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The extracellular matrix protects Bacillus subtilis colonies from Pseudomonas invasion and modulates plant co-colonization
Bacteria of the genera Pseudomonas and Bacillus can promote plant growth and protect plants from pathogens. However, the interactions between these plant-beneficial bacteria are understudied. Here, we explore the interaction between Bacillus subtilis 3610 and Pseudomonas chlororaphis PCL1606. We sho...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478825/ https://www.ncbi.nlm.nih.gov/pubmed/31015472 http://dx.doi.org/10.1038/s41467-019-09944-x |
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author | Molina-Santiago, Carlos Pearson, John R. Navarro, Yurena Berlanga-Clavero, María Victoria Caraballo-Rodriguez, Andrés Mauricio Petras, Daniel García-Martín, María Luisa Lamon, Gaelle Haberstein, Birgit Cazorla, Francisco M. de Vicente, Antonio Loquet, Antoine Dorrestein, Pieter C. Romero, Diego |
author_facet | Molina-Santiago, Carlos Pearson, John R. Navarro, Yurena Berlanga-Clavero, María Victoria Caraballo-Rodriguez, Andrés Mauricio Petras, Daniel García-Martín, María Luisa Lamon, Gaelle Haberstein, Birgit Cazorla, Francisco M. de Vicente, Antonio Loquet, Antoine Dorrestein, Pieter C. Romero, Diego |
author_sort | Molina-Santiago, Carlos |
collection | PubMed |
description | Bacteria of the genera Pseudomonas and Bacillus can promote plant growth and protect plants from pathogens. However, the interactions between these plant-beneficial bacteria are understudied. Here, we explore the interaction between Bacillus subtilis 3610 and Pseudomonas chlororaphis PCL1606. We show that the extracellular matrix protects B. subtilis colonies from infiltration by P. chlororaphis. The absence of extracellular matrix results in increased fluidity and loss of structure of the B. subtilis colony. The P. chlororaphis type VI secretion system (T6SS) is activated upon contact with B. subtilis cells, and stimulates B. subtilis sporulation. Furthermore, we find that B. subtilis sporulation observed prior to direct contact with P. chlororaphis is mediated by histidine kinases KinA and KinB. Finally, we demonstrate the importance of the extracellular matrix and the T6SS in modulating the coexistence of the two species on melon plant leaves and seeds. |
format | Online Article Text |
id | pubmed-6478825 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64788252019-04-25 The extracellular matrix protects Bacillus subtilis colonies from Pseudomonas invasion and modulates plant co-colonization Molina-Santiago, Carlos Pearson, John R. Navarro, Yurena Berlanga-Clavero, María Victoria Caraballo-Rodriguez, Andrés Mauricio Petras, Daniel García-Martín, María Luisa Lamon, Gaelle Haberstein, Birgit Cazorla, Francisco M. de Vicente, Antonio Loquet, Antoine Dorrestein, Pieter C. Romero, Diego Nat Commun Article Bacteria of the genera Pseudomonas and Bacillus can promote plant growth and protect plants from pathogens. However, the interactions between these plant-beneficial bacteria are understudied. Here, we explore the interaction between Bacillus subtilis 3610 and Pseudomonas chlororaphis PCL1606. We show that the extracellular matrix protects B. subtilis colonies from infiltration by P. chlororaphis. The absence of extracellular matrix results in increased fluidity and loss of structure of the B. subtilis colony. The P. chlororaphis type VI secretion system (T6SS) is activated upon contact with B. subtilis cells, and stimulates B. subtilis sporulation. Furthermore, we find that B. subtilis sporulation observed prior to direct contact with P. chlororaphis is mediated by histidine kinases KinA and KinB. Finally, we demonstrate the importance of the extracellular matrix and the T6SS in modulating the coexistence of the two species on melon plant leaves and seeds. Nature Publishing Group UK 2019-04-23 /pmc/articles/PMC6478825/ /pubmed/31015472 http://dx.doi.org/10.1038/s41467-019-09944-x Text en © The Author(s) 2019 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 Molina-Santiago, Carlos Pearson, John R. Navarro, Yurena Berlanga-Clavero, María Victoria Caraballo-Rodriguez, Andrés Mauricio Petras, Daniel García-Martín, María Luisa Lamon, Gaelle Haberstein, Birgit Cazorla, Francisco M. de Vicente, Antonio Loquet, Antoine Dorrestein, Pieter C. Romero, Diego The extracellular matrix protects Bacillus subtilis colonies from Pseudomonas invasion and modulates plant co-colonization |
title | The extracellular matrix protects Bacillus subtilis colonies from Pseudomonas invasion and modulates plant co-colonization |
title_full | The extracellular matrix protects Bacillus subtilis colonies from Pseudomonas invasion and modulates plant co-colonization |
title_fullStr | The extracellular matrix protects Bacillus subtilis colonies from Pseudomonas invasion and modulates plant co-colonization |
title_full_unstemmed | The extracellular matrix protects Bacillus subtilis colonies from Pseudomonas invasion and modulates plant co-colonization |
title_short | The extracellular matrix protects Bacillus subtilis colonies from Pseudomonas invasion and modulates plant co-colonization |
title_sort | extracellular matrix protects bacillus subtilis colonies from pseudomonas invasion and modulates plant co-colonization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478825/ https://www.ncbi.nlm.nih.gov/pubmed/31015472 http://dx.doi.org/10.1038/s41467-019-09944-x |
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