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Int. J. Mol. Sci. 2013, 14(3), 4640-4654; doi:10.3390/ijms14034640
Published: 26 February 2013
Abstract: In the present study we investigated the incidence of bacteriocins produced by 236 lactic acid bacteria (LAB) food isolates against pathogenic or opportunistic pathogenic oral bacteria. This set of LAB contained several strains (≥17%) producing bacteriocins active against food-related bacteria. Interestingly only Streptococcus macedonicus ACA-DC 198 was able to inhibit the growth of Streptococcus oralis, Streptococcus sanguinis and Streptococcus gordonii, while Lactobacillus fermentum ACA-DC 179 and Lactobacillus plantarun ACA-DC 269 produced bacteriocins solely against Streptococcus oralis. Thus, the percentage of strains that were found to produce bacteriocins against oral bacteria was ~1.3%. The rarity of bacteriocins active against oral LAB pathogens produced by food-related LAB was unexpected given their close phylogenetic relationship. Nevertheless, when tested in inhibition assays, the potency of the bacteriocin(s) of S. macedonicus ACA-DC 198 against the three oral streptococci was high. Fourier-transform infrared spectroscopy combined with principal component analysis revealed that exposure of the target cells to the antimicrobial compounds caused major alterations of key cellular constituents. Our findings indicate that bacteriocins produced by food-related LAB against oral LAB may be rare, but deserve further investigation since, when discovered, they can be effective antimicrobials.
Probiotics, defined as “live microorganisms which, when administered in adequate amounts, confer a health benefit on the host” , have become a major topic of lactic acid bacteria (LAB) research over the last two decades. Although a number of health-promoting effects arising from the use of probiotics have been demonstrated, so far the main field of research has been the gastrointestinal tract . Probiotics have been poorly investigated from the oral health perspective. However, this is gradually changing .
Dental plaque is a biofilm that develops naturally on the teeth and is composed of about 700 bacteria species that take part in the complex ecosystem of the oral cavity . Interactions among these bacterial species, from the early stages of colonization to the formation of mature supragingival and subgingival plaque, are the main etiological agents of oral infectious diseases, such as dental caries, gingivitis and periodontitis . Dental caries is a multifactorial disease of bacterial origin that is characterized by acid demineralization of the tooth enamel as a result of the proliferation of streptococci from the mutans group . Gingivitis and periodontitis are largely caused by specific Gram-negative bacterial infections. Such infections lead to the destruction of the connective tissue and the disruption of the underlying alveovar bone and periodontal ligament supporting the teeth . Moreover, in recent years it has been suggested that oral bacteria are associated with many systemic diseases, such as pneumonia and cardiovascular disease [8,9].
Hence, the need for oral care in a systemic health regimen has been emphasized. Generally, dental plaques that have been deposited firmly as biofilms are removed mechanically while antibacterial mouthwashes are also effective in decreasing tooth surface plaque. In general, mouthwashes contain fluorides, alcohols, detergents or antibacterial substances. Ideal antibacterial substances must be effective against pathogenic or opportunistic pathogenic strains related to oral health, act rapidly, maintain activity at low concentrations, and have no side effects . In this context, bacteriocins isolated from food related LAB could be used as alternative antimicrobials [11,12].
In the present study, the aim was to investigate the antimicrobial activity of LAB strains isolated from food products against oral pathogenic or opportunistic pathogenic bacteria. The inhibitory activity of food LAB strains was studied towards both Gram-negative and Gram-positive strains of bacteria associated with oral health. Moreover, the involvement of proteinaceous compound(s) to this activity was examined. Finally, Fourier-transform infrared (FT-IR) spectroscopy was employed in order to unravel the changes at the cellular level caused by these antimicrobial substances on target bacteria.
2. Results and Discussion
2.1. Screening LAB Food Isolates for the Production of Bacteriocins Active against Oral Pathogens
A total of 236 LAB strains of food origin (Table 1) were screened for antimicrobial activity against 10 target strains (3 Gram-negative and 7 Gram-positive).
