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Chemical interplay and complementary adaptative strategies toggle bacterial antagonism and co-existence
Bacterial communities are in a continuous adaptive and evolutionary race for survival. In this work we expand our knowledge on the chemical interplay and specific mutations that modulate the transition from antagonism to co-existence between two plant-beneficial bacteria, Pseudomonas chlororaphis PC...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8333196/ https://www.ncbi.nlm.nih.gov/pubmed/34320359 http://dx.doi.org/10.1016/j.celrep.2021.109449 |
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author | Molina-Santiago, Carlos Vela-Corcía, David Petras, Daniel Díaz-Martínez, Luis Pérez-Lorente, Alicia Isabel Sopeña-Torres, Sara Pearson, John Caraballo-Rodríguez, Andrés Mauricio Dorrestein, Pieter C. de Vicente, Antonio Romero, Diego |
author_facet | Molina-Santiago, Carlos Vela-Corcía, David Petras, Daniel Díaz-Martínez, Luis Pérez-Lorente, Alicia Isabel Sopeña-Torres, Sara Pearson, John Caraballo-Rodríguez, Andrés Mauricio Dorrestein, Pieter C. de Vicente, Antonio Romero, Diego |
author_sort | Molina-Santiago, Carlos |
collection | PubMed |
description | Bacterial communities are in a continuous adaptive and evolutionary race for survival. In this work we expand our knowledge on the chemical interplay and specific mutations that modulate the transition from antagonism to co-existence between two plant-beneficial bacteria, Pseudomonas chlororaphis PCL1606 and Bacillus amyloliquefaciens FZB42. We reveal that the bacteriostatic activity of bacillaene produced by Bacillus relies on an interaction with the protein elongation factor FusA of P. chlororaphis and how mutations in this protein lead to tolerance to bacillaene and other protein translation inhibitors. Additionally, we describe how the unspecific tolerance of B. amyloliquefaciens to antimicrobials associated with mutations in the glycerol kinase GlpK is provoked by a decrease of Bacillus cell membrane permeability, among other pleiotropic responses. We conclude that nutrient specialization and mutations in basic biological functions are bacterial adaptive dynamics that lead to the coexistence of two primary competitive bacterial species rather than their mutual eradication. |
format | Online Article Text |
id | pubmed-8333196 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-83331962021-08-09 Chemical interplay and complementary adaptative strategies toggle bacterial antagonism and co-existence Molina-Santiago, Carlos Vela-Corcía, David Petras, Daniel Díaz-Martínez, Luis Pérez-Lorente, Alicia Isabel Sopeña-Torres, Sara Pearson, John Caraballo-Rodríguez, Andrés Mauricio Dorrestein, Pieter C. de Vicente, Antonio Romero, Diego Cell Rep Article Bacterial communities are in a continuous adaptive and evolutionary race for survival. In this work we expand our knowledge on the chemical interplay and specific mutations that modulate the transition from antagonism to co-existence between two plant-beneficial bacteria, Pseudomonas chlororaphis PCL1606 and Bacillus amyloliquefaciens FZB42. We reveal that the bacteriostatic activity of bacillaene produced by Bacillus relies on an interaction with the protein elongation factor FusA of P. chlororaphis and how mutations in this protein lead to tolerance to bacillaene and other protein translation inhibitors. Additionally, we describe how the unspecific tolerance of B. amyloliquefaciens to antimicrobials associated with mutations in the glycerol kinase GlpK is provoked by a decrease of Bacillus cell membrane permeability, among other pleiotropic responses. We conclude that nutrient specialization and mutations in basic biological functions are bacterial adaptive dynamics that lead to the coexistence of two primary competitive bacterial species rather than their mutual eradication. Cell Press 2021-07-27 /pmc/articles/PMC8333196/ /pubmed/34320359 http://dx.doi.org/10.1016/j.celrep.2021.109449 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Molina-Santiago, Carlos Vela-Corcía, David Petras, Daniel Díaz-Martínez, Luis Pérez-Lorente, Alicia Isabel Sopeña-Torres, Sara Pearson, John Caraballo-Rodríguez, Andrés Mauricio Dorrestein, Pieter C. de Vicente, Antonio Romero, Diego Chemical interplay and complementary adaptative strategies toggle bacterial antagonism and co-existence |
title | Chemical interplay and complementary adaptative strategies toggle bacterial antagonism and co-existence |
title_full | Chemical interplay and complementary adaptative strategies toggle bacterial antagonism and co-existence |
title_fullStr | Chemical interplay and complementary adaptative strategies toggle bacterial antagonism and co-existence |
title_full_unstemmed | Chemical interplay and complementary adaptative strategies toggle bacterial antagonism and co-existence |
title_short | Chemical interplay and complementary adaptative strategies toggle bacterial antagonism and co-existence |
title_sort | chemical interplay and complementary adaptative strategies toggle bacterial antagonism and co-existence |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8333196/ https://www.ncbi.nlm.nih.gov/pubmed/34320359 http://dx.doi.org/10.1016/j.celrep.2021.109449 |
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