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s oralis atcc 9811  (ATCC)


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    Structured Review

    ATCC s oralis atcc 9811
    S Oralis Atcc 9811, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 34 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/s+oralis+atcc+9811/Streptococcus+oralis%3B+Strain+M7A/pmc12766077-21-7-9
    Average 95 stars, based on 34 article reviews
    s oralis atcc 9811 - by Bioz Stars, 2026-10
    95/100 stars

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    other:

    Article Title: A Potent and Narrow-Spectrum Antibacterial against Clostridioides difficile Infection
    Article Snippet: S. oralis ATCC 9811 , 128 , >128 , 64 , 1 , >128 , 32.

    In Silico:

    Article Title: Functional divergence of MdpS and MdpS2 reveals mucin-targeting strategies in Streptococcus oralis
    Article Snippet: .. A genomic study of S. oralis ATCC 9811 revealed that the genes encoding MdpS (Supplementary Figure 1) and MdpS2 (Supplementary Figure 2) are putatively located in the same operon, with a hypothetical protein annotated in silico located between them (Supplementary Figure 3). ..

    Activity Assay:

    Article Title: Potential of microbial-derived biosurfactants for oral applications–a systematic review
    Article Snippet: Bucci A.R. et al. [ ] (2018) , Surfactin , Streptococcus mutans (ATCC 25,175), Streptococcus mitis (ATCC 49,456), Streptococcus salivarius (ATCC 13,419), Porphyromonas gingivalis (ATCC 33,277), Pseudomonas aeruginosa (ATCC 27,853), Staphylococcus aureus (ATCC 25,923), Escherichia coli (ATCC 25,922), Candida albicans (ATCC 10,231) , Terpinen-4-ol (TP) Cetylpyridinium chloride (CPC) Cetyl trimethyl ammonium bromide (CTAB) (all of which with purity above 95% (from Sigma-Aldrich, Brazil)) , 1. Disk diffusion assay 2. Minimum inhibitory concentration 3. Determination of combination index (CI) for micellar solutions 4. Adhesion on test tubes , 1. Inhibition was observed when surfactin was mixed with TP against S. aureus, P. gingivalis , and E. coli , while no inhibition was detected for surfactin against all microorganisms. 2. MIC of surfactin ranged from 22 μg/mL to 700 μg/mL, with no inhibition for P.gingivalis . 3. Combination index for surfactin and TP were synergism for S. mutans and P.gingivalis , slight synergism for C. albicans and E. coli , additive for S. aureus , and antagonism for P. aeruginosa , S. salivarius , and S. mitis . 4. The micellar solution of surfactin and TP showed very high enhancement in antiadhesion activity for two oral pathogens ( C. albicans and P. gingivalis ).. .. Ciandrini E. et al. [ ] (2016) , Biosurfactant from Lactobacillus , Streptococcus mutans ATCC 25,175 and Streptococcus oralis ATCC 9811 , 1% SDS (common chemical surfactant) , 1. Biosurfactants preparation and assessment of the antimicrobial activity by time-killing studies 2. Dialysis of biosurfactants 3. Characterization of dialyzed biosurfactant surface properties 4. Biofilm formation 5. Anti-biofilm effect of dialyzed biosurfactants , 1. Biosurfactants from L. reuteri DSM 17,938, L. acidophilus DDS-1, L. paracasei B21060, and L. rhamnosus ATCC 53,103 showed the greatest antimicrobial activity against S. mutans and S. oralis . They were selected for further studies, and their excreted biosurfactants were purified through dialysis. 2. Biosurfactants excreted by L. reuteri DSM 17,938, L. acidophilus DDS-1, L. rhamnosus ATCC 53,103, and L. paracasei B21060 strains were dialyzed using 1a and 6 kDa methods. 