homologies in all parts of the protein. S. xylosus bap sequences on the other hand, share high homologies among themselves, but differ from S. aureus and S. epidermidis bap genes in some functionally important parts. Namely, they lack long amino acid repeats in region A, harbor slightly different amyloidprone peptide sequences in region B, carry different types of C-repeats and are rather composed of G-rich as to SD-repeats in region D. It is further worth noting that we found a high range of truncated Bap sequences among S. xylosus strains, and also in biofilm positive strains ([12], e.g., S. xylosus C2a, accession: WP_144404228.1). This substantiates our hypothesis that the protein is non-essential for biofilm formation by this species.

3.2. Mutagenesis of the Chromosomal Bap Gene

For mutagenesis of the chromosomal bap gene, 452 nt of the bap promotor region as well as the first 1427 nt of the N-terminal part of the protein in S. xylosus strains TMW 2.1023 and TMW 2.1523 were deleted. To confirm successful knockout of the protein, cell extracts were at first subjected to SDS-PAGE analysis. For TMW 2.1523 a weak band was visible at the expected position for Bap (224 kDa) in the wildtype strain (indicated by arrow) but not in the mutant strain (Figure S2). For TMW 2.1023 no band was detectable at the position of Bap (173 kDa) in neither wildtype nor mutant strain.
Since visibility of S. xylosus Bap on SDS gels was poor and inconclusive namely for strain TMW 2.1023, a high-sensitivity mass-spectrometric analysis of the full proteome was performed. Bap deletion was confirmed by comparing the peptide sequences mapping to Bap in wildtype in contrast to mutant samples. No peptide, except for one in TMW 2.1023 mutant, was found in the full proteome analysis (Table S1). This result confirmed successful knockout of bap.

3.3. Growth Dynamics of Wildtype and Mutant Strains

To ensure that the transformation procedure led to no growth defects as well as to investigate whether Bap deletion has an impact on the growth behavior of S. xylosus, growth curves in different media were recorded. Figure 2 shows the growth dynamics for both strains in TSBN (pH 7.2), TSB+ (pH 7.2), Lac+ (pH 6) and TSB+-HCl (pH 6). While wildtype and mutant strains behave very similar in TSBN and TSB+, curves show higher variation when the growth medium is acidified to pH 6 by either the addition of lactic acid or HCl from the very beginning. However, in general one cannot ascribe any growth deficiencies to the bap mutant strains.

3.4. Biofilm Formation of Bap Wildtypes and Mutants

To determine the impact of Bap on biofilm formation of S. xylosus, we tested the biofilm forming capacities of two wildtype strains and their respective mutants in a 96-well plate assay. Tests were performed on hydrophilic and hydrophobic supports as well as in three different growth media that have previously been shown to promote biofilm formation to various extents in these strains [13]. The results of the biofilm assay are depicted in Figure 3. A significant reduction of biofilm formation on both supports was detectable with strain TMW 2.1523 in TSBN only, thus in a medium where no sugar is present and therefore no pH decrease occurs upon growth. For strain TMW 2.1023, no differences in biofilm formation between wildtype and bap mutant strain were observed.

3.5. Colony Morphology of Bap Wildtype and Mutant Strains on Congo Red Agar

A typical characteristic of Bap positive S. aureus strains is their rough colony morphology on congo red agar as the dye interacts with proteinaceous, fibrillar structures [31]. Loss of Bap causes a transformation of their rough colony morphologies to a smooth type [7]. As shown in Figure 4, we could not observe any differences in colony morphology between wildtype and mutant strains on congo red agar in S. xylosus. Even after a couple of days of inoculation, no switches to Bap positive phenotypes (rough colonies) were observable and colony margins remained smooth.

