Cargando…
Dynamic character displacement among a pair of bacterial phyllosphere commensals in situ
Differences between species promote stable coexistence in a resource-limited environment. These differences can result from interspecies competition leading to character shifts, a process referred to as character displacement. While character displacement is often interpreted as a consequence of gen...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9123166/ https://www.ncbi.nlm.nih.gov/pubmed/35595740 http://dx.doi.org/10.1038/s41467-022-30469-3 |
_version_ | 1784711495739768832 |
---|---|
author | Hemmerle, Lucas Maier, Benjamin A. Bortfeld-Miller, Miriam Ryback, Birgitta Gäbelein, Christoph G. Ackermann, Martin Vorholt, Julia A. |
author_facet | Hemmerle, Lucas Maier, Benjamin A. Bortfeld-Miller, Miriam Ryback, Birgitta Gäbelein, Christoph G. Ackermann, Martin Vorholt, Julia A. |
author_sort | Hemmerle, Lucas |
collection | PubMed |
description | Differences between species promote stable coexistence in a resource-limited environment. These differences can result from interspecies competition leading to character shifts, a process referred to as character displacement. While character displacement is often interpreted as a consequence of genetically fixed trait differences between species, it can also be mediated by phenotypic plasticity in response to the presence of another species. Here, we test whether phenotypic plasticity leads to a shift in proteome allocation during co-occurrence of two bacterial species from the abundant, leaf-colonizing families Sphingomonadaceae and Rhizobiaceae in their natural habitat. Upon mono-colonizing of the phyllosphere, both species exhibit specific and shared protein functions indicating a niche overlap. During co-colonization, quantitative differences in the protein repertoire of both bacterial populations occur as a result of bacterial coexistence in planta. Specifically, the Sphingomonas strain produces enzymes for the metabolization of xylan, while the Rhizobium strain reprograms its metabolism to beta-oxidation of fatty acids fueled via the glyoxylate cycle and adapts its biotin acquisition. We demonstrate the conditional relevance of cross-species facilitation by mutagenesis leading to loss of fitness in competition in planta. Our results show that dynamic character displacement and niche facilitation mediated by phenotypic plasticity can contribute to species coexistence. |
format | Online Article Text |
id | pubmed-9123166 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91231662022-05-22 Dynamic character displacement among a pair of bacterial phyllosphere commensals in situ Hemmerle, Lucas Maier, Benjamin A. Bortfeld-Miller, Miriam Ryback, Birgitta Gäbelein, Christoph G. Ackermann, Martin Vorholt, Julia A. Nat Commun Article Differences between species promote stable coexistence in a resource-limited environment. These differences can result from interspecies competition leading to character shifts, a process referred to as character displacement. While character displacement is often interpreted as a consequence of genetically fixed trait differences between species, it can also be mediated by phenotypic plasticity in response to the presence of another species. Here, we test whether phenotypic plasticity leads to a shift in proteome allocation during co-occurrence of two bacterial species from the abundant, leaf-colonizing families Sphingomonadaceae and Rhizobiaceae in their natural habitat. Upon mono-colonizing of the phyllosphere, both species exhibit specific and shared protein functions indicating a niche overlap. During co-colonization, quantitative differences in the protein repertoire of both bacterial populations occur as a result of bacterial coexistence in planta. Specifically, the Sphingomonas strain produces enzymes for the metabolization of xylan, while the Rhizobium strain reprograms its metabolism to beta-oxidation of fatty acids fueled via the glyoxylate cycle and adapts its biotin acquisition. We demonstrate the conditional relevance of cross-species facilitation by mutagenesis leading to loss of fitness in competition in planta. Our results show that dynamic character displacement and niche facilitation mediated by phenotypic plasticity can contribute to species coexistence. Nature Publishing Group UK 2022-05-20 /pmc/articles/PMC9123166/ /pubmed/35595740 http://dx.doi.org/10.1038/s41467-022-30469-3 Text en © The Author(s) 2022 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 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Hemmerle, Lucas Maier, Benjamin A. Bortfeld-Miller, Miriam Ryback, Birgitta Gäbelein, Christoph G. Ackermann, Martin Vorholt, Julia A. Dynamic character displacement among a pair of bacterial phyllosphere commensals in situ |
title | Dynamic character displacement among a pair of bacterial phyllosphere commensals in situ |
title_full | Dynamic character displacement among a pair of bacterial phyllosphere commensals in situ |
title_fullStr | Dynamic character displacement among a pair of bacterial phyllosphere commensals in situ |
title_full_unstemmed | Dynamic character displacement among a pair of bacterial phyllosphere commensals in situ |
title_short | Dynamic character displacement among a pair of bacterial phyllosphere commensals in situ |
title_sort | dynamic character displacement among a pair of bacterial phyllosphere commensals in situ |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9123166/ https://www.ncbi.nlm.nih.gov/pubmed/35595740 http://dx.doi.org/10.1038/s41467-022-30469-3 |
work_keys_str_mv | AT hemmerlelucas dynamiccharacterdisplacementamongapairofbacterialphyllospherecommensalsinsitu AT maierbenjamina dynamiccharacterdisplacementamongapairofbacterialphyllospherecommensalsinsitu AT bortfeldmillermiriam dynamiccharacterdisplacementamongapairofbacterialphyllospherecommensalsinsitu AT rybackbirgitta dynamiccharacterdisplacementamongapairofbacterialphyllospherecommensalsinsitu AT gabeleinchristophg dynamiccharacterdisplacementamongapairofbacterialphyllospherecommensalsinsitu AT ackermannmartin dynamiccharacterdisplacementamongapairofbacterialphyllospherecommensalsinsitu AT vorholtjuliaa dynamiccharacterdisplacementamongapairofbacterialphyllospherecommensalsinsitu |