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s mutans atcc 25175 strains (ATCC)

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ATCC s mutans atcc 25175 strains
S Mutans Atcc 25175 Strains, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 2875 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/s+mutans+atcc+25175+strains/Streptococcus+mutans+Clarke/10__3390_slash_pr14030537-197-8-10
Average 99 stars, based on 2875 article reviews

s mutans atcc 25175 strains - by Bioz Stars, 2026-09

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Sterility:

Article Title: In vitro evaluation of the effects of various remineralization agents on root caries.
Article Snippet: The supernatant accumulated in the upper part of the tubes was sterilized by filtration with a 0.45 μm injector filter (Minisart, Sartorius, Germany). .. Sterile saliva was stored at -20°C.14 L.casei ATCC 4646 and S.mutans ATCC 25175 strains with international standards were used for bacterial biofilm experiments. ..

Article Title: Comparison of antibacterial activity of five root canal filling materials in primary dentition: an in vitro study
Article Snippet: .. E. faecalis ATCC 29212 and S. mutans ATCC 25175 strains were obtained from the USJ Pathogens Laboratory, and cultured in Petri dishes for E. faecalis and blood agar for S. mutans, over the entire surface in three different directions in a homogeneous way, using a sterile cotton swab. .. Then, Petri dish containing E. faecalis was incubated for 24 hours in an aero-anaerobic atmosphere, and one containing S. mutans in an anaerobic container was incubated for 48 hours at 37°C, with a bag of 5% CO2 (lot No. 0325MJ-4, Mitsubishi Gas Chemical, Japan) in a laboratory oven (model 100-800, Memmert GmbH + Co. KG, Schwabach, Germany).

Incubation:

Article Title: Bacterial Adhesion of Streptococcus mutans to Dental Material Surfaces
Article Snippet: .. The S. mutans ATCC 25175 strains used in this study were selected from culture on blood agar plates incubated at 37 ◦C for 48 h with a CO2 pack for anaerobic conditions. .. The S. mutans overnight culture was made in a BHI (brain–heart infusion) nutrient broth (Biolife, Italiana Srl) (4012302) at 37 ◦C for 18 h to obtain a 109 CFU/mL bacterial suspension.

Article Title: Antibacterial Effectiveness of Four Concentrations of the Hydroalcoholic Extract of Solanum tuberosum ( Tocosh ) against Streptococcus mutans ATCC 25175 TM : A Comparative In Vitro Study
Article Snippet: Petri dishes correctly inoculated with S. mutans ATCC 25175TM strains, each with the same amount of brain heart infusion (BHI) agar HET at 25%, 50%, 75%, and 100% prepared and packaged under sterile conditions .. Petri dishes inoculated with S. mutans ATCC 25175 strains, presenting contamination and/or alterations due to poor incubation or poor operator manipulation HET at concentrations other than those required in the study ..

Article Title: Bacterial Adhesion of Streptococcus mutans to Dental Material Surfaces
Article Snippet: .. The S. mutans ATCC 25175 strains used in this study were selected from culture on blood agar plates incubated at 37 °C for 48 h with a CO 2 pack for anaerobic conditions. .. The S. mutans overnight culture was made in a BHI (brain–heart infusion) nutrient broth (Biolife, Italiana Srl) (4012302) at 37 °C for 18 h to obtain a 10 9 CFU/mL bacterial suspension.

Cell Culture:

Inhibition:

Article Title: Antibacterial and Antibiofilm Activities of Croton pluriglandulosus Carn.-Torres & Riina. Essential Oil and Its Membrane-Disruptive Effects
Article Snippet: .. In contrast, the S. salivarius ATCC 7073 and S. mutans ATCC 25175 strains showed biomass inhibition, but no significant reductions in CFUs. ..

Image Search Results

The effect of tetrahydrocannabinol (THC) on planktonic S mutans . (A) Growth inhibition rate (%) of S mutans cells after THC treatment. THC concentrations of 2 μg/mL and above inhibited 90% of S mutans cell growth. The experiment was performed in triplicate and repeated 3 times. AMP, ampicillin. (B) The pH of the culture medium of planktonic growing S mutans in Brain Heart Infusion with increasing concentrations of THC. The experiment was repeated 3 times but no triplicates. ** P < .01, **** P < .0001.

