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Anaerobic metabolism of Foraminifera thriving below the seafloor

Foraminifera are single-celled eukaryotes (protists) of large ecological importance, as well as environmental and paleoenvironmental indicators and biostratigraphic tools. In addition, they are capable of surviving in anoxic marine environments where they represent a major component of the benthic c...

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Autores principales: Orsi, William D., Morard, Raphaël, Vuillemin, Aurele, Eitel, Michael, Wörheide, Gert, Milucka, Jana, Kucera, Michal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7490399/
https://www.ncbi.nlm.nih.gov/pubmed/32641728
http://dx.doi.org/10.1038/s41396-020-0708-1
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author Orsi, William D.
Morard, Raphaël
Vuillemin, Aurele
Eitel, Michael
Wörheide, Gert
Milucka, Jana
Kucera, Michal
author_facet Orsi, William D.
Morard, Raphaël
Vuillemin, Aurele
Eitel, Michael
Wörheide, Gert
Milucka, Jana
Kucera, Michal
author_sort Orsi, William D.
collection PubMed
description Foraminifera are single-celled eukaryotes (protists) of large ecological importance, as well as environmental and paleoenvironmental indicators and biostratigraphic tools. In addition, they are capable of surviving in anoxic marine environments where they represent a major component of the benthic community. However, the cellular adaptations of Foraminifera to the anoxic environment remain poorly constrained. We sampled an oxic-anoxic transition zone in marine sediments from the Namibian shelf, where the genera Bolivina and Stainforthia dominated the Foraminifera community, and use metatranscriptomics to characterize Foraminifera metabolism across the different geochemical conditions. Relative Foraminifera gene expression in anoxic sediment increased an order of magnitude, which was confirmed in a 10-day incubation experiment where the development of anoxia coincided with a 20–40-fold increase in the relative abundance of Foraminifera protein encoding transcripts, attributed primarily to those involved in protein synthesis, intracellular protein trafficking, and modification of the cytoskeleton. This indicated that many Foraminifera were not only surviving but thriving, under the anoxic conditions. The anaerobic energy metabolism of these active Foraminifera was characterized by fermentation of sugars and amino acids, fumarate reduction, and potentially dissimilatory nitrate reduction. Moreover, the gene expression data indicate that under anoxia Foraminifera use the phosphogen creatine phosphate as an ATP store, allowing reserves of high-energy phosphate pool to be maintained for sudden demands of increased energy during anaerobic metabolism. This was co-expressed alongside genes involved in phagocytosis and clathrin-mediated endocytosis (CME). Foraminifera may use CME to utilize dissolved organic matter as a carbon and energy source, in addition to ingestion of prey cells via phagocytosis. These anaerobic metabolic mechanisms help to explain the ecological success of Foraminifera documented in the fossil record since the Cambrian period more than 500 million years ago.
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spelling pubmed-74903992020-10-01 Anaerobic metabolism of Foraminifera thriving below the seafloor Orsi, William D. Morard, Raphaël Vuillemin, Aurele Eitel, Michael Wörheide, Gert Milucka, Jana Kucera, Michal ISME J Article Foraminifera are single-celled eukaryotes (protists) of large ecological importance, as well as environmental and paleoenvironmental indicators and biostratigraphic tools. In addition, they are capable of surviving in anoxic marine environments where they represent a major component of the benthic community. However, the cellular adaptations of Foraminifera to the anoxic environment remain poorly constrained. We sampled an oxic-anoxic transition zone in marine sediments from the Namibian shelf, where the genera Bolivina and Stainforthia dominated the Foraminifera community, and use metatranscriptomics to characterize Foraminifera metabolism across the different geochemical conditions. Relative Foraminifera gene expression in anoxic sediment increased an order of magnitude, which was confirmed in a 10-day incubation experiment where the development of anoxia coincided with a 20–40-fold increase in the relative abundance of Foraminifera protein encoding transcripts, attributed primarily to those involved in protein synthesis, intracellular protein trafficking, and modification of the cytoskeleton. This indicated that many Foraminifera were not only surviving but thriving, under the anoxic conditions. The anaerobic energy metabolism of these active Foraminifera was characterized by fermentation of sugars and amino acids, fumarate reduction, and potentially dissimilatory nitrate reduction. Moreover, the gene expression data indicate that under anoxia Foraminifera use the phosphogen creatine phosphate as an ATP store, allowing reserves of high-energy phosphate pool to be maintained for sudden demands of increased energy during anaerobic metabolism. This was co-expressed alongside genes involved in phagocytosis and clathrin-mediated endocytosis (CME). Foraminifera may use CME to utilize dissolved organic matter as a carbon and energy source, in addition to ingestion of prey cells via phagocytosis. These anaerobic metabolic mechanisms help to explain the ecological success of Foraminifera documented in the fossil record since the Cambrian period more than 500 million years ago. Nature Publishing Group UK 2020-07-08 2020-10 /pmc/articles/PMC7490399/ /pubmed/32641728 http://dx.doi.org/10.1038/s41396-020-0708-1 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Orsi, William D.
Morard, Raphaël
Vuillemin, Aurele
Eitel, Michael
Wörheide, Gert
Milucka, Jana
Kucera, Michal
Anaerobic metabolism of Foraminifera thriving below the seafloor
title Anaerobic metabolism of Foraminifera thriving below the seafloor
title_full Anaerobic metabolism of Foraminifera thriving below the seafloor
title_fullStr Anaerobic metabolism of Foraminifera thriving below the seafloor
title_full_unstemmed Anaerobic metabolism of Foraminifera thriving below the seafloor
title_short Anaerobic metabolism of Foraminifera thriving below the seafloor
title_sort anaerobic metabolism of foraminifera thriving below the seafloor
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7490399/
https://www.ncbi.nlm.nih.gov/pubmed/32641728
http://dx.doi.org/10.1038/s41396-020-0708-1
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