Evidence map›Paper›PMID 30209339›Full record

ArticleScientific reports2018

Antimicrobial promotion of pig growth is associated with tissue-specific remodeling of bile acid signature and signaling.

Ignacio R Ipharraguerre, Jose J Pastor, Aleix Gavaldà-Navarro, Francesc Villarroya, Alessandro Mereu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 23 citations in OpenAlex.

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  12. Microbiome-immune-metabolic axis in the epidemic of childhood obesity: Evidence and opportunities.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2020
    Review
  13. Frontiers in immunology · 2020
    Article
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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

5 authors at 3 institutions in 2 countries.

Ignacio R IpharraguerreInstitute of Human Nutrition and Food Science, University of Kiel, Hermann-Rodewald-Strasse 6-8, D-24128, Kiel, Germany. ipharraguerre@foodsci.uni-kiel.de.ORCID 0000-0003-1105-6600
Jose J PastorInnovation Division, Lucta S.A., Parc de Recerca UAB, Edifici Eureka, 08193, Bellaterra, Catalonia, Spain.ORCID 0000-0003-2448-2334
Aleix Gavaldà-NavarroDepartament de Bioquímica i Biomedicina Molecular, Institut de Biomedicina (IBUB), Universitat de Barcelona, and CIBER Fisiopatología de la Obesidad y Nutrición, Avinguda Diagonal 645, Edifici nou Pl.-1, 08028, Barcelona, Catalonia, Spain.
Francesc VillarroyaDepartament de Bioquímica i Biomedicina Molecular, Institut de Biomedicina (IBUB), Universitat de Barcelona, and CIBER Fisiopatología de la Obesidad y Nutrición, Avinguda Diagonal 645, Edifici nou Pl.-1, 08028, Barcelona, Catalonia, Spain.
Alessandro MereuInnovation Division, Lucta S.A., Parc de Recerca UAB, Edifici Eureka, 08193, Bellaterra, Catalonia, Spain.
Centro de Investigación Biomédica en Red · ESChristian-Albrechts-Universität zu Kiel · DEUniversidad Nacional de Educación a Distancia · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The spread of bacterial resistance to antimicrobials (AMA) have intensified efforts to discontinue the non-therapeutic use of AMA in animal production. Finding alternatives to AMA, however, is currently encumbered by the obscure mechanism that underlies their growth-promoting action. In this report, we demonstrate that combinations of antibiotics and zinc oxide at doses commonly used for stimulating growth or preventing post-weaning enteritis in pigs converge in promoting microbial production of bile acids (BA) in the intestine. This leads to tissue-specific modifications in the proportion of BA, thereby amplifying BA signaling in intestine, liver, and white adipose tissue (WAT). Activation of BA-regulated pathways ultimately reinforces the intestinal protection against bacterial infection and pathological secretion of fluids and electrolytes, attenuates inflammation in colon and WAT, alters protein and lipid metabolism in liver, and increases the circulating levels of the hormone FGF19. Conceivably, these alterations could spare nutrients for growth and improve the metabolic efficiency of AMA-treated animals. This work provides evidence that BA act as signaling molecules that mediate host physiological, metabolic, and immune responses to the AMA-induced alterations in gut microbial metabolism, eventually permitting the growth-promoting action of AMA. Consequently, BA emerge as a promising target for developing efficacious alternatives to AMA.

Indexed as

Adipose Tissue, WhiteAnimalsAnti-Bacterial AgentsBile Acids and SaltsDrug CombinationsEnteritisFibroblast Growth FactorsIntestinal MucosaIntestinesLipid MetabolismLiverSwineZinc OxideAnti-Bacterial AgentsBile Acids and SaltsDrug CombinationsFibroblast Growth FactorsZinc Oxide

Identifiers

PMID30209339
PMCPMC6135865
OpenAlexW2890926447

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.