Journal: International Dental Journal

Article Title: In Vitro Antimicrobial Effect of Tetrahydrocannabinol on Streptococcus mutans and Its Anticariogenic Potential

doi: 10.1016/j.identj.2025.109386

Figure Lengend Snippet: The effect of tetrahydrocannabinol (THC) on planktonic S mutans . (A) Growth inhibition rate (%) of S mutans cells after THC treatment. THC concentrations of 2 μg/mL and above inhibited 90% of S mutans cell growth. The experiment was performed in triplicate and repeated 3 times. AMP, ampicillin. (B) The pH of the culture medium of planktonic growing S mutans in Brain Heart Infusion with increasing concentrations of THC. The experiment was repeated 3 times but no triplicates. ** P < .01, **** P < .0001.

Article Snippet: The S mutans strain (ATCC 25175) was purchased from the American Type Culture Collection.

Techniques: Inhibition

The effect of tetrahydrocannabinol on S mutans biofilm formation. (A, B) The crystal violet staining was used to detect the biomass of the S mutans biofilm. (C) The live/dead assay was used to determine the viability of the S mutans biofilm. Relative fluorescent units indicate the value of each treatment group normalized to the solvent control. Those results were determined by the TECAN Spark. Each experiment was performed in triplicate and repeated 3 times. **** P < .0001.

Journal: International Dental Journal

Article Title: In Vitro Antimicrobial Effect of Tetrahydrocannabinol on Streptococcus mutans and Its Anticariogenic Potential

doi: 10.1016/j.identj.2025.109386

Figure Lengend Snippet: The effect of tetrahydrocannabinol on S mutans biofilm formation. (A, B) The crystal violet staining was used to detect the biomass of the S mutans biofilm. (C) The live/dead assay was used to determine the viability of the S mutans biofilm. Relative fluorescent units indicate the value of each treatment group normalized to the solvent control. Those results were determined by the TECAN Spark. Each experiment was performed in triplicate and repeated 3 times. **** P < .0001.

Article Snippet: The S mutans strain (ATCC 25175) was purchased from the American Type Culture Collection.

Techniques: Staining, Live Dead Assay, Solvent, Control

The effect of tetrahydrocannabinol (THC) inhibited S mutans biofilm formation, and viability was examined by immunofluorescence. Each experiment was performed twice, and representative images were used. Pie charts show the proportions of integrated fluorescence intensity (IntDen, analyzed with ImageJ) corresponding to PI (red), SYTO 9 (green), and Cascade Blue Dextran (blue) signals. Scale bars represent 20 µm.

Journal: International Dental Journal

Article Title: In Vitro Antimicrobial Effect of Tetrahydrocannabinol on Streptococcus mutans and Its Anticariogenic Potential

doi: 10.1016/j.identj.2025.109386

Figure Lengend Snippet: The effect of tetrahydrocannabinol (THC) inhibited S mutans biofilm formation, and viability was examined by immunofluorescence. Each experiment was performed twice, and representative images were used. Pie charts show the proportions of integrated fluorescence intensity (IntDen, analyzed with ImageJ) corresponding to PI (red), SYTO 9 (green), and Cascade Blue Dextran (blue) signals. Scale bars represent 20 µm.

Article Snippet: The S mutans strain (ATCC 25175) was purchased from the American Type Culture Collection.

Techniques: Immunofluorescence, Fluorescence

The effect of tetrahydrocannabinol (THC) on the preformed S mutans biofilm. (A, B) The crystal violet staining was used to detect the biomass of the S mutans biofilm. (C-F) The live/dead assay was used to determine the viability of the S mutans biofilm after 1, 3, 6, and 24 hours of treatment. (G) The methylthiazolyldiphenyl tetrazolium bromide (MTT) assay was used to detect the metabolic activity of the S mutans biofilm. (H, I) The timeline of the live cells and dead cells after THC treatment for 1, 3, 6, and 24 hours. Those results were determined by the TECAN Spark. Each experiment was performed 3 times in triplicate. * P < .05, ** P < .01, *** P < .001, **** P < .0001.

Journal: International Dental Journal

Article Title: In Vitro Antimicrobial Effect of Tetrahydrocannabinol on Streptococcus mutans and Its Anticariogenic Potential

doi: 10.1016/j.identj.2025.109386

Figure Lengend Snippet: The effect of tetrahydrocannabinol (THC) on the preformed S mutans biofilm. (A, B) The crystal violet staining was used to detect the biomass of the S mutans biofilm. (C-F) The live/dead assay was used to determine the viability of the S mutans biofilm after 1, 3, 6, and 24 hours of treatment. (G) The methylthiazolyldiphenyl tetrazolium bromide (MTT) assay was used to detect the metabolic activity of the S mutans biofilm. (H, I) The timeline of the live cells and dead cells after THC treatment for 1, 3, 6, and 24 hours. Those results were determined by the TECAN Spark. Each experiment was performed 3 times in triplicate. * P < .05, ** P < .01, *** P < .001, **** P < .0001.

