A Phytase-Based Reporter System for Identification of Functional Secretion Signals in Bifidobacteria

Health-promoting effects have been attributed to a number of Bifidobacterium sp. strains. These effects as well as the ability to colonise the host depend on secreted proteins. Moreover, rational design of protein secretion systems bears the potential for the generation of novel probiotic bifidobacteria with improved health-promoting or therapeutic properties. To date, there is only very limited data on secretion signals of bifidobacteria available. Using in silico analysis, we demonstrate that all bifidobacteria encode the major components of Sec-dependent secretion machineries but only B. longum strains harbour Tat protein translocation systems. A reporter plasmid for secretion signals in bifidobacteria was established by fusing the coding sequence of the signal peptide of a sialidase of Bifidobacterium bifidum S17 to the phytase gene appA of E. coli. The recombinant strain showed increased phytase activity in spent culture supernatants and reduced phytase levels in crude extracts compared to the control indicating efficient phytase secretion. The reporter plasmid was used to screen seven predicted signal peptides in B. bifidum S17 and B. longum E18. The tested signal peptides differed substantially in their efficacy to mediate protein secretion in different host strains. An efficient signal peptide was used for expression and secretion of a therapeutically relevant protein in B. bifidum S17. Expression of a secreted cytosine deaminase led to a 100-fold reduced sensitivity of B. bifidum S17 to 5-fluorocytosine compared to the non-secreted cytosine deaminase suggesting efficient conversion of 5-fluorocytosine to the cytotoxic cancer drug 5-fluorouracil by cytosine deaminase occurred outside the bacterial cell. Selection of appropriate signal peptides for defined protein secretion might improve therapeutic efficacy as well as probiotic properties of bifidobacteria.


Introduction
Bifidobacteria are an important component of the normal human gastrointestinal microbiota and, besides lactobacilli, the most frequently used microbial supplements in functional foods and probiotic formulations [1]. The concept of functional foods containing live microbial supplements, i.e. probiotics, is based on the observation that some of the commensal bacteria of the human microbiota have beneficial effects in different in vitro settings, small animal models or clinical trials [1,2]. These beneficial effects are, in most cases, strain-specific and include maintenance of remission in paediatric ulcerative colitis (UC), prevention of Clostridium difficileand antibiotic-associated diarrhoea, and a reduced mortality in necrotizing enterocolitis (NEC) [2].
Some of the health-promoting effects of probiotics and bifidobacteria seem to be mediated by secreted factors. Several anti-inflammatory factors of bifidobacteria potentially involved in their effects in UC and NEC are secreted proteins. One example is a eukaryotic-type serine protease inhibitor (serpin). Serpin was initially identified in the genome sequence of B. longum NCC2705 [3] and shown to inhibit pancreatic and neutrophil elastases [4]. Later, serpin-like proteases were also identified in other bifidobacteria [5,6]. Serpin is hypothesized to confer protection against proteolysis by pancreatic elastase in the gastrointestinal environment as well as to inhibit proteolytic damage by neutrophil elastase during intestinal inflammation [4]. A secreted protein of B. animalis subsp. lactis was shown to inhibit inflammatory chemokine secretion by TNF-α challenged cultured intestinal epithelial cells. Similarly, a released peptide factor of B. infantis was able to prevent loss of epithelial integrity in response to TNF-α or IFNγ challenge in an in vitro setting [7].
The ability to exert a health-promoting effect via secreted proteins depends on an active metabolism and, thus, on acquisition of nutrients. Various strains and species of bifidobacteria were shown to ferment different high molecular weight substrates derived from both the host and its diet including mucus [8], human milk oligosaccharides [9,10], starch [11], and other plant-derived polysaccharides [12]. All these substrates require degradation by extracellular enzymes prior to uptake and further breakdown for energy conservation. The ability to utilize these substrates is thought to provide a selective advantage over other bacteria, aiding the colonization of breast-fed infants and persistence during later stages of life [13][14][15][16] and hence support their health-promoting effects.
