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Nutrient Transitions Are a Source of Persisters in Escherichia coli Biofilms
Chronic and recurrent infections have been attributed to persisters in biofilms, and despite this importance, the mechanisms of persister formation in biofilms remain unclear. The plethora of biofilm characteristics that could give rise to persisters, including slower growth, quorum signaling, oxida...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3965526/ https://www.ncbi.nlm.nih.gov/pubmed/24667358 http://dx.doi.org/10.1371/journal.pone.0093110 |
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author | Amato, Stephanie M. Brynildsen, Mark P. |
author_facet | Amato, Stephanie M. Brynildsen, Mark P. |
author_sort | Amato, Stephanie M. |
collection | PubMed |
description | Chronic and recurrent infections have been attributed to persisters in biofilms, and despite this importance, the mechanisms of persister formation in biofilms remain unclear. The plethora of biofilm characteristics that could give rise to persisters, including slower growth, quorum signaling, oxidative stress, and nutrient heterogeneity, have complicated efforts to delineate formation pathways that generate persisters during biofilm development. Here we sought to specifically determine whether nutrient transitions, which are a common metabolic stress encountered within surface-attached communities, stimulate persister formation in biofilms and if so, to then identify the pathway. To accomplish this, we established an experimental methodology where nutrient availability to biofilm cells could be controlled exogenously, and then used that method to discover that diauxic carbon source transitions stimulated persister formation in Escherichia coli biofilms. Previously, we found that carbon source transitions stimulate persister formation in planktonic E. coli cultures, through a pathway that involved ppGpp and nucleoid-associated proteins, and therefore, tested the functionality of that pathway in biofilms. Biofilm persister formation was also found to be dependent on ppGpp and nucleoid-associated proteins, but the importance of specific proteins and enzymes between biofilm and planktonic lifestyles was significantly different. Data presented here support the increasingly appreciated role of ppGpp as a central mediator of bacterial persistence and demonstrate that nutrient transitions can be a source of persisters in biofilms. |
format | Online Article Text |
id | pubmed-3965526 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39655262014-03-27 Nutrient Transitions Are a Source of Persisters in Escherichia coli Biofilms Amato, Stephanie M. Brynildsen, Mark P. PLoS One Research Article Chronic and recurrent infections have been attributed to persisters in biofilms, and despite this importance, the mechanisms of persister formation in biofilms remain unclear. The plethora of biofilm characteristics that could give rise to persisters, including slower growth, quorum signaling, oxidative stress, and nutrient heterogeneity, have complicated efforts to delineate formation pathways that generate persisters during biofilm development. Here we sought to specifically determine whether nutrient transitions, which are a common metabolic stress encountered within surface-attached communities, stimulate persister formation in biofilms and if so, to then identify the pathway. To accomplish this, we established an experimental methodology where nutrient availability to biofilm cells could be controlled exogenously, and then used that method to discover that diauxic carbon source transitions stimulated persister formation in Escherichia coli biofilms. Previously, we found that carbon source transitions stimulate persister formation in planktonic E. coli cultures, through a pathway that involved ppGpp and nucleoid-associated proteins, and therefore, tested the functionality of that pathway in biofilms. Biofilm persister formation was also found to be dependent on ppGpp and nucleoid-associated proteins, but the importance of specific proteins and enzymes between biofilm and planktonic lifestyles was significantly different. Data presented here support the increasingly appreciated role of ppGpp as a central mediator of bacterial persistence and demonstrate that nutrient transitions can be a source of persisters in biofilms. Public Library of Science 2014-03-25 /pmc/articles/PMC3965526/ /pubmed/24667358 http://dx.doi.org/10.1371/journal.pone.0093110 Text en © 2014 Amato, Brynildsen http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Amato, Stephanie M. Brynildsen, Mark P. Nutrient Transitions Are a Source of Persisters in Escherichia coli Biofilms |
title | Nutrient Transitions Are a Source of Persisters in Escherichia coli Biofilms |
title_full | Nutrient Transitions Are a Source of Persisters in Escherichia coli Biofilms |
title_fullStr | Nutrient Transitions Are a Source of Persisters in Escherichia coli Biofilms |
title_full_unstemmed | Nutrient Transitions Are a Source of Persisters in Escherichia coli Biofilms |
title_short | Nutrient Transitions Are a Source of Persisters in Escherichia coli Biofilms |
title_sort | nutrient transitions are a source of persisters in escherichia coli biofilms |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3965526/ https://www.ncbi.nlm.nih.gov/pubmed/24667358 http://dx.doi.org/10.1371/journal.pone.0093110 |
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