Article Snippet: The S mutans strain (ATCC 25175) was purchased from the American Type Culture Collection.

Techniques: Staining, Live Dead Assay, MTT Assay, Activity Assay

The effect of tetrahydrocannabinol (THC) on the preformed S mutans biofilm viability. Biofilms were photographed under a fluorescence microscope after live/dead staining. The live cells are shown in green, and the dead cells in red. The figure shows a merged color of green and red, evaluating the viability of S mutans biofilm. At the 1-hour, 3-hour, and 6-hour time points, compared with the methanol group, the biofilm was more yellow and even red in the THC groups, and as the THC concentration increased, the color of the biofilm became redder, indicating a dose-dependent change. In the different concentration groups, as time increased, the color of the biofilm became increasingly red from 1 to 6 hours, while there was no obvious change in the methanol group, illustrating a time-dependent change. In the 24-hour group, the color of the biofilms in the THC groups was not as red as at 6 hours, consistent with the TECAN results. As shown in Figure 4H-I, the live cells increased, and the dead cells did not change much, suggesting that the effect of THC gradually diminished over 6 to 24 hours. Each experiment was performed twice, and representative images were used. Pie charts show the proportions of integrated fluorescence intensity (IntDen, analyzed with ImageJ) corresponding to PI (red) and SYTO 9 (green) signals. Scale bars represent 20 µm.

Journal: International Dental Journal

Article Title: In Vitro Antimicrobial Effect of Tetrahydrocannabinol on Streptococcus mutans and Its Anticariogenic Potential

doi: 10.1016/j.identj.2025.109386

Figure Lengend Snippet: The effect of tetrahydrocannabinol (THC) on the preformed S mutans biofilm viability. Biofilms were photographed under a fluorescence microscope after live/dead staining. The live cells are shown in green, and the dead cells in red. The figure shows a merged color of green and red, evaluating the viability of S mutans biofilm. At the 1-hour, 3-hour, and 6-hour time points, compared with the methanol group, the biofilm was more yellow and even red in the THC groups, and as the THC concentration increased, the color of the biofilm became redder, indicating a dose-dependent change. In the different concentration groups, as time increased, the color of the biofilm became increasingly red from 1 to 6 hours, while there was no obvious change in the methanol group, illustrating a time-dependent change. In the 24-hour group, the color of the biofilms in the THC groups was not as red as at 6 hours, consistent with the TECAN results. As shown in Figure 4H-I, the live cells increased, and the dead cells did not change much, suggesting that the effect of THC gradually diminished over 6 to 24 hours. Each experiment was performed twice, and representative images were used. Pie charts show the proportions of integrated fluorescence intensity (IntDen, analyzed with ImageJ) corresponding to PI (red) and SYTO 9 (green) signals. Scale bars represent 20 µm.

Article Snippet: The S mutans strain (ATCC 25175) was purchased from the American Type Culture Collection.

Techniques: Fluorescence, Microscopy, Staining, Concentration Assay

The effect of tetrahydrocannabinol (THC) on S mutans membrane potential. (A) Performance and validation of negative (black bars) and positive (gray bars) controls for the membrane potential assays performed simultaneously in a 96-well microplate under harmonized conditions (Brain Heart Infusion medium, cellular density OD 600 = 0.03) using S mutans in the absence of cannabinoids. (B) The effect of different concentrations of THC on S mutans after a 5-minute treatment. ** P < .01, **** P < .0001.

Journal: International Dental Journal

Article Title: In Vitro Antimicrobial Effect of Tetrahydrocannabinol on Streptococcus mutans and Its Anticariogenic Potential

doi: 10.1016/j.identj.2025.109386

Figure Lengend Snippet: The effect of tetrahydrocannabinol (THC) on S mutans membrane potential. (A) Performance and validation of negative (black bars) and positive (gray bars) controls for the membrane potential assays performed simultaneously in a 96-well microplate under harmonized conditions (Brain Heart Infusion medium, cellular density OD 600 = 0.03) using S mutans in the absence of cannabinoids. (B) The effect of different concentrations of THC on S mutans after a 5-minute treatment. ** P < .01, **** P < .0001.

Article Snippet: The S mutans strain (ATCC 25175) was purchased from the American Type Culture Collection.

Techniques: Membrane, Biomarker Discovery

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s mutans atcc 25175 strains (ATCC)

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