Disruption of hindgut microbiome homeostasis promotes postpartum energy metabolism disorders in dairy ruminants by inhibiting acetate-mediated hepatic AMPK-PPARA axis.

IF 13.8 1区 生物学 Q1 MICROBIOLOGY
Shuo Wang, Fanlin Kong, Xinyue Zhang, Dongwen Dai, Chen Li, Zhijun Cao, Yajing Wang, Wei Wang, Shengli Li
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引用次数: 0

Abstract

Background: Postpartum energy metabolism disorders pose a significant challenge to the health and productivity of dairy ruminants, yet their underlying pathogenesis remains poorly understood. The critical role of the gut microbiota in regulating host metabolic processes via the "gut-liver axis" has garnered increasing attention, but its specific mechanisms in dairy ruminant energy metabolism disorders are still unclear. This study uses dairy cows as a model and employs a large-scale case-control analysis to systematically investigate the pathophysiological basis of postpartum energy metabolism disorders through the lens of the "gut-liver axis."

Results: Postpartum energy metabolism disorders in dairy cows are characterized by elevated blood β-hydroxybutyrate (BHB) and aspartate aminotransferase (AST) levels, and hepatic steatosis. A random forest model based on gut microbiota effectively predicts disease occurrence (AUC = 0.74). Multi-omics (metagenomics, metabolomics, and transcriptomics) analysis further identified key microbes, including Faecousia species (sp017465625 and sp017380435), Methanosphaera species (sp016282985), and Bifidobacterium globosum. These microbes regulate acetate concentration in the gut, which is significantly correlated with key genes in the hepatic PPAR and PI3K-AKT pathways, as well as with blood BHB levels. Primary hepatocyte culture experiments further confirmed that sodium acetate effectively inhibits hepatic fat deposition induced by mixed fatty acids through the hepatic AMPK-PPARA axis and reduces the production of BHB in the culture medium.

Conclusion: This study demonstrates that key gut microbes and their metabolic product (acetate) inhibit the occurrence of metabolic disorders through the hepatic AMPK-PPARA axis. These findings provide new insights and potential therapeutic targets for understanding and mitigating postpartum metabolic disorders in dairy ruminants. Video Abstract.

后肠道微生物群稳态的破坏通过抑制醋酸盐介导的肝脏AMPK-PPARA轴促进乳反刍动物产后能量代谢紊乱。
背景:产后能量代谢紊乱对乳反刍动物的健康和生产能力构成了重大挑战,但其潜在的发病机制尚不清楚。肠道菌群通过“肠-肝轴”调节宿主代谢过程的关键作用已引起越来越多的关注,但其在乳反刍动物能量代谢紊乱中的具体机制尚不清楚。本研究以奶牛为模型,采用大规模病例对照分析,通过“肠肝轴”的视角,系统探讨产后能量代谢紊乱的病理生理基础。结果:奶牛产后能量代谢紊乱表现为血液中β-羟基丁酸酯(BHB)和天冬氨酸转氨酶(AST)水平升高,肝脏脂肪变性。基于肠道菌群的随机森林模型能有效预测疾病发生(AUC = 0.74)。多组学(宏基因组学、代谢组学和转录组学)分析进一步确定了关键微生物,包括Faecousia种(sp017465625和sp017380435)、Methanosphaera种(sp016282985)和Bifidobacterium globosum。这些微生物调节肠道内的醋酸盐浓度,这与肝脏PPAR和PI3K-AKT通路中的关键基因以及血液BHB水平显著相关。原代肝细胞培养实验进一步证实,乙酸钠通过肝脏AMPK-PPARA轴有效抑制混合脂肪酸诱导的肝脏脂肪沉积,减少培养基中BHB的产生。结论:本研究表明,关键肠道微生物及其代谢产物(醋酸酯)通过肝脏AMPK-PPARA轴抑制代谢紊乱的发生。这些发现为了解和减轻乳反刍动物产后代谢紊乱提供了新的见解和潜在的治疗靶点。视频摘要。
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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
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