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Polysorbates prevent biofilm formation and pathogenesis of Escherichia coli O104:H4.
Sloup, Rudolph E; Cieza, Roberto J; Needle, David B; Abramovitch, Robert B; Torres, Alfredo G; Waters, Christopher M.
Afiliação
  • Sloup RE; a Department of Microbiology and Molecular Genetics , Michigan State University , East Lansing , MI , USA.
  • Cieza RJ; c Department of Microbiology and Immunology , Sealy Center for Vaccine Development, University of Texas Medical Branch , Galveston , TX , USA.
  • Needle DB; a Department of Microbiology and Molecular Genetics , Michigan State University , East Lansing , MI , USA.
  • Abramovitch RB; a Department of Microbiology and Molecular Genetics , Michigan State University , East Lansing , MI , USA.
  • Torres AG; c Department of Microbiology and Immunology , Sealy Center for Vaccine Development, University of Texas Medical Branch , Galveston , TX , USA.
  • Waters CM; a Department of Microbiology and Molecular Genetics , Michigan State University , East Lansing , MI , USA.
Biofouling ; 32(9): 1131-1140, 2016 Oct.
Article em En | MEDLINE | ID: mdl-27667095
ABSTRACT
Escherichia coli biotype O104H4 recently caused the deadliest E. coli outbreak ever reported. Based on prior results, it was hypothesized that compounds inhibiting biofilm formation by O104H4 would reduce its pathogenesis. The nonionic surfactants polysorbate 80 (PS80) and polysorbate 20 (PS20) were found to reduce biofilms by ≥ 90% at submicromolar concentrations and elicited nearly complete dispersal of preformed biofilms. PS80 did not significantly impact in vivo colonization in a mouse infection model; however, mice treated with PS80 exhibited almost no intestinal inflammation or tissue damage while untreated mice exhibited robust pathology. As PS20 and PS80 are classified as 'Generally Recognized as Safe' (GRAS) compounds by the Food and Drug Administration (FDA), these compounds have clinical potential to treat future O104H4 outbreaks.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies Idioma: En Ano de publicação: 2016 Tipo de documento: Article