In addition to their reported health-promoting effects, some strains of bifidobacteria were shown colonise solid tumours in various mouse models [17][18][19][20] and thus have gained increasing interest as vectors for delivery of therapeutic genes in cancer therapy [21][22][23]. The most widely used approach in bacterial tumour targeting is expression of enzymes that convert nontoxic prodrugs to therapeutically active compounds [24]. One example of a well-studied prodrug-converting enzyme (PCE) is cytosine deaminase (CD). This enzyme converts the nontoxic prodrug 5-fluorocytosine to 5-fluorouracil, which interferes with DNA synthesis and thus inhibits proliferation of tumour cells. In order to improve the efficacy of prodrug conversion, while at the same time avoiding inhibitory effects on the proliferation of the delivery vector, PCEs are mostly used as secreted proteins.
Altogether, these findings indicate that secreted proteins might be important for establishment and maintenance of stable bifidobacterial populations in the gastrointestinal tract. Moreover, efficient protein secretion is crucial for functionality of bifidobacteria as probiotics and gene delivery vectors for tumour targeting approaches. In bacteria, the majority of extracellular proteins is secreted by either the Sec or the Twin arginine translocation (Tat) pathway [25,26]. The Sec pathway exports proteins across the cytoplasma membrane in an unfolded state, whereas the Tat-pathway transports folded proteins [27,28]. Both pathways depend on secretion signals usually located in the N-terminus of the substrate that are distinct yet share structural similarities [27].
In bifidobacteria, protein secretion has not been analysed in great detail and there is only one study employing a nuclease reporter to identify bifidobacterial signal sequences [29]. In the present study, we aim at providing a more systematic analysis of protein secretion and associated signal peptides of bifidobacteria, developing a system to analyse these SPs, and devising a tool for efficient expression of extracellular proteins in bifidobacteria.

Materials and Methods
Bacterial strains, plasmids and growth conditions All strains and plasmids used in this study are listed in S1 Table. E. coli DH10B was used as cloning host and for propagation of plasmids and grown in Luria broth (LB) at 37°C. Bifidobacteria were grown anaerobically at 37°C in Reinforced Clostridial Medium (RCM, BD Difco, Germany) or Lactobacilli MRS (BD Difco, Germany) broth supplemented with 0.5 g/L L-cysteine hydrochloride-monohydrate (MRSc). For cultivation of E. coli and Bifidobacterium sp. strains harbouring plasmids, 100 μg/ml spectinomycin were added to culture media. All media were prepared with ultrapure water.

Cloning procedures
Genomic DNA of E. coli DH10B was used as template for amplification of appA. Coding sequences of predicted SPs were amplified from genomic DNA of B. bifidum S17 or B. longum E18. PCRs were performed using Phusion DNA Polymerase (Thermo Scientific, Germany). All primers used in this study (S2 Table) were purchased from Eurofins Genomics GmbH (Germany). Thermo cycling was performed on a FlexCycler (Analytik Jena, Germany) with annealing temperature optimized for each primer pair. The appA gene of E. coli K-12 encoding a phytase was amplified without its native signal peptide sequence using primers PhytF and PhytR. The obtained PCR product was digested with restriction enzymes XhoI and HindIII and ligated to the 4,423 bp fragment of similarly digested pMDY23-P gap [30], i.e. the vector backbone including P gap but lacking the gusA gene. This yielded pMgapP, which harbours the appA gene fused directly to P gap without any signal sequence.
Coding sequences of signal peptides were fused to the appA gene by splicing-by-overlapextension (SOEing) PCR [31]. The coding sequences for different SPs were amplified using a forward primer and a SOEing reverse primer. The PCR was designed to include two additional amino acid residues after the predicted cleavage site to preserve the recognition sequence for cleavage. In parallel, a SOEing forward primer with complementary sequence to the SP reverse primer was used together with primer PhytR for amplification of appA. To fuse the SP coding sequence to appA, a second round of PCR was performed using the two PCR products of the first round as template, the SP forward primer, and primer PhytR. To increase specificity, DMSO was added to the PCR reaction to a final concentration of 5% (v/v) and annealing temperature was set to 70°C. The obtained PCR products were digested with restriction enzymes XhoI and HindIII and ligated to the 4,423 bp fragment of XhoI/HindIII cut pMDY23-P gap yielding plasmids with exact translational fusions of the different SPs to AppA.