3. A reduction of the interfacial tension from 47.92 to 34.81 mN/m was observed compared to MRS broth’s surface tension (53.0 mN/m). The highest emulsifying activity was obtained from the dialyzed 6 kDa biosurfactant of L. paracasei B21060 (61.11%). 4. All 1 and 6 kDa dialyzed BSFs effectively inhibited S. mutans ATCC 25,175 and S. oralis ATCC 9811 biofilm growth. Biomass analysis highlighted the dose-dependent effect of all the dialyzed biosurfactants (1 and 6 kDa), particularly remarkable in the case of biofilm formation inhibition of S. oralis ATCC 9811. 5. The 6 kDa dialyzed BSFs possess antibiofilm activity against S. mutans ATCC 25,175 and S. oralis ATCC 9811 with optical density of 0.329 (± 0.026) for BSF of L. reuteri DSM 17,938, 0.280 (± 0.009) for L. acidophilus DDS-1, 0.356 (± 0.025) for L. rhamnosus ATCC 53,103, and 0.261 (± 0.012) for L. paracasei B21060.. .. Farias J.M. et al. [ ] (2019) , Biosurfactant Pseudomonas aeruginosa (PB), Bacillus cereus (BB), Candida bombicola (CB) , C. albicans ATCC 1106 S. aureus ATCC 15,656 E. coli ATCC 25,922 L. acidophilus ATCC 4356 S. salivarius ATCC 25,975 S. mutans ATCC 25,175 , Chitosan (extracted from the cell wall of Mucor javanicus (UCP 69)), Peppermint essential oil (POE) , 1. Characterization of biosurfactants 2. Formulation of mouthwash 3. Determination of antimicrobial activity 4. Analysis of fraction inhibitory concentration 5. Evaluation of toxicity of formulated mouthwashes , 1. The biosurfactants obtained from C. bombicola , B. cereus , and P. aeruginosa (respectively designated as CB, BB, and PB) were capable of reducing the surface tension of water from 70 mN/m to 30, 29, and 26.5 mN/m, respectively. 2. The formulation consists of biosurfactant, peppermint essential oil, and chitosan solution (diluted in 1% acetic acid), the solid components (sodium benzoate and sodium saccharine) in a fine powder, followed by distilled water to complete 100 mL. The pH of the formulation was adjusted to 7.0 with NaOH 1 N. 3. The biosurfactant PB was the most effective against S. aureus , E. coli , and S. salivarius (MIC: 20 μg/mL), while PB and CB had similar effects on S. mutans (MIC: 20 μg/mL). All biosurfactants exhibited uniform effects on C. albicans and L. acidophilus (MIC: 40 μg/mL). Combining biosurfactants with chitosan reduced MIC for all microorganisms. When combined with peppermint essential oils, the MIC for C. albicans either increased (CB + POE and BB + POE: 30 μg/mL) or remained the same (PB + POE: 20 μg/mL). The low MIC combination for L. acidophilus (20 μg/mL) was peppermint essential oil with PB. For S. mutans , only CB + POE maintained the biosurfactant’s MIC, with reductions observed in all other combinations. 4. The combinations of the CB and PB with chitosan demonstrated an additive effect on the majority of microorganisms tested and an indifferent effect on E. coli and C. albicans . The combinations of CB and BB with the peppermint essential oil exhibited an additive effect only on the gram-negative bacterium E. coli and an indifferent effect on the other microorganisms tested. 5. The results demonstrate that the test mouthwashes were classified as non-toxic to the fibroblast line, with cell inhibition rates lower than 20%. However, the mouthwash containing the biosurfactant extracted from C. bombicola + peppermint essential oil + chitosan exhibited moderate toxicity to the macrophage line (66% inhibition)..

