Evidence map›Paper›PMID 36849975›Full record

ArticleMicrobiome2023

Rapid remodeling of the soil lipidome in response to a drying-rewetting event.

Sneha P Couvillion, Robert E Danczak, Dan Naylor, Montana L Smith, Kelly G Stratton, Vanessa L Paurus, Kent J Bloodsworth, Yuliya Farris, Darren J Schmidt, Rachel E Richardson and 8 more

Open access · goldAbstract readVideo-Audio Media
In one paragraph

Article in Microbiome, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
23.6field-weighted citation impact, top 1% of its field
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

13 citing papers in PubMed, 39 citations in OpenAlex.

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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

18 authors at 3 institutions in 1 country.

Sneha P CouvillionEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Robert E DanczakEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Dan NaylorEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Montana L SmithEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Kelly G StrattonEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Vanessa L PaurusEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Kent J BloodsworthEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Yuliya FarrisEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Darren J SchmidtEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Rachel E RichardsonNational Security Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Lisa M BramerEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Sarah J FanslerEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Ernesto S NakayasuEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Jason E McDermottEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Thomas O MetzEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Mary S LiptonEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Janet K JanssonEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Kirsten S HofmockelEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA. kirsten.hofmockel@pnnl.gov.
Pacific Northwest National Laboratory · USIowa State University · USOregon Health & Science University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMicrobiomes contribute to multiple ecosystem services by transforming organic matter in the soil. Extreme shifts in the environment, such as drying-rewetting cycles during drought, can impact the microbial metabolism of organic matter by altering microbial physiology and function. These physiological responses are mediated in part by lipids that are responsible for regulating interactions between cells and the environment. Despite this critical role in regulating the microbial response to stress, little is known about microbial lipids and metabolites in the soil or how they influence phenotypes that are expressed under drying-rewetting cycles. To address this knowledge gap, we conducted a soil incubation experiment to simulate soil drying during a summer drought of an arid grassland, then measured the response of the soil lipidome and metabolome during the first 3 h after wet-up.

resultsReduced nutrient access during soil drying incurred a replacement of membrane phospholipids, resulting in a diminished abundance of multiple phosphorus-rich membrane lipids. The hot and dry conditions increased the prevalence of sphingolipids and lipids containing long-chain polyunsaturated fatty acids, both of which are associated with heat and osmotic stress-mitigating properties in fungi. This novel finding suggests that lipids commonly present in eukaryotes such as fungi may play a significant role in supporting community resilience displayed by arid land soil microbiomes during drought. As early as 10 min after rewetting dry soil, distinct changes were observed in several lipids that had bacterial signatures including a rapid increase in the abundance of glycerophospholipids with saturated and short fatty acid chains, prototypical of bacterial membrane lipids. Polar metabolites including disaccharides, nucleic acids, organic acids, inositols, and amino acids also increased in abundance upon rewetting. This rapid metabolic reactivation and growth after rewetting coincided with an increase in the relative abundance of firmicutes, suggesting that members of this phylum were positively impacted by rewetting.

conclusionsOur study revealed specific changes in lipids and metabolites that are indicative of stress adaptation, substrate use, and cellular recovery during soil drying and subsequent rewetting. The drought-induced nutrient limitation was reflected in the lipidome and polar metabolome, both of which rapidly shifted (within hours) upon rewet. Reduced nutrient access in dry soil caused the replacement of glycerophospholipids with phosphorus-free lipids and impeded resource-expensive osmolyte accumulation. Elevated levels of ceramides and lipids with long-chain polyunsaturated fatty acids in dry soil suggest that lipids likely play an important role in the drought tolerance of microbial taxa capable of synthesizing these lipids. An increasing abundance of bacterial glycerophospholipids and triacylglycerols with fatty acids typical of bacteria and polar metabolites suggest a metabolic recovery in representative bacteria once the environmental conditions are conducive for growth. These results underscore the importance of the soil lipidome as a robust indicator of microbial community responses, especially at the short time scales of cell-environment reactions. Video Abstract.

Indexed as

EcosystemLipidomicsAcclimatizationCeramidesFatty AcidsFatty Acids, UnsaturatedCeramidesFatty AcidsFatty Acids, UnsaturatedDrying-rewettingLipidomicsMetabolomicsSoilSummer drought

Identifiers

PMID36849975
PMCPMC9969633
OpenAlexW4322504564

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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.