Metagenomic Insights Into the Microbial Iron Cycle of Subseafloor Habitats

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

Abstract

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.

Funder

National Nuclear Security Administration

Publisher

Frontiers Media SA

Subject

Microbiology (medical),Microbiology

Reference127 articles.

1. Characterization and expression of the co-transcribed cyc1 and cyc2 genes encoding the cytochrome cR (cSSP) and a high-molecular-mass cytochrome c from Thiobacillus ferrooxidans ATCC 33020.;Appia-Ayme;FEMS Microbiol. Lett.,1998

2. Rates and microbial players of iron-driven anaerobic oxidation of methane in methanic marine sediments.;Aromokeye;Front. Microbiol.,2020

3. Some compositional and kinetic controls on the bioenergetic landscapes in oceanic basement.;Bach;Front. Microbiol.,2016

4. Iron and sulfide oxidation within the basaltic ocean crust: implications for chemolithoautotrophic microbial biomass production.;Bach;Geochim. Cosmochim. Acta,2003

5. SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing.;Bankevich;J. Comput. Biol.,2012

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