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Biofilm Formation Drives Transfer of the Conjugative Element ICEBs1 in Bacillus subtilis

Horizontal gene transfer by integrative and conjugative elements (ICEs) is a very important mechanism for spreading antibiotic resistance in various bacterial species. In environmental and clinical settings, most bacteria form biofilms as a way to protect themselves against extracellular stress. How...

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Autores principales: Lécuyer, Frédéric, Bourassa, Jean-Sébastien, Gélinas, Martin, Charron-Lamoureux, Vincent, Burrus, Vincent, Beauregard, Pascale B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6158512/
https://www.ncbi.nlm.nih.gov/pubmed/30258041
http://dx.doi.org/10.1128/mSphere.00473-18
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author Lécuyer, Frédéric
Bourassa, Jean-Sébastien
Gélinas, Martin
Charron-Lamoureux, Vincent
Burrus, Vincent
Beauregard, Pascale B.
author_facet Lécuyer, Frédéric
Bourassa, Jean-Sébastien
Gélinas, Martin
Charron-Lamoureux, Vincent
Burrus, Vincent
Beauregard, Pascale B.
author_sort Lécuyer, Frédéric
collection PubMed
description Horizontal gene transfer by integrative and conjugative elements (ICEs) is a very important mechanism for spreading antibiotic resistance in various bacterial species. In environmental and clinical settings, most bacteria form biofilms as a way to protect themselves against extracellular stress. However, much remains to be known about ICE transfer in biofilms. Using ICEBs1 from Bacillus subtilis, we show that the natural conjugation efficiency of this ICE is greatly affected by the ability of the donor and recipient to form a biofilm. ICEBs1 transfer considerably increases in biofilm, even at low donor/recipient ratios. Also, while there is a clear temporal correlation between biofilm formation and ICEBs1 transfer, biofilms do not alter the level of ICEBs1 excision in donor cells. Conjugative transfer appears to be favored by the biophysical context of biofilms. Indeed, extracellular matrix production, particularly from the recipient cells, is essential for biofilms to promote ICEBs1 transfer. Our study provides basic new knowledge on the high rate of conjugative transfer of ICEs in biofilms, a widely preponderant bacterial lifestyle in the environment, which could have a major impact on our understanding of horizontal gene transfer in natural and clinical environments. IMPORTANCE Transfer of mobile genetic elements from one bacterium to another is the principal cause of the spread of antibiotic resistance. However, the dissemination of these elements in environmental contexts is poorly understood. In clinical and environmental settings, bacteria are often found living in multicellular communities encased in a matrix, a structure known as a biofilm. In this study, we examined how forming a biofilm influences the transmission of an integrative and conjugative element (ICE). Using the model Gram-positive bacterium B. subtilis, we observed that biofilm formation highly favors ICE transfer. This increase in conjugative transfer is due to the production of extracellular matrix, which creates an ideal biophysical context. Our study provides important insights into the role of the biofilm structure in driving conjugative transfer, which is of major importance since biofilm is a widely preponderant bacterial lifestyle for clinically relevant bacterial strains.
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spelling pubmed-61585122018-10-02 Biofilm Formation Drives Transfer of the Conjugative Element ICEBs1 in Bacillus subtilis Lécuyer, Frédéric Bourassa, Jean-Sébastien Gélinas, Martin Charron-Lamoureux, Vincent Burrus, Vincent Beauregard, Pascale B. mSphere Research Article Horizontal gene transfer by integrative and conjugative elements (ICEs) is a very important mechanism for spreading antibiotic resistance in various bacterial species. In environmental and clinical settings, most bacteria form biofilms as a way to protect themselves against extracellular stress. However, much remains to be known about ICE transfer in biofilms. Using ICEBs1 from Bacillus subtilis, we show that the natural conjugation efficiency of this ICE is greatly affected by the ability of the donor and recipient to form a biofilm. ICEBs1 transfer considerably increases in biofilm, even at low donor/recipient ratios. Also, while there is a clear temporal correlation between biofilm formation and ICEBs1 transfer, biofilms do not alter the level of ICEBs1 excision in donor cells. Conjugative transfer appears to be favored by the biophysical context of biofilms. Indeed, extracellular matrix production, particularly from the recipient cells, is essential for biofilms to promote ICEBs1 transfer. Our study provides basic new knowledge on the high rate of conjugative transfer of ICEs in biofilms, a widely preponderant bacterial lifestyle in the environment, which could have a major impact on our understanding of horizontal gene transfer in natural and clinical environments. IMPORTANCE Transfer of mobile genetic elements from one bacterium to another is the principal cause of the spread of antibiotic resistance. However, the dissemination of these elements in environmental contexts is poorly understood. In clinical and environmental settings, bacteria are often found living in multicellular communities encased in a matrix, a structure known as a biofilm. In this study, we examined how forming a biofilm influences the transmission of an integrative and conjugative element (ICE). Using the model Gram-positive bacterium B. subtilis, we observed that biofilm formation highly favors ICE transfer. This increase in conjugative transfer is due to the production of extracellular matrix, which creates an ideal biophysical context. Our study provides important insights into the role of the biofilm structure in driving conjugative transfer, which is of major importance since biofilm is a widely preponderant bacterial lifestyle for clinically relevant bacterial strains. American Society for Microbiology 2018-09-26 /pmc/articles/PMC6158512/ /pubmed/30258041 http://dx.doi.org/10.1128/mSphere.00473-18 Text en Copyright © 2018 Lécuyer et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Lécuyer, Frédéric
Bourassa, Jean-Sébastien
Gélinas, Martin
Charron-Lamoureux, Vincent
Burrus, Vincent
Beauregard, Pascale B.
Biofilm Formation Drives Transfer of the Conjugative Element ICEBs1 in Bacillus subtilis
title Biofilm Formation Drives Transfer of the Conjugative Element ICEBs1 in Bacillus subtilis
title_full Biofilm Formation Drives Transfer of the Conjugative Element ICEBs1 in Bacillus subtilis
title_fullStr Biofilm Formation Drives Transfer of the Conjugative Element ICEBs1 in Bacillus subtilis
title_full_unstemmed Biofilm Formation Drives Transfer of the Conjugative Element ICEBs1 in Bacillus subtilis
title_short Biofilm Formation Drives Transfer of the Conjugative Element ICEBs1 in Bacillus subtilis
title_sort biofilm formation drives transfer of the conjugative element icebs1 in bacillus subtilis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6158512/
https://www.ncbi.nlm.nih.gov/pubmed/30258041
http://dx.doi.org/10.1128/mSphere.00473-18
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