Your browser doesn't support javascript.
loading
Inhibitory effects of Myricetin derivatives on curli-dependent biofilm formation in Escherichia coli.
Arita-Morioka, Ken-Ichi; Yamanaka, Kunitoshi; Mizunoe, Yoshimitsu; Tanaka, Yoshihiko; Ogura, Teru; Sugimoto, Shinya.
Afiliación
  • Arita-Morioka KI; Advanced Science Research Center, Fukuoka Dental College, Fukuoka, Japan.
  • Yamanaka K; Department of Molecular Cell Biology, Institute of Molecular Embryology and Genetics, Kumamoto University, Kumamoto, Japan.
  • Mizunoe Y; Department of Molecular Cell Biology, Institute of Molecular Embryology and Genetics, Kumamoto University, Kumamoto, Japan.
  • Tanaka Y; Department of Bacteriology, The Jikei University School of Medicine, Tokyo, Japan.
  • Ogura T; Jikei Center for Biofilm Research and Technology, The Jikei University School of Medicine, Tokyo, Japan.
  • Sugimoto S; Advanced Science Research Center, Fukuoka Dental College, Fukuoka, Japan.
Sci Rep ; 8(1): 8452, 2018 05 31.
Article en En | MEDLINE | ID: mdl-29855532
Biofilms are well-organised communities of microbes embedded in a self-produced extracellular matrix (e.g., curli amyloid fibers) and are associated with chronic infections. Therefore, development of anti-biofilm drugs is important to combat with these infections. Previously, we found that flavonol Myricetin inhibits curli-dependent biofilm formation by Escherichia coli (IC50 = 46.2 µM). In this study, we tested activities of seven Myricetin-derivatives to inhibit biofilm formation by E. coli K-12 in liquid culture. Among them, only Epigallocatechin gallate (EGCG), a major catechin in green tea, inhibited biofilm formation of K-12 (IC50 = 5.9 µM) more efficiently than Myricetin. Transmission electron microscopy and immunoblotting analyses demonstrated that EGCG prevented curli production by suppressing the expression of curli-related proteins. Quantitative RT-PCR analysis revealed that the transcripts of csgA, csgB, and csgD were significantly reduced in the presence of EGCG. Interestingly, the cellular level of RpoS, a stationary-phase specific alternative sigma factor, was reduced in the presence of EGCG, whereas the rpoS transcript was not affected. Antibiotic-chase experiments and genetic analyses revealed that EGCG accelerated RpoS degradation by ATP-dependent protease ClpXP in combination with its adaptor RssB. Collectively, these results provide significant insights into the development of drugs to treat chronic biofilm-associated infections.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Bacterianas / Flavonoides / Biopelículas / Escherichia coli Idioma: En Revista: Sci Rep Año: 2018 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Bacterianas / Flavonoides / Biopelículas / Escherichia coli Idioma: En Revista: Sci Rep Año: 2018 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Reino Unido