Evidence map›Paper›PMID 34539592›Full record

ArticleFrontiers in microbiology2021

Metagenomic Insights Into the Microbial Iron Cycle of Subseafloor Habitats.

Arkadiy I Garber, Ashley B Cohen, Kenneth H Nealson, Gustavo A Ramírez, Roman A Barco, Tristan C Enzingmüller-Bleyl, Michelle M Gehringer, Nancy Merino

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Microbial Catalysis for COCold Spring Harbor perspectives in biology · 2024
    Review
  7. Article
  8. Microorganisms · 2022
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Arkadiy I GarberSchool of Life Sciences, Arizona State University, Tempe, AZ, United States.
Ashley B CohenSchool of Marine and Atmospheric Sciences, Stony Brook University, Stony Brook, NY, United States.
Kenneth H NealsonDepartment of Earth Sciences, University of Southern California, Los Angeles, CA, United States.
Gustavo A RamírezDepartment of Marine Biology, Leon H. Charney School of Marine Sciences, University of Haifa, Haifa, Israel.
Roman A BarcoDepartment of Earth Sciences, University of Southern California, Los Angeles, CA, United States.
Tristan C Enzingmüller-BleylDepartment of Microbiology, Technical University of Kaiserslautern, Kaiserslautern, Germany.
Michelle M GehringerDepartment of Microbiology, Technical University of Kaiserslautern, Kaiserslautern, Germany.
Nancy MerinoBiosciences & Biotechnology Division, Lawrence Livermore National Laboratory, Livermore, CA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

FeGenieiron acquisitioniron cyclingiron oxidationiron reductionmarine aquifermarine sedimentmetagenomics

Identifiers

PMID34539592
PMCPMC8446621

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.