In order to generate a vector for expression of a secreted cytosine deaminase (CD), the signal peptide of the bbif_1734 gene encoding a sialidase was amplified from B. bifidum S17 chromosomal DNA by PCR using primers SP_fw_SalI and SP_rev_HindIII. The codA gene was amplified from E. coli K-12 chromosomal DNA with the primers codA_fw_HindIII and codA_rev_SacII by PCR. Both PCR products were digested with HindIII and subsequently joined by a ligase reaction. The fusion was then amplified by PCR using primers SP_fw_SalI codA_rev_SacII and the product was digested with SalI and SacII and ligated to the 4,423 bp fragment of SalI/SacII cut pMGS-P gap -bopAHis 6 [32] containing P gap to yield pAO-S0-CD. The control plasmid pAO-CD, which contains a SP-less CD construct, was obtained by amplifying codA with primers codA_fw_SalI and codA_rev_HindIII and ligation of the SalI/HindIII digested PCR product to to the 4,423 bp fragment of SalI /HindIII cut pMGS-P gap -bopAHis 6 .
Following transformation into E. coli, plasmids of spectinomycin resistant colonies were checked for correct inserts by PCR. Plasmids of positive clones were verified by restriction analysis and Sanger sequencing and constructs with correct sequences were transformed into either B. bifidum S17 or B. longum E18 as described elsewhere [33].

Phytase assay
For phytase samples, special attention is needed to deplete potential free phosphate contamination. All related reagents and medium were prepared in ultrapure ddH 2 O (18 MOÁcm; Millipore, USA).
Recombinant B. bifidum S17 or B. longum E18 strains were grown in 50 ml RCM containing 100 μg/ml spectinomycin under anaerobic conditions. At the indicated time points, 5 ml of the cultures were harvested and centrifuged (5 000 × g, 5 min, 4°C). Supernatants were filter-sterilized and used for determination of extracellular phytase activity. Bacterial pellets were washed twice in 1 ml of 0.2 M sodium citrate buffer, pH 5.5, and resuspended in 500 μl of the same buffer. Bacterial suspensions were transferred to cryotubes containing 250 μg glass beads and disrupted during 2 cycles of 35 s at 6500 rpm in a Precellys 24 homogenisator (PEQLAB Biotechnologie GmbH, Germany). Lysates were centrifuged (13 000 × g, 5 min, 4°C) and the supernatant was retained as crude extracts for determination of intracellular phytase activity. Total protein in crude extracts was quantified using the Pierce BCA protein assay kit (Thermo Scientific, Germany).
Phytase activity in supernatants and crude extracts was quantified using an assay described elsewhere [34] with minor modifications. Briefly, 100 μl sample (supernatant or crude extract) were pre-incubated for 5 min at 37°C and then mixed with 100 μl 10.8 mM sodium phytate (50% (w/w) phytic acid diluted in 0.2 M sodium citrate buffer). The reaction was carried out at 37°C for 15 min, and then stopped by adding 200 μl 15% tricholoroacetic acid (TCA). After centrifugation (14 000 × g, 2 min), an aliquot of 20 μl was mixed with 480 μl ultrapure ddH 2 O and 500 μl color reagent (mix of 1M sulfuric acid, 2.5% (w/v) ammonium molybdate in ddH 2 O, and 10% (w/v) ascorbic acid in ddH 2 O at a ratio of 3:1:1). The mixture was incubated at 50°C for 15 min, and 100 μl were transferred to a transparent 96-well microtiter plate (Thermo Scientific, Germany). Absorbance at 820 nm was measured in triplicate using an Infinite M200 multimode microplate reader (Tecan, Switzerland). Phytase activity equivalents were calculated using to a standard curve of two-fold serial dilutions of a 9 mM potassium dihydrogen phosphate in water. Phytase activity equivalents were defined as the amount of enzyme that catalyses the release of 1 μmol of inorganic phosphate per minute from 5.4 mM sodium phytate (i.e. 100 μl sample + 100 μl 10.8 mM sodium phytate solution, see above) under the conditions of the assay. Activities were expressed as relative phytase units (RPU) per ml in supernatant and RPU/mg in crude extracts.

