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Alkyl quinolones mediate heterogeneous colony biofilm architecture that improves community-level survival.
Weaver, Abigail A; Jia, Jin; Cutri, Allison R; Madukoma, Chinedu S; Vaerewyck, Catherine M; Bohn, Paul W; Shrout, Joshua D.
Afiliación
  • Weaver AA; Department of Civil and Environmental Engineering and Earth Sciences, University of Notre Dame, Notre Dame, Indiana, USA.
  • Jia J; Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana, USA.
  • Cutri AR; Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana, USA.
  • Madukoma CS; Department of Civil and Environmental Engineering and Earth Sciences, University of Notre Dame, Notre Dame, Indiana, USA.
  • Vaerewyck CM; Department of Civil and Environmental Engineering and Earth Sciences, University of Notre Dame, Notre Dame, Indiana, USA.
  • Bohn PW; Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana, USA.
  • Shrout JD; Department of Chemical and Biomolecular Engineering, University of Notre Dame, Notre Dame, Indiana, USA.
J Bacteriol ; 206(4): e0009524, 2024 04 18.
Article en En | MEDLINE | ID: mdl-38564677
ABSTRACT
Bacterial communities exhibit complex self-organization that contributes to their survival. To better understand the molecules that contribute to transforming a small number of cells into a heterogeneous surface biofilm community, we studied acellular aggregates, structures seen by light microscopy in Pseudomonas aeruginosa colony biofilms using light microscopy and chemical imaging. These structures differ from cellular aggregates, cohesive clusters of cells important for biofilm formation, in that they are visually distinct from cells using light microscopy and are reliant on metabolites for assembly. To investigate how these structures benefit a biofilm community we characterized three recurrent types of acellular aggregates with distinct geometries that were each abundant in specific areas of these biofilms. Alkyl quinolones (AQs) were essential for the formation of all aggregate types with AQ signatures outside the aggregates below the limit of detection. These acellular aggregates spatially sequester AQs and differentiate the biofilm space. However, the three types of aggregates showed differing properties in their size, associated cell death, and lipid content. The largest aggregate type co-localized with spatially confined cell death that was not mediated by Pf4 bacteriophage. Biofilms lacking AQs were absent of localized cell death but exhibited increased, homogeneously distributed cell death. Thus, these AQ-rich aggregates regulate metabolite accessibility, differentiate regions of the biofilm, and promote survival in biofilms.IMPORTANCEPseudomonas aeruginosa is an opportunistic pathogen with the ability to cause infection in the immune-compromised. It is well established that P. aeruginosa biofilms exhibit resilience that includes decreased susceptibility to antimicrobial treatment. This work examines the self-assembled heterogeneity in biofilm communities studying acellular aggregates, regions of condensed matter requiring alkyl quinolones (AQs). AQs are important to both virulence and biofilm formation. Aggregate structures described here spatially regulate the accessibility of these AQs, differentiate regions of the biofilm community, and despite their association with autolysis, correlate with improved P. aeruginosa colony biofilm survival.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Infecciones por Pseudomonas / Quinolonas Límite: Humans Idioma: En Revista: J Bacteriol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Infecciones por Pseudomonas / Quinolonas Límite: Humans Idioma: En Revista: J Bacteriol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos