Evidence map›Paper›PMID 42277887›Full record

ArticleJournal of animal science and biotechnology2026

Uncovering how selected potent bacteriocins reshape the broiler chicken gut microbiome in a PolyFermS continuous in vitro model.

Amal Mamjoud, Séverine Zirah, Sylvie Rebuffat, Éric Biron, Ismail Fliss

Abstract read
In one paragraph

Article in Journal of animal science and biotechnology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Amal MamjoudUnit Molecules of Communication and Adaptation of Microorganisms (MCAM), UMR 7245 CNRS- MNHN, Paris, 75005, France.
Séverine ZirahUnit Molecules of Communication and Adaptation of Microorganisms (MCAM), UMR 7245 CNRS- MNHN, Paris, 75005, France. severine.zirah@mnhn.fr.
Sylvie RebuffatUnit Molecules of Communication and Adaptation of Microorganisms (MCAM), UMR 7245 CNRS- MNHN, Paris, 75005, France.
Éric BironInstitute of Nutrition and Functional Foods, Université Laval, Quebec, QC, G1V 0A6, Canada.
Ismail FlissFood Science Department, Food and Agriculture Faculty, Université Laval, Quebec, QC, G1V 0A6, Canada. ismail.fliss@fsaa.ulaval.ca.

Funding

CRIBIQ 2014-022-C12IDRC-Innovet-Initiative 109048-001NSERC IRCPJ 499946-15
6 · The paper itself

Abstract

backgroundBacteriocins are promising alternatives to antibiotics in poultry production, offering pathogen control with minimal disruption to gut microbiota and reduced risk of resistance dissemination. This study compared the impact of three bacteriocins-microcin J25, nisin Z, and pediocin PA-1-against bacitracin as a positive control, specifically evaluating their effects on gut microbiota composition and metabolic activity. The study utilized the PolyFermS continuous fermentation model to simulate chicken caecal conditions.

results16S rRNA sequencing revealed that bacitracin and nisin Z significantly altered the microbiota composition, reducing key families such as Lactobacillaceae and Ruminococcaceae, while microcin J25 and pediocin PA-1 had negligible effects. Short-chain fatty acid analysis revealed a significant time-dependent decrease in butyrate levels following nisin Z and bacitracin treatments, with the most pronounced reduction observed at 48 h post-injection. Conversely, microcin J25 and pediocin PA-1 maintained stable profiles. Untargeted LC-MS metabolomics indicated a marked metabolic shift under nisin Z treatment, including increased amino acids and cyclic dipeptide levels, while microcin J25 had minimal impact. Stability assays confirmed that microcin J25 remained active up to 24 h, whereas nisin Z and pediocin PA-1 lost antimicrobial activity rapidly.

conclusionsThese findings support the selective use of bacteriocins as alternatives to antibiotics in poultry farming, with microcin J25 demonstrating the most favorable profile for microbiota preservation and metabolic stability. Future research will focus on in vivo trials in broiler chickens to confirm these findings and evaluate the practical application of microcin J25 in a production environment.

Indexed as

AntibioticsBacteriocinsMicrobiotaMicrocin J25NisinPediocinPolyFermSPoultry

Identifiers

PMID42277887
PMCPMC13262205

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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.