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Genomic reconstruction of fossil and living microorganisms in ancient Siberian permafrost

BACKGROUND: Total DNA (intracellular, iDNA and extracellular, eDNA) from ancient permafrost records the mixed genetic repository of the past and present microbial populations through geological time. Given the exceptional preservation of eDNA under perennial frozen conditions, typical metagenomic se...

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Autores principales: Liang, Renxing, Li, Zhou, Lau Vetter, Maggie C. Y., Vishnivetskaya, Tatiana A., Zanina, Oksana G., Lloyd, Karen G., Pfiffner, Susan M., Rivkina, Elizaveta M., Wang, Wei, Wiggins, Jessica, Miller, Jennifer, Hettich, Robert L., Onstott, Tullis C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8130349/
https://www.ncbi.nlm.nih.gov/pubmed/34001281
http://dx.doi.org/10.1186/s40168-021-01057-2
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author Liang, Renxing
Li, Zhou
Lau Vetter, Maggie C. Y.
Vishnivetskaya, Tatiana A.
Zanina, Oksana G.
Lloyd, Karen G.
Pfiffner, Susan M.
Rivkina, Elizaveta M.
Wang, Wei
Wiggins, Jessica
Miller, Jennifer
Hettich, Robert L.
Onstott, Tullis C.
author_facet Liang, Renxing
Li, Zhou
Lau Vetter, Maggie C. Y.
Vishnivetskaya, Tatiana A.
Zanina, Oksana G.
Lloyd, Karen G.
Pfiffner, Susan M.
Rivkina, Elizaveta M.
Wang, Wei
Wiggins, Jessica
Miller, Jennifer
Hettich, Robert L.
Onstott, Tullis C.
author_sort Liang, Renxing
collection PubMed
description BACKGROUND: Total DNA (intracellular, iDNA and extracellular, eDNA) from ancient permafrost records the mixed genetic repository of the past and present microbial populations through geological time. Given the exceptional preservation of eDNA under perennial frozen conditions, typical metagenomic sequencing of total DNA precludes the discrimination between fossil and living microorganisms in ancient cryogenic environments. DNA repair protocols were combined with high throughput sequencing (HTS) of separate iDNA and eDNA fraction to reconstruct metagenome-assembled genomes (MAGs) from ancient microbial DNA entrapped in Siberian coastal permafrost. RESULTS: Despite the severe DNA damage in ancient permafrost, the coupling of DNA repair and HTS resulted in a total of 52 MAGs from sediments across a chronosequence (26–120 kyr). These MAGs were compared with those derived from the same samples but without utilizing DNA repair protocols. The MAGs from the youngest stratum showed minimal DNA damage and thus likely originated from viable, active microbial species. Many MAGs from the older and deeper sediment appear related to past aerobic microbial populations that had died upon freezing. MAGs from anaerobic lineages, including Asgard archaea, however exhibited minimal DNA damage and likely represent extant living microorganisms that have become adapted to the cryogenic and anoxic environments. The integration of aspartic acid racemization modeling and metaproteomics further constrained the metabolic status of the living microbial populations. Collectively, combining DNA repair protocols with HTS unveiled the adaptive strategies of microbes to long-term survivability in ancient permafrost. CONCLUSIONS: Our results indicated that coupling of DNA repair protocols with simultaneous sequencing of iDNA and eDNA fractions enabled the assembly of MAGs from past and living microorganisms in ancient permafrost. The genomic reconstruction from the past and extant microbial populations expanded our understanding about the microbial successions and biogeochemical alterations from the past paleoenvironment to the present-day frozen state. Furthermore, we provided genomic insights into long-term survival mechanisms of microorganisms under cryogenic conditions through geological time. The combined strategies in this study can be extrapolated to examine other ancient non-permafrost environments and constrain the search for past and extant extraterrestrial life in permafrost and ice deposits on Mars. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-021-01057-2.
