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Weaponizing volatiles to inhibit competitor biofilms from a distance

The soil bacterium Bacillus subtilis forms beneficial biofilms that induce plant defences and prevent the growth of pathogens. It is naturally found in the rhizosphere, where microorganisms coexist in an extremely competitive environment, and thus have evolved a diverse arsenal of defence mechanisms...

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Autores principales: Hou, Qihui, Keren-Paz, Alona, Korenblum, Elisa, Oved, Rela, Malitsky, Sergey, Kolodkin-Gal, Ilana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7785731/
https://www.ncbi.nlm.nih.gov/pubmed/33402677
http://dx.doi.org/10.1038/s41522-020-00174-4
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author Hou, Qihui
Keren-Paz, Alona
Korenblum, Elisa
Oved, Rela
Malitsky, Sergey
Kolodkin-Gal, Ilana
author_facet Hou, Qihui
Keren-Paz, Alona
Korenblum, Elisa
Oved, Rela
Malitsky, Sergey
Kolodkin-Gal, Ilana
author_sort Hou, Qihui
collection PubMed
description The soil bacterium Bacillus subtilis forms beneficial biofilms that induce plant defences and prevent the growth of pathogens. It is naturally found in the rhizosphere, where microorganisms coexist in an extremely competitive environment, and thus have evolved a diverse arsenal of defence mechanisms. In this work, we found that volatile compounds produced by B. subtilis biofilms inhibited the development of competing biofilm colonies, by reducing extracellular matrix gene expression, both within and across species. This effect was dose-dependent, with the structural defects becoming more pronounced as the number of volatile-producing colonies increased. This inhibition was mostly mediated by organic volatiles, and we identified the active molecules as 3-methyl-1-butanol and 1-butanol. Similar results were obtained with biofilms formed by phylogenetically distinct bacterium sharing the same niche, Escherichia coli, which produced the biofilm-inhibiting 3-methyl-1-butanol and 2-nonanon. The ability of established biofilms to inhibit the development and spreading of new biofilms from afar might be a general mechanism utilized by bacterial biofilms to protect an occupied niche from the invasion of competing bacteria.
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spelling pubmed-77857312021-01-14 Weaponizing volatiles to inhibit competitor biofilms from a distance Hou, Qihui Keren-Paz, Alona Korenblum, Elisa Oved, Rela Malitsky, Sergey Kolodkin-Gal, Ilana NPJ Biofilms Microbiomes Article The soil bacterium Bacillus subtilis forms beneficial biofilms that induce plant defences and prevent the growth of pathogens. It is naturally found in the rhizosphere, where microorganisms coexist in an extremely competitive environment, and thus have evolved a diverse arsenal of defence mechanisms. In this work, we found that volatile compounds produced by B. subtilis biofilms inhibited the development of competing biofilm colonies, by reducing extracellular matrix gene expression, both within and across species. This effect was dose-dependent, with the structural defects becoming more pronounced as the number of volatile-producing colonies increased. This inhibition was mostly mediated by organic volatiles, and we identified the active molecules as 3-methyl-1-butanol and 1-butanol. Similar results were obtained with biofilms formed by phylogenetically distinct bacterium sharing the same niche, Escherichia coli, which produced the biofilm-inhibiting 3-methyl-1-butanol and 2-nonanon. The ability of established biofilms to inhibit the development and spreading of new biofilms from afar might be a general mechanism utilized by bacterial biofilms to protect an occupied niche from the invasion of competing bacteria. Nature Publishing Group UK 2021-01-05 /pmc/articles/PMC7785731/ /pubmed/33402677 http://dx.doi.org/10.1038/s41522-020-00174-4 Text en © The Author(s) 2021 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
Hou, Qihui
Keren-Paz, Alona
Korenblum, Elisa
Oved, Rela
Malitsky, Sergey
Kolodkin-Gal, Ilana
Weaponizing volatiles to inhibit competitor biofilms from a distance
title Weaponizing volatiles to inhibit competitor biofilms from a distance
title_full Weaponizing volatiles to inhibit competitor biofilms from a distance
title_fullStr Weaponizing volatiles to inhibit competitor biofilms from a distance
title_full_unstemmed Weaponizing volatiles to inhibit competitor biofilms from a distance
title_short Weaponizing volatiles to inhibit competitor biofilms from a distance
title_sort weaponizing volatiles to inhibit competitor biofilms from a distance
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7785731/
https://www.ncbi.nlm.nih.gov/pubmed/33402677
http://dx.doi.org/10.1038/s41522-020-00174-4
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