3.6. pH Changes of S. xylosus during Growth in Glucose Supplemented Media

In S. aureus the formation of Bap-based amyloid structures starts with the entry of S. aureus cells into stationary phase when the pH drops under pH 5 [9]. The mechanism of Bap-based aggregation is very sensible to pH changes, best functioning when the environment reaches pH values close to the isoelectric point of the protein. However, pH measurements over time of S. xylosus strains in TSB+ show, that S. xylosus is not lowering the pH below 5.0 (see Figure S3). After 24 h of pH measurement, S. xylosus incubated in TSB+ yielded values between 5.1 ± 0.2 and 5.0 ± 0.1 for TMW 21023 and TMW 2.1523, respectively. The observed accelerated acidification of TMW 2.1023 compared to TMW 2.1523 is in concurrence with the observed, faster growth of this particular strain.

3.7. Calcium Does Not Impair Biofilm Formation of Bap Positive S. xylosus Wildtype Strains

Since calcium has been described as a negative effector on biofilm formation in S. aureus V329 and addition of calcium to the growth medium completely abolished Bap mediated biofilm formation [10], the role of Ca2+ on S. xylosus biofilm formation was investigated. Therefore, CaCl2 was added to a concentration of 20 mM to the wells and biofilm formation was quantified again. As shown in Figure 5 (the respective staining results are shown in Figure S4), no biofilm-eradicating effect of calcium was found on neither of the tested supports nor in any of the tested growth media. This result leads us to hypothesize that Bap is not a major factor of S. xylosus biofilm formation in these strains.

3.8. Formation of Cell Aggregates in Wildtype and Mutant Strains

Previous studies with S. aureus V329 have shown that Bap is engaged in intercellular interactions, promoting aggregate formation under acidic conditions [9]. We found that S. xylosus is prone to aggregation in an acidic environment, too. However, neither the absence of Bap nor addition of CaCl2 can impair cell aggregation as it has been described for S. aureus V329. As shown in Figure 6, all cultures showed heavy cell clumping with cells precipitating either at the bottom of the tube or building a top layer at the air-liquid interface when incubated in TSB+.
Generally, the formation of multicellular aggregates is much weaker when strains are incubated in TSBN, where pH remains in a neutral to basic range. Still, in neither of the media tested, any differences between wildtype and mutant strains were detectable. We further tested the aggregation and biofilm behavior of S. xylosus strains when incubated in medium acidified with 1 M HCl to pH 4.5. However, no growth was detectable and thus neither aggregation nor biofilm formation could be observed. Acidification to pH 4.5 of the cells, which had been grown at neutral pH, did not lead to a change to a clumping phenotype either. Cells remained in a turbid suspension, comparable to when they were grown under neutral conditions (TSBN).

3.9. Proteomic Analysis of Expression Levels of Bap under Planktonic versus Sessile Conditions

Since visibility of Bap on SDS page was poor, we decided to use a full proteome analysis to confirm that Bap is expressed and to monitor the expression of Bap under different conditions. Therefore, we compared the measured intensity values for Bap of both S. xylosus strains when planktonic growth in Lac+ occurred compared to sessile growth in the same medium. Hereby, detected Bap amounts did not change significantly (TMW 2.1023) or only to a minor degree (1.15 log2 fold, TMW 2.1523) between the two compared conditions; however, one should keep in mind that cells grown planktonically in Lac+ show heavy cell aggregation which is closely related to biofilm formation. On the other hand, when Bap amounts are compared in cells grown in TSBN, the protein shows a more than fivefold reduction in biofilm stages compared to planktonic growth (Table 2, Figure S4, note: TSBN data only available for TMW 2.1523).
Further, Bap expression is significantly higher (+2.97) when TMW 2.1523 planktonic cells are grown in TSBN compared to Lac+.
In order to obtain a better understanding of whether Bap of S. xylosus is a protein with a generally low abundance in the cell, Bap intensity values were not just compared between samples obtained from cells at different growth stages but also within samples. Plotting all protein intensities measured in one sample under one condition, reveals that Bap is not a highly abundant protein such as, for example, ribosomal proteins are. However, Bap expression is not remarkably low either (compare Figure S6).