    Purification:

    Article Title: Potential of microbial-derived biosurfactants for oral applications–a systematic review
    Article Snippet: Bucci A.R. et al. [ ] (2018) , Surfactin , Streptococcus mutans (ATCC 25,175), Streptococcus mitis (ATCC 49,456), Streptococcus salivarius (ATCC 13,419), Porphyromonas gingivalis (ATCC 33,277), Pseudomonas aeruginosa (ATCC 27,853), Staphylococcus aureus (ATCC 25,923), Escherichia coli (ATCC 25,922), Candida albicans (ATCC 10,231) , Terpinen-4-ol (TP) Cetylpyridinium chloride (CPC) Cetyl trimethyl ammonium bromide (CTAB) (all of which with purity above 95% (from Sigma-Aldrich, Brazil)) , 1. Disk diffusion assay 2. Minimum inhibitory concentration 3. Determination of combination index (CI) for micellar solutions 4. Adhesion on test tubes , 1. Inhibition was observed when surfactin was mixed with TP against S. aureus, P. gingivalis , and E. coli , while no inhibition was detected for surfactin against all microorganisms. 2. MIC of surfactin ranged from 22 μg/mL to 700 μg/mL, with no inhibition for P.gingivalis . 3. Combination index for surfactin and TP were synergism for S. mutans and P.gingivalis , slight synergism for C. albicans and E. coli , additive for S. aureus , and antagonism for P. aeruginosa , S. salivarius , and S. mitis . 4. The micellar solution of surfactin and TP showed very high enhancement in antiadhesion activity for two oral pathogens ( C. albicans and P. gingivalis ).. .. Ciandrini E. et al. [ ] (2016) , Biosurfactant from Lactobacillus , Streptococcus mutans ATCC 25,175 and Streptococcus oralis ATCC 9811 , 1% SDS (common chemical surfactant) , 1. Biosurfactants preparation and assessment of the antimicrobial activity by time-killing studies 2. Dialysis of biosurfactants 3. Characterization of dialyzed biosurfactant surface properties 4. Biofilm formation 5. Anti-biofilm effect of dialyzed biosurfactants , 1. Biosurfactants from L. reuteri DSM 17,938, L. acidophilus DDS-1, L. paracasei B21060, and L. rhamnosus ATCC 53,103 showed the greatest antimicrobial activity against S. mutans and S. oralis . They were selected for further studies, and their excreted biosurfactants were purified through dialysis. 2. Biosurfactants excreted by L. reuteri DSM 17,938, L. acidophilus DDS-1, L. rhamnosus ATCC 53,103, and L. paracasei B21060 strains were dialyzed using 1a and 6 kDa methods. 3. A reduction of the interfacial tension from 47.92 to 34.81 mN/m was observed compared to MRS broth’s surface tension (53.0 mN/m). The highest emulsifying activity was obtained from the dialyzed 6 kDa biosurfactant of L. paracasei B21060 (61.11%). 4. All 1 and 6 kDa dialyzed BSFs effectively inhibited S. mutans ATCC 25,175 and S. oralis ATCC 9811 biofilm growth. Biomass analysis highlighted the dose-dependent effect of all the dialyzed biosurfactants (1 and 6 kDa), particularly remarkable in the case of biofilm formation inhibition of S. oralis ATCC 9811. 5. The 6 kDa dialyzed BSFs possess antibiofilm activity against S. mutans ATCC 25,175 and S. oralis ATCC 9811 with optical density of 0.329 (± 0.026) for BSF of L. reuteri DSM 17,938, 0.280 (± 0.009) for L. acidophilus DDS-1, 0.356 (± 0.025) for L. rhamnosus ATCC 53,103, and 0.261 (± 0.012) for L. paracasei B21060.. .. Farias J.M. et al. [ ] (2019) , Biosurfactant Pseudomonas aeruginosa (PB), Bacillus cereus (BB), Candida bombicola (CB) , C. albicans ATCC 1106 S. aureus ATCC 15,656 E. coli ATCC 25,922 L. acidophilus ATCC 4356 S. salivarius ATCC 25,975 S. mutans ATCC 25,175 , Chitosan (extracted from the cell wall of Mucor javanicus (UCP 69)), Peppermint essential oil (POE) , 1. Characterization of biosurfactants 2. Formulation of mouthwash 3. Determination of antimicrobial activity 4. Analysis of fraction inhibitory concentration 5. Evaluation of toxicity of formulated mouthwashes , 1. The biosurfactants obtained from C. bombicola , B. cereus , and P. aeruginosa (respectively designated as CB, BB, and PB) were capable of reducing the surface tension of water from 70 mN/m to 30, 29, and 26.5 mN/m, respectively. 2. The formulation consists of biosurfactant, peppermint essential oil, and chitosan solution (diluted in 1% acetic acid), the solid components (sodium benzoate and sodium saccharine) in a fine powder, followed by distilled water to complete 100 mL. The pH of the formulation was adjusted to 7.0 with NaOH 1 N. 3. The biosurfactant PB was the most effective against S. aureus , E. coli , and S. salivarius (MIC: 20 μg/mL), while PB and CB had similar effects on S. mutans (MIC: 20 μg/mL). All biosurfactants exhibited uniform effects on C. albicans and L. acidophilus (MIC: 40 μg/mL). Combining biosurfactants with chitosan reduced MIC for all microorganisms. When combined with peppermint essential oils, the MIC for C. albicans either increased (CB + POE and BB + POE: 30 μg/mL) or remained the same (PB + POE: 20 μg/mL). The low MIC combination for L. acidophilus (20 μg/mL) was peppermint essential oil with PB. For S. mutans , only CB + POE maintained the biosurfactant’s MIC, with reductions observed in all other combinations. 4. The combinations of the CB and PB with chitosan demonstrated an additive effect on the majority of microorganisms tested and an indifferent effect on E. coli and C. albicans . The combinations of CB and BB with the peppermint essential oil exhibited an additive effect only on the gram-negative bacterium E. coli and an indifferent effect on the other microorganisms tested. 5. The results demonstrate that the test mouthwashes were classified as non-toxic to the fibroblast line, with cell inhibition rates lower than 20%. However, the mouthwash containing the biosurfactant extracted from C. bombicola + peppermint essential oil + chitosan exhibited moderate toxicity to the macrophage line (66% inhibition)..

