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Metagenomic Insights Into the Microbial Iron Cycle of Subseafloor Habitats

Microbial iron cycling influences the flux of major nutrients in the environment (e.g., through the adsorptive capacity of iron oxides) and includes biotically induced iron oxidation and reduction processes. The ecological extent of microbial iron cycling is not well understood, even with increased...

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Autores principales: Garber, Arkadiy I., Cohen, Ashley B., Nealson, Kenneth H., Ramírez, Gustavo A., Barco, Roman A., Enzingmüller-Bleyl, Tristan C., Gehringer, Michelle M., Merino, Nancy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8446621/
https://www.ncbi.nlm.nih.gov/pubmed/34539592
http://dx.doi.org/10.3389/fmicb.2021.667944
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author Garber, Arkadiy I.
Cohen, Ashley B.
Nealson, Kenneth H.
Ramírez, Gustavo A.
Barco, Roman A.
Enzingmüller-Bleyl, Tristan C.
Gehringer, Michelle M.
Merino, Nancy
author_facet Garber, Arkadiy I.
Cohen, Ashley B.
Nealson, Kenneth H.
Ramírez, Gustavo A.
Barco, Roman A.
Enzingmüller-Bleyl, Tristan C.
Gehringer, Michelle M.
Merino, Nancy
author_sort Garber, Arkadiy I.
collection PubMed
description Microbial iron cycling influences the flux of major nutrients in the environment (e.g., through the adsorptive capacity of iron oxides) and includes biotically induced iron oxidation and reduction processes. The ecological extent of microbial iron cycling is not well understood, even with increased sequencing efforts, in part due to limitations in gene annotation pipelines and limitations in experimental studies linking phenotype to genotype. This is particularly true for the marine subseafloor, which remains undersampled, but represents the largest contiguous habitat on Earth. To address this limitation, we used FeGenie, a database and bioinformatics tool that identifies microbial iron cycling genes and enables the development of testable hypotheses on the biogeochemical cycling of iron. Herein, we survey the microbial iron cycle in diverse subseafloor habitats, including sediment-buried crustal aquifers, as well as surficial and deep sediments. We inferred the genetic potential for iron redox cycling in 32 of the 46 metagenomes included in our analysis, demonstrating the prevalence of these activities across underexplored subseafloor ecosystems. We show that while some processes (e.g., iron uptake and storage, siderophore transport potential, and iron gene regulation) are near-universal, others (e.g., iron reduction/oxidation, siderophore synthesis, and magnetosome formation) are dependent on local redox and nutrient status. Additionally, we detected niche-specific differences in strategies used for dissimilatory iron reduction, suggesting that geochemical constraints likely play an important role in dictating the dominant mechanisms for iron cycling. Overall, our survey advances the known distribution, magnitude, and potential ecological impact of microbe-mediated iron cycling and utilization in sub-benthic ecosystems.
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spelling pubmed-84466212021-09-18 Metagenomic Insights Into the Microbial Iron Cycle of Subseafloor Habitats Garber, Arkadiy I. Cohen, Ashley B. Nealson, Kenneth H. Ramírez, Gustavo A. Barco, Roman A. Enzingmüller-Bleyl, Tristan C. Gehringer, Michelle M. Merino, Nancy Front Microbiol Microbiology Microbial iron cycling influences the flux of major nutrients in the environment (e.g., through the adsorptive capacity of iron oxides) and includes biotically induced iron oxidation and reduction processes. The ecological extent of microbial iron cycling is not well understood, even with increased sequencing efforts, in part due to limitations in gene annotation pipelines and limitations in experimental studies linking phenotype to genotype. This is particularly true for the marine subseafloor, which remains undersampled, but represents the largest contiguous habitat on Earth. To address this limitation, we used FeGenie, a database and bioinformatics tool that identifies microbial iron cycling genes and enables the development of testable hypotheses on the biogeochemical cycling of iron. Herein, we survey the microbial iron cycle in diverse subseafloor habitats, including sediment-buried crustal aquifers, as well as surficial and deep sediments. We inferred the genetic potential for iron redox cycling in 32 of the 46 metagenomes included in our analysis, demonstrating the prevalence of these activities across underexplored subseafloor ecosystems. We show that while some processes (e.g., iron uptake and storage, siderophore transport potential, and iron gene regulation) are near-universal, others (e.g., iron reduction/oxidation, siderophore synthesis, and magnetosome formation) are dependent on local redox and nutrient status. Additionally, we detected niche-specific differences in strategies used for dissimilatory iron reduction, suggesting that geochemical constraints likely play an important role in dictating the dominant mechanisms for iron cycling. Overall, our survey advances the known distribution, magnitude, and potential ecological impact of microbe-mediated iron cycling and utilization in sub-benthic ecosystems. Frontiers Media S.A. 2021-09-03 /pmc/articles/PMC8446621/ /pubmed/34539592 http://dx.doi.org/10.3389/fmicb.2021.667944 Text en Copyright © 2021 Garber, Cohen, Nealson, Ramírez, Barco, Enzingmüller-Bleyl, Gehringer and Merino. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Garber, Arkadiy I.
Cohen, Ashley B.
Nealson, Kenneth H.
Ramírez, Gustavo A.
Barco, Roman A.
Enzingmüller-Bleyl, Tristan C.
Gehringer, Michelle M.
Merino, Nancy
Metagenomic Insights Into the Microbial Iron Cycle of Subseafloor Habitats
title Metagenomic Insights Into the Microbial Iron Cycle of Subseafloor Habitats
title_full Metagenomic Insights Into the Microbial Iron Cycle of Subseafloor Habitats
title_fullStr Metagenomic Insights Into the Microbial Iron Cycle of Subseafloor Habitats
title_full_unstemmed Metagenomic Insights Into the Microbial Iron Cycle of Subseafloor Habitats
title_short Metagenomic Insights Into the Microbial Iron Cycle of Subseafloor Habitats
title_sort metagenomic insights into the microbial iron cycle of subseafloor habitats
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8446621/
https://www.ncbi.nlm.nih.gov/pubmed/34539592
http://dx.doi.org/10.3389/fmicb.2021.667944
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