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Lipid analysis of CO(2)-rich subsurface aquifers suggests an autotrophy-based deep biosphere with lysolipids enriched in CPR bacteria

Sediment-hosted CO(2)-rich aquifers deep below the Colorado Plateau (USA) contain a remarkable diversity of uncultivated microorganisms, including Candidate Phyla Radiation (CPR) bacteria that are putative symbionts unable to synthesize membrane lipids. The origin of organic carbon in these ecosyste...

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Autores principales: Probst, Alexander J., Elling, Felix J., Castelle, Cindy J., Zhu, Qingzeng, Elvert, Marcus, Birarda, Giovanni, Holman, Hoi-Ying N., Lane, Katherine R., Ladd, Bethany, Ryan, M. Cathryn, Woyke, Tanja, Hinrichs, Kai-Uwe, Banfield, Jillian F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7242380/
https://www.ncbi.nlm.nih.gov/pubmed/32203118
http://dx.doi.org/10.1038/s41396-020-0624-4
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author Probst, Alexander J.
Elling, Felix J.
Castelle, Cindy J.
Zhu, Qingzeng
Elvert, Marcus
Birarda, Giovanni
Holman, Hoi-Ying N.
Lane, Katherine R.
Ladd, Bethany
Ryan, M. Cathryn
Woyke, Tanja
Hinrichs, Kai-Uwe
Banfield, Jillian F.
author_facet Probst, Alexander J.
Elling, Felix J.
Castelle, Cindy J.
Zhu, Qingzeng
Elvert, Marcus
Birarda, Giovanni
Holman, Hoi-Ying N.
Lane, Katherine R.
Ladd, Bethany
Ryan, M. Cathryn
Woyke, Tanja
Hinrichs, Kai-Uwe
Banfield, Jillian F.
author_sort Probst, Alexander J.
collection PubMed
description Sediment-hosted CO(2)-rich aquifers deep below the Colorado Plateau (USA) contain a remarkable diversity of uncultivated microorganisms, including Candidate Phyla Radiation (CPR) bacteria that are putative symbionts unable to synthesize membrane lipids. The origin of organic carbon in these ecosystems is unknown and the source of CPR membrane lipids remains elusive. We collected cells from deep groundwater brought to the surface by eruptions of Crystal Geyser, sequenced the community, and analyzed the whole community lipidome over time. Characteristic stable carbon isotopic compositions of microbial lipids suggest that bacterial and archaeal CO(2) fixation ongoing in the deep subsurface provides organic carbon for the complex communities that reside there. Coupled lipidomic-metagenomic analysis indicates that CPR bacteria lack complete lipid biosynthesis pathways but still possess regular lipid membranes. These lipids may therefore originate from other community members, which also adapt to high in situ pressure by increasing fatty acid unsaturation. An unusually high abundance of lysolipids attributed to CPR bacteria may represent an adaptation to membrane curvature stress induced by their small cell sizes. Our findings provide new insights into the carbon cycle in the deep subsurface and suggest the redistribution of lipids into putative symbionts within this community.
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spelling pubmed-72423802020-05-29 Lipid analysis of CO(2)-rich subsurface aquifers suggests an autotrophy-based deep biosphere with lysolipids enriched in CPR bacteria Probst, Alexander J. Elling, Felix J. Castelle, Cindy J. Zhu, Qingzeng Elvert, Marcus Birarda, Giovanni Holman, Hoi-Ying N. Lane, Katherine R. Ladd, Bethany Ryan, M. Cathryn Woyke, Tanja Hinrichs, Kai-Uwe Banfield, Jillian F. ISME J Article Sediment-hosted CO(2)-rich aquifers deep below the Colorado Plateau (USA) contain a remarkable diversity of uncultivated microorganisms, including Candidate Phyla Radiation (CPR) bacteria that are putative symbionts unable to synthesize membrane lipids. The origin of organic carbon in these ecosystems is unknown and the source of CPR membrane lipids remains elusive. We collected cells from deep groundwater brought to the surface by eruptions of Crystal Geyser, sequenced the community, and analyzed the whole community lipidome over time. Characteristic stable carbon isotopic compositions of microbial lipids suggest that bacterial and archaeal CO(2) fixation ongoing in the deep subsurface provides organic carbon for the complex communities that reside there. Coupled lipidomic-metagenomic analysis indicates that CPR bacteria lack complete lipid biosynthesis pathways but still possess regular lipid membranes. These lipids may therefore originate from other community members, which also adapt to high in situ pressure by increasing fatty acid unsaturation. An unusually high abundance of lysolipids attributed to CPR bacteria may represent an adaptation to membrane curvature stress induced by their small cell sizes. Our findings provide new insights into the carbon cycle in the deep subsurface and suggest the redistribution of lipids into putative symbionts within this community. Nature Publishing Group UK 2020-03-13 2020-06 /pmc/articles/PMC7242380/ /pubmed/32203118 http://dx.doi.org/10.1038/s41396-020-0624-4 Text en © The Author(s) 2020 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
Probst, Alexander J.
Elling, Felix J.
Castelle, Cindy J.
Zhu, Qingzeng
Elvert, Marcus
Birarda, Giovanni
Holman, Hoi-Ying N.
Lane, Katherine R.
Ladd, Bethany
Ryan, M. Cathryn
Woyke, Tanja
Hinrichs, Kai-Uwe
Banfield, Jillian F.
Lipid analysis of CO(2)-rich subsurface aquifers suggests an autotrophy-based deep biosphere with lysolipids enriched in CPR bacteria
title Lipid analysis of CO(2)-rich subsurface aquifers suggests an autotrophy-based deep biosphere with lysolipids enriched in CPR bacteria
title_full Lipid analysis of CO(2)-rich subsurface aquifers suggests an autotrophy-based deep biosphere with lysolipids enriched in CPR bacteria
title_fullStr Lipid analysis of CO(2)-rich subsurface aquifers suggests an autotrophy-based deep biosphere with lysolipids enriched in CPR bacteria
title_full_unstemmed Lipid analysis of CO(2)-rich subsurface aquifers suggests an autotrophy-based deep biosphere with lysolipids enriched in CPR bacteria
title_short Lipid analysis of CO(2)-rich subsurface aquifers suggests an autotrophy-based deep biosphere with lysolipids enriched in CPR bacteria
title_sort lipid analysis of co(2)-rich subsurface aquifers suggests an autotrophy-based deep biosphere with lysolipids enriched in cpr bacteria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7242380/
https://www.ncbi.nlm.nih.gov/pubmed/32203118
http://dx.doi.org/10.1038/s41396-020-0624-4
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