4. Discussion

In this study different experimental approaches were used to evaluate the impact of Bap in S. xylosus on its anticipated general role in biofilm formation and multicellular behavior. Therefore two S. xylosus wildtype strains were chosen, that have previously been shown to display different biofilm positive phenotypes [13]. After genetic and phenotypic comparison of the two strains and their isogenic bap mutants we found that the role of Bap in S. xylosus is most likely non-essential for biofilm formation, apparently strain-specific, and predictively more diverse than anticipated. Upon deletion of bap, a significant reduction in biofilm formation was only observed with S. xylosus TMW 2.1523 under neutral pH environmental conditions. It did not affect its aggregation behavior and had no effect on any of the investigated traits of S. xylosus TMW 2.1023. This is in contrast to studies on S. aureus V329 [7] and S. epidermidis C533 [11], which showed that disruption of bap led to complete abolishment of biofilm formation. We therefore conclude that, firstly, bap orthologs do not necessarily have the same function in other staphylococcal species as the one previously determined for single strains of S. aureus and S. epidermidis and secondly, that biofilm formation and aggregation of S. xylosus involves different mechanisms. This view is supported by our previous study, which revealed that different S. xylosus strains encode a variable set of biofilm related genes in their genomes and display a biofilm phenotype that is dependent on environmental conditions in a strain-specific manner [13]. It is also supported by the observation that S. xylosus C2a has been described as a strong biofilm producer [12], even though we found that Bap is truncated by a premature stop codon in region B in this strain. Given this, it appears likely that either other factors dominate biofilm formation of the species, such as eDNA, which has been named as an important component of S. xylosus C2a biofilm matrix [32], or that Bap does not have a predominant role in S. xylosus biofilm formation, due to either low expression or functional differences of the protein.
Congo red is commonly used as amyloid dye and has been shown to interact with amyloidogenic structures formed by the N-terminal part of Bap [9,31] resulting in rough colony phenotypes of Bap positive strains on CRA. Loss of Bap has subsequently been shown to transform rough colonies to colonies with smooth margins [31]. Even though S. xylosus strains TMW 2.1023 and TMW 2.1523 are Bap positive, no colony morphology changes in wildtype versus mutant strains could be observed. Both strains and their respective mutants displayed smooth colony margins, suggesting that in contrary to Bap positive S. aureus strains, (Bap based-) amyloid formation seems to be different or at least under the conditions tested, not existent in S. xylosus. Another factor supporting a minor role of Bap in biofilm formation of S. xylosus is that calcium addition (20 mM) had neither an inhibiting effect on cell aggregation in culture tubes nor on biofilm formation. In S. aureus V329 adding as little as 6 mM calcium to the growth medium already abolishes any kind of aggregation and biofilm formation behavior [10]. If Bap binds calcium ions with low affinity, the molten globule conformation of the protein is stabilized in a way that no subsequent assembly to amyloid structures occurs. The effect of calcium binding and stabilization is attributed to EF domains 2 and 3 in the B region of the protein. However, even though BapXYL harbors the exact same EF hand motifs in its B region as BapAUR, no aggregation/biofilm reducing effects were observed upon calcium addition. On the contrary, in some cases one could rather predict a trend towards an enhancing effect on biofilm formation especially on hydrophobic support. If and to which extent the increased number of EF hand motifs found in BapXYL, compared to BapAUR, is related to this observation remains speculative.
