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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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.
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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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