Cargando…
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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1785018213318262784 |
---|---|
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. |
format | Online Article Text |
id | pubmed-10066038 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT seymourcaleo hyperactivenanobacteriawithhostdependenttraitspervadeomnitrophota AT palmermarike hyperactivenanobacteriawithhostdependenttraitspervadeomnitrophota AT becraftericd hyperactivenanobacteriawithhostdependenttraitspervadeomnitrophota AT stepanauskasramunas hyperactivenanobacteriawithhostdependenttraitspervadeomnitrophota AT frielarield hyperactivenanobacteriawithhostdependenttraitspervadeomnitrophota AT schulzfrederik hyperactivenanobacteriawithhostdependenttraitspervadeomnitrophota AT woyketanja hyperactivenanobacteriawithhostdependenttraitspervadeomnitrophota AT eloefadroshemiley hyperactivenanobacteriawithhostdependenttraitspervadeomnitrophota AT laidengxun hyperactivenanobacteriawithhostdependenttraitspervadeomnitrophota AT jiaojianyu hyperactivenanobacteriawithhostdependenttraitspervadeomnitrophota AT huazhengshuang hyperactivenanobacteriawithhostdependenttraitspervadeomnitrophota AT liulan hyperactivenanobacteriawithhostdependenttraitspervadeomnitrophota AT lianzhenghan hyperactivenanobacteriawithhostdependenttraitspervadeomnitrophota AT liwenjun hyperactivenanobacteriawithhostdependenttraitspervadeomnitrophota AT chuvochinamaria hyperactivenanobacteriawithhostdependenttraitspervadeomnitrophota AT finleybriannak hyperactivenanobacteriawithhostdependenttraitspervadeomnitrophota AT kochbenjaminj hyperactivenanobacteriawithhostdependenttraitspervadeomnitrophota AT schwartzegbert hyperactivenanobacteriawithhostdependenttraitspervadeomnitrophota AT dijkstrapaul hyperactivenanobacteriawithhostdependenttraitspervadeomnitrophota AT moserduanep hyperactivenanobacteriawithhostdependenttraitspervadeomnitrophota AT hungatebrucea hyperactivenanobacteriawithhostdependenttraitspervadeomnitrophota AT hedlundbrianp hyperactivenanobacteriawithhostdependenttraitspervadeomnitrophota |