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Inhibitory effects of antibiofilm compound 1 against Staphylococcus aureus biofilms.
Shrestha, Looniva; Kayama, Shizuo; Sasaki, Michiko; Kato, Fuminori; Hisatsune, Junzo; Tsuruda, Keiko; Koizumi, Kazuhisa; Tatsukawa, Nobuyuki; Yu, Liansheng; Takeda, Kei; Sugai, Motoyuki.
Afiliación
  • Shrestha L; Department of Bacteriology, Hiroshima University Graduate School of Biomedical Sciences.
  • Kayama S; Department of Bacteriology, Hiroshima University Graduate School of Biomedical Sciences.
  • Sasaki M; Project Research Center for Nosocomial Infectious Disease, Hiroshima University.
  • Kato F; Department of Synthetic Organic Chemistry, Hiroshima University Graduate School of Biomedical Sciences, 1-2-3 Kasumi Minami-ku Hiroshima 734-8551, Japan.
  • Hisatsune J; Department of Bacteriology, Hiroshima University Graduate School of Biomedical Sciences.
  • Tsuruda K; Project Research Center for Nosocomial Infectious Disease, Hiroshima University.
  • Koizumi K; Department of Bacteriology, Hiroshima University Graduate School of Biomedical Sciences.
  • Tatsukawa N; Project Research Center for Nosocomial Infectious Disease, Hiroshima University.
  • Yu L; Department of Bacteriology, Hiroshima University Graduate School of Biomedical Sciences.
  • Takeda K; Department of Bacteriology, Hiroshima University Graduate School of Biomedical Sciences.
  • Sugai M; Project Research Center for Nosocomial Infectious Disease, Hiroshima University.
Microbiol Immunol ; 60(3): 148-59, 2016 Mar.
Article en En | MEDLINE | ID: mdl-26786482
ABSTRACT
A novel benzimidazole molecule that was identified in a small-molecule screen and is known as antibiofilm compound 1 (ABC-1) has been found to prevent bacterial biofilm formation by multiple bacterial pathogens, including Staphylococcus aureus, without affecting bacterial growth. Here, the biofilm inhibiting ability of 156 µM ABC-1 was tested in various biofilm-forming strains of S. aureus. It was demonstrated that ABC-1 inhibits biofilm formation by these strains at micromolar concentrations regardless of the strains' dependence on Polysaccharide Intercellular Adhesin (PIA), cell wall-associated protein dependent or cell wall- associated extracellular DNA (eDNA). Of note, ABC-1 treatment primarily inhibited Protein A (SpA) expression in all strains tested. spa gene disruption showed decreased biofilm formation; however, the mutants still produced more biofilm than ABC-1 treated strains, implying that ABC-1 affects not only SpA but also other factors. Indeed, ABC-1 also attenuated the accumulation of PIA and eDNA on cell surface. Our results suggest that ABC-1 has pleotropic effects on several biofilm components and thus inhibits biofilm formation by S. aureus.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Staphylococcus aureus / Bencimidazoles / Biopelículas / Antibacterianos Tipo de estudio: Prognostic_studies Idioma: En Revista: Microbiol Immunol Año: 2016 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Staphylococcus aureus / Bencimidazoles / Biopelículas / Antibacterianos Tipo de estudio: Prognostic_studies Idioma: En Revista: Microbiol Immunol Año: 2016 Tipo del documento: Article