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Horizontal acquisition of a patchwork Calvin cycle by symbiotic and free-living Campylobacterota (formerly Epsilonproteobacteria)

Most autotrophs use the Calvin–Benson–Bassham (CBB) cycle for carbon fixation. In contrast, all currently described autotrophs from the Campylobacterota (previously Epsilonproteobacteria) use the reductive tricarboxylic acid cycle (rTCA) instead. We discovered campylobacterotal epibionts (“Candidatu...

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Autores principales: Assié, Adrien, Leisch, Nikolaus, Meier, Dimitri V., Gruber-Vodicka, Harald, Tegetmeyer, Halina E., Meyerdierks, Anke, Kleiner, Manuel, Hinzke, Tjorven, Joye, Samantha, Saxton, Matthew, Dubilier, Nicole, Petersen, Jillian M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6908604/
https://www.ncbi.nlm.nih.gov/pubmed/31562384
http://dx.doi.org/10.1038/s41396-019-0508-7
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author Assié, Adrien
Leisch, Nikolaus
Meier, Dimitri V.
Gruber-Vodicka, Harald
Tegetmeyer, Halina E.
Meyerdierks, Anke
Kleiner, Manuel
Hinzke, Tjorven
Joye, Samantha
Saxton, Matthew
Dubilier, Nicole
Petersen, Jillian M.
author_facet Assié, Adrien
Leisch, Nikolaus
Meier, Dimitri V.
Gruber-Vodicka, Harald
Tegetmeyer, Halina E.
Meyerdierks, Anke
Kleiner, Manuel
Hinzke, Tjorven
Joye, Samantha
Saxton, Matthew
Dubilier, Nicole
Petersen, Jillian M.
author_sort Assié, Adrien
collection PubMed
description Most autotrophs use the Calvin–Benson–Bassham (CBB) cycle for carbon fixation. In contrast, all currently described autotrophs from the Campylobacterota (previously Epsilonproteobacteria) use the reductive tricarboxylic acid cycle (rTCA) instead. We discovered campylobacterotal epibionts (“Candidatus Thiobarba”) of deep-sea mussels that have acquired a complete CBB cycle and may have lost most key genes of the rTCA cycle. Intriguingly, the phylogenies of campylobacterotal CBB cycle genes suggest they were acquired in multiple transfers from Gammaproteobacteria closely related to sulfur-oxidizing endosymbionts associated with the mussels, as well as from Betaproteobacteria. We hypothesize that “Ca. Thiobarba” switched from the rTCA cycle to a fully functional CBB cycle during its evolution, by acquiring genes from multiple sources, including co-occurring symbionts. We also found key CBB cycle genes in free-living Campylobacterota, suggesting that the CBB cycle may be more widespread in this phylum than previously known. Metatranscriptomics and metaproteomics confirmed high expression of CBB cycle genes in mussel-associated “Ca. Thiobarba”. Direct stable isotope fingerprinting showed that “Ca. Thiobarba” has typical CBB signatures, suggesting that it uses this cycle for carbon fixation. Our discovery calls into question current assumptions about the distribution of carbon fixation pathways in microbial lineages, and the interpretation of stable isotope measurements in the environment.
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spelling pubmed-69086042019-12-13 Horizontal acquisition of a patchwork Calvin cycle by symbiotic and free-living Campylobacterota (formerly Epsilonproteobacteria) Assié, Adrien Leisch, Nikolaus Meier, Dimitri V. Gruber-Vodicka, Harald Tegetmeyer, Halina E. Meyerdierks, Anke Kleiner, Manuel Hinzke, Tjorven Joye, Samantha Saxton, Matthew Dubilier, Nicole Petersen, Jillian M. ISME J Article Most autotrophs use the Calvin–Benson–Bassham (CBB) cycle for carbon fixation. In contrast, all currently described autotrophs from the Campylobacterota (previously Epsilonproteobacteria) use the reductive tricarboxylic acid cycle (rTCA) instead. We discovered campylobacterotal epibionts (“Candidatus Thiobarba”) of deep-sea mussels that have acquired a complete CBB cycle and may have lost most key genes of the rTCA cycle. Intriguingly, the phylogenies of campylobacterotal CBB cycle genes suggest they were acquired in multiple transfers from Gammaproteobacteria closely related to sulfur-oxidizing endosymbionts associated with the mussels, as well as from Betaproteobacteria. We hypothesize that “Ca. Thiobarba” switched from the rTCA cycle to a fully functional CBB cycle during its evolution, by acquiring genes from multiple sources, including co-occurring symbionts. We also found key CBB cycle genes in free-living Campylobacterota, suggesting that the CBB cycle may be more widespread in this phylum than previously known. Metatranscriptomics and metaproteomics confirmed high expression of CBB cycle genes in mussel-associated “Ca. Thiobarba”. Direct stable isotope fingerprinting showed that “Ca. Thiobarba” has typical CBB signatures, suggesting that it uses this cycle for carbon fixation. Our discovery calls into question current assumptions about the distribution of carbon fixation pathways in microbial lineages, and the interpretation of stable isotope measurements in the environment. Nature Publishing Group UK 2019-09-27 2020-01 /pmc/articles/PMC6908604/ /pubmed/31562384 http://dx.doi.org/10.1038/s41396-019-0508-7 Text en © The Author(s) 2019 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/.
spellingShingle Article
Assié, Adrien
Leisch, Nikolaus
Meier, Dimitri V.
Gruber-Vodicka, Harald
Tegetmeyer, Halina E.
Meyerdierks, Anke
Kleiner, Manuel
Hinzke, Tjorven
Joye, Samantha
Saxton, Matthew
Dubilier, Nicole
Petersen, Jillian M.
Horizontal acquisition of a patchwork Calvin cycle by symbiotic and free-living Campylobacterota (formerly Epsilonproteobacteria)
title Horizontal acquisition of a patchwork Calvin cycle by symbiotic and free-living Campylobacterota (formerly Epsilonproteobacteria)
title_full Horizontal acquisition of a patchwork Calvin cycle by symbiotic and free-living Campylobacterota (formerly Epsilonproteobacteria)
title_fullStr Horizontal acquisition of a patchwork Calvin cycle by symbiotic and free-living Campylobacterota (formerly Epsilonproteobacteria)
title_full_unstemmed Horizontal acquisition of a patchwork Calvin cycle by symbiotic and free-living Campylobacterota (formerly Epsilonproteobacteria)
title_short Horizontal acquisition of a patchwork Calvin cycle by symbiotic and free-living Campylobacterota (formerly Epsilonproteobacteria)
title_sort horizontal acquisition of a patchwork calvin cycle by symbiotic and free-living campylobacterota (formerly epsilonproteobacteria)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6908604/
https://www.ncbi.nlm.nih.gov/pubmed/31562384
http://dx.doi.org/10.1038/s41396-019-0508-7
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