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A glimpse of the paleome in endolithic microbial communities
BACKGROUND: The terrestrial subsurface is home to a significant proportion of the Earth’s microbial biomass. Our understanding about terrestrial subsurface microbiomes is almost exclusively derived from groundwater and porous sediments mainly by using 16S rRNA gene surveys. To obtain more insights a...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10518947/ https://www.ncbi.nlm.nih.gov/pubmed/37749660 http://dx.doi.org/10.1186/s40168-023-01647-2 |
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author | Wegner, Carl-Eric Stahl, Raphaela Velsko, Irina Hübner, Alex Fagernäs, Zandra Warinner, Christina Lehmann, Robert Ritschel, Thomas Totsche, Kai U. Küsel, Kirsten |
author_facet | Wegner, Carl-Eric Stahl, Raphaela Velsko, Irina Hübner, Alex Fagernäs, Zandra Warinner, Christina Lehmann, Robert Ritschel, Thomas Totsche, Kai U. Küsel, Kirsten |
author_sort | Wegner, Carl-Eric |
collection | PubMed |
description | BACKGROUND: The terrestrial subsurface is home to a significant proportion of the Earth’s microbial biomass. Our understanding about terrestrial subsurface microbiomes is almost exclusively derived from groundwater and porous sediments mainly by using 16S rRNA gene surveys. To obtain more insights about biomass of consolidated rocks and the metabolic status of endolithic microbiomes, we investigated interbedded limestone and mudstone from the vadose zone, fractured aquifers, and deep aquitards. RESULTS: By adapting methods from microbial archaeology and paleogenomics, we could recover sufficient DNA for downstream metagenomic analysis from seven rock specimens independent of porosity, lithology, and depth. Based on the extracted DNA, we estimated between 2.81 and 4.25 × 10(5) cells × g(−1) rock. Analyzing DNA damage patterns revealed paleome signatures (genetic records of past microbial communities) for three rock specimens, all obtained from the vadose zone. DNA obtained from deep aquitards isolated from surface input was not affected by DNA decay indicating that water saturation and not flow is controlling subsurface microbial survival. Decoding the taxonomy and functional potential of paleome communities revealed increased abundances for sequences affiliated with chemolithoautotrophs and taxa such as Cand. Rokubacteria. We also found a broader metabolic potential in terms of aromatic hydrocarbon breakdown, suggesting a preferred utilization of sedimentary organic matter in the past. CONCLUSIONS: Our study suggests that limestones function as archives for genetic records of past microbial communities including those sensitive to environmental stress at modern times, due to their specific conditions facilitating long-term DNA preservation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01647-2. |
format | Online Article Text |
id | pubmed-10518947 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-105189472023-09-26 A glimpse of the paleome in endolithic microbial communities Wegner, Carl-Eric Stahl, Raphaela Velsko, Irina Hübner, Alex Fagernäs, Zandra Warinner, Christina Lehmann, Robert Ritschel, Thomas Totsche, Kai U. Küsel, Kirsten Microbiome Research BACKGROUND: The terrestrial subsurface is home to a significant proportion of the Earth’s microbial biomass. Our understanding about terrestrial subsurface microbiomes is almost exclusively derived from groundwater and porous sediments mainly by using 16S rRNA gene surveys. To obtain more insights about biomass of consolidated rocks and the metabolic status of endolithic microbiomes, we investigated interbedded limestone and mudstone from the vadose zone, fractured aquifers, and deep aquitards. RESULTS: By adapting methods from microbial archaeology and paleogenomics, we could recover sufficient DNA for downstream metagenomic analysis from seven rock specimens independent of porosity, lithology, and depth. Based on the extracted DNA, we estimated between 2.81 and 4.25 × 10(5) cells × g(−1) rock. Analyzing DNA damage patterns revealed paleome signatures (genetic records of past microbial communities) for three rock specimens, all obtained from the vadose zone. DNA obtained from deep aquitards isolated from surface input was not affected by DNA decay indicating that water saturation and not flow is controlling subsurface microbial survival. Decoding the taxonomy and functional potential of paleome communities revealed increased abundances for sequences affiliated with chemolithoautotrophs and taxa such as Cand. Rokubacteria. We also found a broader metabolic potential in terms of aromatic hydrocarbon breakdown, suggesting a preferred utilization of sedimentary organic matter in the past. CONCLUSIONS: Our study suggests that limestones function as archives for genetic records of past microbial communities including those sensitive to environmental stress at modern times, due to their specific conditions facilitating long-term DNA preservation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01647-2. BioMed Central 2023-09-25 /pmc/articles/PMC10518947/ /pubmed/37749660 http://dx.doi.org/10.1186/s40168-023-01647-2 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Wegner, Carl-Eric Stahl, Raphaela Velsko, Irina Hübner, Alex Fagernäs, Zandra Warinner, Christina Lehmann, Robert Ritschel, Thomas Totsche, Kai U. Küsel, Kirsten A glimpse of the paleome in endolithic microbial communities |
title | A glimpse of the paleome in endolithic microbial communities |
title_full | A glimpse of the paleome in endolithic microbial communities |
title_fullStr | A glimpse of the paleome in endolithic microbial communities |
title_full_unstemmed | A glimpse of the paleome in endolithic microbial communities |
title_short | A glimpse of the paleome in endolithic microbial communities |
title_sort | glimpse of the paleome in endolithic microbial communities |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10518947/ https://www.ncbi.nlm.nih.gov/pubmed/37749660 http://dx.doi.org/10.1186/s40168-023-01647-2 |
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