Phytate degradation assays
To test for phytate degradation an agar plate assay developed for yeasts [35] was adapted for bifidobacteria using RCM agar (RCA) containing calcium phytate (Ca-phytate) as substrate. RCM phytate agar was prepared by adding 3 g/l calcium carbonate (Sigma, Germany) and 1.5 ml of a 50% (w/w) phytic acid solution in H 2 O (Sigma) to standard RCM agar prior to autoclaving. 2 μl of an overnight culture of the tested recombinant bifidobacteria were spotted onto a freshly prepared agar plate. Following incubation for 48 h under standard conditions, phytate degradation can be observed by clear zones in the otherwise opaque agar around the bacterial spots on the plate.

Growth inhibition by 5-FC
The effect of the conversion of 5-FC to 5-FU by cytosine deaminase was determined for B. bifidum S17 wildtype and its isogenic derivatives carrying plasmids pAO-CD or pAO-S0_CD. OD 600 of overnight cultures grown in MRSc was adjusted to 0.1 in fresh medium containing 5-FC at 5, 1, 0.5, 0.1, 0.05, 0.01, 0.005 or 0.001 mg/ml (final concentration). 200 μl aliquots were pipetted into wells of a 96-well microtiter plate in four technical replicates per strain and concentration. After 24 h of anaerobic incubation at 37°C, OD 600 was measured using an Infinite M200 multimode reader.

Analysis of protein secretion pathways in bifidobacteria
As a basis to establish a protein secretion reporter in bifidobacteria, the genome sequences of a number of representative Bifidobacterium sp. strains were analysed. As expected, all analysed genomes harboured genes for SecY, SecE, and SecG, i.e. the major components of the Sec translocon, and the associated ATPase SecA with reasonable homology to the respective proteins of E. coli K12-W3110 (Table 1). By contrast, genes for Tat-dependent protein secretion were only found in the genomes of B. longum E18 (Table 1) and other strains of this species (data not shown).

Construction of a secretion reporter for bifidobacteria
We next extracted a list of all proteins of B. bifidum S17 predicted to be localized to the extracellular compartment. The N-terminal 60 residues of all proteins retrieved were analysed in silico for potential SPs ( Table 2). The SP of a sialidase (BBIF_1734) had the highest PSORTb Escore for extracellular localization and the second highest SignalP D-score for SP prediction. Moreover, the sialidase of Micromonospora viridifaciens, a closely related member of the phylum Actinobacteria, has been experimentally confirmed to be secreted into the extracellular environment [40,41]. Thus, the SP of BBIF_1734 was named S0 and selected to develop a secretion reporter using the phytase gene appA of E. coli DH10B.
The S0 sequence was fused to the appA gene by SOEing PCR and cloned into pMDY23-P gap under the control of P gap , replacing the glucuronidase reporter gene gusA (Fig 1A) to yield pMgapS0P. As a control vector, pMgapP was constructed, which harbours an identical appA construct fused directly to P gap without a signal sequence.
