Cargando…

Sulfur-cycling chemolithoautotrophic microbial community dominates a cold, anoxic, hypersaline Arctic spring

BACKGROUND: Gypsum Hill Spring, located in Nunavut in the Canadian High Arctic, is a rare example of a cold saline spring arising through thick permafrost. It perennially discharges cold (~ 7 °C), hypersaline (7–8% salinity), anoxic (~ 0.04 ppm O(2)), and highly reducing (~ − 430 mV) brines rich in...

Descripción completa

Detalles Bibliográficos
Autores principales: Magnuson, Elisse, Altshuler, Ianina, Freyria, Nastasia J., Leveille, Richard J., Whyte, Lyle G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10494364/
https://www.ncbi.nlm.nih.gov/pubmed/37697305
http://dx.doi.org/10.1186/s40168-023-01628-5
_version_ 1785104675089940480
author Magnuson, Elisse
Altshuler, Ianina
Freyria, Nastasia J.
Leveille, Richard J.
Whyte, Lyle G.
author_facet Magnuson, Elisse
Altshuler, Ianina
Freyria, Nastasia J.
Leveille, Richard J.
Whyte, Lyle G.
author_sort Magnuson, Elisse
collection PubMed
description BACKGROUND: Gypsum Hill Spring, located in Nunavut in the Canadian High Arctic, is a rare example of a cold saline spring arising through thick permafrost. It perennially discharges cold (~ 7 °C), hypersaline (7–8% salinity), anoxic (~ 0.04 ppm O(2)), and highly reducing (~ − 430 mV) brines rich in sulfate (2.2 g.L(−1)) and sulfide (9.5 ppm), making Gypsum Hill an analog to putative sulfate-rich briny habitats on extraterrestrial bodies such as Mars. RESULTS: Genome-resolved metagenomics and metatranscriptomics were utilized to describe an active microbial community containing novel metagenome-assembled genomes and dominated by sulfur-cycling Desulfobacterota and Gammaproteobacteria. Sulfate reduction was dominated by hydrogen-oxidizing chemolithoautotrophic Desulfovibrionaceae sp. and was identified in phyla not typically associated with sulfate reduction in novel lineages of Spirochaetota and Bacteroidota. Highly abundant and active sulfur-reducing Desulfuromusa sp. highly transcribed non-coding RNAs associated with transcriptional regulation, showing potential evidence of putative metabolic flexibility in response to substrate availability. Despite low oxygen availability, sulfide oxidation was primarily attributed to aerobic chemolithoautotrophic Halothiobacillaceae. Low abundance and transcription of photoautotrophs indicated sulfur-based chemolithoautotrophy drives primary productivity even during periods of constant illumination. CONCLUSIONS: We identified a rare surficial chemolithoautotrophic, sulfur-cycling microbial community active in a unique anoxic, cold, hypersaline Arctic spring. We detected Mars-relevant metabolisms including hydrogenotrophic sulfate reduction, sulfur reduction, and sulfide oxidation, which indicate the potential for microbial life in analogous S-rich brines on past and present Mars. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01628-5.
format Online
Article
Text
id pubmed-10494364
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-104943642023-09-12 Sulfur-cycling chemolithoautotrophic microbial community dominates a cold, anoxic, hypersaline Arctic spring Magnuson, Elisse Altshuler, Ianina Freyria, Nastasia J. Leveille, Richard J. Whyte, Lyle G. Microbiome Research BACKGROUND: Gypsum Hill Spring, located in Nunavut in the Canadian High Arctic, is a rare example of a cold saline spring arising through thick permafrost. It perennially discharges cold (~ 7 °C), hypersaline (7–8% salinity), anoxic (~ 0.04 ppm O(2)), and highly reducing (~ − 430 mV) brines rich in sulfate (2.2 g.L(−1)) and sulfide (9.5 ppm), making Gypsum Hill an analog to putative sulfate-rich briny habitats on extraterrestrial bodies such as Mars. RESULTS: Genome-resolved metagenomics and metatranscriptomics were utilized to describe an active microbial community containing novel metagenome-assembled genomes and dominated by sulfur-cycling Desulfobacterota and Gammaproteobacteria. Sulfate reduction was dominated by hydrogen-oxidizing chemolithoautotrophic Desulfovibrionaceae sp. and was identified in phyla not typically associated with sulfate reduction in novel lineages of Spirochaetota and Bacteroidota. Highly abundant and active sulfur-reducing Desulfuromusa sp. highly transcribed non-coding RNAs associated with transcriptional regulation, showing potential evidence of putative metabolic flexibility in response to substrate availability. Despite low oxygen availability, sulfide oxidation was primarily attributed to aerobic chemolithoautotrophic Halothiobacillaceae. Low abundance and transcription of photoautotrophs indicated sulfur-based chemolithoautotrophy drives primary productivity even during periods of constant illumination. CONCLUSIONS: We identified a rare surficial chemolithoautotrophic, sulfur-cycling microbial community active in a unique anoxic, cold, hypersaline Arctic spring. We detected Mars-relevant metabolisms including hydrogenotrophic sulfate reduction, sulfur reduction, and sulfide oxidation, which indicate the potential for microbial life in analogous S-rich brines on past and present Mars. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01628-5. BioMed Central 2023-09-11 /pmc/articles/PMC10494364/ /pubmed/37697305 http://dx.doi.org/10.1186/s40168-023-01628-5 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
Magnuson, Elisse
Altshuler, Ianina
Freyria, Nastasia J.
Leveille, Richard J.
Whyte, Lyle G.
Sulfur-cycling chemolithoautotrophic microbial community dominates a cold, anoxic, hypersaline Arctic spring
title Sulfur-cycling chemolithoautotrophic microbial community dominates a cold, anoxic, hypersaline Arctic spring
title_full Sulfur-cycling chemolithoautotrophic microbial community dominates a cold, anoxic, hypersaline Arctic spring
title_fullStr Sulfur-cycling chemolithoautotrophic microbial community dominates a cold, anoxic, hypersaline Arctic spring
title_full_unstemmed Sulfur-cycling chemolithoautotrophic microbial community dominates a cold, anoxic, hypersaline Arctic spring
title_short Sulfur-cycling chemolithoautotrophic microbial community dominates a cold, anoxic, hypersaline Arctic spring
title_sort sulfur-cycling chemolithoautotrophic microbial community dominates a cold, anoxic, hypersaline arctic spring
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10494364/
https://www.ncbi.nlm.nih.gov/pubmed/37697305
http://dx.doi.org/10.1186/s40168-023-01628-5
work_keys_str_mv AT magnusonelisse sulfurcyclingchemolithoautotrophicmicrobialcommunitydominatesacoldanoxichypersalinearcticspring
AT altshulerianina sulfurcyclingchemolithoautotrophicmicrobialcommunitydominatesacoldanoxichypersalinearcticspring
AT freyrianastasiaj sulfurcyclingchemolithoautotrophicmicrobialcommunitydominatesacoldanoxichypersalinearcticspring
AT leveillerichardj sulfurcyclingchemolithoautotrophicmicrobialcommunitydominatesacoldanoxichypersalinearcticspring
AT whytelyleg sulfurcyclingchemolithoautotrophicmicrobialcommunitydominatesacoldanoxichypersalinearcticspring