Within the set of strains to be tested as bacteriocin-producers against oral bacteria, there were a number of strains that had been screened in our laboratory against food-related bacteria and were found to produce bacteriocins (Supplementary Table 1). From the total of 236 strains, approximately 140 had been previously screened and from those 41 were found positive based on the well diffusion assay (WDA, see Experimental Section). Thus, a conservative estimate of the percentage of bacteriocin-producing strains in the total of strains tested in the present study would be ≥17%. Different sets of target strains were used including common indicator strains employed by different laboratories in similar studies (e.g., Lactococcus lactis CNRZ 117, Lactobacillus sakei LMG 2313, Listeria innocua BL86/26, etc.), as well as in-house indicator strains (e.g., Lactococcus lactis ACA-DC 49, Streptococcus thermophilus ACA-DC 4, Lactobacillus delbrueckii subsp. bulgaricus ACA-DC 84, etc.). Even though for some of the commonly used indicator strains their food origin is established (e.g., for Lactobacillus helveticus ATCC 15009 and L. lactis CNRZ 117, which are isolated from dairy products), for others (e.g., L. innocua BL86/26) the isolation source is not available in the literature or in the databases of culture collections. Our in-house indicator strains were all food isolates of dairy origin.
In the current screening assay, in order to increase the possibility for bacteriocin production, all potential producers were grown in three different culture media, namely skim milk containing yeast extract, MRS and M17. The respective cell-free culture supernatants (CFCSs) were tested towards the target bacteria by the WDA. In case of positive results, the 10-fold concentrated CFCSs, obtained after ammonium sulfate precipitation, were also tested for antimicrobial activity against the sensitive bacteria by the WDA.
None of the LAB strains was able to inhibit any of the Gram-negative strains used as target strains, apart from three strains, namely Lactococcus lactis ACA-DC 46 (Formaela cheese isolate), and E. faecium ACA-DC 3350 and ACA-DC 3359 (both Feta cheese isolates). More precisely, the milk CFCS of L. lactis, as well as the MRS CFCSs of both E. faecium strains gave a “borderline” inhibition (i.e., less colonies of the target strain around the well) towards Porphyromonas gingivalis DSM 20709T. Treatment with proteinase K revealed that this antimicrobial effect was not due to bacetriocin(s).
Regarding the Gram-positive target strains tested, only three LAB strains, namely Lactobacillus fermentum ACA-DC 179 (Kasseri cheese isolate), Lactobacillus plantarum ACA-DC 269 (Feta cheese isolate) and Streptococcus macedonicus ACA-DC 198 (Kasseri cheese isolate), showed antimicrobial activity towards Streptococcus strains (Table 2). More specifically, the MRS CFCS of L. fermentum ACA-DC 179 and milk CFCS of L. plantarum ACA-DC 269 were active against S. oralis LMG 14532T. On the other hand, the milk CFCS of S. macedonicus ACA-DC 198 exhibited inhibitory activity against S. oralis LMG 14532T, S. sanguinis DSM 20068 and S. gordonii LMG 14518T, while the M17 CFCS of S. macedonicus ACA-DC 198 towards S. sanguinis DSM 20068 and S. gordonii LMG 14518T. In all cases, the antimicrobial activity increased with the respective 10-fold concentrated CFCSs (Table 2). No activity was detected with both M17 and milk CFCS of L. fermentum ACA-DC 179, as well as the MRS CFCS of S. macedonicus ACA-DC 198 in accordance to previous experiments . In addition, no activity was detected with both MRS and M17 CFCS of L. plantarum ACA-DC 269. In addition, the proteinaceous nature of the substances responsible for all inhibitions observed was verified after treatment with proteinase K that resulted in complete loss of antimicrobial activity.
Lactic acid bacteria, and especially strains of the genera Lactobacillus and Streptococcus, are known to play a role in the health of the oral cavity . In the present study, the rarity of bacteriocins produced by food-related LAB that were active against oral LAB was unexpected. Despite the presence of at least 41 bacteriocin producers, corresponding to ≥17% of the 236 LAB strains of food origin as mentioned above, six were able to inhibit the oral pathogenic or opportunistic pathogenic bacteria tested as target strains. Among these six LAB strains, only three showed antimicrobial activity that could be correlated to bacteriocin production, representing ~1.3% of the strains tested. This difference of more than 10-fold in the number of strains inhibiting food vs. oral indicator strains is intriguing given the close phylogenetic relationship between food and oral LAB that should favor the existence of bacteriocins produced by members of the one group active against members of the other. It could be hypothesized that a correlation between the ecological niche and the antimicrobial spectrum of bacteriocins exists. Bacteriocins produced by bacteria in an ecological niche may have evolved to target mostly species/strains present in this particular niche. However, more experimental evidence is needed to validate this hypothesis.
