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The evolutionary origin of host association in the Rickettsiales

The evolution of obligate host-association of bacterial symbionts and pathogens remains poorly understood. The Rickettsiales are an alphaproteobacterial order of obligate endosymbionts and parasites that infect a wide variety of eukaryotic hosts, including humans, livestock, insects and protists. In...

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Autores principales: Schön, Max E., Martijn, Joran, Vosseberg, Julian, Köstlbacher, Stephan, Ettema, Thijs J. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9352585/
https://www.ncbi.nlm.nih.gov/pubmed/35798888
http://dx.doi.org/10.1038/s41564-022-01169-x
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author Schön, Max E.
Martijn, Joran
Vosseberg, Julian
Köstlbacher, Stephan
Ettema, Thijs J. G.
author_facet Schön, Max E.
Martijn, Joran
Vosseberg, Julian
Köstlbacher, Stephan
Ettema, Thijs J. G.
author_sort Schön, Max E.
collection PubMed
description The evolution of obligate host-association of bacterial symbionts and pathogens remains poorly understood. The Rickettsiales are an alphaproteobacterial order of obligate endosymbionts and parasites that infect a wide variety of eukaryotic hosts, including humans, livestock, insects and protists. Induced by their host-associated lifestyle, Rickettsiales genomes have undergone reductive evolution, leading to small, AT-rich genomes with limited metabolic capacities. Here we uncover eleven deep-branching alphaproteobacterial metagenome assembled genomes from aquatic environments, including data from the Tara Oceans initiative and other publicly available datasets, distributed over three previously undescribed Rickettsiales-related clades. Phylogenomic analyses reveal that two of these clades, Mitibacteraceae and Athabascaceae, branch sister to all previously sampled Rickettsiales. The third clade, Gamibacteraceae, branch sister to the recently identified ectosymbiotic ‘Candidatus Deianiraea vastatrix’. Comparative analyses indicate that the gene complement of Mitibacteraceae and Athabascaceae is reminiscent of that of free-living and biofilm-associated bacteria. Ancestral genome content reconstruction across the Rickettsiales species tree further suggests that the evolution of host association in Rickettsiales was a gradual process that may have involved the repurposing of a type IV secretion system.
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spelling pubmed-93525852022-08-06 The evolutionary origin of host association in the Rickettsiales Schön, Max E. Martijn, Joran Vosseberg, Julian Köstlbacher, Stephan Ettema, Thijs J. G. Nat Microbiol Article The evolution of obligate host-association of bacterial symbionts and pathogens remains poorly understood. The Rickettsiales are an alphaproteobacterial order of obligate endosymbionts and parasites that infect a wide variety of eukaryotic hosts, including humans, livestock, insects and protists. Induced by their host-associated lifestyle, Rickettsiales genomes have undergone reductive evolution, leading to small, AT-rich genomes with limited metabolic capacities. Here we uncover eleven deep-branching alphaproteobacterial metagenome assembled genomes from aquatic environments, including data from the Tara Oceans initiative and other publicly available datasets, distributed over three previously undescribed Rickettsiales-related clades. Phylogenomic analyses reveal that two of these clades, Mitibacteraceae and Athabascaceae, branch sister to all previously sampled Rickettsiales. The third clade, Gamibacteraceae, branch sister to the recently identified ectosymbiotic ‘Candidatus Deianiraea vastatrix’. Comparative analyses indicate that the gene complement of Mitibacteraceae and Athabascaceae is reminiscent of that of free-living and biofilm-associated bacteria. Ancestral genome content reconstruction across the Rickettsiales species tree further suggests that the evolution of host association in Rickettsiales was a gradual process that may have involved the repurposing of a type IV secretion system. Nature Publishing Group UK 2022-07-07 2022 /pmc/articles/PMC9352585/ /pubmed/35798888 http://dx.doi.org/10.1038/s41564-022-01169-x 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
Schön, Max E.
Martijn, Joran
Vosseberg, Julian
Köstlbacher, Stephan
Ettema, Thijs J. G.
The evolutionary origin of host association in the Rickettsiales
title The evolutionary origin of host association in the Rickettsiales
title_full The evolutionary origin of host association in the Rickettsiales
title_fullStr The evolutionary origin of host association in the Rickettsiales
title_full_unstemmed The evolutionary origin of host association in the Rickettsiales
title_short The evolutionary origin of host association in the Rickettsiales
title_sort evolutionary origin of host association in the rickettsiales
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9352585/
https://www.ncbi.nlm.nih.gov/pubmed/35798888
http://dx.doi.org/10.1038/s41564-022-01169-x
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