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The rise of diversity in metabolic platforms across the Candidate Phyla Radiation

BACKGROUND: A unifying feature of the bacterial Candidate Phyla Radiation (CPR) is a limited and highly variable repertoire of biosynthetic capabilities. However, the distribution of metabolic traits across the CPR and the evolutionary processes underlying them are incompletely resolved. RESULTS: He...

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Autores principales: Jaffe, Alexander L., Castelle, Cindy J., Matheus Carnevali, Paula B., Gribaldo, Simonetta, Banfield, Jillian F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7304191/
https://www.ncbi.nlm.nih.gov/pubmed/32560683
http://dx.doi.org/10.1186/s12915-020-00804-5
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author Jaffe, Alexander L.
Castelle, Cindy J.
Matheus Carnevali, Paula B.
Gribaldo, Simonetta
Banfield, Jillian F.
author_facet Jaffe, Alexander L.
Castelle, Cindy J.
Matheus Carnevali, Paula B.
Gribaldo, Simonetta
Banfield, Jillian F.
author_sort Jaffe, Alexander L.
collection PubMed
description BACKGROUND: A unifying feature of the bacterial Candidate Phyla Radiation (CPR) is a limited and highly variable repertoire of biosynthetic capabilities. However, the distribution of metabolic traits across the CPR and the evolutionary processes underlying them are incompletely resolved. RESULTS: Here, we selected ~ 1000 genomes of CPR bacteria from diverse environments to construct a robust internal phylogeny that was consistent across two unlinked marker sets. Mapping of glycolysis, the pentose phosphate pathway, and pyruvate metabolism onto the tree showed that some components of these pathways are sparsely distributed and that similarity between metabolic platforms is only partially predicted by phylogenetic relationships. To evaluate the extent to which gene loss and lateral gene transfer have shaped trait distribution, we analyzed the patchiness of gene presence in a phylogenetic context, examined the phylogenetic depth of clades with shared traits, and compared the reference tree topology with those of specific metabolic proteins. While the central glycolytic pathway in CPR is widely conserved and has likely been shaped primarily by vertical transmission, there is evidence for both gene loss and transfer especially in steps that convert glucose into fructose 1,6-bisphosphate and glycerate 3P into pyruvate. Additionally, the distribution of Group 3 and Group 4-related NiFe hydrogenases is patchy and suggests multiple events of ancient gene transfer. CONCLUSIONS: We infer that patterns of gene gain and loss in CPR, including acquisition of accessory traits in independent transfer events, could have been driven by shifts in host-derived resources and led to sparse but varied genetic inventories.
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spelling pubmed-73041912020-06-22 The rise of diversity in metabolic platforms across the Candidate Phyla Radiation Jaffe, Alexander L. Castelle, Cindy J. Matheus Carnevali, Paula B. Gribaldo, Simonetta Banfield, Jillian F. BMC Biol Research Article BACKGROUND: A unifying feature of the bacterial Candidate Phyla Radiation (CPR) is a limited and highly variable repertoire of biosynthetic capabilities. However, the distribution of metabolic traits across the CPR and the evolutionary processes underlying them are incompletely resolved. RESULTS: Here, we selected ~ 1000 genomes of CPR bacteria from diverse environments to construct a robust internal phylogeny that was consistent across two unlinked marker sets. Mapping of glycolysis, the pentose phosphate pathway, and pyruvate metabolism onto the tree showed that some components of these pathways are sparsely distributed and that similarity between metabolic platforms is only partially predicted by phylogenetic relationships. To evaluate the extent to which gene loss and lateral gene transfer have shaped trait distribution, we analyzed the patchiness of gene presence in a phylogenetic context, examined the phylogenetic depth of clades with shared traits, and compared the reference tree topology with those of specific metabolic proteins. While the central glycolytic pathway in CPR is widely conserved and has likely been shaped primarily by vertical transmission, there is evidence for both gene loss and transfer especially in steps that convert glucose into fructose 1,6-bisphosphate and glycerate 3P into pyruvate. Additionally, the distribution of Group 3 and Group 4-related NiFe hydrogenases is patchy and suggests multiple events of ancient gene transfer. CONCLUSIONS: We infer that patterns of gene gain and loss in CPR, including acquisition of accessory traits in independent transfer events, could have been driven by shifts in host-derived resources and led to sparse but varied genetic inventories. BioMed Central 2020-06-19 /pmc/articles/PMC7304191/ /pubmed/32560683 http://dx.doi.org/10.1186/s12915-020-00804-5 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Jaffe, Alexander L.
Castelle, Cindy J.
Matheus Carnevali, Paula B.
Gribaldo, Simonetta
Banfield, Jillian F.
The rise of diversity in metabolic platforms across the Candidate Phyla Radiation
title The rise of diversity in metabolic platforms across the Candidate Phyla Radiation
title_full The rise of diversity in metabolic platforms across the Candidate Phyla Radiation
title_fullStr The rise of diversity in metabolic platforms across the Candidate Phyla Radiation
title_full_unstemmed The rise of diversity in metabolic platforms across the Candidate Phyla Radiation
title_short The rise of diversity in metabolic platforms across the Candidate Phyla Radiation
title_sort rise of diversity in metabolic platforms across the candidate phyla radiation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7304191/
https://www.ncbi.nlm.nih.gov/pubmed/32560683
http://dx.doi.org/10.1186/s12915-020-00804-5
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