Evidence map›Paper›PMID 37858269›Full record

ArticleMicrobiome2023

Four functional profiles for fibre and mucin metabolism in the human gut microbiome.

Simon Labarthe, Sandra Plancade, Sebastien Raguideau, Florian Plaza Oñate, Emmanuelle Le Chatelier, Marion Leclerc, Beatrice Laroche

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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

7 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
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  3. Apple Pomace Fermented with Non-International journal of molecular sciences · 2026
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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

7 authors at 7 institutions in 3 countries.

Simon LabartheUniversité Paris-Saclay, INRAE, MaIAGE, 78350, Jouy-en-Josas, France. simon.labarthe@inrae.fr.
Sandra PlancadeUniversité Paris-Saclay, INRAE, MaIAGE, 78350, Jouy-en-Josas, France.
Sebastien RaguideauUniversité Paris-Saclay, INRAE, MaIAGE, 78350, Jouy-en-Josas, France.
Florian Plaza OñateUniversité Paris-Saclay, INRAE, MGP, 78350, Jouy-en-Josas, France.
Emmanuelle Le ChatelierUniversité Paris-Saclay, INRAE, MGP, 78350, Jouy-en-Josas, France.
Marion LeclercUniversité Paris-Saclay, INRAE, Micalis, 78350, Jouy-en-Josas, France.
Beatrice LarocheUniversité Paris-Saclay, INRAE, MaIAGE, 78350, Jouy-en-Josas, France.
CEA CESTA · FRDépartement Mathématiques et Informatique Appliquées · FREarlham Institute · GBFulcrum Therapeutics (United States) · USInstitut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement · FRMathématiques et Informatique Appliquées du Génome à l'Environnement · FRUniversité Paris-Saclay · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWith the emergence of metagenomic data, multiple links between the gut microbiome and the host health have been shown. Deciphering these complex interactions require evolved analysis methods focusing on the microbial ecosystem functions. Despite the fact that host or diet-derived fibres are the most abundant nutrients available in the gut, the presence of distinct functional traits regarding fibre and mucin hydrolysis, fermentation and hydrogenotrophic processes has never been investigated.

resultsAfter manually selecting 91 KEGG orthologies and 33 glycoside hydrolases further aggregated in 101 functional descriptors representative of fibre and mucin degradation pathways in the gut microbiome, we used nonnegative matrix factorization to mine metagenomic datasets. Four distinct metabolic profiles were further identified on a training set of 1153 samples, thoroughly validated on a large database of 2571 unseen samples from 5 external metagenomic cohorts and confirmed with metatranscriptomic data. Profiles 1 and 2 are the main contributors to the fibre-degradation-related metagenome: they present contrasted involvement in fibre degradation and sugar metabolism and are differentially linked to dysbiosis, metabolic disease and inflammation. Profile 1 takes over Profile 2 in healthy samples, and unbalance of these profiles characterize dysbiotic samples. Furthermore, high fibre diet favours a healthy balance between profiles 1 and profile 2. Profile 3 takes over profile 2 during Crohn's disease, inducing functional reorientations towards unusual metabolism such as fucose and H2S degradation or propionate, acetone and butanediol production. Profile 4 gathers under-represented functions, like methanogenesis. Two taxonomic makes up of the profiles were investigated, using either the covariation of 203 prevalent genomes or metagenomic species, both providing consistent results in line with their functional characteristics. This taxonomic characterization showed that profiles 1 and 2 were respectively mainly composed of bacteria from the phyla Bacteroidetes and Firmicutes while profile 3 is representative of Proteobacteria and profile 4 of methanogens.

conclusionsIntegrating anaerobic microbiology knowledge with statistical learning can narrow down the metagenomic analysis to investigate functional profiles. Applying this approach to fibre degradation in the gut ended with 4 distinct functional profiles that can be easily monitored as markers of diet, dysbiosis, inflammation and disease. Video Abstract.

Indexed as

Gastrointestinal MicrobiomeMicrobiotaDietary FiberDysbiosisHumansInflammationMetagenomeMetagenomicsMucinsDietary FiberMucinsFunctional profilingMetagenomicsNMFStatistical learning

Identifiers

PMID37858269
PMCPMC10588041
OpenAlexW4313425413

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.