    Inhibition:

    Article Title: Potential of microbial-derived biosurfactants for oral applications–a systematic review
    Article Snippet: Bucci A.R. et al. [ ] (2018) , Surfactin , Streptococcus mutans (ATCC 25,175), Streptococcus mitis (ATCC 49,456), Streptococcus salivarius (ATCC 13,419), Porphyromonas gingivalis (ATCC 33,277), Pseudomonas aeruginosa (ATCC 27,853), Staphylococcus aureus (ATCC 25,923), Escherichia coli (ATCC 25,922), Candida albicans (ATCC 10,231) , Terpinen-4-ol (TP) Cetylpyridinium chloride (CPC) Cetyl trimethyl ammonium bromide (CTAB) (all of which with purity above 95% (from Sigma-Aldrich, Brazil)) , 1. Disk diffusion assay 2. Minimum inhibitory concentration 3. Determination of combination index (CI) for micellar solutions 4. Adhesion on test tubes , 1. Inhibition was observed when surfactin was mixed with TP against S. aureus, P. gingivalis , and E. coli , while no inhibition was detected for surfactin against all microorganisms. 2. MIC of surfactin ranged from 22 μg/mL to 700 μg/mL, with no inhibition for P.gingivalis . 3. Combination index for surfactin and TP were synergism for S. mutans and P.gingivalis , slight synergism for C. albicans and E. coli , additive for S. aureus , and antagonism for P. aeruginosa , S. salivarius , and S. mitis . 4. The micellar solution of surfactin and TP showed very high enhancement in antiadhesion activity for two oral pathogens ( C. albicans and P. gingivalis ).. .. Ciandrini E. et al. [ ] (2016) , Biosurfactant from Lactobacillus , Streptococcus mutans ATCC 25,175 and Streptococcus oralis ATCC 9811 , 1% SDS (common chemical surfactant) , 1. Biosurfactants preparation and assessment of the antimicrobial activity by time-killing studies 2. Dialysis of biosurfactants 3. Characterization of dialyzed biosurfactant surface properties 4. Biofilm formation 5. Anti-biofilm effect of dialyzed biosurfactants , 1. Biosurfactants from L. reuteri DSM 17,938, L. acidophilus DDS-1, L. paracasei B21060, and L. rhamnosus ATCC 53,103 showed the greatest antimicrobial activity against S. mutans and S. oralis . They were selected for further studies, and their excreted biosurfactants were purified through dialysis. 2. Biosurfactants excreted by L. reuteri DSM 17,938, L. acidophilus DDS-1, L. rhamnosus ATCC 53,103, and L. paracasei B21060 strains were dialyzed using 1a and 6 kDa methods. 3. A reduction of the interfacial tension from 47.92 to 34.81 mN/m was observed compared to MRS broth’s surface tension (53.0 mN/m). The highest emulsifying activity was obtained from the dialyzed 6 kDa biosurfactant of L. paracasei B21060 (61.11%). 4. All 1 and 6 kDa dialyzed BSFs effectively inhibited S. mutans ATCC 25,175 and S. oralis ATCC 9811 biofilm growth. Biomass analysis highlighted the dose-dependent effect of all the dialyzed biosurfactants (1 and 6 kDa), particularly remarkable in the case of biofilm formation inhibition of S. oralis ATCC 9811. 5. The 6 kDa dialyzed BSFs possess antibiofilm activity against S. mutans ATCC 25,175 and S. oralis ATCC 9811 with optical density of 0.329 (± 0.026) for BSF of L. reuteri DSM 17,938, 0.280 (± 0.009) for L. acidophilus DDS-1, 0.356 (± 0.025) for L. rhamnosus ATCC 53,103, and 0.261 (± 0.012) for L. paracasei B21060.. .. Farias J.M. et al. [ ] (2019) , Biosurfactant Pseudomonas aeruginosa (PB), Bacillus cereus (BB), Candida bombicola (CB) , C. albicans ATCC 1106 S. aureus ATCC 15,656 E. coli ATCC 25,922 L. acidophilus ATCC 4356 S. salivarius ATCC 25,975 S. mutans ATCC 25,175 , Chitosan (extracted from the cell wall of Mucor javanicus (UCP 69)), Peppermint essential oil (POE) , 1. Characterization of biosurfactants 2. Formulation of mouthwash 3. Determination of antimicrobial activity 4. Analysis of fraction inhibitory concentration 5. Evaluation of toxicity of formulated mouthwashes , 1. The biosurfactants obtained from C. bombicola , B. cereus , and P. aeruginosa (respectively designated as CB, BB, and PB) were capable of reducing the surface tension of water from 70 mN/m to 30, 29, and 26.5 mN/m, respectively. 2. The formulation consists of biosurfactant, peppermint essential oil, and chitosan solution (diluted in 1% acetic acid), the solid components (sodium benzoate and sodium saccharine) in a fine powder, followed by distilled water to complete 100 mL. The pH of the formulation was adjusted to 7.0 with NaOH 1 N. 3. The biosurfactant PB was the most effective against S. aureus , E. coli , and S. salivarius (MIC: 20 μg/mL), while PB and CB had similar effects on S. mutans (MIC: 20 μg/mL). All biosurfactants exhibited uniform effects on C. albicans and L. acidophilus (MIC: 40 μg/mL). Combining biosurfactants with chitosan reduced MIC for all microorganisms. When combined with peppermint essential oils, the MIC for C. albicans either increased (CB + POE and BB + POE: 30 μg/mL) or remained the same (PB + POE: 20 μg/mL). The low MIC combination for L. acidophilus (20 μg/mL) was peppermint essential oil with PB. For S. mutans , only CB + POE maintained the biosurfactant’s MIC, with reductions observed in all other combinations. 4. The combinations of the CB and PB with chitosan demonstrated an additive effect on the majority of microorganisms tested and an indifferent effect on E. coli and C. albicans . The combinations of CB and BB with the peppermint essential oil exhibited an additive effect only on the gram-negative bacterium E. coli and an indifferent effect on the other microorganisms tested. 5. The results demonstrate that the test mouthwashes were classified as non-toxic to the fibroblast line, with cell inhibition rates lower than 20%. However, the mouthwash containing the biosurfactant extracted from C. bombicola + peppermint essential oil + chitosan exhibited moderate toxicity to the macrophage line (66% inhibition)..