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spelling pubmed-81303492021-05-18 Genomic reconstruction of fossil and living microorganisms in ancient Siberian permafrost Liang, Renxing Li, Zhou Lau Vetter, Maggie C. Y. Vishnivetskaya, Tatiana A. Zanina, Oksana G. Lloyd, Karen G. Pfiffner, Susan M. Rivkina, Elizaveta M. Wang, Wei Wiggins, Jessica Miller, Jennifer Hettich, Robert L. Onstott, Tullis C. Microbiome Research BACKGROUND: Total DNA (intracellular, iDNA and extracellular, eDNA) from ancient permafrost records the mixed genetic repository of the past and present microbial populations through geological time. Given the exceptional preservation of eDNA under perennial frozen conditions, typical metagenomic sequencing of total DNA precludes the discrimination between fossil and living microorganisms in ancient cryogenic environments. DNA repair protocols were combined with high throughput sequencing (HTS) of separate iDNA and eDNA fraction to reconstruct metagenome-assembled genomes (MAGs) from ancient microbial DNA entrapped in Siberian coastal permafrost. RESULTS: Despite the severe DNA damage in ancient permafrost, the coupling of DNA repair and HTS resulted in a total of 52 MAGs from sediments across a chronosequence (26–120 kyr). These MAGs were compared with those derived from the same samples but without utilizing DNA repair protocols. The MAGs from the youngest stratum showed minimal DNA damage and thus likely originated from viable, active microbial species. Many MAGs from the older and deeper sediment appear related to past aerobic microbial populations that had died upon freezing. MAGs from anaerobic lineages, including Asgard archaea, however exhibited minimal DNA damage and likely represent extant living microorganisms that have become adapted to the cryogenic and anoxic environments. The integration of aspartic acid racemization modeling and metaproteomics further constrained the metabolic status of the living microbial populations. Collectively, combining DNA repair protocols with HTS unveiled the adaptive strategies of microbes to long-term survivability in ancient permafrost. CONCLUSIONS: Our results indicated that coupling of DNA repair protocols with simultaneous sequencing of iDNA and eDNA fractions enabled the assembly of MAGs from past and living microorganisms in ancient permafrost. The genomic reconstruction from the past and extant microbial populations expanded our understanding about the microbial successions and biogeochemical alterations from the past paleoenvironment to the present-day frozen state. Furthermore, we provided genomic insights into long-term survival mechanisms of microorganisms under cryogenic conditions through geological time. The combined strategies in this study can be extrapolated to examine other ancient non-permafrost environments and constrain the search for past and extant extraterrestrial life in permafrost and ice deposits on Mars. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-021-01057-2. BioMed Central 2021-05-17 /pmc/articles/PMC8130349/ /pubmed/34001281 http://dx.doi.org/10.1186/s40168-021-01057-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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
Liang, Renxing
Li, Zhou
Lau Vetter, Maggie C. Y.
Vishnivetskaya, Tatiana A.
Zanina, Oksana G.
Lloyd, Karen G.
Pfiffner, Susan M.
Rivkina, Elizaveta M.
Wang, Wei
Wiggins, Jessica
Miller, Jennifer
Hettich, Robert L.
Onstott, Tullis C.
Genomic reconstruction of fossil and living microorganisms in ancient Siberian permafrost
title Genomic reconstruction of fossil and living microorganisms in ancient Siberian permafrost
title_full Genomic reconstruction of fossil and living microorganisms in ancient Siberian permafrost
title_fullStr Genomic reconstruction of fossil and living microorganisms in ancient Siberian permafrost
title_full_unstemmed Genomic reconstruction of fossil and living microorganisms in ancient Siberian permafrost
title_short Genomic reconstruction of fossil and living microorganisms in ancient Siberian permafrost
title_sort genomic reconstruction of fossil and living microorganisms in ancient siberian permafrost
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8130349/
https://www.ncbi.nlm.nih.gov/pubmed/34001281
http://dx.doi.org/10.1186/s40168-021-01057-2
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