pH plays an important factor in Bap-mediated biofilm formation, as self-assembly of the protein into amyloid fibers occurs under acidic conditions only. When S. aureus V329 is incubated in medium containing glucose, pH drops below 5 as soon as stationary phase is entered, thereby approaching the pI of the aggregation prone B region of the protein, which facilitates amyloid structure formation [9]. S. xylosus differs in two points. First, the calculated pI of Region B of BapBXYL is 4.4 compared to BapBAUR 4.6, thus, considerably lower. Secondly, S. xylosus is not lowering the pH below 5 in medium containing glucose. Hence, even though amyloidogenic potential of BapBXYL was predicted by several amyloid finders in silico, peptide self-assembly into amyloids is impeded, as a pH close to the pI of BapBXYL is not reached during sugar fermentation of the organism. A final pH of 5 and not lower, after glucose fermentation by S. xylosus, is in consistence with our observation that S. xylosus, contrary to S. aureus [9], did not show any growth in medium with pH 4.5.
While glucose has been discussed to indirectly regulate biofilm formation of S. aureus [33] and acidosis related to glucose metabolism is essential for biofilm formation in Bap+ S. aureus strains [9], it is noteworthy that S. xylosus is a well biofilm former under neutral to basic conditions (TSBN) and that pH decrease during growth is, in contrast to S. aureus V329, not necessary to induce biofilm formation. Additionally, the only reduction in biofilm formation between wildtype and mutant strain we observed was when strain TMW 2.1523 was grown under neutral conditions. Besides the already mentioned fact that the pH drop during growth of S. xylosus might not be low enough to induce Bap derived peptide aggregation, one could also argue that Bap might not be expressed in sufficient amounts, especially under acidic conditions, to promote formation of multicellular aggregates. This is substantiated by the results obtained from full proteome analysis which revealed a significantly higher amount of Bap2.1523 in neutral (TSBN) compared to acidic (Lac+) medium. Moreover, even though multiple authors reported good visibility of Bap on SDS gels [7,10], S. xylosus Bap was poorly visible on the gel, and only a slight band was detectable for strain TMW 2.1523 when grown in TSBN. This leads us to hypothesize that BapAUR is expressed to a higher extent than BapXYL. Whether BapXYL visibility on SDS gels is impaired by any processing that occurs, as described for BapAUR under acidic conditions [9], cannot be ruled out and should be kept in mind.
Another difference between the two species to be considered is the structural organization of the proteins. While Bap of S. epidermidis, S. chromogenes, S. hyicus and S. simulans share almost 100% protein similarity with BapAUR [11], BapXYL and BapAUR show only around 50 (our study) to 80% [11] protein identity. Thus, different functions cannot be excluded, especially since the correlation between Bap and staphylococcal biofilm formation has mainly been studied extensively in strain S. aureus V329 and a function has been solely assigned to the N-terminal region of the protein so far. A large part of the protein (C-terminal part) remains bound to the cell surface, with a still unknown purpose for the cell. Lastly, small but predictively important sequence differences need to be considered, for example two short peptide sequences that have been predicted to show high amyloidogenic potential in BapAUR [9] are not conserved across the two species. Also, BapAUR Region D is rich in SD repeats and C-terminal SD repeats have previously been described to be an important structural attribute in staphylococcal surface adhesins [34,35]. BapXYL lacks any of those SD repeat rich regions.
