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...

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Autores principales: Benny Lemaire, Peter Vandamme, Vincent Merckx, Erik Smets, Steven Dessein
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Publicado: Public Library of Science (PLoS) 2011
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Acceso en línea:https://doaj.org/article/307ab7c90a91415996238c8a1a1322ac
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spelling oai:doaj.org-article:307ab7c90a91415996238c8a1a1322ac2021-11-18T06:46:32ZBacterial leaf symbiosis in angiosperms: host specificity without co-speciation.1932-620310.1371/journal.pone.0024430https://doaj.org/article/307ab7c90a91415996238c8a1a1322ac2011-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21915326/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203Bacterial 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.Benny LemairePeter VandammeVincent MerckxErik SmetsSteven DesseinPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 6, Iss 9, p e24430 (2011)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Benny Lemaire
Peter Vandamme
Vincent Merckx
Erik Smets
Steven Dessein
Bacterial leaf symbiosis in angiosperms: host specificity without co-speciation.
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 article
author Benny Lemaire
Peter Vandamme
Vincent Merckx
Erik Smets
Steven Dessein
author_facet Benny Lemaire
Peter Vandamme
Vincent Merckx
Erik Smets
Steven Dessein
author_sort Benny Lemaire
title Bacterial leaf symbiosis in angiosperms: host specificity without co-speciation.
title_short 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_sort bacterial leaf symbiosis in angiosperms: host specificity without co-speciation.
publisher Public Library of Science (PLoS)
publishDate 2011
url https://doaj.org/article/307ab7c90a91415996238c8a1a1322ac
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AT petervandamme bacterialleafsymbiosisinangiospermshostspecificitywithoutcospeciation
AT vincentmerckx bacterialleafsymbiosisinangiospermshostspecificitywithoutcospeciation
AT eriksmets bacterialleafsymbiosisinangiospermshostspecificitywithoutcospeciation
AT stevendessein bacterialleafsymbiosisinangiospermshostspecificitywithoutcospeciation
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