2.2. Sensitivity of Oral Streptococci towards the Antimicrobial Activity of the Food LAB Strains
Since the potency of the antimicrobial substance is the most important factor, we preceded with in vitro inhibition assays in order to determine the effectiveness of the antimicrobials produced by food LAB. In addition, since oral bacteria have been suggested to adopt a feast and famine lifestyle in the oral cavity , we also attempted to assess the sensitivity of the target strains in different growth phases. Concerning the antimicrobial activity of the two Lactobacillus strains, only the MRS CFCS of L. fermentum ACA-DC 179 was included in these experiments as it was the most active one. In addition, only the milk CFCS of S. macedonicus ACA-DC 198 was tested as it was active towards more target strains than the M17 CFCS of the same strain. The antimicrobial activity of the two active CFCSs was studied against target cells corresponding to three different phases of bacterial growth (lag, logarithmic and stationary). In all experiments, the 10-fold concentrated supernatants of L. fermentum ACA-DC 179 and S. macedonicus ACA-DC 198 were used.
The antimicrobial activity of the MRS CFCS of L. fermentum against S. oralis LMG 14532T was not evident by the in vitro inhibition assay. Only in the case of the stationary phase cells, a viability difference, less than 1 log, was detected between S. oralis cells treated with the supernatant and those treated with the control sample (data not shown).
On the contrary, growth phase of the three Streptococcus strains affected their sensitivity to the milk CFCS of S. macedonicus ACA-DC 198. As shown in Figure 1, in most cases lag and logarithmic phase cells were killed rapidly (≥99% cell-death within the first 2 h). In details, for S. oralis LMG 14532T (Figure 1A), viability differences were detected mainly for lag and logarithmic phase cells (2 log decrease after 2 h of incubation). For S. sanguinis DSM 20068, the milk CFCS of S. macedonicus affected similarly both lag and stationary phase cells (2 log decreases after 2 h of incubation) but not the logarithmic phase cells (Figure 1B). Finally, S. gordonii cells at lag phase were more sensitive (4 log decrease after 2 h of incubation) than logarithmic phase cells (3 log decrease after 2 h of incubation) while less activity was detected against stationary phase cells (Figure 1C). A recovery of cells after 24 h of incubation was observed that in our opinion deserves further investigation.
According to the inhibition assays performed, lag phase cells of all three sensitive Streptococcus strains were the most sensitive to the antimicrobial compound(s) of the milk CFCS of S. macedonicus ACA-DC 198. Differences in the effect of the target cells’ growth phase on their sensitivity to active bacteriocins or bacteriocin-like inhibitory substances have also been reported in the past [16–18]. Lag and exponential phase cells seem to be less resistant than stationary phase cells as during these phases biosynthesis of the target cell membrane is more vigorous, enhancing the initial electrostatic attraction of the bacteriocin that is thought to be the driving force for subsequent events .
2.3. FT-IR Analysis
The FT-IR spectroscopy was applied in order to specify global biochemical changes of target Streptococcus cells after incubation with the 10-fold concentrated milk CFCS of S. macedonicus ACA-DC 198. It has been previously established that in milk S. macedonicus produces the bacteriocin macedocin . We also included samples of the target strains treated with the pure bacteriocin molecule for comparison. We adjusted the concentration of purified macedocin so as to be equal in arbitrary anits (AU)/mL to that of the CFCS during treatment. For all target strains, FT-IR spectra were recorded for lag phase cells treated for 2 h with the active supernatant or pure bacteriocin. Figure 2 shows the mean FT-IR spectra of S. gordonii LMG 14518T cells in all four characteristic spectral regions [21,22]. Region I (3000 to 2800 cm−1) is the region dominated by the fatty acids of the bacterial cell membrane, and peaks at 2960 cm−1, 2925 cm−1, and 2860 cm−1 are assigned to the asymmetric or symmetric stretches of their methyl or methylene groups [23,24]. Region II (1800 to 1500 cm−1) reflects mainly the proteinaceous content of the cells as the two intense peaks at 1650 and 1550 cm−1 are due to the vibrations of amide I and II bands, respectively . Region III (1500 to 1200 cm−1) is considered a mixed region, as it is informative for proteins, fatty acids, and other phosphate-carrying compounds. Peak at 1455 cm−1 can be assigned to the asymmetric bending of methyl or methylene groups of proteins, while peak at 1400 cm−1 can be attributed to the symmetric bending of the same groups as well as the C-O symmetric stretching of carbohydrates. In addition, peak at 1240 cm−1 is due to the symmetric stretching of phosphodiester groups in nucleic acids or phospholipids . Finally, region IV (1200 to 900 cm−1) is the region influenced by polysaccharides of the cell wall, as the broad band at 1100 to 950 cm−1 arises from the stretching vibrations of the C-O polysaccharides moieties .