Proteins containing a YSIRK signal peptide and an LPxTG cell anchor motif have been discussed in different contexts in the past and different functions including peptidase and hydrolase activity have been assigned to those proteins [36,37]. Furthermore, Bhp, a Bap homolog found in S. epidermidis, has been speculated to mediate biofilm formation at first [11]; however, disruption of bhp did not result in any biofilm reduced phenotypes [38]. Thus, we suggest that biofilm formation in S. xylosus does not necessarily require Bap, and that its dominant role in biofilm formation is currently rather restricted to strains of selected species such as S. aureus and S. epidermidis [9,11]. Our findings further suggest that conclusions on the function of Bap drawn from studies conducted with S. aureus V329 should be carefully applied to other organisms carrying Bap orthologs when experimental proof is lacking. Furthermore, it appears that other proteins/mechanisms must be involved in multicellular behavior and biofilm formation of S. xylosus.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/microorganisms9122610/s1, Figure S1: Bap sequence alignment of selected S. xylosus strains with two Bap-dependent biofilm formers: S. epidermidis C533 and S. aureus V329. Only functionally important parts of the alignment are shown. A. shows the YSIRK-Signal peptide sequence as well the difference in A-region repeat length between S. epidermidis/S. aureus and S. xylosus. B. shows the sequence differences between the two amyloidprone peptides (defined by Taglialegna et al. [8]) of Bap Region B (marked in yellow). C. displays the conservation across species of EF hand domains 2 and 3 (pink). D. shows the differences in D-repeats between the species. While S. aureus and S. epidermidis region D is rich in SD repeats, S. xylosus encodes G-rich repeats, Figure S2: Analysis of cell extract protein preparations on SDS-PAGE. Left: TMW 2.1523 wildtype (Wt) and mutant (Mt) strain, Right: TMW 2.1023 Wt and Mt. The black arrow indicates a possible location of Bap in TMW 2.1523–Wt, Figure S3: pH changes of S. xylosus TMW 2.1023 (grey) and 2.1523 (black) incubated in TSB+ aerobically at 37 °C. Changes in pH were recorded over 12 h, OD600 at t0 was set to 0.1. Curves display the mean of 3 biological replicates, Figure S4: Calcium (20 mM) does not impair biofilm formation of selected S. xylosus strains (incubated in TSB+, 24 h, 37 °C, stained with safranin-O), Figure S5: Boxplot of log2 transformed LFQ intensities measured for Bap in TMW 2.1023 (A) under planktonic and sessile conditions in Lac+, for TMW 2.1523 (B) under planktonic and sessile conditions in Lac+ and TSBN, Figure S6: Intensity based absolute quantification (iBAQ)—intensities of proteins expressed in TMW 2.1023 under planktonic (A) or sessile (B) conditions and TMW 2.1523 under planktonic Lac+ (A), sessile Lac+ (B), planktonic TSBN (C) and sessile TSBN (D) conditions. Bap is marked in red, highly abundant ribosomal proteins (50S) are marked in green for comparison. Table S1: Identified peptide sequences (intensity values) mapping on Bap in wildtype and mutant strains of TWW strains 2.1023 and 2.1523.