Both plasmids were transformed into B. bifidum S17 and phytase activity in crude extracts (intracellular) and culture supernatants (extracellular) of the recombinant strains was measured at various time points during growth. Both strains displayed almost identical growth (data not shown) ruling out any effect of plasmids on growth or phytase activity. Phytase activity markedly increased over time in supernatants of B. bifidum S17/pMgapS0P (Fig 1B). By contrast, phytase activity in supernatants of the control strain B. bifidum S17/pMgapP were barely above background until later time points during growth, i.e. stationary growth phase (Fig 1B). On the other hand, phytase activities were higher in crude extracts of B. bifidum S17/ pMgapP than in the strain harbouring pMgapS0P, i.e. the construct with a SP, throughout the experiment (Fig 1C). Comparative analysis of various SPs in different Bifidobacterium sp. hosts Following the successful establishment of appA as a secretion reporter in B. bifidum S17, this system was used to test various other bifidobacterial SPs. For this purpose, a total of six SPs with high D-scores according to the SignalP prediction were selected (Table 3). Of these SPs, two belong to proteins from B. bifidum S17 (BBIF_1681 and BBIF_1761) and two other to proteins from B. longum E18 (BLONG_1728 and BLONG_0476). Moreover, two SPs of (putative) Tat-secreted proteins of B. longum E18 (BLONG_0223 and BLONG_1620) were included. To test their functionality, all SPs were fused to the appA reporter by SOEing PCR, cloned into pMDY23-P gap replacing the gusA reporter gene, and the obtained plasmids were introduced into B. bifidum S17 or B. longum E18 by electroporation. Monitoring of growth in RCM broth indicated that all recombinant strains show the same growth pattern (data not shown). All recombinant strains were analysed for phytase secretion using a phenotypic assay based on the degradation of insoluble Ca-phytate in solid medium (Fig 2). Clear zones of Ca-phytate degradation were observed for B. bifidum S17 strains harbouring pMgapS0P, pMgapS1P, pMgapS3P, pMgapS4P, and pMgapS6. By contrast, strains harbouring plasmids pMgapS2P and pMgapS5P did not display Ca-phytate degradation above background levels (pMgapP). A similar pattern of Ca-phytate degradation was observed for B. longum E18 strains, however at somewhat lower levels. In order to get a more quantitative comparison of protein secretion effected by the different SPs, phytase activity was measured in the supernatants of all strains generated. Using S0, highest levels of phytase activity in supernatants of B. bifidum S17 were observed in stationary growth phase (Fig 1). The sequence upstream of the SP-appA constructs including the promoter (P gap ) and all elements relevant for translation, i.e. ribosome binding site, start codon, and the sequence and distance between them, were identical in all strains. Thus, equal levels of expression at least amongst derivatives of the same strain was assumed and samples were collected from cultures grown for 16 h, i.e. early stationary growth phase, for determination of phytase activity. For B. bifidum S17 strains, highest levels of phytase activity were observed for S6 and somewhat lower yet still efficient secretion was observed when S0, S1 and S4 were used as SP (Fig 3A). Statistical analysis suggests that protein secretion mediated by S4 and S6 is significant different (higher) compared to all other SPs and no difference is observed between S0 and S1 (Fig 3A; S3 Table). In B. longum E18, S0 and S1 were the most efficient secretion signals (Fig 3B). Again no statistically significant difference between S0 and S1 was observed but both SPs differed from all other SPs (Fig 3B; S3 Table). bifidum S17/pMgapP (S17 pMgapP) and B. bifidum S17/pMgapS0P (S17 pMgaS0P) during growth in RCM batch cultures. Values are relative phytase units (RPU) per ml supernatant (B) or mg protein in crude extracts (C) and are mean +/-standard deviation of three independent cultures measured in technical triplicates.
doi:10.1371/journal.pone.0128802.g001 Table 3. Signal peptides used to establish or tested in the phytase reporter assay and corresponding information on the predicted localization.

Secretion of cytosine deaminase
In order to demonstrate applicability of the identified SPs for secretion of a therapeutically relevant protein, we aimed at implementing a PCE approach using CD. For this purpose, we selected S0 based on the efficient secretion of phytase by both B. bifidum S17 and B. longum E18. The coding sequence of S0 was fused to the codA gene of E. coli K12. The fusion was cloned under control of P gap resulting in pAO-S0_CD, which was transformed into B. bifidum S17. As a control, codA was cloned under control of P gap without a SP in the same vector backbone (pAO-CD). Growth of all strains was comparable in the absence of 5-FC (data not shown). Both recombinant strains as well as the wildtype were tested for growth inhibition by the prodrug 5-FC (Fig 4). This revealed that B. bifidum S17 showed good resistance to the prodrug and growth was only inhibited at the highest prodrug concentration tested (5 mg/ml). Expression of CD without a SP markedly increased sensitivity of the recombinant strain (B. bifidum S17/pAO-CD). Growth of this strain was already inhibited at 0.005 mg/ml 5-FC. By contrast, growth of B. bifidum S17/pAO-S0_CD was comparable to that of the wild type in the presence of up to 0.1 mg/ml 5-FC. A slight inhibition of growth was observed only at 5-FC concentrations of 0.5 mg/ml and above but final OD 600 were higher than that of the strain expressing the SP-less CD at all concentrations tested. Thus, the sensitivity to 5-FC was reduced by expressing CD as a secreted protein by two orders of magnitude suggesting efficient protein export.