Principal component analysis (PCA) was performed for each spectral region separately and distinct sample clusters were observed among the cells of S. gordonii LMG 14518T treated with the CFCS, the pure bacteriocin sample and those treated with the control samples (milk supernatant or distilled water) in all spectral regions (Figure 4). Discrete grouping of samples was readily evident within the first three PCs, accounting for 87% to 98% of the variability in the original data depending on the spectral region. These findings clearly demonstrate that the bacteriocin(s) activity within the CFCS of the S. macedonicus culture had resulted in alterations of the composition of all major cellular constituents of S. gordonii. Similar results were obtained when S. sanguinis DSM 20068 and S. oralis LMG 14532T were used as target strains (data not shown).
We detected important changes in the FT-IR spectral features for the target strain S. gordonii LMG 14518T after treatment with the CFCS or the purified macedocin. Non-treated and treated cells were clustered in distinct groups according to the PCA of their second derivative transformed FT-IR spectra. Consequently, our findings clearly support that the chemical composition of the target cells changed radically due to the antimicrobial effect of the milk CFCS of S. macedonicus ACA-DC 198 or the bacteriocin treatment. The magnitude of the alterations on the cellular composition of the sensitive cells, determined during FT-IR analysis, seems to be extensive (i.e., affecting all major cellular constituents) and coincides with the detrimental effect of the antimicrobial compound(s). In fact, it could be hypothesized that these changes in the chemistry of the cell could be the reason for the potency of the bacteriocin produced by S. macedonicus ACA-DC 198. Nevertheless, the actual underlying mechanism needs to be elucidated.
It should be emphasized that control samples could be readily distinguished from the treated samples within the first PC that carries the major part of the variability within the dataset. In fact, the differences in PC values for the two control groups were significantly less than the difference of each control group with its respective treated sample (i.e., treated with CFCS or pure baceriocin), indicating that the chemical composition of control samples was similar. For example, the two control groups occupied the same space in the PC graph in the case of spectral region I. Furthermore, treated samples also exhibited minor differences in the PC1 axis, supporting that chemical changes at the cellular level have the same major trend with the exception of spectral region I, where the two groups of treated samples were distributed in opposite directions of the control samples. This phenomenon deserves further investigation, since it indicates that substances in the CFCS that are not present in the purified macedocin preparation may also contribute to the observed changes (and potentially the killing effect).
3. Experimental Section
3.1. Bacterial Strains and Culture Conditions
A total of 236 LAB strains, namely 139 lactobacilli and 97 cocci, were included in the present study as potential producers of antimicrobial activity (Table 1). Identification of LAB strains was performed with 16s rRNA gene sequencing followed by phenotypic tests, including API 50 CH tests (bioMérieux, Inc., Marcy l’Etoile, France). The strains were isolated mainly from dairy products and are held at the ACA-DC Collection (Laboratory of Dairy Research, Agricultural University of Athens, Athens, Greece). They were stored at −80 °C in MRS (Biokar Diagnostics, Beauvais, France) or M17 broth (Biokar Diagnostics), supplemented with 20% (v/v) glycerol.
Ten strains, among them 3 Gram-negative and 7 Gram-positive, belonging to bacteria species related to the oral health were used as target strains. Fusobacterium nucleatum subsp. vincentii DSM 19507T and Porphyromonas gingivalis DSM 20709T were grown in BHI supplemented with yeast extract (0.5% w/v, Biokar Diagnostics), hemin (5 μg/mL, Sigma, St. Louis, MO, USA) and menadione (1 μg/mL, Sigma) at 37 °C, anaerobically (GasPak kit, Beckton Dickinson, USA). Aggregatibacter actinomycetemcomitans DSM 11123 was cultured in BHI (Biokar Diagnostics) enriched with yeast extract (0.5% w/v, Biokar Diagnostics) at 37 °C. Finally, Staphylococcus aureus DSM 21705 and six Streptococcus strains, namely Streptococcus gordonii LMG 14518T, Streptococcus mutans LMG 14558T, Streptococcus oralis LMG 14532T, Streptococcus salivarius LMG 11489T, Streptococcus sanguinis DSM 20068, and Streptococcus sobrinus LMG 14641T, were grown in BHI (Biokar Diagnostics) at 37 °C.
