Integrative multi-omics and bioinformatics analysis of the effects of BaiRui YuPingFeng Powder on intestinal health in broilers.

IF 2.6 2区 农林科学 Q1 VETERINARY SCIENCES
Frontiers in Veterinary Science Pub Date : 2025-06-18 eCollection Date: 2025-01-01 DOI:10.3389/fvets.2025.1606531
Haonan Xu, Fang Zhang, Yan Che, Yu Cui, Qisheng Yao, Yueqin Guan, Hao Chen, Yuying Huang
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Histopathological examination indicated that high-dose TCYP significantly enhanced villus height and the villus-to-crypt ratio (V/C) in the duodenum, jejunum, and ileum compared to the CON group (<i>p</i> < 0.05). 16S rRNA sequencing analysis revealed that TCYP treatment significantly modified the <i>β</i>-diversity of cecal microbiota (<i>p</i> < 0.01). Compared to the CON group, ATB treatment increased the abundance of <i>Faecalibacterium and Lachnospiraceae_unclassified</i> but reduced <i>Ruminococcaceae_unclassified and Firmicutes_unclassified</i>. Notably, dietary TCYP supplementation maintained gut microbiota profiles similar to the CON group, demonstrating its stabilizing effect on microbial community structure in broilers. Metabolomic analysis identified differential metabolites primarily involved in lipid and lipid-like molecules, organic heterocyclic compounds, and organic acids and derivatives. 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引用次数: 0

Abstract

Introduction: In recent years, global poultry consumption has increased rapidly, making chicken the most widely consumed meat worldwide by 2019. To increase livestock development, antibiotics are often added to animal feed as growth promoters. But overuse of antibiotics may alter the gut microbiota, make people more resistant to them, and raise the possibility that they will spread antibiotic resistance genes to the human microbiome. Therefore, identifying safe and effective alternatives to antibiotics in livestock production is crucial for maintaining and improving gut microbial balance, ultimately promoting poultry health. The aim of this study was to investigate the mechanisms behind the impacts of BaiRui YuPingFeng Powder (TCYP) on intestinal health in broilers using combined metabolomics, bioinformatics analysis, and 16S rRNA sequencing.

Methods: In a 42-day feeding trial, 300 one-day-old broilers were randomly divided into five groups (six replicates per group; 10 broilers per replicate) fed a basal diet with or without supplements: control (CON), antibiotic (ATB), and TCYP at 500, 1000, and 1500 mg/kg. Growth performance, serum biochemical parameters, intestinal morphology, cecal microbiota composition, and metabolomic profiles were analyzed. Bioinformatics analysis was used to identify potential targets and pathways, followed by qPCR validation of key genes.

Results: Compared with the CON group, TCYP administration dose-dependently reduced the feed-to-gain ratio (F/G) and average daily feed intake (ADFI) while increasing average daily gain (ADG), with the high-dose TCYP showing more pronounced effects (p < 0.05). Serum biochemical analysis revealed that TCYP treatment significantly decreased serum levels of total cholesterol (T-CHO), triglycerides (TG), lactate dehydrogenase (LDH), and alanine aminotransferase (ALT) in a dose-dependent manner, while elevating albumin (ALB) content. These beneficial effects were particularly marked in the high-dose TCYP group (p < 0.05). Histopathological examination indicated that high-dose TCYP significantly enhanced villus height and the villus-to-crypt ratio (V/C) in the duodenum, jejunum, and ileum compared to the CON group (p < 0.05). 16S rRNA sequencing analysis revealed that TCYP treatment significantly modified the β-diversity of cecal microbiota (p < 0.01). Compared to the CON group, ATB treatment increased the abundance of Faecalibacterium and Lachnospiraceae_unclassified but reduced Ruminococcaceae_unclassified and Firmicutes_unclassified. Notably, dietary TCYP supplementation maintained gut microbiota profiles similar to the CON group, demonstrating its stabilizing effect on microbial community structure in broilers. Metabolomic analysis identified differential metabolites primarily involved in lipid and lipid-like molecules, organic heterocyclic compounds, and organic acids and derivatives. Spearman correlation analysis revealed significant associations between Lachnospiraceae_unclassified and metabolites such as Gly-Leu, fumarate, and phenylpyruvic acid (|r| > 0.5, p < 0.05). Bioinformatics analysis suggested that TCYP may improve intestinal health by regulating key targets, including MMP9, TGFB1, and PPARG, as well as the peroxisome proliferator-activated receptor (PPAR) signaling pathway. Quantitative PCR (qPCR) results showed that, compared to the CON group, TCYP dose-dependently significantly upregulated the mRNA expression of PPARG, PDPK1, and Bcl2 in jejunal tissues (p < 0.05), while significantly downregulating the expression of MMP1 and Bax (p < 0.05).

