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Microbial survival strategies in ancient permafrost: insights from metagenomics
In permafrost (perennially frozen ground) microbes survive oligotrophic conditions, sub-zero temperatures, low water availability and high salinity over millennia. Viable life exists in permafrost tens of thousands of years old but we know little about the metabolic and physiological adaptations to...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607373/ https://www.ncbi.nlm.nih.gov/pubmed/28696425 http://dx.doi.org/10.1038/ismej.2017.93 |
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author | Mackelprang, Rachel Burkert, Alexander Haw, Monica Mahendrarajah, Tara Conaway, Christopher H Douglas, Thomas A Waldrop, Mark P |
author_facet | Mackelprang, Rachel Burkert, Alexander Haw, Monica Mahendrarajah, Tara Conaway, Christopher H Douglas, Thomas A Waldrop, Mark P |
author_sort | Mackelprang, Rachel |
collection | PubMed |
description | In permafrost (perennially frozen ground) microbes survive oligotrophic conditions, sub-zero temperatures, low water availability and high salinity over millennia. Viable life exists in permafrost tens of thousands of years old but we know little about the metabolic and physiological adaptations to the challenges presented by life in frozen ground over geologic time. In this study we asked whether increasing age and the associated stressors drive adaptive changes in community composition and function. We conducted deep metagenomic and 16 S rRNA gene sequencing across a Pleistocene permafrost chronosequence from 19 000 to 33 000 years before present (kyr). We found that age markedly affected community composition and reduced diversity. Reconstruction of paleovegetation from metagenomic sequence suggests vegetation differences in the paleo record are not responsible for shifts in community composition and function. Rather, we observed shifts consistent with long-term survival strategies in extreme cryogenic environments. These include increased reliance on scavenging detrital biomass, horizontal gene transfer, chemotaxis, dormancy, environmental sensing and stress response. Our results identify traits that may enable survival in ancient cryoenvironments with no influx of energy or new materials. |
format | Online Article Text |
id | pubmed-5607373 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-56073732017-10-01 Microbial survival strategies in ancient permafrost: insights from metagenomics Mackelprang, Rachel Burkert, Alexander Haw, Monica Mahendrarajah, Tara Conaway, Christopher H Douglas, Thomas A Waldrop, Mark P ISME J Original Article In permafrost (perennially frozen ground) microbes survive oligotrophic conditions, sub-zero temperatures, low water availability and high salinity over millennia. Viable life exists in permafrost tens of thousands of years old but we know little about the metabolic and physiological adaptations to the challenges presented by life in frozen ground over geologic time. In this study we asked whether increasing age and the associated stressors drive adaptive changes in community composition and function. We conducted deep metagenomic and 16 S rRNA gene sequencing across a Pleistocene permafrost chronosequence from 19 000 to 33 000 years before present (kyr). We found that age markedly affected community composition and reduced diversity. Reconstruction of paleovegetation from metagenomic sequence suggests vegetation differences in the paleo record are not responsible for shifts in community composition and function. Rather, we observed shifts consistent with long-term survival strategies in extreme cryogenic environments. These include increased reliance on scavenging detrital biomass, horizontal gene transfer, chemotaxis, dormancy, environmental sensing and stress response. Our results identify traits that may enable survival in ancient cryoenvironments with no influx of energy or new materials. Nature Publishing Group 2017-10 2017-07-11 /pmc/articles/PMC5607373/ /pubmed/28696425 http://dx.doi.org/10.1038/ismej.2017.93 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Original Article Mackelprang, Rachel Burkert, Alexander Haw, Monica Mahendrarajah, Tara Conaway, Christopher H Douglas, Thomas A Waldrop, Mark P Microbial survival strategies in ancient permafrost: insights from metagenomics |
title | Microbial survival strategies in ancient permafrost: insights from metagenomics |
title_full | Microbial survival strategies in ancient permafrost: insights from metagenomics |
title_fullStr | Microbial survival strategies in ancient permafrost: insights from metagenomics |
title_full_unstemmed | Microbial survival strategies in ancient permafrost: insights from metagenomics |
title_short | Microbial survival strategies in ancient permafrost: insights from metagenomics |
title_sort | microbial survival strategies in ancient permafrost: insights from metagenomics |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607373/ https://www.ncbi.nlm.nih.gov/pubmed/28696425 http://dx.doi.org/10.1038/ismej.2017.93 |
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