Evidence map›Paper›PMID 39557655›Full record

ArticleFEMS microbiology ecology2024

A respiro-fermentative strategy to survive nanoxia in Acidobacterium capsulatum.

Daniela Trojan, Emilio García-Robledo, Bela Hausmann, Niels Peter Revsbech, Dagmar Woebken, Stephanie A Eichorst

Abstract read
In one paragraph

Article in FEMS microbiology ecology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

6 authors.

Daniela TrojanDepartment of Microbiology and Ecosystem Science, Centre for Microbiology and Environmental Systems Science, University of Vienna, 1030 Vienna, Austria.ORCID 0000-0001-6748-5311
Emilio García-RobledoDepartment of Biology, Faculty of Marine and Environmental Sciences, University of Cádiz, 11002 Cádiz, Spain.ORCID 0000-0002-4337-6433
Bela HausmannDepartment of Microbiology and Ecosystem Science, Centre for Microbiology and Environmental Systems Science, University of Vienna, 1030 Vienna, Austria.ORCID 0000-0002-0846-1202
Niels Peter RevsbechWATEC, Department of Biology, Aarhus University, 8000 Aarhus, Denmark.ORCID 0000-0002-2193-262X
Dagmar WoebkenDepartment of Microbiology and Ecosystem Science, Centre for Microbiology and Environmental Systems Science, University of Vienna, 1030 Vienna, Austria.ORCID 0000-0002-1314-9926
Stephanie A EichorstDepartment of Microbiology and Ecosystem Science, Centre for Microbiology and Environmental Systems Science, University of Vienna, 1030 Vienna, Austria.ORCID 0000-0002-9017-7461

Funding

Austrian Science FundEuropean Research Council 636928Spanish Research Agency PID2020-117340RA-I00
6 · The paper itself

Abstract

Microbial soil habitats are characterized by rapid shifts in substrate and nutrient availabilities, as well as chemical and physical parameters. One such parameter that can vary in soil is oxygen; thus, microbial survival is dependent on adaptation to this substrate. To better understand the metabolic abilities and adaptive strategies to oxygen-deprived environments, we combined genomics with transcriptomics of a model organism, Acidobacterium capsulatum, to explore the effect of decreasing, environmentally relevant oxygen concentrations. The decrease from 10 to 0.1 µM oxygen (3.6 to 0.036 pO2% present atmospheric level, respectively) caused the upregulation of the transcription of genes involved in signal transduction mechanisms, energy production and conversion and secondary metabolites biosynthesis, transport, and catabolism based on clusters of orthologous group categories. Contrary to established observations for aerobic metabolism, key genes in oxidative stress response were significantly upregulated at lower oxygen concentrations, presumably due to an NADH/NAD+ redox ratio imbalance as the cells transitioned into nanoxia. Furthermore, A. capsulatum adapted to nanoxia by inducing a respiro-fermentative metabolism and rerouting fluxes of its central carbon and energy pathways to adapt to high NADH/NAD+ redox ratios. Our results reveal physiological features and metabolic capabilities that allowed A. capsulatum to adapt to oxygen-limited conditions, which could expand into other environmentally relevant soil strains.

Indexed as

OxygenAcidobacteriaAdaptation, PhysiologicalFermentationGene Expression Regulation, BacterialOxidation-ReductionOxidative StressSoil MicrobiologyOxygenAcidobacteriotafermentationmicroaerobic respirationNADH imbalancesoxygen limitationtranscriptome

Identifiers

PMID39557655
PMCPMC11636273

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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.