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    Temporal analysis of S. <t>oralis</t> biofilm growth <t>and</t> <t>mdpS/mdpS2</t> mRNA expression. (A) Bacterial growth (CFU/mL) of S. oralis ATCC 9811 grown on MUC5B-coated surfaces over 48 hours. Biofilm growth increased steadily over 3 hours and continued with a minor increase up to 24 hours, followed by both conditions experiencing a 98.5% reduction between 24 and 48 hours. A solid line is used between 3 and 24 hours due to consistent CFU/mL values across replicates, while a dashed line between 24 and 48 hours reflects the variability in the decline phase. (B) Relative mRNA expression of mdpS and mdpS2 were quantified using RT-PCR using ef-tu as the reference gene, where expression was calculated using the ΔΔCt method. Data are shown as mean ± standard deviation from biological triplicates. Asterisks indicate significant differences (* p < 0.05, ** p < 0.01) compared to the 0-hour time point. Statistical analysis was performed using two-way ANOVA with Dunnett's multiple comparison test. Time 0 samples were collected prior to MUC5B exposure and were biologically equivalent across conditions. Although the RNA yield was insufficient for RT-qPCR, this time point served as a shared baseline for fold-change analysis, with a set fold change of 1 reflecting equal mRNA levels in both conditions.
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    Image Search Results


    Temporal analysis of S. oralis biofilm growth and mdpS/mdpS2 mRNA expression. (A) Bacterial growth (CFU/mL) of S. oralis ATCC 9811 grown on MUC5B-coated surfaces over 48 hours. Biofilm growth increased steadily over 3 hours and continued with a minor increase up to 24 hours, followed by both conditions experiencing a 98.5% reduction between 24 and 48 hours. A solid line is used between 3 and 24 hours due to consistent CFU/mL values across replicates, while a dashed line between 24 and 48 hours reflects the variability in the decline phase. (B) Relative mRNA expression of mdpS and mdpS2 were quantified using RT-PCR using ef-tu as the reference gene, where expression was calculated using the ΔΔCt method. Data are shown as mean ± standard deviation from biological triplicates. Asterisks indicate significant differences (* p < 0.05, ** p < 0.01) compared to the 0-hour time point. Statistical analysis was performed using two-way ANOVA with Dunnett's multiple comparison test. Time 0 samples were collected prior to MUC5B exposure and were biologically equivalent across conditions. Although the RNA yield was insufficient for RT-qPCR, this time point served as a shared baseline for fold-change analysis, with a set fold change of 1 reflecting equal mRNA levels in both conditions.

