Evidence map›Paper›PMID 32762019›Full record

ArticleMicrobiologyOpen2020

Snow microbiome functional analyses reveal novel aspects of microbial metabolism of complex organic compounds.

Chengsheng Zhu, Maximilian Miller, Nicholas Lusskin, Benoît Bergk Pinto, Lorrie Maccario, Max Häggblom, Timothy Vogel, Catherine Larose, Yana Bromberg

Open access · goldAbstract read
In one paragraph

Article in MicrobiologyOpen, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

6 citing papers in PubMed, 9 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

9 authors at 2 institutions in 4 countries.

Chengsheng ZhuDepartment of Biochemistry and Microbiology, Rutgers University, New Brunswick, NJ, USA.
Maximilian MillerDepartment of Biochemistry and Microbiology, Rutgers University, New Brunswick, NJ, USA.
Nicholas LusskinDepartment of Biochemistry and Microbiology, Rutgers University, New Brunswick, NJ, USA.
Benoît Bergk PintoEnvironmental Microbial Genomics, Laboratoire Ampere, Ecole Centrale de Lyon, CNRS UMR 5005, Université de Lyon, Ecully, France.
Lorrie MaccarioEnvironmental Microbial Genomics, Laboratoire Ampere, Ecole Centrale de Lyon, CNRS UMR 5005, Université de Lyon, Ecully, France.
Max HäggblomDepartment of Biochemistry and Microbiology, Rutgers University, New Brunswick, NJ, USA.
Timothy VogelEnvironmental Microbial Genomics, Laboratoire Ampere, Ecole Centrale de Lyon, CNRS UMR 5005, Université de Lyon, Ecully, France.
Catherine LaroseEnvironmental Microbial Genomics, Laboratoire Ampere, Ecole Centrale de Lyon, CNRS UMR 5005, Université de Lyon, Ecully, France.
Yana BrombergDepartment of Biochemistry and Microbiology, Rutgers University, New Brunswick, NJ, USA.ORCID 0000-0002-8351-0844
Rutgers, The State University of New Jersey · USUniversité Claude Bernard Lyon 1 · FR

Funding

AVA,Dx: Analysis of Variation for Association with DiseaseU01GM115486 · NIGMS · RUTGERS, THE STATE UNIV OF N.J. · PI BROMBERG, YANA · 2015 to 2018
$1.2M
NIGMS NIH HHS U01 GM115486
6 · The paper itself

Abstract

Microbes active in extreme cold are not as well explored as those of other extreme environments. Studies have revealed a substantial microbial diversity and identified cold-specific microbiome molecular functions. We analyzed the metagenomes and metatranscriptomes of 20 snow samples collected in early and late spring in Svalbard, Norway using mi-faser, our read-based computational microbiome function annotation tool. Our results reveal a more diverse microbiome functional capacity and activity in the early- vs. late-spring samples. We also find that functional dissimilarity between the same-sample metagenomes and metatranscriptomes is significantly higher in early than late spring samples. These findings suggest that early spring samples may contain a larger fraction of DNA of dormant (or dead) organisms, while late spring samples reflect a new, metabolically active community. We further show that the abundance of sequencing reads mapping to the fatty acid synthesis-related microbial pathways in late spring metagenomes and metatranscriptomes is significantly correlated with the organic acid levels measured in these samples. Similarly, the organic acid levels correlate with the pathway read abundances of geraniol degradation and inversely correlate with those of styrene degradation, suggesting a possible nutrient change. Our study thus highlights the activity of microbial degradation pathways of complex organic compounds previously unreported at low temperatures.

Indexed as

Acyclic MonoterpenesBacteriaCarbonFatty AcidsMetabolic Networks and PathwaysMetagenomeMicrobiotaNorwayOrganic ChemicalsSeasonsSnowStyreneTranscriptomeAcyclic MonoterpenesCarbonFatty AcidsgeraniolOrganic ChemicalsStyrenemetagenomemetatranscriptomemi-fasersnow microbiome

Identifiers

PMID32762019
PMCPMC7520998
OpenAlexW3048163270

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.