Discussion
A number of traits of bacteria require extracellular proteins. These traits include acquisition of nutrients e.g. by secretion of glycosyl hydrolases for degradation of polysaccharides [42]. Extracellular proteins are not only required for mere survival, but are also involved in the interaction with the host. Thus, survival and interaction with the host of most bacteria crucially depends on secretion of functional proteins. Bifidobacteria as members of the normal human gut microbiota are no exception to this rule. In fact, in the highly competitive environment of the are mean +/-standard deviation of three independent cultures measured in technical triplicates. Statistical analysis was performed by one-way ANOVA with Bonferroni post-tests for multiple comparisons. Phytase activity in the supernatants of each strain was compared to all other strains. Letters indicate statistical significance of the difference (a: p < 0.001 for all comparisons; b: p < 0.001 for all comparisons except S0 vs. S1; differences for all other signal peptides were significant at p<0001 for less than 5 other signal peptides). For complete results of the analysis see S3 Table. doi:10.1371/journal.pone.0128802.g003 Secretion Reporter in Bifidobacteria gastrointestinal tract, secretion of proteins might be even more important than in other less densely populated habitats [42]. The vast majority of bacterial proteins are transported by the Sec pathway. Tat-dependent secretion is essential in only a few bacteria [25][26][27] and was shown to be important for virulence of a wide range of bacterial pathogens [43]. All Bifidobacterium sp. genomes analysed harboured genes for a Sec translocon. By contrast, only the B. longum genomes contained genes for Tat protein export machineries. This is consistent with the conservation and distribution of Sec and Tat systems amongst bacteria.
Various bifidobacterial signal sequences have been used for expression of secreted recombinant proteins. These include the SPs of the galacto-N-biose/lacto-N-biose I-binding protein [44] and exo-xylanase [45][46][47] of B. longum, the β-galactosidase of B. bifidum [48], and Sec2 and ApuB of B. breve [49,50]. However, in none of these cases the authors provide a rationale for selecting the respective SP and in most cases the sequences have not been analysed. Comparative and systematic studies on secretion systems and signal peptides of bifidobacteria are largely missing. In one study, a nuclease reporter was used to screen a genomic library of B. breve UCC2003 for signal sequences in E. coli and subsequent confirmation of positive clones in L. lactis [29]. This identified three Sec-dependent SPs and three signal sequences of putative membrane proteins. Further analysis of these SPs confirmed that the three Sec-dependent SP are functional for secretion but quantitative analysis of nuclease activity in the supernatants showed no differences in efficiency of protein export.
We used a slightly different approach by selecting SPs of potentially secreted proteins of different bifidobacterial species predicted in silico. Using the predicted SPs of the sialidase BBIF_1734, we were able to establish a reporter system for protein secretion in bifidobacteria employing the phytase AppA of E. coli lacking its native SP. Heterologous expression and secretion of a phytase has previously been demonstrated in lactic acid bacteria [51,52]. The relative levels of extra-and intracellular phytase activity in B. bifidum S17/pMgapS0P compared to B. bifidum S17/pMgapP (the strain expressing AppA without SP) suggest that S0 mediates efficient secretion of phytase. Although it is not possible to quantitatively compare levels of intracellular and extracellular levels of phytase due to intrinsic limitations of the Phytex method (RPU/mg of protein in crude extracts vs. RPU/ml supernatant), our results demonstrate that phytase is a valuable reporter system for the identification and analysis of secretion signals in bifidobacteria. The enzyme is resistant against proteases, active in a wide range of pH values, and activity is optimal at pH 4-5, which is the normal pH in stationary phase batch fermentations of bifidobacteria [53].
Bifidobacteria do not encode appA homologues since BLAST searches revealed no significant hits in the genus Bifidobacterium (data not shown). Nevertheless, phytase activity has been detected in different Bifidobacterium sp. [54,55]. Recently, two enzymes of bifidobacteria with phytase activity have been characterized. Based on sequence comparisons, the enzymes belong to a different phylogenetic cluster than the E. coli AppA enzyme and are more closely related to the phytases of plants, fungi and vertebrates [56]. Intrinsic activity of non-AppA phytases or other phosphatases might explain the slight background observed for B. bifidum S17/pMgapP.