    Journal: Journal of Oral Microbiology

    Article Title: Functional divergence of MdpS and MdpS2 reveals mucin-targeting strategies in Streptococcus oralis

    doi: 10.1080/20002297.2025.2571186

    Figure Lengend Snippet: Temporal analysis of S. oralis biofilm growth and mdpS/mdpS2 mRNA expression. (A) Bacterial growth (CFU/mL) of S. oralis ATCC 9811 grown on MUC5B-coated surfaces over 48 hours. Biofilm growth increased steadily over 3 hours and continued with a minor increase up to 24 hours, followed by both conditions experiencing a 98.5% reduction between 24 and 48 hours. A solid line is used between 3 and 24 hours due to consistent CFU/mL values across replicates, while a dashed line between 24 and 48 hours reflects the variability in the decline phase. (B) Relative mRNA expression of mdpS and mdpS2 were quantified using RT-PCR using ef-tu as the reference gene, where expression was calculated using the ΔΔCt method. Data are shown as mean ± standard deviation from biological triplicates. Asterisks indicate significant differences (* p < 0.05, ** p < 0.01) compared to the 0-hour time point. Statistical analysis was performed using two-way ANOVA with Dunnett's multiple comparison test. Time 0 samples were collected prior to MUC5B exposure and were biologically equivalent across conditions. Although the RNA yield was insufficient for RT-qPCR, this time point served as a shared baseline for fold-change analysis, with a set fold change of 1 reflecting equal mRNA levels in both conditions.

    Article Snippet: The subcellular localisation of MdpS2 was assessed by analysing three distinct fractions of planktonic S. oralis ATCC 9811: lysate (intracellular and cell-wall associated), surface-associated (papain-digested), and extracellular (culture supernatant).

    Techniques: Expressing, Reverse Transcription Polymerase Chain Reaction, Standard Deviation, Comparison, Quantitative RT-PCR

    Enzyme-induced dispersal from S. oralis biofilms by MdpS and MdpS2. Biofilms of S. oralis ATCC 9811 were grown on MUC5B-coated surfaces and treated with MdpS, MdpS2, or buffer (control). After 24 hour treatment, viable counts (CFU/mL) were determined from both the supernatant (representing dispersed cells) and the intact (attached) biofilm, which was resuspended prior to plating. Dispersal was quantified as the ratio of supernatant CFUs to intact biofilm CFUs, normalised to the control (set to 1). Data are shown as mean ± standard deviation from technical replicates. Statistical analysis was performed using Kruskal Wallis ANOVA with Dunn's multiple comparison test (ns = p > 0.05, * p < 0.05).

    Journal: Journal of Oral Microbiology

    Article Title: Functional divergence of MdpS and MdpS2 reveals mucin-targeting strategies in Streptococcus oralis

    doi: 10.1080/20002297.2025.2571186

    Figure Lengend Snippet: Enzyme-induced dispersal from S. oralis biofilms by MdpS and MdpS2. Biofilms of S. oralis ATCC 9811 were grown on MUC5B-coated surfaces and treated with MdpS, MdpS2, or buffer (control). After 24 hour treatment, viable counts (CFU/mL) were determined from both the supernatant (representing dispersed cells) and the intact (attached) biofilm, which was resuspended prior to plating. Dispersal was quantified as the ratio of supernatant CFUs to intact biofilm CFUs, normalised to the control (set to 1). Data are shown as mean ± standard deviation from technical replicates. Statistical analysis was performed using Kruskal Wallis ANOVA with Dunn's multiple comparison test (ns = p > 0.05, * p < 0.05).

    Article Snippet: The subcellular localisation of MdpS2 was assessed by analysing three distinct fractions of planktonic S. oralis ATCC 9811: lysate (intracellular and cell-wall associated), surface-associated (papain-digested), and extracellular (culture supernatant).

    Techniques: Control, Standard Deviation, Comparison