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Phenotypic plasticity and a new small molecule are involved in a fungal-bacterial interaction

Nitrogen-fixing bacteria have been extensively studied in the context of interactions with their host plants; however, little is known about the phenotypic plasticity of these microorganisms in nonmutualistic interactions with other eukaryotes. A dual-species coculture model was developed by using t...

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Autores principales: Andrade-Domínguez, Andrés, Trejo-Hernández, Abigail, Vargas-Lagunas, Carmen, Encarnación-Guevara, Sergio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8479133/
https://www.ncbi.nlm.nih.gov/pubmed/34584120
http://dx.doi.org/10.1038/s41598-021-98474-y
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author Andrade-Domínguez, Andrés
Trejo-Hernández, Abigail
Vargas-Lagunas, Carmen
Encarnación-Guevara, Sergio
author_facet Andrade-Domínguez, Andrés
Trejo-Hernández, Abigail
Vargas-Lagunas, Carmen
Encarnación-Guevara, Sergio
author_sort Andrade-Domínguez, Andrés
collection PubMed
description Nitrogen-fixing bacteria have been extensively studied in the context of interactions with their host plants; however, little is known about the phenotypic plasticity of these microorganisms in nonmutualistic interactions with other eukaryotes. A dual-species coculture model was developed by using the plant symbiotic bacterium Rhizobium etli and the well-studied eukaryote Saccharomyces cerevisiae as a tractable system to explore the molecular mechanisms used by R. etli in nonmutual interactions. Here, we show that the fungus promotes the growth of the bacterium and that together, these organisms form a mixed biofilm whose biomass is ~ 3 times greater and is more structured than that of either single-species biofilm. We found that these biofilm traits are dependent on a symbiotic plasmid encoding elements involved in the phenotypic plasticity of the bacterium, mitochondrial function and in the production of a yeast-secreted sophoroside. Interestingly, the promoters of 3 genes that are key in plant bacteria-interaction (nifH, fixA and nodA) were induced when R. etli coexists with yeast. These results show that investigating interactions between species that do not naturally coexist is a new approach to discover gene functions and specialized metabolites in model organisms.
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spelling pubmed-84791332021-09-30 Phenotypic plasticity and a new small molecule are involved in a fungal-bacterial interaction Andrade-Domínguez, Andrés Trejo-Hernández, Abigail Vargas-Lagunas, Carmen Encarnación-Guevara, Sergio Sci Rep Article Nitrogen-fixing bacteria have been extensively studied in the context of interactions with their host plants; however, little is known about the phenotypic plasticity of these microorganisms in nonmutualistic interactions with other eukaryotes. A dual-species coculture model was developed by using the plant symbiotic bacterium Rhizobium etli and the well-studied eukaryote Saccharomyces cerevisiae as a tractable system to explore the molecular mechanisms used by R. etli in nonmutual interactions. Here, we show that the fungus promotes the growth of the bacterium and that together, these organisms form a mixed biofilm whose biomass is ~ 3 times greater and is more structured than that of either single-species biofilm. We found that these biofilm traits are dependent on a symbiotic plasmid encoding elements involved in the phenotypic plasticity of the bacterium, mitochondrial function and in the production of a yeast-secreted sophoroside. Interestingly, the promoters of 3 genes that are key in plant bacteria-interaction (nifH, fixA and nodA) were induced when R. etli coexists with yeast. These results show that investigating interactions between species that do not naturally coexist is a new approach to discover gene functions and specialized metabolites in model organisms. Nature Publishing Group UK 2021-09-28 /pmc/articles/PMC8479133/ /pubmed/34584120 http://dx.doi.org/10.1038/s41598-021-98474-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Andrade-Domínguez, Andrés
Trejo-Hernández, Abigail
Vargas-Lagunas, Carmen
Encarnación-Guevara, Sergio
Phenotypic plasticity and a new small molecule are involved in a fungal-bacterial interaction
title Phenotypic plasticity and a new small molecule are involved in a fungal-bacterial interaction
title_full Phenotypic plasticity and a new small molecule are involved in a fungal-bacterial interaction
title_fullStr Phenotypic plasticity and a new small molecule are involved in a fungal-bacterial interaction
title_full_unstemmed Phenotypic plasticity and a new small molecule are involved in a fungal-bacterial interaction
title_short Phenotypic plasticity and a new small molecule are involved in a fungal-bacterial interaction
title_sort phenotypic plasticity and a new small molecule are involved in a fungal-bacterial interaction
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8479133/
https://www.ncbi.nlm.nih.gov/pubmed/34584120
http://dx.doi.org/10.1038/s41598-021-98474-y
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