The target strains presented in supplementary Table 1 were cultivated as follows: Clostridium tyrobutyricum NCDO 1754 was grown anaerobically (GasPak kit) in RCM (Biokar Diagnostics) at 37 °C, Listeria innocua BL86/26 in BHI at 30 °C, lactobacilli in MRS at appropriate temperatures and enterococci, lactococci and streptococci in M17, also at appropriate temperatures.
3.2. Preparation of Cell-Free Culture Supernatants (CFCSs) and of Pure Macedocin
CFCSs of the potential producer strains were collected after growth in skim milk (10% w/v, Oxoid) containing 0.3% (w/v) yeast extract (Biokar Diagnostics), MRS and M17 broth. Fresh overnight culture supernatants were collected by centrifugation (12,000 ×g, 15 min, 4 °C), adjusted to pH 6.5 and filtered (0.22 μm Millex Syringe Filter, Millipore, Billerica, MA, USA). Skim milk containing yeast extract, MRS and M17 broth also adjusted to pH 6.5 and filtered were used as controls. Neutralizing the pH of the supernatant was considered necessary to avoid false positive results in the WDA due to acidity-mediated inhibition of the indicator strain.
In order to obtain the 10-fold concentrated CFCSs, pellets of the above supernatants, obtained after ammonium sulfate precipitation (50% saturation), were diluted in the appropriate volume of sterilized distilled water. Non-inoculated growth medium (skim milk containing yeast extract, MRS and M17), adjusted to pH 6.5, filtered and concentrated (10-fold) after ammonium sulfate treatment were used as controls. Before use, all concentrated supernatants were once more centrifuged (12,000 ×g, 15 min, 4 °C) in order to avoid further precipitation during the experiments.
CFCSs of strains presented in supplementary Table 1 were prepared as above from fresh overnight cultures of lactobacilli, leuconostocs and pediococci grown in MRS and enterococci, lactococci and streptococci grown in M17, with the exception of Streptococcus macecdonicus ACA-DC 198 that was grown in skim milk supplemented with 0.3% (w/v) yeast extract.
Pure macedocin was prepared as previously described . After dialysis, active fractions were lyophilized and resuspended in distilled water (data not shown).
3.3. Detection of Antimicrobial Activity
CFCSs were screened for antimicrobial activity using the well diffusion assay (WDA). Briefly, 5 × 105–1 × 106 cfu/mL of the target strain was incorporated into the appropriate soft agar (1% w/v) plates. CFCSs (50 μL) of the potential producer strains were transferred to holes (5 mm diameter) drilled into the agar. The plates were then incubated at the appropriate conditions, depending on the target strain, and the antimicrobial activity was recorded as growth-free inhibition zones (diameter) around the well. To assess the effect of proteinase K on the CFCSs antimicrobial activity, proteinase K (Applichem, Darmstadt, Germany) was added in a well next to the well containing the CFCSs at a final concentration of 2 mg/mL. The effect was attributed to the production of bacteriocins if the inhibition zone totally disappeared after proteinase K treatment.
3.4. Inhibition Assays
The inhibitory activity of CFCSs towards sensitive strains was studied by an in vitro inhibition assay designed to target cells at different bacterial growth phases, namely lag, logarithmic and stationary phase cells.
To obtain target cells, an inoculum (2% v/v) of fresh 18 h culture was transferred to 5 mL of BHI broth and incubated at 37 °C. For lag phase cells, cells were incubated for 2 h (S. oralis LMG 14532T and S. sanguinis DSM 20068) or 2.5 h (S. gordonii LMG 14518T). For logarithmic phase cells, cells were incubated for 3, 4 and 5 h (S. oralis LMG 14532T, S. sanguinis DSM 20068, and S. gordonii LMG 14518T, respectively). Finally, for stationary phase cells, cells were incubated for 18 h for all three Streptococcus strains. After incubation, cells were collected by centrifugation, washed twice with phosphate-buffered saline (PBS; pH 7.2) and resuspended in the same volume of fresh BHI broth (5 mL). Target cell suspensions were then mixed with equal volume (5 mL) of active CFCS or the control supernatant and incubated at 37 °C for 24 h. At various time intervals, the surviving cells were determined by plating on the appropriate growth medium. Three independent experiments were performed.