Author Contributions

C.J.S.: Conceptualization, Investigation, Methodology, Software, Visualization, Writing—Original Draft preparation; M.A.: Methodology, Software, Writing—Review and Editing; M.A.E.: Conceptualization, Supervision, Writing—Review & Editing; R.F.V.: Funding Aquisition, Project Administration, Supervision, Writing—Review & Editing. All authors have read and agreed to the published version of the manuscript.

Funding

Part of this work was funded by the German Federal Ministry for Economic Affairs and Energy via the German Federation of Industrial Research Associations (AiF) and the Forschungskreis der Ernährungsindustrie E.V. (FEI), project AiF 19690N. M. Abele was supported by the EU Horizon 2020 grant Epic-XS.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The proteomics raw data, MaxQuant search results and used protein sequence databases have been deposited with the ProteomeXchange Consortium via the PRIDE partner repository [29] and can be accessed using the data set identifier PXD029728. Sequencing data of TMW 2.1023 and TMW 2.1523 is accessible under JAEMUG000000000 and CP066721-CP066725, respectively.

Conflicts of Interest

The authors received research grants from the AiF, which did not influence the aims or setup of this study, and declare no conflict of interest.

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Microorganisms 09 02610 g001 550
Figure 1. Amyloidogenic structure prediction of different protein sequences from S. xylosus TMW 2.1023, TMW 2.1523 and S. aureus V329. Prediction based on aggrescan (A), waltz (B), fold amyloid (C) and tango (D).
Figure 1. Amyloidogenic structure prediction of different protein sequences from S. xylosus TMW 2.1023, TMW 2.1523 and S. aureus V329. Prediction based on aggrescan (A), waltz (B), fold amyloid (C) and tango (D).
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Figure 2. Growth curves of wildtype and mutant strains of S. xylosus TMW 2.1023 and TMW 2.1523 in different growth media (as indicated). Curves were recorded in 96-well plates in a plate reader (37 °C, aerobic conditions) every 30 min over a period of 33 h— – 023-WT, – 023-mut, – 523-WT, – 523-mut. Data are shown as mean of three biological replicates.
Figure 2. Growth curves of wildtype and mutant strains of S. xylosus TMW 2.1023 and TMW 2.1523 in different growth media (as indicated). Curves were recorded in 96-well plates in a plate reader (37 °C, aerobic conditions) every 30 min over a period of 33 h— – 023-WT, – 023-mut, – 523-WT, – 523-mut. Data are shown as mean of three biological replicates.
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Figure 3. Biofilm formation of S. xylosus strains TMW 2.1023 and TMW 2.1523 and its bap mutants on hydrophilic (upper row) and hydrophobic (lower row) support in TSBN, TSB+ and Lac+ (as indicated). Significant differences of means are marked by * (p-value < 0.05). Mean ± SE.
Figure 3. Biofilm formation of S. xylosus strains TMW 2.1023 and TMW 2.1523 and its bap mutants on hydrophilic (upper row) and hydrophobic (lower row) support in TSBN, TSB+ and Lac+ (as indicated). Significant differences of means are marked by * (p-value < 0.05). Mean ± SE.
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Figure 4. Colony morphology of S. xylosus strains on congo red agar. Bacterial overnight cultures were either streaked out for single colonies (left, middle) or applied as drops to the agar (right). Scale bar indicates 10 mm.
Figure 4. Colony morphology of S. xylosus strains on congo red agar. Bacterial overnight cultures were either streaked out for single colonies (left, middle) or applied as drops to the agar (right). Scale bar indicates 10 mm.
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Figure 5. Effect of calcium on biofilm formation of S. xylosus. Biofilm formation was quantified of S. xylosus TMW 2.1023 and 2.1523 in three different media on hydrophilic (upper row) and hydrophobic (lower row) support. CaCl2 (dark grey bars) was added to the respective growth medium to a final concentration of 20 mM.
Figure 5. Effect of calcium on biofilm formation of S. xylosus. Biofilm formation was quantified of S. xylosus TMW 2.1023 and 2.1523 in three different media on hydrophilic (upper row) and hydrophobic (lower row) support. CaCl2 (dark grey bars) was added to the respective growth medium to a final concentration of 20 mM.
