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Filamentous Bacteriophage Promote Biofilm Assembly and Function.
Secor, Patrick R; Sweere, Johanna M; Michaels, Lia A; Malkovskiy, Andrey V; Lazzareschi, Daniel; Katznelson, Ethan; Rajadas, Jayakumar; Birnbaum, Michael E; Arrigoni, Allison; Braun, Kathleen R; Evanko, Stephen P; Stevens, David A; Kaminsky, Werner; Singh, Pradeep K; Parks, William C; Bollyky, Paul L.
Afiliação
  • Secor PR; Departments of Medicine and Microbiology, University of Washington, Seattle, WA 98195, USA. Electronic address: psecor@uw.edu.
  • Sweere JM; Department of Medicine, Stanford University, Stanford, CA 94305, USA; Stanford Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Michaels LA; Departments of Medicine and Microbiology, University of Washington, Seattle, WA 98195, USA.
  • Malkovskiy AV; Department of Medicine, Stanford University, Stanford, CA 94305, USA.
  • Lazzareschi D; Department of Medicine, Stanford University, Stanford, CA 94305, USA.
  • Katznelson E; Department of Medicine, Stanford University, Stanford, CA 94305, USA.
  • Rajadas J; Department of Medicine, Stanford University, Stanford, CA 94305, USA.
  • Birnbaum ME; Stanford Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Arrigoni A; Benaroya Research Institute, Seattle, WA 98101, USA.
  • Braun KR; Benaroya Research Institute, Seattle, WA 98101, USA.
  • Evanko SP; Benaroya Research Institute, Seattle, WA 98101, USA.
  • Stevens DA; California Institute for Medical Research, San Jose, CA 95128, USA.
  • Kaminsky W; Department of Chemistry, University of Washington, Seattle, WA 98195, USA.
  • Singh PK; Departments of Medicine and Microbiology, University of Washington, Seattle, WA 98195, USA.
  • Parks WC; Department of Medicine (Pulmonary and Critical Care Medicine), Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA.
  • Bollyky PL; Department of Medicine, Stanford University, Stanford, CA 94305, USA.
Cell Host Microbe ; 18(5): 549-59, 2015 Nov 11.
Article em En | MEDLINE | ID: mdl-26567508
ABSTRACT
Biofilms-communities of bacteria encased in a polymer-rich matrix-confer bacteria with the ability to persist in pathologic host contexts, such as the cystic fibrosis (CF) airways. How bacteria assemble polymers into biofilms is largely unknown. We find that the extracellular matrix produced by Pseudomonas aeruginosa self-assembles into a liquid crystal through entropic interactions between polymers and filamentous Pf bacteriophages, which are long, negatively charged filaments. This liquid crystalline structure enhances biofilm function by increasing adhesion and tolerance to desiccation and antibiotics. Pf bacteriophages are prevalent among P. aeruginosa clinical isolates and were detected in CF sputum. The addition of Pf bacteriophage to sputum polymers or serum was sufficient to drive their rapid assembly into viscous liquid crystals. Fd, a related bacteriophage of Escherichia coli, has similar biofilm-building capabilities. Targeting filamentous bacteriophage or the liquid crystalline organization of the biofilm matrix may represent antibacterial strategies.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Polímeros / Pseudomonas aeruginosa / Fagos de Pseudomonas / Inovirus / Biofilmes Limite: Humans Idioma: En Revista: Cell Host Microbe Assunto da revista: MICROBIOLOGIA Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Polímeros / Pseudomonas aeruginosa / Fagos de Pseudomonas / Inovirus / Biofilmes Limite: Humans Idioma: En Revista: Cell Host Microbe Assunto da revista: MICROBIOLOGIA Ano de publicação: 2015 Tipo de documento: Article