Evidence map›Paper›PMID 32616808›Full record

ArticleScientific reports2020

Integrated network modeling approach defines key metabolic responses of soil microbiomes to perturbations.

Ryan S McClure, Joon-Yong Lee, Taniya Roy Chowdhury, Eric M Bottos, Richard Allen White, Young-Mo Kim, Carrie D Nicora, Thomas O Metz, Kirsten S Hofmockel, Janet K Jansson and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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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

11 authors.

Ryan S McClure *Biological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA.
Joon-Yong Lee *Biological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA.
Taniya Roy ChowdhuryBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA.
Eric M BottosBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA.
Richard Allen WhiteBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA.
Young-Mo KimBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA.
Carrie D NicoraBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA.
Thomas O MetzBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA.
Kirsten S HofmockelBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA.
Janet K JanssonBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA.
Hyun-Seob SongBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA. hsong5@unl.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The soil environment is constantly changing due to shifts in soil moisture, nutrient availability and other conditions. To contend with these changes, soil microorganisms have evolved a variety of ways to adapt to environmental perturbations, including regulation of gene expression. However, it is challenging to untangle the complex phenotypic response of the soil to environmental change, partly due to the absence of predictive modeling frameworks that can mechanistically link molecular-level changes in soil microorganisms to a community's functional phenotypes (or metaphenome). Towards filling this gap, we performed a combined analysis of metabolic and gene co-expression networks to explore how the soil microbiome responded to changes in soil moisture and nutrient conditions and to determine which genes were expressed under a given condition. Our integrated modeling approach revealed previously unknown, but critically important aspects of the soil microbiomes' response to environmental perturbations. Incorporation of metabolomic and transcriptomic data into metabolic reaction networks identified condition-specific signature genes that are uniquely associated with dry, wet, and glycine-amended conditions. A subsequent gene co-expression network analysis revealed that drought-associated genes occupied more central positions in a network model of the soil community, compared to the genes associated with wet, and glycine-amended conditions. These results indicate the occurrence of system-wide metabolic coordination when soil microbiomes cope with moisture or nutrient perturbations. Importantly, the approach that we demonstrate here to analyze large-scale multi-omics data from a natural soil environment is applicable to other microbiome systems for which multi-omics data are available.

Indexed as

Metabolic Networks and PathwaysMicrobiotaSoil MicrobiologyBacterial ProteinsDroughtsEnzymesGene Expression Regulation, BacterialGene Regulatory NetworksGlycineHumidityKansasTranscriptomeBacterial ProteinsEnzymesGlycine

Identifiers

PMID32616808
PMCPMC7331712

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LicenceCC BY
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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.