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Abrupt permafrost thaw triggers activity of copiotrophs and microbiome predators

Permafrost soils store a substantial part of the global soil carbon and nitrogen. However, global warming causes abrupt erosion and gradual thaw, which make these stocks vulnerable to microbial decomposition into greenhouse gases. Here, we investigated the microbial response to abrupt in situ permaf...

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Autores principales: Scheel, Maria, Zervas, Athanasios, Rijkers, Ruud, Tveit, Alexander T, Ekelund, Flemming, Campuzano Jiménez, Francisco, Christensen, Torben R, Jacobsen, Carsten S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10599396/
https://www.ncbi.nlm.nih.gov/pubmed/37796894
http://dx.doi.org/10.1093/femsec/fiad123
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author Scheel, Maria
Zervas, Athanasios
Rijkers, Ruud
Tveit, Alexander T
Ekelund, Flemming
Campuzano Jiménez, Francisco
Christensen, Torben R
Jacobsen, Carsten S
author_facet Scheel, Maria
Zervas, Athanasios
Rijkers, Ruud
Tveit, Alexander T
Ekelund, Flemming
Campuzano Jiménez, Francisco
Christensen, Torben R
Jacobsen, Carsten S
author_sort Scheel, Maria
collection PubMed
description Permafrost soils store a substantial part of the global soil carbon and nitrogen. However, global warming causes abrupt erosion and gradual thaw, which make these stocks vulnerable to microbial decomposition into greenhouse gases. Here, we investigated the microbial response to abrupt in situ permafrost thaw. We sequenced the total RNA of a 1 m deep soil core consisting of up to 26 500-year-old permafrost material from an active abrupt erosion site. We analysed the microbial community in the active layer soil, the recently thawed, and the intact permafrost, and found maximum RNA:DNA ratios in recently thawed permafrost indicating a high microbial activity. In thawed permafrost, potentially copiotrophic Burkholderiales and Sphingobacteriales, but also microbiome predators dominated the community. Overall, both thaw-dependent and long-term soil properties significantly correlated with changes in community composition, as did microbiome predator abundance. Bacterial predators were dominated in shallower depths by Myxococcota, while protozoa, especially Cercozoa and Ciliophora, almost tripled in relative abundance in thawed layers. Our findings highlight the ecological importance of a diverse interkingdom and active microbial community highly abundant in abruptly thawing permafrost, as well as predation as potential biological control mechanism.
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spelling pubmed-105993962023-10-26 Abrupt permafrost thaw triggers activity of copiotrophs and microbiome predators Scheel, Maria Zervas, Athanasios Rijkers, Ruud Tveit, Alexander T Ekelund, Flemming Campuzano Jiménez, Francisco Christensen, Torben R Jacobsen, Carsten S FEMS Microbiol Ecol Research Article Permafrost soils store a substantial part of the global soil carbon and nitrogen. However, global warming causes abrupt erosion and gradual thaw, which make these stocks vulnerable to microbial decomposition into greenhouse gases. Here, we investigated the microbial response to abrupt in situ permafrost thaw. We sequenced the total RNA of a 1 m deep soil core consisting of up to 26 500-year-old permafrost material from an active abrupt erosion site. We analysed the microbial community in the active layer soil, the recently thawed, and the intact permafrost, and found maximum RNA:DNA ratios in recently thawed permafrost indicating a high microbial activity. In thawed permafrost, potentially copiotrophic Burkholderiales and Sphingobacteriales, but also microbiome predators dominated the community. Overall, both thaw-dependent and long-term soil properties significantly correlated with changes in community composition, as did microbiome predator abundance. Bacterial predators were dominated in shallower depths by Myxococcota, while protozoa, especially Cercozoa and Ciliophora, almost tripled in relative abundance in thawed layers. Our findings highlight the ecological importance of a diverse interkingdom and active microbial community highly abundant in abruptly thawing permafrost, as well as predation as potential biological control mechanism. Oxford University Press 2023-10-05 /pmc/articles/PMC10599396/ /pubmed/37796894 http://dx.doi.org/10.1093/femsec/fiad123 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of FEMS. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Scheel, Maria
Zervas, Athanasios
Rijkers, Ruud
Tveit, Alexander T
Ekelund, Flemming
Campuzano Jiménez, Francisco
Christensen, Torben R
Jacobsen, Carsten S
Abrupt permafrost thaw triggers activity of copiotrophs and microbiome predators
title Abrupt permafrost thaw triggers activity of copiotrophs and microbiome predators
title_full Abrupt permafrost thaw triggers activity of copiotrophs and microbiome predators
title_fullStr Abrupt permafrost thaw triggers activity of copiotrophs and microbiome predators
title_full_unstemmed Abrupt permafrost thaw triggers activity of copiotrophs and microbiome predators
title_short Abrupt permafrost thaw triggers activity of copiotrophs and microbiome predators
title_sort abrupt permafrost thaw triggers activity of copiotrophs and microbiome predators
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10599396/
https://www.ncbi.nlm.nih.gov/pubmed/37796894
http://dx.doi.org/10.1093/femsec/fiad123
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