Hu Fan, Gebeyew Kefyalew, Wu Zhiwu, Chen Bingrui, Jiao Jinzhen, Tan Zhiliang, Tian Di, He Zhixiong
State Key Laboratory of Forage Breeding-by-Design and Utilization, National Engineering Laboratory for Pollution Control and Waste Utilization in Livestock and Poultry Production, and Hunan Provincial Key Laboratory of Animal Nutritional Physiology and Metabolic Process, Institute of Subtropical Agriculture, Chinese Academy of Sciences, Changsha, 410125, Hunan, China.
College of Advanced Agricultural Sciences, University of Chinese Academy of Sciences, Beijing, 100049, China.
J Anim Sci Biotechnol. 2025 Jun 5;16(1):81. doi: 10.1186/s40104-025-01214-9.
The ketogenic diet that forces adenosine triphosphate (ATP) production by beta-oxidation of fatty acids instead of carbohydrate glycolysis, has gained consensus on host metabolism. However, the mechanisms how a ketogenic diet alters gastrointestinal microbiome and its downstream consequences on microbial nutrient availability and energy metabolism remain to be elucidated. Here, we used the sheep model fed with fat-rich diet to evaluate the symbiotic microbiome across three regions of the gastrointestinal tract (rumen, ileum, and colon) to gain a comprehensive understanding of the microbial energy metabolism and microbe-mediated ATP biosynthesis.
Results showed that sheep fed a fat-rich diet had a greater ADG and increased reliance on fat oxidation for fuel utilization. Metagenomics analysis showed the loss of the specialized fiber-degrading bacteria (genus_Fibrobacter) in the rumen and enrichment of genera RUG420 and Eubacterium, which are involved in lipid metabolism and bile acid processing, in the ileum. A significant functional shift related to energy metabolism was shared across three regions of the gastrointestinal microbiomes. These shifts were dominated by glycolysis/gluconeogenesis and TCA cycle in the rumen and by fatty acid degradation and bile acid transformation in the ileum, indicating adaptation to nutrient availability and energy acquisition. Notably, the abundance of substrate-level phosphorylation (SLP) enzymes was significantly increased in the rumen, ileum and colon, while the ATP-producing capacity through electron transport phosphorylation (ETP) by family_Bacteroidaceae in rumen and Acutalibacteraceae in ileum of sheep with fat-rich diet.
Altogether, the ATP-related microbiome encoding SLP and ETP in rumen, ileum, and colon contributed 36.95% to the host's weight variation. Our study is the first one demonstrating the microbial potential in the ATP synthesis under the shift in dietary energy source, providing a new perspective on the energy metabolism and precise human macronutrients nutrition.
生酮饮食通过脂肪酸的β-氧化而非碳水化合物糖酵解来迫使三磷酸腺苷(ATP)生成,这在宿主代谢方面已达成共识。然而,生酮饮食如何改变胃肠道微生物群及其对微生物养分可利用性和能量代谢的下游影响的机制仍有待阐明。在此,我们使用喂食高脂饮食的绵羊模型来评估胃肠道三个区域(瘤胃、回肠和结肠)的共生微生物群,以全面了解微生物能量代谢和微生物介导的ATP生物合成。
结果表明,喂食高脂饮食的绵羊具有更高的平均日增重,并且在燃料利用方面对脂肪氧化的依赖性增加。宏基因组学分析显示,瘤胃中专门的纤维降解细菌(纤维杆菌属)减少,回肠中参与脂质代谢和胆汁酸加工的RUG420属和真杆菌属富集。胃肠道微生物群的三个区域都出现了与能量代谢相关的显著功能转变。这些转变在瘤胃中以糖酵解/糖异生和三羧酸循环为主,在回肠中以脂肪酸降解和胆汁酸转化为主,表明对养分可利用性和能量获取的适应。值得注意的是,底物水平磷酸化(SLP)酶的丰度在瘤胃、回肠和结肠中显著增加,而喂食高脂饮食的绵羊瘤胃中的拟杆菌科和回肠中的锐杆菌科通过电子传递磷酸化(ETP)产生ATP的能力增强。
总之,瘤胃、回肠和结肠中编码SLP和ETP的与ATP相关的微生物群对宿主体重变化的贡献率为36.95%。我们的研究首次证明了在饮食能量来源转变下微生物在ATP合成中的潜力,为能量代谢和精确的人类常量营养素营养提供了新的视角。