Evidence map›Paper›PMID 32703946›Full record

ArticleNature communications2020

Bile acids drive the newborn's gut microbiota maturation.

N van Best, U Rolle-Kampczyk, F G Schaap, M Basic, S W M Olde Damink, A Bleich, P H M Savelkoul, M von Bergen, J Penders, M W Hornef

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 133 papers.

0numbers the graph read from it
0cells of the map it votes in
133citing papers in PubMed
11.2field-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

133 citing papers in PubMed, 235 citations in OpenAlex.

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73 more citing papers are in PubMed but not listed here.

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

10 authors at 5 institutions in 2 countries.

N van BestInstitute of Medical Microbiology, RWTH University Hospital Aachen, RWTH University, Aachen, Germany.ORCID http://orcid.org/0000-0003-3577-7285
U Rolle-KampczykDepartment of Molecular Systems Biology, UFZ-Helmholtz Centre for Environmental Research, Leipzig, Germany.ORCID http://orcid.org/0000-0002-7728-6284
F G SchaapDepartment of General Surgery, NUTRIM, Maastricht University, Maastricht, The Netherlands.ORCID http://orcid.org/0000-0002-1597-572X
M BasicInstitute for Laboratory Animal Science, Hannover Medical School, Hannover, Germany.
S W M Olde DaminkDepartment of General Surgery, NUTRIM, Maastricht University, Maastricht, The Netherlands.ORCID http://orcid.org/0000-0002-5202-9345
A BleichInstitute for Laboratory Animal Science, Hannover Medical School, Hannover, Germany.ORCID http://orcid.org/0000-0002-3438-0254
P H M SavelkoulDepartment of Medical Microbiology, School of Nutrition and Translational Research in Metabolism (NUTRIM), Maastricht University, Maastricht, The Netherlands.
M von BergenDepartment of Molecular Systems Biology, UFZ-Helmholtz Centre for Environmental Research, Leipzig, Germany.
J Penders *Department of Medical Microbiology, School of Nutrition and Translational Research in Metabolism (NUTRIM), Maastricht University, Maastricht, The Netherlands. j.penders@maastrichtuniversity.nl.ORCID http://orcid.org/0000-0001-9146-5919
M W Hornef *Institute of Medical Microbiology, RWTH University Hospital Aachen, RWTH University, Aachen, Germany. mhornef@ukaachen.de.ORCID http://orcid.org/0000-0001-6096-9110
Maastricht University · NLHelmholtz Centre for Environmental Research · DEMedizinische Hochschule Hannover · DEMaastricht University Medical Centre · NLUniversitätsklinikum Aachen · DE

Funding

National Metabolomics Data Repository - nextgen Metabolomics WorkbenchU2CDK119886 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SUBRAMANIAM, SHANKAR · 2018 to 2021
$12.7M
NIDDK NIH HHS U2C DK119886
6 · The paper itself

Abstract

Following birth, the neonatal intestine is exposed to maternal and environmental bacteria that successively form a dense and highly dynamic intestinal microbiota. Whereas the effect of exogenous factors has been extensively investigated, endogenous, host-mediated mechanisms have remained largely unexplored. Concomitantly with microbial colonization, the liver undergoes functional transition from a hematopoietic organ to a central organ of metabolic regulation and immune surveillance. The aim of the present study was to analyze the influence of the developing hepatic function and liver metabolism on the early intestinal microbiota. Here, we report on the characterization of the colonization dynamics and liver metabolism in the murine gastrointestinal tract (n = 6-10 per age group) using metabolomic and microbial profiling in combination with multivariate analysis. We observed major age-dependent microbial and metabolic changes and identified bile acids as potent drivers of the early intestinal microbiota maturation. Consistently, oral administration of tauro-cholic acid or β-tauro-murocholic acid to newborn mice (n = 7-14 per group) accelerated postnatal microbiota maturation.

Indexed as

Gastrointestinal MicrobiomeAdministration, OralAnimalsAnimals, NewbornBile Acids and SaltsIntestinal AbsorptionKineticsLactobacillusLiverMetabolomicsMice, Inbred C57BLPhylogenyPrincipal Component AnalysisBile Acids and Salts

Identifiers

PMID32703946
PMCPMC7378201
OpenAlexW3044002524

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.