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Metagenomics of Antarctic Marine Sediment Reveals Potential for Diverse Chemolithoautotrophy

The microbial biogeochemical processes occurring in marine sediment in Antarctica remain underexplored due to limited access. Further, these polar habitats are unique, as they are being exposed to significant changes in their climate. To explore how microbes drive biogeochemistry in these sediments,...

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Autores principales: Garber, Arkadiy I., Zehnpfennig, Jessica R., Sheik, Cody S., Henson, Michael W., Ramírez, Gustavo A., Mahon, Andrew R., Halanych, Kenneth M., Learman, Deric R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8612310/
https://www.ncbi.nlm.nih.gov/pubmed/34817234
http://dx.doi.org/10.1128/mSphere.00770-21
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author Garber, Arkadiy I.
Zehnpfennig, Jessica R.
Sheik, Cody S.
Henson, Michael W.
Ramírez, Gustavo A.
Mahon, Andrew R.
Halanych, Kenneth M.
Learman, Deric R.
author_facet Garber, Arkadiy I.
Zehnpfennig, Jessica R.
Sheik, Cody S.
Henson, Michael W.
Ramírez, Gustavo A.
Mahon, Andrew R.
Halanych, Kenneth M.
Learman, Deric R.
author_sort Garber, Arkadiy I.
collection PubMed
description The microbial biogeochemical processes occurring in marine sediment in Antarctica remain underexplored due to limited access. Further, these polar habitats are unique, as they are being exposed to significant changes in their climate. To explore how microbes drive biogeochemistry in these sediments, we performed a shotgun metagenomic survey of marine surficial sediment (0 to 3 cm of the seafloor) collected from 13 locations in western Antarctica and assembled 16 high-quality metagenome assembled genomes for focused interrogation of the lifestyles of some abundant lineages. We observe an abundance of genes from pathways for the utilization of reduced carbon, sulfur, and nitrogen sources. Although organotrophy is pervasive, nitrification and sulfide oxidation are the dominant lithotrophic pathways and likely fuel carbon fixation via the reverse tricarboxylic acid and Calvin cycles. Oxygen-dependent terminal oxidases are common, and genes for reduction of oxidized nitrogen are sporadically present in our samples. Our results suggest that the underlying benthic communities are well primed for the utilization of settling organic matter, which is consistent with findings from highly productive surface water. Despite the genetic potential for nitrate reduction, the net catabolic pathway in our samples remains aerobic respiration, likely coupled to the oxidation of sulfur and nitrogen imported from the highly productive Antarctic water column above. IMPORTANCE The impacts of climate change in polar regions, like Antarctica, have the potential to alter numerous ecosystems and biogeochemical cycles. Increasing temperature and freshwater runoff from melting ice can have profound impacts on the cycling of organic and inorganic nutrients between the pelagic and benthic ecosystems. Within the benthos, sediment microbial communities play a critical role in carbon mineralization and the cycles of essential nutrients like nitrogen and sulfur. Metagenomic data collected from sediment samples from the continental shelf of western Antarctica help to examine this unique system and document the metagenomic potential for lithotrophic metabolisms and the cycles of both nitrogen and sulfur, which support not only benthic microbes but also life in the pelagic zone.
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spelling pubmed-86123102021-11-29 Metagenomics of Antarctic Marine Sediment Reveals Potential for Diverse Chemolithoautotrophy Garber, Arkadiy I. Zehnpfennig, Jessica R. Sheik, Cody S. Henson, Michael W. Ramírez, Gustavo A. Mahon, Andrew R. Halanych, Kenneth M. Learman, Deric R. mSphere Research Article The microbial biogeochemical processes occurring in marine sediment in Antarctica remain underexplored due to limited access. Further, these polar habitats are unique, as they are being exposed to significant changes in their climate. To explore how microbes drive biogeochemistry in these sediments, we performed a shotgun metagenomic survey of marine surficial sediment (0 to 3 cm of the seafloor) collected from 13 locations in western Antarctica and assembled 16 high-quality metagenome assembled genomes for focused interrogation of the lifestyles of some abundant lineages. We observe an abundance of genes from pathways for the utilization of reduced carbon, sulfur, and nitrogen sources. Although organotrophy is pervasive, nitrification and sulfide oxidation are the dominant lithotrophic pathways and likely fuel carbon fixation via the reverse tricarboxylic acid and Calvin cycles. Oxygen-dependent terminal oxidases are common, and genes for reduction of oxidized nitrogen are sporadically present in our samples. Our results suggest that the underlying benthic communities are well primed for the utilization of settling organic matter, which is consistent with findings from highly productive surface water. Despite the genetic potential for nitrate reduction, the net catabolic pathway in our samples remains aerobic respiration, likely coupled to the oxidation of sulfur and nitrogen imported from the highly productive Antarctic water column above. IMPORTANCE The impacts of climate change in polar regions, like Antarctica, have the potential to alter numerous ecosystems and biogeochemical cycles. Increasing temperature and freshwater runoff from melting ice can have profound impacts on the cycling of organic and inorganic nutrients between the pelagic and benthic ecosystems. Within the benthos, sediment microbial communities play a critical role in carbon mineralization and the cycles of essential nutrients like nitrogen and sulfur. Metagenomic data collected from sediment samples from the continental shelf of western Antarctica help to examine this unique system and document the metagenomic potential for lithotrophic metabolisms and the cycles of both nitrogen and sulfur, which support not only benthic microbes but also life in the pelagic zone. American Society for Microbiology 2021-11-24 /pmc/articles/PMC8612310/ /pubmed/34817234 http://dx.doi.org/10.1128/mSphere.00770-21 Text en Copyright © 2021 Garber et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Garber, Arkadiy I.
Zehnpfennig, Jessica R.
Sheik, Cody S.
Henson, Michael W.
Ramírez, Gustavo A.
Mahon, Andrew R.
Halanych, Kenneth M.
Learman, Deric R.
Metagenomics of Antarctic Marine Sediment Reveals Potential for Diverse Chemolithoautotrophy
title Metagenomics of Antarctic Marine Sediment Reveals Potential for Diverse Chemolithoautotrophy
title_full Metagenomics of Antarctic Marine Sediment Reveals Potential for Diverse Chemolithoautotrophy
title_fullStr Metagenomics of Antarctic Marine Sediment Reveals Potential for Diverse Chemolithoautotrophy
title_full_unstemmed Metagenomics of Antarctic Marine Sediment Reveals Potential for Diverse Chemolithoautotrophy
title_short Metagenomics of Antarctic Marine Sediment Reveals Potential for Diverse Chemolithoautotrophy
title_sort metagenomics of antarctic marine sediment reveals potential for diverse chemolithoautotrophy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8612310/
https://www.ncbi.nlm.nih.gov/pubmed/34817234
http://dx.doi.org/10.1128/mSphere.00770-21
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