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Experimental evolution of Bacillus subtilis on Arabidopsis thaliana roots reveals fast adaptation and improved root colonization
Bacillus subtilis is known to promote plant growth and protect plants against disease. B. subtilis rapidly adapts to Arabidopsis thaliana root colonization, as evidenced by improved root colonizers already after 12 consecutive transfers between seedlings in a hydroponic setup. Re-sequencing of singl...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9157203/ https://www.ncbi.nlm.nih.gov/pubmed/35663012 http://dx.doi.org/10.1016/j.isci.2022.104406 |
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author | Nordgaard, Mathilde Blake, Christopher Maróti, Gergely Hu, Guohai Wang, Yue Strube, Mikael Lenz Kovács, Ákos T. |
author_facet | Nordgaard, Mathilde Blake, Christopher Maróti, Gergely Hu, Guohai Wang, Yue Strube, Mikael Lenz Kovács, Ákos T. |
author_sort | Nordgaard, Mathilde |
collection | PubMed |
description | Bacillus subtilis is known to promote plant growth and protect plants against disease. B. subtilis rapidly adapts to Arabidopsis thaliana root colonization, as evidenced by improved root colonizers already after 12 consecutive transfers between seedlings in a hydroponic setup. Re-sequencing of single evolved isolates and endpoint populations revealed mutations in genes related to different bacterial traits, in accordance with evolved isolates displaying increased root colonization associated with robust biofilm formation in response to the plant polysaccharide xylan and impaired motility. Interestingly, evolved isolates suffered a fitness disadvantage in a non-selective environment, demonstrating an evolutionary cost of adaptation to the plant root. Finally, increased root colonization by an evolved isolate was also demonstrated in the presence of resident soil microbes. Our findings highlight how a plant growth-promoting rhizobacterium rapidly adapts to an ecologically relevant environment and reveal evolutionary consequences that are fundamental to consider when evolving strains for biocontrol purposes. |
format | Online Article Text |
id | pubmed-9157203 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-91572032022-06-02 Experimental evolution of Bacillus subtilis on Arabidopsis thaliana roots reveals fast adaptation and improved root colonization Nordgaard, Mathilde Blake, Christopher Maróti, Gergely Hu, Guohai Wang, Yue Strube, Mikael Lenz Kovács, Ákos T. iScience Article Bacillus subtilis is known to promote plant growth and protect plants against disease. B. subtilis rapidly adapts to Arabidopsis thaliana root colonization, as evidenced by improved root colonizers already after 12 consecutive transfers between seedlings in a hydroponic setup. Re-sequencing of single evolved isolates and endpoint populations revealed mutations in genes related to different bacterial traits, in accordance with evolved isolates displaying increased root colonization associated with robust biofilm formation in response to the plant polysaccharide xylan and impaired motility. Interestingly, evolved isolates suffered a fitness disadvantage in a non-selective environment, demonstrating an evolutionary cost of adaptation to the plant root. Finally, increased root colonization by an evolved isolate was also demonstrated in the presence of resident soil microbes. Our findings highlight how a plant growth-promoting rhizobacterium rapidly adapts to an ecologically relevant environment and reveal evolutionary consequences that are fundamental to consider when evolving strains for biocontrol purposes. Elsevier 2022-05-14 /pmc/articles/PMC9157203/ /pubmed/35663012 http://dx.doi.org/10.1016/j.isci.2022.104406 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Nordgaard, Mathilde Blake, Christopher Maróti, Gergely Hu, Guohai Wang, Yue Strube, Mikael Lenz Kovács, Ákos T. Experimental evolution of Bacillus subtilis on Arabidopsis thaliana roots reveals fast adaptation and improved root colonization |
title | Experimental evolution of Bacillus subtilis on Arabidopsis thaliana roots reveals fast adaptation and improved root colonization |
title_full | Experimental evolution of Bacillus subtilis on Arabidopsis thaliana roots reveals fast adaptation and improved root colonization |
title_fullStr | Experimental evolution of Bacillus subtilis on Arabidopsis thaliana roots reveals fast adaptation and improved root colonization |
title_full_unstemmed | Experimental evolution of Bacillus subtilis on Arabidopsis thaliana roots reveals fast adaptation and improved root colonization |
title_short | Experimental evolution of Bacillus subtilis on Arabidopsis thaliana roots reveals fast adaptation and improved root colonization |
title_sort | experimental evolution of bacillus subtilis on arabidopsis thaliana roots reveals fast adaptation and improved root colonization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9157203/ https://www.ncbi.nlm.nih.gov/pubmed/35663012 http://dx.doi.org/10.1016/j.isci.2022.104406 |
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