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Fungal–bacterial interaction selects for quorum sensing mutants with increased production of natural antifungal compounds
Soil microorganisms coexist and interact showing antagonistic or mutualistic behaviors. Here, we show that an environmental strain of Bacillus subtilis undergoes heritable phenotypic variation upon interaction with the soil fungal pathogen Setophoma terrestris (ST). Metabolomics analysis revealed di...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7661731/ https://www.ncbi.nlm.nih.gov/pubmed/33184402 http://dx.doi.org/10.1038/s42003-020-01342-0 |
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author | Albarracín Orio, Andrea G. Petras, Daniel Tobares, Romina A. Aksenov, Alexander A. Wang, Mingxun Juncosa, Florencia Sayago, Pamela Moyano, Alejandro J. Dorrestein, Pieter C. Smania, Andrea M. |
author_facet | Albarracín Orio, Andrea G. Petras, Daniel Tobares, Romina A. Aksenov, Alexander A. Wang, Mingxun Juncosa, Florencia Sayago, Pamela Moyano, Alejandro J. Dorrestein, Pieter C. Smania, Andrea M. |
author_sort | Albarracín Orio, Andrea G. |
collection | PubMed |
description | Soil microorganisms coexist and interact showing antagonistic or mutualistic behaviors. Here, we show that an environmental strain of Bacillus subtilis undergoes heritable phenotypic variation upon interaction with the soil fungal pathogen Setophoma terrestris (ST). Metabolomics analysis revealed differential profiles in B. subtilis before (pre-ST) and after (post-ST) interacting with the fungus, which paradoxically involved the absence of lipopeptides surfactin and plipastatin and yet acquisition of antifungal activity in post-ST variants. The profile of volatile compounds showed that 2-heptanone and 2-octanone were the most discriminating metabolites present at higher concentrations in post-ST during the interaction process. Both ketones showed strong antifungal activity, which was lost with the addition of exogenous surfactin. Whole-genome analyses indicate that mutations in ComQPXA quorum-sensing system, constituted the genetic bases of post-ST conversion, which rewired B. subtilis metabolism towards the depletion of surfactins and the production of antifungal compounds during its antagonistic interaction with S. terrestris. |
format | Online Article Text |
id | pubmed-7661731 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76617312020-11-17 Fungal–bacterial interaction selects for quorum sensing mutants with increased production of natural antifungal compounds Albarracín Orio, Andrea G. Petras, Daniel Tobares, Romina A. Aksenov, Alexander A. Wang, Mingxun Juncosa, Florencia Sayago, Pamela Moyano, Alejandro J. Dorrestein, Pieter C. Smania, Andrea M. Commun Biol Article Soil microorganisms coexist and interact showing antagonistic or mutualistic behaviors. Here, we show that an environmental strain of Bacillus subtilis undergoes heritable phenotypic variation upon interaction with the soil fungal pathogen Setophoma terrestris (ST). Metabolomics analysis revealed differential profiles in B. subtilis before (pre-ST) and after (post-ST) interacting with the fungus, which paradoxically involved the absence of lipopeptides surfactin and plipastatin and yet acquisition of antifungal activity in post-ST variants. The profile of volatile compounds showed that 2-heptanone and 2-octanone were the most discriminating metabolites present at higher concentrations in post-ST during the interaction process. Both ketones showed strong antifungal activity, which was lost with the addition of exogenous surfactin. Whole-genome analyses indicate that mutations in ComQPXA quorum-sensing system, constituted the genetic bases of post-ST conversion, which rewired B. subtilis metabolism towards the depletion of surfactins and the production of antifungal compounds during its antagonistic interaction with S. terrestris. Nature Publishing Group UK 2020-11-12 /pmc/articles/PMC7661731/ /pubmed/33184402 http://dx.doi.org/10.1038/s42003-020-01342-0 Text en © The Author(s) 2020 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 Albarracín Orio, Andrea G. Petras, Daniel Tobares, Romina A. Aksenov, Alexander A. Wang, Mingxun Juncosa, Florencia Sayago, Pamela Moyano, Alejandro J. Dorrestein, Pieter C. Smania, Andrea M. Fungal–bacterial interaction selects for quorum sensing mutants with increased production of natural antifungal compounds |
title | Fungal–bacterial interaction selects for quorum sensing mutants with increased production of natural antifungal compounds |
title_full | Fungal–bacterial interaction selects for quorum sensing mutants with increased production of natural antifungal compounds |
title_fullStr | Fungal–bacterial interaction selects for quorum sensing mutants with increased production of natural antifungal compounds |
title_full_unstemmed | Fungal–bacterial interaction selects for quorum sensing mutants with increased production of natural antifungal compounds |
title_short | Fungal–bacterial interaction selects for quorum sensing mutants with increased production of natural antifungal compounds |
title_sort | fungal–bacterial interaction selects for quorum sensing mutants with increased production of natural antifungal compounds |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7661731/ https://www.ncbi.nlm.nih.gov/pubmed/33184402 http://dx.doi.org/10.1038/s42003-020-01342-0 |
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