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Real-time optotracing of curli and cellulose in live Salmonella biofilms using luminescent oligothiophenes

Extracellular matrix (ECM) is the protein- and polysaccharide-rich backbone of bacterial biofilms that provides a defensive barrier in clinical, environmental and industrial settings. Understanding the dynamics of biofilm formation in native environments has been hindered by a lack of research tools...

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Autores principales: Choong, Ferdinand X, Bäck, Marcus, Fahlén, Sara, Johansson, Leif BG, Melican, Keira, Rhen, Mikael, Nilsson, K Peter R, Richter-Dahlfors, Agneta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5515270/
https://www.ncbi.nlm.nih.gov/pubmed/28721253
http://dx.doi.org/10.1038/npjbiofilms.2016.24
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author Choong, Ferdinand X
Bäck, Marcus
Fahlén, Sara
Johansson, Leif BG
Melican, Keira
Rhen, Mikael
Nilsson, K Peter R
Richter-Dahlfors, Agneta
author_facet Choong, Ferdinand X
Bäck, Marcus
Fahlén, Sara
Johansson, Leif BG
Melican, Keira
Rhen, Mikael
Nilsson, K Peter R
Richter-Dahlfors, Agneta
author_sort Choong, Ferdinand X
collection PubMed
description Extracellular matrix (ECM) is the protein- and polysaccharide-rich backbone of bacterial biofilms that provides a defensive barrier in clinical, environmental and industrial settings. Understanding the dynamics of biofilm formation in native environments has been hindered by a lack of research tools. Here we report a method for simultaneous, real-time, in situ detection and differentiation of the Salmonella ECM components curli and cellulose, using non-toxic, luminescent conjugated oligothiophenes (LCOs). These flexible conjugated polymers emit a conformation-dependent fluorescence spectrum, which we use to kinetically define extracellular appearance of curli fibres and cellulose polysaccharides during bacterial growth. The scope of this technique is demonstrated by defining biofilm morphotypes of Salmonella enterica serovars Enteritidis and Typhimurium, and their isogenic mutants in liquid culture and on solid media, and by visualising the ECM components in native biofilms. Our reported use of LCOs across a number of platforms, including intracellular cellulose production in eukaryotic cells and in infected tissues, demonstrates the versatility of this optotracing technology, and its ability to redefine biofilm research.
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spelling pubmed-55152702017-07-18 Real-time optotracing of curli and cellulose in live Salmonella biofilms using luminescent oligothiophenes Choong, Ferdinand X Bäck, Marcus Fahlén, Sara Johansson, Leif BG Melican, Keira Rhen, Mikael Nilsson, K Peter R Richter-Dahlfors, Agneta NPJ Biofilms Microbiomes Article Extracellular matrix (ECM) is the protein- and polysaccharide-rich backbone of bacterial biofilms that provides a defensive barrier in clinical, environmental and industrial settings. Understanding the dynamics of biofilm formation in native environments has been hindered by a lack of research tools. Here we report a method for simultaneous, real-time, in situ detection and differentiation of the Salmonella ECM components curli and cellulose, using non-toxic, luminescent conjugated oligothiophenes (LCOs). These flexible conjugated polymers emit a conformation-dependent fluorescence spectrum, which we use to kinetically define extracellular appearance of curli fibres and cellulose polysaccharides during bacterial growth. The scope of this technique is demonstrated by defining biofilm morphotypes of Salmonella enterica serovars Enteritidis and Typhimurium, and their isogenic mutants in liquid culture and on solid media, and by visualising the ECM components in native biofilms. Our reported use of LCOs across a number of platforms, including intracellular cellulose production in eukaryotic cells and in infected tissues, demonstrates the versatility of this optotracing technology, and its ability to redefine biofilm research. Nature Publishing Group 2016-11-23 /pmc/articles/PMC5515270/ /pubmed/28721253 http://dx.doi.org/10.1038/npjbiofilms.2016.24 Text en Copyright © 2016 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Choong, Ferdinand X
Bäck, Marcus
Fahlén, Sara
Johansson, Leif BG
Melican, Keira
Rhen, Mikael
Nilsson, K Peter R
Richter-Dahlfors, Agneta
Real-time optotracing of curli and cellulose in live Salmonella biofilms using luminescent oligothiophenes
title Real-time optotracing of curli and cellulose in live Salmonella biofilms using luminescent oligothiophenes
title_full Real-time optotracing of curli and cellulose in live Salmonella biofilms using luminescent oligothiophenes
title_fullStr Real-time optotracing of curli and cellulose in live Salmonella biofilms using luminescent oligothiophenes
title_full_unstemmed Real-time optotracing of curli and cellulose in live Salmonella biofilms using luminescent oligothiophenes
title_short Real-time optotracing of curli and cellulose in live Salmonella biofilms using luminescent oligothiophenes
title_sort real-time optotracing of curli and cellulose in live salmonella biofilms using luminescent oligothiophenes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5515270/
https://www.ncbi.nlm.nih.gov/pubmed/28721253
http://dx.doi.org/10.1038/npjbiofilms.2016.24
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