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Gene gain facilitated endosymbiotic evolution of Chlamydiae
Chlamydiae is a bacterial phylum composed of obligate animal and protist endosymbionts. However, other members of the Planctomycetes–Verrucomicrobia–Chlamydiae superphylum are primarily free living. How Chlamydiae transitioned to an endosymbiotic lifestyle is still largely unresolved. Here we recons...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9816063/ https://www.ncbi.nlm.nih.gov/pubmed/36604515 http://dx.doi.org/10.1038/s41564-022-01284-9 |
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author | Dharamshi, Jennah E. Köstlbacher, Stephan Schön, Max E. Collingro, Astrid Ettema, Thijs J. G. Horn, Matthias |
author_facet | Dharamshi, Jennah E. Köstlbacher, Stephan Schön, Max E. Collingro, Astrid Ettema, Thijs J. G. Horn, Matthias |
author_sort | Dharamshi, Jennah E. |
collection | PubMed |
description | Chlamydiae is a bacterial phylum composed of obligate animal and protist endosymbionts. However, other members of the Planctomycetes–Verrucomicrobia–Chlamydiae superphylum are primarily free living. How Chlamydiae transitioned to an endosymbiotic lifestyle is still largely unresolved. Here we reconstructed Planctomycetes–Verrucomicrobia–Chlamydiae species relationships and modelled superphylum genome evolution. Gene content reconstruction from 11,996 gene families suggests a motile and facultatively anaerobic last common Chlamydiae ancestor that had already gained characteristic endosymbiont genes. Counter to expectations for genome streamlining in strict endosymbionts, we detected substantial gene gain within Chlamydiae. We found that divergence in energy metabolism and aerobiosis observed in extant lineages emerged later during chlamydial evolution. In particular, metabolic and aerobic genes characteristic of the more metabolically versatile protist-infecting chlamydiae were gained, such as respiratory chain complexes. Our results show that metabolic complexity can increase during endosymbiont evolution, adding an additional perspective for understanding symbiont evolutionary trajectories across the tree of life. |
format | Online Article Text |
id | pubmed-9816063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98160632023-01-07 Gene gain facilitated endosymbiotic evolution of Chlamydiae Dharamshi, Jennah E. Köstlbacher, Stephan Schön, Max E. Collingro, Astrid Ettema, Thijs J. G. Horn, Matthias Nat Microbiol Article Chlamydiae is a bacterial phylum composed of obligate animal and protist endosymbionts. However, other members of the Planctomycetes–Verrucomicrobia–Chlamydiae superphylum are primarily free living. How Chlamydiae transitioned to an endosymbiotic lifestyle is still largely unresolved. Here we reconstructed Planctomycetes–Verrucomicrobia–Chlamydiae species relationships and modelled superphylum genome evolution. Gene content reconstruction from 11,996 gene families suggests a motile and facultatively anaerobic last common Chlamydiae ancestor that had already gained characteristic endosymbiont genes. Counter to expectations for genome streamlining in strict endosymbionts, we detected substantial gene gain within Chlamydiae. We found that divergence in energy metabolism and aerobiosis observed in extant lineages emerged later during chlamydial evolution. In particular, metabolic and aerobic genes characteristic of the more metabolically versatile protist-infecting chlamydiae were gained, such as respiratory chain complexes. Our results show that metabolic complexity can increase during endosymbiont evolution, adding an additional perspective for understanding symbiont evolutionary trajectories across the tree of life. Nature Publishing Group UK 2023-01-05 2023 /pmc/articles/PMC9816063/ /pubmed/36604515 http://dx.doi.org/10.1038/s41564-022-01284-9 Text en © The Author(s) 2023 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 Dharamshi, Jennah E. Köstlbacher, Stephan Schön, Max E. Collingro, Astrid Ettema, Thijs J. G. Horn, Matthias Gene gain facilitated endosymbiotic evolution of Chlamydiae |
title | Gene gain facilitated endosymbiotic evolution of Chlamydiae |
title_full | Gene gain facilitated endosymbiotic evolution of Chlamydiae |
title_fullStr | Gene gain facilitated endosymbiotic evolution of Chlamydiae |
title_full_unstemmed | Gene gain facilitated endosymbiotic evolution of Chlamydiae |
title_short | Gene gain facilitated endosymbiotic evolution of Chlamydiae |
title_sort | gene gain facilitated endosymbiotic evolution of chlamydiae |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9816063/ https://www.ncbi.nlm.nih.gov/pubmed/36604515 http://dx.doi.org/10.1038/s41564-022-01284-9 |
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