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Hyperactive nanobacteria with host-dependent traits pervade Omnitrophota

Candidate bacterial phylum Omnitrophota has not been isolated and is poorly understood. We analysed 72 newly sequenced and 349 existing Omnitrophota genomes representing 6 classes and 276 species, along with Earth Microbiome Project data to evaluate habitat, metabolic traits and lifestyles. We appli...

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Autores principales: Seymour, Cale O., Palmer, Marike, Becraft, Eric D., Stepanauskas, Ramunas, Friel, Ariel D., Schulz, Frederik, Woyke, Tanja, Eloe-Fadrosh, Emiley, Lai, Dengxun, Jiao, Jian-Yu, Hua, Zheng-Shuang, Liu, Lan, Lian, Zheng-Han, Li, Wen-Jun, Chuvochina, Maria, Finley, Brianna K., Koch, Benjamin J., Schwartz, Egbert, Dijkstra, Paul, Moser, Duane P., Hungate, Bruce A., Hedlund, Brian P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10066038/
https://www.ncbi.nlm.nih.gov/pubmed/36928026
http://dx.doi.org/10.1038/s41564-022-01319-1
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author Seymour, Cale O.
Palmer, Marike
Becraft, Eric D.
Stepanauskas, Ramunas
Friel, Ariel D.
Schulz, Frederik
Woyke, Tanja
Eloe-Fadrosh, Emiley
Lai, Dengxun
Jiao, Jian-Yu
Hua, Zheng-Shuang
Liu, Lan
Lian, Zheng-Han
Li, Wen-Jun
Chuvochina, Maria
Finley, Brianna K.
Koch, Benjamin J.
Schwartz, Egbert
Dijkstra, Paul
Moser, Duane P.
Hungate, Bruce A.
Hedlund, Brian P.
author_facet Seymour, Cale O.
Palmer, Marike
Becraft, Eric D.
Stepanauskas, Ramunas
Friel, Ariel D.
Schulz, Frederik
Woyke, Tanja
Eloe-Fadrosh, Emiley
Lai, Dengxun
Jiao, Jian-Yu
Hua, Zheng-Shuang
Liu, Lan
Lian, Zheng-Han
Li, Wen-Jun
Chuvochina, Maria
Finley, Brianna K.
Koch, Benjamin J.
Schwartz, Egbert
Dijkstra, Paul
Moser, Duane P.
Hungate, Bruce A.
Hedlund, Brian P.
author_sort Seymour, Cale O.
collection PubMed
description Candidate bacterial phylum Omnitrophota has not been isolated and is poorly understood. We analysed 72 newly sequenced and 349 existing Omnitrophota genomes representing 6 classes and 276 species, along with Earth Microbiome Project data to evaluate habitat, metabolic traits and lifestyles. We applied fluorescence-activated cell sorting and differential size filtration, and showed that most Omnitrophota are ultra-small (~0.2 μm) cells that are found in water, sediments and soils. Omnitrophota genomes in 6 classes are reduced, but maintain major biosynthetic and energy conservation pathways, including acetogenesis (with or without the Wood-Ljungdahl pathway) and diverse respirations. At least 64% of Omnitrophota genomes encode gene clusters typical of bacterial symbionts, suggesting host-associated lifestyles. We repurposed quantitative stable-isotope probing data from soils dominated by andesite, basalt or granite weathering and identified 3 families with high isotope uptake consistent with obligate bacterial predators. We propose that most Omnitrophota inhabit various ecosystems as predators or parasites.
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spelling pubmed-100660382023-04-02 Hyperactive nanobacteria with host-dependent traits pervade Omnitrophota Seymour, Cale O. Palmer, Marike Becraft, Eric D. Stepanauskas, Ramunas Friel, Ariel D. Schulz, Frederik Woyke, Tanja Eloe-Fadrosh, Emiley Lai, Dengxun Jiao, Jian-Yu Hua, Zheng-Shuang Liu, Lan Lian, Zheng-Han Li, Wen-Jun Chuvochina, Maria Finley, Brianna K. Koch, Benjamin J. Schwartz, Egbert Dijkstra, Paul Moser, Duane P. Hungate, Bruce A. Hedlund, Brian P. Nat Microbiol Analysis Candidate bacterial phylum Omnitrophota has not been isolated and is poorly understood. We analysed 72 newly sequenced and 349 existing Omnitrophota genomes representing 6 classes and 276 species, along with Earth Microbiome Project data to evaluate habitat, metabolic traits and lifestyles. We applied fluorescence-activated cell sorting and differential size filtration, and showed that most Omnitrophota are ultra-small (~0.2 μm) cells that are found in water, sediments and soils. Omnitrophota genomes in 6 classes are reduced, but maintain major biosynthetic and energy conservation pathways, including acetogenesis (with or without the Wood-Ljungdahl pathway) and diverse respirations. At least 64% of Omnitrophota genomes encode gene clusters typical of bacterial symbionts, suggesting host-associated lifestyles. We repurposed quantitative stable-isotope probing data from soils dominated by andesite, basalt or granite weathering and identified 3 families with high isotope uptake consistent with obligate bacterial predators. We propose that most Omnitrophota inhabit various ecosystems as predators or parasites. Nature Publishing Group UK 2023-03-16 2023 /pmc/articles/PMC10066038/ /pubmed/36928026 http://dx.doi.org/10.1038/s41564-022-01319-1 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 Analysis
Seymour, Cale O.
Palmer, Marike
Becraft, Eric D.
Stepanauskas, Ramunas
Friel, Ariel D.
Schulz, Frederik
Woyke, Tanja
Eloe-Fadrosh, Emiley
Lai, Dengxun
Jiao, Jian-Yu
Hua, Zheng-Shuang
Liu, Lan
Lian, Zheng-Han
Li, Wen-Jun
Chuvochina, Maria
Finley, Brianna K.
Koch, Benjamin J.
Schwartz, Egbert
Dijkstra, Paul
Moser, Duane P.
Hungate, Bruce A.
Hedlund, Brian P.
Hyperactive nanobacteria with host-dependent traits pervade Omnitrophota
title Hyperactive nanobacteria with host-dependent traits pervade Omnitrophota
title_full Hyperactive nanobacteria with host-dependent traits pervade Omnitrophota
title_fullStr Hyperactive nanobacteria with host-dependent traits pervade Omnitrophota
title_full_unstemmed Hyperactive nanobacteria with host-dependent traits pervade Omnitrophota
title_short Hyperactive nanobacteria with host-dependent traits pervade Omnitrophota
title_sort hyperactive nanobacteria with host-dependent traits pervade omnitrophota
topic Analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10066038/
https://www.ncbi.nlm.nih.gov/pubmed/36928026
http://dx.doi.org/10.1038/s41564-022-01319-1
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