3.5. FT-IR Sample Preparation and Measurements
Lag phase cell suspensions of the target strain (5 mL) were mixed with equal volume (5 mL) of active CFCS or the control supernatant and incubated at 37 °C. Purified macedocin was used in the same concentration to that of the CFCS in AU/mL. After 2 h of incubation, cells were collected by centrifugation, washed twice with PBS (pH 7.2) and resuspended in 30 μL of sterile double-distilled water. FT-IR sample preparation and measurements were performed according to the methodology described before . In brief, 10 μL of the resulting suspension were spotted at the center of an IR transparent ZnSe optical disc. Samples were then air dried under laminar flow in order to achieve the formation of a homogenous dried film of bacterial cells. Nicolet 6700 spectrometer (DTGS detector; Nichrome source; KBr beamsplitter; Thermo Electron Corporation, Madison, WI, USA) was used to record FT-IR bacterial spectra. Spectra were recorded in absorbance between wave numbers 4000 to 600 cm−1 at a 4 cm−1 spectral resolution and each spectrum was obtained by co-adding 100 scans.
3.6. FT-IR Data Analysis
Omnic software (Version 7.3, Thermo Electron Corporation) was used to conduct spectral processing. FT-IR spectra were smoothed, baseline corrected and normalized using the automatic functions and the algorithms built into the aforementioned software. Furthermore, the second derivative transformation of each pre-processed spectrum was calculated with the Savitzky-Golay derivative filter and default parameters (7-point, 4 cm−1 resolution, polynomial degree 3). Data from the second derivative transformed spectra were imported into Statgraphics Centurion software (Version XV, Statpoint Technologies Inc., VA, USA) and principal component analysis (PCA) was employed in order to statistically evaluate these data.
After a screening of an important number of LAB food isolates for the production of bacteriocins active against a set of known bacteria implicated in oral disease, we report that this seems to be a rare property. Overall, only three out of 236 LAB strains, namely L. plantarum ACA-DC 269, L. fermentum ACA-DC 179 and S. macedonicus ACA-DC 198 showed inhibitory activity against bacteria related to oral health that could be attributed to bacteriocin(s) present in their cell-free culture supernatants, even though at least 41 bacteriocin-producing LAB strains were included in the set of strains used in this experiment. This conclusion is rather unexpected due to the close phylogenetic relationship between food- and oral-related LAB. The effect of the S. macedonicus ACA-DC 198 milk CFCS or purified macedocin was more prominent against target cells at the lag phase of growth and could be correlated to major alterations in the chemistry of the cells as a whole. Thus, the antimicrobial compounds investigated here could be further studied for their role in oral infections. Our findings indicate that this chase for appropriate antibiotics towards oral pathogens within food LAB must be continued.
The present work has been carried out through financial support from the Greek Ministry of Health and Social Solidarity.
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|Table 1. Genus and species of the lactic acid bacteria used as potential producers of bacteriocins.|
|Genus/species||Number of strains|
|Lactobacillus delbrueckii subsp. bulgaricus||11|
|Lactobacillus delbrueckii subsp. delbrueckii||1|
|Lactobacillus delbrueckii subsp. lactis||4|
|Lactobacillus paracasei subsp. paracasei||17|
|Lactobacillus paracasei subsp. tolerans||1|
|Leuconostoc mesenteroides subsp. dextranicum||4|
|Table 2. Antimicrobial activity of cell-free culture supernatants (CFCSs) of L. fermentum ACA-DC 179, L. plantarum ACA-DC 269 and S. macedonicus ACA-DC 198 towards three Streptococcus strains as determined by the well diffusion assay.|
|Target strain||Inhibition (diameter; mm ± SD) a|
|L. fermentum ACA-DC 179||L. plantarum ACA-DC 269||S. macedonicus ACA-DC 198|
|MRS CFCS||10-fold concentrated MRS CFCS||Milk CFCS||10-fold concentrated milk CFCS||Milk CFCS||10-fold concentrated milk CFCS||M17 CFCS||10-fold concentrated M17 CFCS|
|S. oralis LMG 14532T||0.7 ± 0.10||1.1 ± 0.10||0.5 ± 0.06||0.9 ± 0.06||1.0 ± 0.06||1.1 ± 0.10||– b||–|
|S. sanguinis DSM 20068||–||–||–||–||1.0 ± 0.06||1.1 ± 0.12||0.9 ± 0.06||1.2 ± 0.12|
|S. gordonii LMG 14518T||–||–||–||–||1.2 ± 0.06||1.6 ± 0.10||1.0 ± 0.06||1.4 ± 0.12|
aValues are means of the results of three independent experiments;bNo inhibition.
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