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Dynamic Remodeling of Microbial Biofilms by Functionally Distinct Exopolysaccharides
Biofilms are densely populated communities of microbial cells protected and held together by a matrix of extracellular polymeric substances. The structure and rheological properties of the matrix at the microscale influence the retention and transport of molecules and cells in the biofilm, thereby d...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Microbiology
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4128364/ https://www.ncbi.nlm.nih.gov/pubmed/25096883 http://dx.doi.org/10.1128/mBio.01536-14 |
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author | Chew, Su Chuen Kundukad, Binu Seviour, Thomas van der Maarel, Johan R. C. Yang, Liang Rice, Scott A. Doyle, Patrick Kjelleberg, Staffan |
author_facet | Chew, Su Chuen Kundukad, Binu Seviour, Thomas van der Maarel, Johan R. C. Yang, Liang Rice, Scott A. Doyle, Patrick Kjelleberg, Staffan |
author_sort | Chew, Su Chuen |
collection | PubMed |
description | Biofilms are densely populated communities of microbial cells protected and held together by a matrix of extracellular polymeric substances. The structure and rheological properties of the matrix at the microscale influence the retention and transport of molecules and cells in the biofilm, thereby dictating population and community behavior. Despite its importance, quantitative descriptions of the matrix microstructure and microrheology are limited. Here, particle-tracking microrheology in combination with genetic approaches was used to spatially and temporally study the rheological contributions of the major exopolysaccharides Pel and Psl in Pseudomonas aeruginosa biofilms. Psl increased the elasticity and effective cross-linking within the matrix, which strengthened its scaffold and appeared to facilitate the formation of microcolonies. Conversely, Pel reduced effective cross-linking within the matrix. Without Psl, the matrix becomes more viscous, which facilitates biofilm spreading. The wild-type biofilm decreased in effective cross-linking over time, which would be advantageous for the spreading and colonization of new surfaces. This suggests that there are regulatory mechanisms to control production of the exopolysaccharides that serve to remodel the matrix of developing biofilms. The exopolysaccharides were also found to have profound effects on the spatial organization and integration of P. aeruginosa in a mixed-species biofilm model of P. aeruginosa-Staphylococcus aureus. Pel was required for close association of the two species in mixed-species microcolonies. In contrast, Psl was important for P. aeruginosa to form single-species biofilms on top of S. aureus biofilms. Our results demonstrate that Pel and Psl have distinct physical properties and functional roles during biofilm formation. |
format | Online Article Text |
id | pubmed-4128364 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Society of Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-41283642014-08-12 Dynamic Remodeling of Microbial Biofilms by Functionally Distinct Exopolysaccharides Chew, Su Chuen Kundukad, Binu Seviour, Thomas van der Maarel, Johan R. C. Yang, Liang Rice, Scott A. Doyle, Patrick Kjelleberg, Staffan mBio Research Article Biofilms are densely populated communities of microbial cells protected and held together by a matrix of extracellular polymeric substances. The structure and rheological properties of the matrix at the microscale influence the retention and transport of molecules and cells in the biofilm, thereby dictating population and community behavior. Despite its importance, quantitative descriptions of the matrix microstructure and microrheology are limited. Here, particle-tracking microrheology in combination with genetic approaches was used to spatially and temporally study the rheological contributions of the major exopolysaccharides Pel and Psl in Pseudomonas aeruginosa biofilms. Psl increased the elasticity and effective cross-linking within the matrix, which strengthened its scaffold and appeared to facilitate the formation of microcolonies. Conversely, Pel reduced effective cross-linking within the matrix. Without Psl, the matrix becomes more viscous, which facilitates biofilm spreading. The wild-type biofilm decreased in effective cross-linking over time, which would be advantageous for the spreading and colonization of new surfaces. This suggests that there are regulatory mechanisms to control production of the exopolysaccharides that serve to remodel the matrix of developing biofilms. The exopolysaccharides were also found to have profound effects on the spatial organization and integration of P. aeruginosa in a mixed-species biofilm model of P. aeruginosa-Staphylococcus aureus. Pel was required for close association of the two species in mixed-species microcolonies. In contrast, Psl was important for P. aeruginosa to form single-species biofilms on top of S. aureus biofilms. Our results demonstrate that Pel and Psl have distinct physical properties and functional roles during biofilm formation. American Society of Microbiology 2014-08-05 /pmc/articles/PMC4128364/ /pubmed/25096883 http://dx.doi.org/10.1128/mBio.01536-14 Text en Copyright © 2014 Chew et al. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-ShareAlike 3.0 Unported license (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Chew, Su Chuen Kundukad, Binu Seviour, Thomas van der Maarel, Johan R. C. Yang, Liang Rice, Scott A. Doyle, Patrick Kjelleberg, Staffan Dynamic Remodeling of Microbial Biofilms by Functionally Distinct Exopolysaccharides |
title | Dynamic Remodeling of Microbial Biofilms by Functionally Distinct Exopolysaccharides |
title_full | Dynamic Remodeling of Microbial Biofilms by Functionally Distinct Exopolysaccharides |
title_fullStr | Dynamic Remodeling of Microbial Biofilms by Functionally Distinct Exopolysaccharides |
title_full_unstemmed | Dynamic Remodeling of Microbial Biofilms by Functionally Distinct Exopolysaccharides |
title_short | Dynamic Remodeling of Microbial Biofilms by Functionally Distinct Exopolysaccharides |
title_sort | dynamic remodeling of microbial biofilms by functionally distinct exopolysaccharides |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4128364/ https://www.ncbi.nlm.nih.gov/pubmed/25096883 http://dx.doi.org/10.1128/mBio.01536-14 |
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