Using the phytase reporter, we were able to screen a number of other SPs of potentially secreted proteins of B. bifidum S17 and B. longum E18. All strains were initially screened for secreted phytase by detection of Ca-phytate degradation in agar plates and measuring phytase activity in culture supernatants. Some of the SPs did not produce zones of phytate degradation on agar, but phytase activity well above background was measured in the supernatants. Thus, Ca-phytate degradation in agar plates is rather a first, but not definite, indicator for the functionality of highly efficient SPs and measuring phytase activity in supernatants allows a more quantitative analysis.
All SPs analysed yielded phytase activities above background in both B. bifidum S17 and B. longum E18, suggesting that bifidobacterial SPs might be functional in other Bifidobacterium sp. besides their original hosts. Despite their annotation as (putative) Tat substrates, SPs S1 and S2 mediated phytase export in B. bifidum S17, which lacks a Tat system. Further in silico analysis revealed that both SPs yielded no prediction for Tat recognition using TATFIND and no Tat motifs were found by TatP (data not shown). Moreover, S1 and S2 had D-scores of 0.865 and 0.772, respectively, in the SignalP analysis. Collectively, this suggests that the predicted Tat-dependence of these SPs might be false and they might actually be Sec-dependent secretion signals.
Amongst the tested SPs, the SP of BBIF_1734 (S0) mediated efficient protein secretion in both B. bifidum S17 and B. longum E18. Thus, we selected S0 to clone a vector for expression and secretion of a therapeutically relevant protein. A number of bacteria including bifidobacteria are investigated as gene delivery vectors for cancer therapy. One of the approaches pursued, is the so-called Bacterial Directed Enzyme Prodrug Therapy (BDEPT), i.e. the use of recombinant bacteria expressing secreted enzymes for conversion of non-toxic prodrugs into their active, cytotoxic form [24]. An enzyme frequently used in BDEPT is the cytosine deaminase [24]. This enzyme is present in a wide range of microorganisms but not in mammalian cells. Its physiological role is deamination of cytosine to uracil and, as a non-specific, nonphysiologic side reaction, also catalyses conversion of the prodrug 5-FC to the tumour therapeutic 5-FU.
In a proof-of-principle approach, a construct was generated for expression of a secreted form of the CodA cytosine deaminase of E. coli in bifidobacteria using the P gap promoter and S0 to achieve secretion. B. bifidum S17/pAO-S0P tolerate doses of 5-FC of 0.2 mg/ml without inhibition of growth. By contrast, growth of the isogenic strain expressing a non-secreted CD is inhibited at concentration of 0.005 mg/ml and above. This demonstrates that a therapeutically relevant protein can be expressed and secreted in its active form using the SP of BBIF_1734. Moreover, the highest systemic concentration of 5-FC that is tolerated during therapy without adverse side effects is 0.1 mg/ml [57]. Thus, expression of CD as a secreted form by B. bifidum S17 renders this strain tolerant to therapeutically relevant doses.
A number of genetically engineered bifidobacteria expressing various therapeutic genes were successfully used to inhibit tumour growth in mouse models [58][59][60][61][62]. CD has also been expressed in bifidobacteria [63,64] and one of these recombinant strains was successfully used in combination with 5-FC to inhibit growth of a subcutaneous tumours of a melanoma cell line in mice [64]. Expression CD and other proteins in secreted form by bifidobacteria using appropriate secretion signals might improve their therapeutic efficacy.
In summary, our data shows that we have successfully developed a reporter system for identification and analysis of secretion signals in bifidobacteria. We furthermore demonstrated that an SP identified using this report is functional in mediating secretion of a therapeutically relevant protein. Rationally designed systems for secreted proteins might improve the efficacy of recombinant bifidobacteria as probiotic supplements in functional foods or in therapeutic applications such as cancer therapy.
Supporting Information S1 Data. Amino acid sequences of Sec and Tat homologues of representative Bifidobacterium sp. (DOCX) S1