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Figure 6. Aggregation behavior of S. xylosus TMW 2.1023 (.023), TMW 2.1523 (.523) and the corresponding bap mutants grown for 24 h in TSB+ at 37 °C (200 rpm). Measured pH values are specified in the top left corner. CaCl2 was added to a concentration of 20 mM when indicated.
Figure 6. Aggregation behavior of S. xylosus TMW 2.1023 (.023), TMW 2.1523 (.523) and the corresponding bap mutants grown for 24 h in TSB+ at 37 °C (200 rpm). Measured pH values are specified in the top left corner. CaCl2 was added to a concentration of 20 mM when indicated.
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Table
Table 1. Sequence comparison of Bap originating from S. xylosus TMW 2.1023, TMW 2.1523 and S. aureus V329. Different characteristics such as protein size, length of each region of the multidomain protein, molecular weight (MW), isoelectric point (pI) as well as number (#) of repeats and EF-hand motifs are listed.
Table 1. Sequence comparison of Bap originating from S. xylosus TMW 2.1023, TMW 2.1523 and S. aureus V329. Different characteristics such as protein size, length of each region of the multidomain protein, molecular weight (MW), isoelectric point (pI) as well as number (#) of repeats and EF-hand motifs are listed.
BapS. xylosus 2.1023S. xylosus 2.1523S. aureus V329
AccessionJGY91_02455JGY88_01140-45AAK38834
Length total (aa)165121612276
YSIRK Signal Peptide1–441–441–44
Region A316316316
Region B458458458
Region C (incl. spacer)64411601321
Region D (incl LPXTG)189183137
TM helix 1624–16412134–21512249–2266
MW (kDa)173.1224.3238.5
pI_Bap4.013.903.90
pI_BapB4.414.394.61
# RepeatsA222
sequenceTAEDNTAEDNAQDDDNIKEDSNTQEESTNTSSQSSEVPQTKK
# RepeatsC71314
type of C repeatsig-like domain type 6ig-like domain type 6ig-like domain type 3
# RepeatsD17167
sequence13× GTGENP, 1× GKGENP, 1× GGGENP, 1× GIGENP,1× GTGENT14× GTGENP, 1× GAGENP, 1× GTGENT2× SDDNSDNGNN
1× SDDNSGNGDN
1× SDDNSDN
1× SGAGDTSD
2× SGAGDNSD
%p.identity_Xyl vs Aur45.1358.97-
%p.identity_B_Xyl vs Aur80.1879.96-
# EF motifs774
seq_EF2DYDKDGLLDRYERDYDKDGLLDRYERDYDKDGLLDRYER
seq_EF3DTDGDGKNDGDEVDTDGDGKNDGDEVDTDGDGKNDGDEV
%p.identity EF2_Xyl vs. Aur100100-
%p.identity EF3_Xyl vs. Aur100100-
Table
Table 2. LFQ intensities determined during full proteome analysis for two different S. xylosus strains in two different growth media. Indicated are log2 fold change of intensity values, adjusted (Benjamini-Hochberg method) p-values and whether the change in expression between the compared conditions is considered as statistically significant (α = 0.05, True vs. False). If the log2 fold change was <2, true is written in italics.
Table 2. LFQ intensities determined during full proteome analysis for two different S. xylosus strains in two different growth media. Indicated are log2 fold change of intensity values, adjusted (Benjamini-Hochberg method) p-values and whether the change in expression between the compared conditions is considered as statistically significant (α = 0.05, True vs. False). If the log2 fold change was <2, true is written in italics.
Biofilm Associated Protein (Bap)
TMW 2.1023 JGY91_02455
plankt. vs. sessile, Lac+log2 fold change0.901
p.val (adj.)0.158
significantFALSE
TMW 2.1523 JGY88_01140-45
plankt. vs. sessile, Lac+log2 fold change1.15
p.val (adj.)0.0189
significantTRUE
plankt. vs. sessile, TSBNlog2 fold change5.11
p.val (adj.)0.0000231
significantTRUE
Lac+ vs. TSBN (plankt.)log2 fold change−2.97
p.val (adj.)0.000139
significantTRUE
Lac+ vs. TSBN (sessil)log2 fold change0.981
p.val (adj.)0.0356
significantFALSE
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Schiffer, C.J.; Abele, M.; Ehrmann, M.A.; Vogel, R.F. Bap-Independent Biofilm Formation in Staphylococcus xylosus. Microorganisms 2021, 9, 2610. https://doi.org/10.3390/microorganisms9122610

AMA Style

Schiffer CJ, Abele M, Ehrmann MA, Vogel RF. Bap-Independent Biofilm Formation in Staphylococcus xylosus. Microorganisms. 2021; 9(12):2610. https://doi.org/10.3390/microorganisms9122610

Chicago/Turabian Style

Schiffer, Carolin J., Miriam Abele, Matthias A. Ehrmann, and Rudi F. Vogel. 2021. "Bap-Independent Biofilm Formation in Staphylococcus xylosus" Microorganisms 9, no. 12: 2610. https://doi.org/10.3390/microorganisms9122610

APA Style

Schiffer, C. J., Abele, M., Ehrmann, M. A., & Vogel, R. F. (2021). Bap-Independent Biofilm Formation in Staphylococcus xylosus. Microorganisms, 9(12), 2610. https://doi.org/10.3390/microorganisms9122610

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