Evidence map›Paper›PMID 41857540›Full record

ArticleBMC microbiology2026

Synergistic regulation of selenium yeast and vitamin E on the rumen microbiota-VFA-liver axis in lambs.

Shangwu Ma, Yuzhu Sha, Xiaoyong Ma, Haibo Wang, Shengguo Zhao, Ting Jiao

Abstract read
In one paragraph

Article in BMC microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Shangwu MaCollege of Animal Science and Technology, Gansu Agricultural University, Lanzhou, 730070, China.
Yuzhu ShaCollege of Animal Science and Technology, Gansu Agricultural University, Lanzhou, 730070, China.
Xiaoyong MaCollege of Animal Science and Technology, Gansu Agricultural University, Lanzhou, 730070, China.
Haibo WangCollege of Animal Science and Technology, Gansu Agricultural University, Lanzhou, 730070, China.
Shengguo ZhaoCollege of Animal Science and Technology, Gansu Agricultural University, Lanzhou, 730070, China. zhaosg@gsau.edu.cn.
Ting JiaoCollege of Pratacultural Science, Gansu Agricultural University, Lanzhou, 730070, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn intensive livestock production, various environmental and management stressors often compromise the oxidative and immune homeostasis of lambs, thereby impairing their growth performance and health. Selenium and vitamin E are well-established antioxidant nutrients; but their combined regulatory effects via the rumen-liver axis remain insufficiently understood. To investigate this, twenty-four healthy lambs (average body weight: 20.39 ± 1.52 kg) were randomly assigned to four dietary treatment groups (n = 6 per group) and housed individually. The groups were as follows: a control (CON) group fed a basal diet; an SY group fed the basal diet supplemented with 0.6 mg/kg selenium yeast (SY); a VE group fed the basal diet supplemented with 200 IU/kg vitamin E (VE); and a MIX group fed the basal diet supplemented with both 0.6 mg/kg SY and 200 IU/kg VE. This study aimed to elucidate the underlying regulatory pathways of the rumen-liver axis by assessing lamb growth performance, immune function, antioxidant capacity, rumen fermentation parameters, and liver transcriptome profiles, and by analyzing the interrelationships among these variables.

resultsLambs in the MIX group exhibited significantly higher average daily gain, serum concentrations of growth hormone and immunoglobulins, and enhanced serum antioxidant capacity compared to other groups (P < 0.05). Concurrently, the rumen environment was notably improved, characterized by reduced pH and ammonia–nitrogen concentration, increased volatile fatty acid (VFA) production, and an elevated abundance of beneficial bacteria such as Firmicutes and Prevotella. Liver transcriptomic analysis further revealed that differentially expressed genes (DEGs) were significantly enriched in pathways related to immune and antioxidant functions, notably arachidonic acid metabolism. Furthermore, correlation analysis suggested that rumen microbiota influence hepatic gene expression profiles through modulation of VFA metabolism.

conclusionThe findings of this study demonstrate that the combined dietary supplementation of SY and VE enhances antioxidant and immune functions, and synergistically improves the growth performance and health status of lambs. These beneficial effects are closely associated with alterations in a "rumen microbiota–VFA–liver" axis.

Indexed as

Fatty Acids, VolatileGastrointestinal MicrobiomeLiverRumenSeleniumVitamin EAnimal FeedAnimalsAntioxidantsBacteriaDietDietary SupplementsFermentationSheepAntioxidantsFatty Acids, VolatileSeleniumVitamin EAntioxidantImmunityMicrobiotaTranscriptomeVFA

Identifiers

PMID41857540
PMCPMC13122907

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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.