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Bacterial Leaf Symbiosis in Angiosperms: Host Specificity without Co-Speciation
Bacterial leaf symbiosis is a unique and intimate interaction between bacteria and flowering plants, in which endosymbionts are organized in specialized leaf structures. Previously, bacterial leaf symbiosis has been described as a cyclic and obligate interaction in which the endosymbionts are vertic...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3168474/ https://www.ncbi.nlm.nih.gov/pubmed/21915326 http://dx.doi.org/10.1371/journal.pone.0024430 |
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author | Lemaire, Benny Vandamme, Peter Merckx, Vincent Smets, Erik Dessein, Steven |
author_facet | Lemaire, Benny Vandamme, Peter Merckx, Vincent Smets, Erik Dessein, Steven |
author_sort | Lemaire, Benny |
collection | PubMed |
description | Bacterial leaf symbiosis is a unique and intimate interaction between bacteria and flowering plants, in which endosymbionts are organized in specialized leaf structures. Previously, bacterial leaf symbiosis has been described as a cyclic and obligate interaction in which the endosymbionts are vertically transmitted between plant generations and lack autonomous growth. Theoretically this allows for co-speciation between leaf nodulated plants and their endosymbionts. We sequenced the nodulated Burkholderia endosymbionts of 54 plant species from known leaf nodulated angiosperm genera, i.e. Ardisia, Pavetta, Psychotria and Sericanthe. Phylogenetic reconstruction of bacterial leaf symbionts and closely related free-living bacteria indicates the occurrence of multiple horizontal transfers of bacteria from the environment to leaf nodulated plant species. This rejects the hypothesis of a long co-speciation process between the bacterial endosymbionts and their host plants. Our results indicate a recent evolutionary process towards a stable and host specific interaction confirming the proposed maternal transmission mode of the endosymbionts through the seeds. Divergence estimates provide evidence for a relatively recent origin of bacterial leaf symbiosis, dating back to the Miocene (5–23 Mya). This geological epoch was characterized by cool and arid conditions, which may have triggered the origin of bacterial leaf symbiosis. |
format | Online Article Text |
id | pubmed-3168474 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-31684742011-09-13 Bacterial Leaf Symbiosis in Angiosperms: Host Specificity without Co-Speciation Lemaire, Benny Vandamme, Peter Merckx, Vincent Smets, Erik Dessein, Steven PLoS One Research Article Bacterial leaf symbiosis is a unique and intimate interaction between bacteria and flowering plants, in which endosymbionts are organized in specialized leaf structures. Previously, bacterial leaf symbiosis has been described as a cyclic and obligate interaction in which the endosymbionts are vertically transmitted between plant generations and lack autonomous growth. Theoretically this allows for co-speciation between leaf nodulated plants and their endosymbionts. We sequenced the nodulated Burkholderia endosymbionts of 54 plant species from known leaf nodulated angiosperm genera, i.e. Ardisia, Pavetta, Psychotria and Sericanthe. Phylogenetic reconstruction of bacterial leaf symbionts and closely related free-living bacteria indicates the occurrence of multiple horizontal transfers of bacteria from the environment to leaf nodulated plant species. This rejects the hypothesis of a long co-speciation process between the bacterial endosymbionts and their host plants. Our results indicate a recent evolutionary process towards a stable and host specific interaction confirming the proposed maternal transmission mode of the endosymbionts through the seeds. Divergence estimates provide evidence for a relatively recent origin of bacterial leaf symbiosis, dating back to the Miocene (5–23 Mya). This geological epoch was characterized by cool and arid conditions, which may have triggered the origin of bacterial leaf symbiosis. Public Library of Science 2011-09-07 /pmc/articles/PMC3168474/ /pubmed/21915326 http://dx.doi.org/10.1371/journal.pone.0024430 Text en Lemaire et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Lemaire, Benny Vandamme, Peter Merckx, Vincent Smets, Erik Dessein, Steven Bacterial Leaf Symbiosis in Angiosperms: Host Specificity without Co-Speciation |
title | Bacterial Leaf Symbiosis in Angiosperms: Host Specificity without Co-Speciation |
title_full | Bacterial Leaf Symbiosis in Angiosperms: Host Specificity without Co-Speciation |
title_fullStr | Bacterial Leaf Symbiosis in Angiosperms: Host Specificity without Co-Speciation |
title_full_unstemmed | Bacterial Leaf Symbiosis in Angiosperms: Host Specificity without Co-Speciation |
title_short | Bacterial Leaf Symbiosis in Angiosperms: Host Specificity without Co-Speciation |
title_sort | bacterial leaf symbiosis in angiosperms: host specificity without co-speciation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3168474/ https://www.ncbi.nlm.nih.gov/pubmed/21915326 http://dx.doi.org/10.1371/journal.pone.0024430 |
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