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How do environment-dependent switching rates between susceptible and persister cells affect the dynamics of biofilms faced with antibiotics?
Persisters form sub-populations of stress-tolerant cells that play a major role in the capacity of biofilms to survive and recover from disturbances such as antibiotic treatments. The mechanisms of persistence are diverse and influenced by environmental conditions, and persister populations are more...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5854711/ https://www.ncbi.nlm.nih.gov/pubmed/29560270 http://dx.doi.org/10.1038/s41522-018-0049-2 |
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author | Carvalho, Gabriel Balestrino, Damien Forestier, Christiane Mathias, Jean-Denis |
author_facet | Carvalho, Gabriel Balestrino, Damien Forestier, Christiane Mathias, Jean-Denis |
author_sort | Carvalho, Gabriel |
collection | PubMed |
description | Persisters form sub-populations of stress-tolerant cells that play a major role in the capacity of biofilms to survive and recover from disturbances such as antibiotic treatments. The mechanisms of persistence are diverse and influenced by environmental conditions, and persister populations are more heterogeneous than formerly suspected. We used computational modeling to assess the impact of three switching strategies between susceptible and persister cells on the capacity of bacterial biofilms to grow, survive and recover from antibiotic treatments. The strategies tested were: (1) constant switches, (2) substrate-dependent switches and (3) antibiotic-dependent switches. We implemented these strategies in an individual-based biofilm model and simulated antibiotic shocks on virtual biofilms. Because of limited available data on switching rates in the literature, nine parameter sets were assessed for each strategy. Substrate and antibiotic-dependent switches allowed high switching rates without affecting the growth of the biofilms. Compared to substrate-dependent switches, constant and antibiotic-dependent switches were associated with higher proportions of persisters in the top of the biofilms, close to the substrate source, which probably confers a competitive advantage within multi-species biofilms. The constant and substrate-dependent strategies need a compromise between limiting the wake-up and death of persisters during treatments and leaving the persister state fast enough to recover quickly after antibiotic-removal. Overall, the simulations gave new insights into the relationships between the dynamics of persister populations in biofilms and their dynamics of growth, survival and recovery when faced with disturbances. |
format | Online Article Text |
id | pubmed-5854711 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58547112018-03-20 How do environment-dependent switching rates between susceptible and persister cells affect the dynamics of biofilms faced with antibiotics? Carvalho, Gabriel Balestrino, Damien Forestier, Christiane Mathias, Jean-Denis NPJ Biofilms Microbiomes Article Persisters form sub-populations of stress-tolerant cells that play a major role in the capacity of biofilms to survive and recover from disturbances such as antibiotic treatments. The mechanisms of persistence are diverse and influenced by environmental conditions, and persister populations are more heterogeneous than formerly suspected. We used computational modeling to assess the impact of three switching strategies between susceptible and persister cells on the capacity of bacterial biofilms to grow, survive and recover from antibiotic treatments. The strategies tested were: (1) constant switches, (2) substrate-dependent switches and (3) antibiotic-dependent switches. We implemented these strategies in an individual-based biofilm model and simulated antibiotic shocks on virtual biofilms. Because of limited available data on switching rates in the literature, nine parameter sets were assessed for each strategy. Substrate and antibiotic-dependent switches allowed high switching rates without affecting the growth of the biofilms. Compared to substrate-dependent switches, constant and antibiotic-dependent switches were associated with higher proportions of persisters in the top of the biofilms, close to the substrate source, which probably confers a competitive advantage within multi-species biofilms. The constant and substrate-dependent strategies need a compromise between limiting the wake-up and death of persisters during treatments and leaving the persister state fast enough to recover quickly after antibiotic-removal. Overall, the simulations gave new insights into the relationships between the dynamics of persister populations in biofilms and their dynamics of growth, survival and recovery when faced with disturbances. Nature Publishing Group UK 2018-03-15 /pmc/articles/PMC5854711/ /pubmed/29560270 http://dx.doi.org/10.1038/s41522-018-0049-2 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Carvalho, Gabriel Balestrino, Damien Forestier, Christiane Mathias, Jean-Denis How do environment-dependent switching rates between susceptible and persister cells affect the dynamics of biofilms faced with antibiotics? |
title | How do environment-dependent switching rates between susceptible and persister cells affect the dynamics of biofilms faced with antibiotics? |
title_full | How do environment-dependent switching rates between susceptible and persister cells affect the dynamics of biofilms faced with antibiotics? |
title_fullStr | How do environment-dependent switching rates between susceptible and persister cells affect the dynamics of biofilms faced with antibiotics? |
title_full_unstemmed | How do environment-dependent switching rates between susceptible and persister cells affect the dynamics of biofilms faced with antibiotics? |
title_short | How do environment-dependent switching rates between susceptible and persister cells affect the dynamics of biofilms faced with antibiotics? |
title_sort | how do environment-dependent switching rates between susceptible and persister cells affect the dynamics of biofilms faced with antibiotics? |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5854711/ https://www.ncbi.nlm.nih.gov/pubmed/29560270 http://dx.doi.org/10.1038/s41522-018-0049-2 |
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