Evidence map›Paper›PMID 37394428›Full record

ArticleMicrobiome2023

Gut barrier-microbiota imbalances in early life lead to higher sensitivity to inflammation in a murine model of C-section delivery.

M Barone, Y Ramayo-Caldas, J Estellé, K Tambosco, S Chadi, F Maillard, M Gallopin, J Planchais, F Chain, C Kropp and 5 more

Erratum issuedOpen 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. An erratum has been issued. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

15 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
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  9. Microbiome: A Key Regulator of Body-Brain Interactions.Advances in experimental medicine and biology · 2025
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 5 institutions in 3 countries.

M Barone *Microbiomics Unit, Department of Medical and Surgical Sciences, University of Bologna, 40138, Bologna, Italy.
Y Ramayo-Caldas *INRAE, AgroParisTech, GABI, Paris-Saclay University, 78350, Jouy-en-Josas, France.
J EstelléINRAE, AgroParisTech, GABI, Paris-Saclay University, 78350, Jouy-en-Josas, France.
K TamboscoINRAE, AgroParisTech, Micalis Institut,, Paris-Saclay University, 78350, Jouy-en-Josas, France.
S ChadiINRAE, AgroParisTech, Micalis Institut,, Paris-Saclay University, 78350, Jouy-en-Josas, France.
F MaillardINRAE, AgroParisTech, Micalis Institut,, Paris-Saclay University, 78350, Jouy-en-Josas, France.
M GallopinCNRS, CEA, l'Institut de Biologie Intégrative de La Cellule (I2BC), Paris-Saclay University, 91405, Orsay, France.
J PlanchaisINRAE, AgroParisTech, Micalis Institut,, Paris-Saclay University, 78350, Jouy-en-Josas, France.
F ChainINRAE, AgroParisTech, Micalis Institut,, Paris-Saclay University, 78350, Jouy-en-Josas, France.
C KroppINRAE, AgroParisTech, Micalis Institut,, Paris-Saclay University, 78350, Jouy-en-Josas, France.
D Rios-CovianINRAE, AgroParisTech, Micalis Institut,, Paris-Saclay University, 78350, Jouy-en-Josas, France.
H SokolINRAE, AgroParisTech, Micalis Institut,, Paris-Saclay University, 78350, Jouy-en-Josas, France.
P BrigidiMicrobiomics Unit, Department of Medical and Surgical Sciences, University of Bologna, 40138, Bologna, Italy.
P LangellaINRAE, AgroParisTech, Micalis Institut,, Paris-Saclay University, 78350, Jouy-en-Josas, France.
R MartínINRAE, AgroParisTech, Micalis Institut,, Paris-Saclay University, 78350, Jouy-en-Josas, France. rebeca.martin-rosique@inrae.fr.
AgroParisTech · FRUniversity of Bologna · ITCentre National de la Recherche Scientifique · FRInserm · FRMicrobiologie de l’alimentation au service de la santé · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMost interactions between the host and its microbiota occur at the gut barrier, and primary colonizers are essential in the gut barrier maturation in the early life. The mother-offspring transmission of microorganisms is the most important factor influencing microbial colonization in mammals, and C-section delivery (CSD) is an important disruptive factor of this transfer. Recently, the deregulation of symbiotic host-microbe interactions in early life has been shown to alter the maturation of the immune system, predisposing the host to gut barrier dysfunction and inflammation. The main goal of this study is to decipher the role of the early-life gut microbiota-barrier alterations and its links with later-life risks of intestinal inflammation in a murine model of CSD.

resultsThe higher sensitivity to chemically induced inflammation in CSD mice is related to excessive exposure to a too diverse microbiota too early in life. This early microbial stimulus has short-term consequences on the host homeostasis. It switches the pup's immune response to an inflammatory context and alters the epithelium structure and the mucus-producing cells, disrupting gut homeostasis. This presence of a too diverse microbiota in the very early life involves a disproportionate short-chain fatty acids ratio and an excessive antigen exposure across the vulnerable gut barrier in the first days of life, before the gut closure. Besides, as shown by microbiota transfer experiments, the microbiota is causal in the high sensitivity of CSD mice to chemical-induced colitis and in most of the phenotypical parameters found altered in early life. Finally, supplementation with lactobacilli, the main bacterial group impacted by CSD in mice, reverts the higher sensitivity to inflammation in ex-germ-free mice colonized by CSD pups' microbiota.

conclusionsEarly-life gut microbiota-host crosstalk alterations related to CSD could be the linchpin behind the phenotypic effects that lead to increased susceptibility to an induced inflammation later in life in mice. Video Abstract.

Indexed as

ColitisGastrointestinal MicrobiomeMicrobiotaAnimalsDisease Models, AnimalInflammationMammalsMiceC-section deliveryEarly lifeGut barrierInflammationMicrobiotaMurine modelPrimary colonization

Identifiers

PMID37394428
PMCPMC10316582
OpenAlexW4382893256

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.