Conclusion: TCYP enhances growth performance and intestinal health in broilers through multiple mechanisms, including maintaining cecal microbial homeostasis, modulating lipid and amino acid metabolism, with potential involvement of the PPAR signaling pathway based on bioinformatics and gene expression analysis.

百瑞玉屏风散对肉鸡肠道健康影响的综合多组学和生物信息学分析。
导读:近年来,全球家禽消费迅速增长,到2019年,鸡肉将成为全球消费最广泛的肉类。为了促进牲畜的生长,抗生素经常作为生长促进剂添加到动物饲料中。但过度使用抗生素可能会改变肠道微生物群,使人们对它们产生更强的耐药性,并增加它们将抗生素抗性基因传播给人类微生物群的可能性。因此,在畜牧生产中寻找安全有效的抗生素替代品对于维持和改善肠道微生物平衡,最终促进家禽健康至关重要。本研究旨在通过代谢组学、生物信息学分析和16S rRNA测序技术,探讨百瑞玉屏风散(TCYP)对肉仔鸡肠道健康影响的机制。方法:选取300只1日龄肉仔鸡,随机分为5组(每组6个重复;每重复10只,分别饲喂基础饲粮,添加或不添加对照组(CON)、抗生素(ATB)和TCYP(500、1000和1500 mg/kg)。分析了生长性能、血清生化指标、肠道形态、盲肠菌群组成和代谢组学特征。利用生物信息学分析确定潜在的靶点和途径,然后对关键基因进行qPCR验证。结果:与CON组相比,TCYP剂量依赖性地降低了料重比(F/G)和平均日采食量(ADFI),提高了平均日增重(ADG),且高剂量TCYP效果更显著(p < 0.05)。血清生化分析显示,TCYP治疗显著降低血清总胆固醇(T-CHO)、甘油三酯(TG)、乳酸脱氢酶(LDH)和丙氨酸转氨酶(ALT)水平,并呈剂量依赖性,同时升高白蛋白(ALB)含量。这些有益作用在高剂量TCYP组尤为显著(p < 0.05)。组织病理学检查显示,与CON组相比,高剂量TCYP显著提高了十二指肠、空肠和回肠的绒毛高度和绒毛/隐窝比(V/C) (p < 0.05)。16S rRNA测序分析显示,TCYP处理显著改变了盲肠微生物群的β-多样性(p < 0.01)。与CON组相比,ATB处理增加了Faecalibacterium和Lachnospiraceae_unclassified的丰度,但减少了Ruminococcaceae_unclassified和Firmicutes_unclassified。值得注意的是,饲粮中添加TCYP维持了与CON组相似的肠道菌群分布,表明其对肉仔鸡微生物群落结构具有稳定作用。代谢组学分析确定了主要涉及脂质和类脂分子、有机杂环化合物、有机酸及其衍生物的差异代谢物。Spearman相关分析显示,lachnospirace_unclassified与代谢物Gly-Leu、富马酸盐、苯丙酮酸有显著相关性(|r| >.5, p < 0.05)。生物信息学分析提示,TCYP可能通过调控关键靶点,包括MMP9、TGFB1和PPAR,以及过氧化物酶体增殖物激活受体(PPAR)信号通路,改善肠道健康。定量PCR (qPCR)结果显示,与CON组相比,TCYP剂量依赖性地显著上调空肠组织中PPARG、PDPK1、Bcl2 mRNA的表达(p < 0.05),显著下调MMP1、Bax mRNA的表达(p < 0.05)。结论:TCYP通过维持盲肠微生物稳态、调节脂质和氨基酸代谢等多种机制改善肉鸡生长性能和肠道健康,基于生物信息学和基因表达分析,TCYP可能参与PPAR信号通路。
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来源期刊
Frontiers in Veterinary Science
Frontiers in Veterinary Science Veterinary-General Veterinary
CiteScore
4.80
自引率
9.40%
发文量
1870
审稿时长
14 weeks
期刊介绍: Frontiers in Veterinary Science is a global, peer-reviewed, Open Access journal that bridges animal and human health, brings a comparative approach to medical and surgical challenges, and advances innovative biotechnology and therapy. Veterinary research today is interdisciplinary, collaborative, and socially relevant, transforming how we understand and investigate animal health and disease. Fundamental research in emerging infectious diseases, predictive genomics, stem cell therapy, and translational modelling is grounded within the integrative social context of public and environmental health, wildlife conservation, novel biomarkers, societal well-being, and cutting-edge clinical practice and specialization. Frontiers in Veterinary Science brings a 21st-century approach—networked, collaborative, and Open Access—to communicate this progress and innovation to both the specialist and to the wider audience of readers in the field. Frontiers in Veterinary Science publishes articles on outstanding discoveries across a wide spectrum of translational, foundational, and clinical research. The journal''s mission is to bring all relevant veterinary sciences together on a single platform with the goal of improving animal and human health.
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