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Inhibitory effects of tea catechin epigallocatechin-3-gallate against biofilms formed from Streptococcus mutans and a probiotic lactobacillus strain.
Wu, Ching-Yi; Su, Tzu-Yi; Wang, Mao-Yu; Yang, Shue-Fen; Mar, Kwei; Hung, Shan-Ling.
Affiliation
  • Wu CY; Institute of Oral Biology, National Yang-Ming University, Taipei, Taiwan; Department of Stomatology, Taipei Veterans General Hospital, Taipei, Taiwan.
  • Su TY; Institute of Oral Biology, National Yang-Ming University, Taipei, Taiwan.
  • Wang MY; Institute of Oral Biology, National Yang-Ming University, Taipei, Taiwan.
  • Yang SF; Department of Stomatology, Taipei Veterans General Hospital, Taipei, Taiwan; School of Dentistry, National Yang-Ming University, Taipei, Taiwan.
  • Mar K; Department of Community Dentistry, Zhong-Xiao Branch, Taipei City Hospital, Taipei, Taiwan; Faculty of Medicine, National Yang-Ming University, Taipei, Taiwan. Electronic address: DAH83@tpech.gov.tw.
  • Hung SL; Institute of Oral Biology, National Yang-Ming University, Taipei, Taiwan; Department of Stomatology, Taipei Veterans General Hospital, Taipei, Taiwan; Department of Community Dentistry, Zhong-Xiao Branch, Taipei City Hospital, Taipei, Taiwan. Electronic address: slhung@ym.edu.tw.
Arch Oral Biol ; 94: 69-77, 2018 Oct.
Article in En | MEDLINE | ID: mdl-29979975
OBJECTIVE: Effects of tea catechin epigallocatechin-3-gallate (EGCG) against biofilm formation by Streptococcus mutans and probiotic Lactobacillus casei in Yakult® (LcY) were examined. DESIGN: Biofilms were formed by S. mutans alone (Sm) and co-culture of S. mutans and LcY (Sm + LcY) in the absence or presence of EGCG. The biomass of biofilms, which were sonicated or not, was measured by the crystal violet assay. Biofilm morphology was observed by scanning electron microscopy. Bacterial viability and extracellular polysaccharides were determined by SYTO9/propidium iodide and dextran-conjugated fluorescein staining, respectively, and confocal microscopy. Gene expression of glucosyltransferase was determined by quantitative polymerase chain reaction. RESULTS: While 250 µg/ml EGCG significantly decreased the biomass and acid production of Sm biofilms, 500 µg/ml EGCG was required to inhibit Sm + LcY biofilm formation and acid production. EGCG decreased the amount of live bacteria present in both Sm and Sm + LcY biofilms. The level of dead bacteria in Sm + LcY biofilms was higher than in Sm biofilms when formed in the presence of 250 µg/ml EGCG. EGCG decreased levels of extracellular polysaccharides in Sm and Sm + LcY biofilms. The extent of biofilm removal by sonication was not different between Sm and Sm+LcY biofilms formed in the absence or presence of 62.5 or 125 µg/ml EGCG. The level of Sm gtfB and gtfD expression in Sm + LcY biofilms was higher than those in the Sm biofilms when formed in the presence of EGCG at 250 µg/ml. CONCLUSION: The results indicated that LcY might interfere the inhibitory effects of EGCG against biofilm formation by S. mutans.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Streptococcus mutans / Tea / Catechin / Biofilms / Probiotics / Lacticaseibacillus casei / Anti-Bacterial Agents Language: En Journal: Arch Oral Biol Year: 2018 Document type: Article Affiliation country: Taiwan Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Streptococcus mutans / Tea / Catechin / Biofilms / Probiotics / Lacticaseibacillus casei / Anti-Bacterial Agents Language: En Journal: Arch Oral Biol Year: 2018 Document type: Article Affiliation country: Taiwan Country of publication: United kingdom