青藏高原藏羊和湖羊瘤胃微生物群-肝脏糖异生-线粒体相互作用差异的研究

IF 2.7 2区 农林科学 Q1 AGRICULTURE, DAIRY & ANIMAL SCIENCE
Animals Pub Date : 2025-05-30 DOI:10.3390/ani15111603
Qianling Chen, Yuzhu Sha, Xiu Liu, Min Gao, Xiaowei Chen, Wenxin Yang, Wei Huang, Jiqing Wang, Yapeng He, Xu Gao, Yanyu He
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引用次数: 0

摘要

湖羊是中国优质绵羊种质资源,具有生长发育快、繁殖力强、耐旱耐寒等特点。西藏羊适应了高海拔环境,具有较强的环境适应性。为探讨青藏高原藏羊和湖羊瘤胃微生物菌群、肝脏糖异生和线粒体功能相互作用的差异,本研究系统比较分析了相同饲养管理条件下藏羊和湖羊瘤胃菌群密度、肝脏糖异生和线粒体功能相关关键酶活性及相关基因表达水平。然后进行相关分析。结果表明:湖羊的淀粉和蛋白质降解相关反刍杆菌(Ram)和琥珀酸纤维杆菌(Fs)密度极显著高于对照组(p < 0.01);叉头箱O1 (FOXO1)表达量、丙酮酸羧化酶(PC)活性和三磷酸腺苷(ATP)含量也极显著高于藏羊(p < 0.01)。藏羊溶纤维丁酸弧菌(Bf)、白色瘤胃球菌(Ra)、黄瘤球菌(Rf)等细菌密度较高,与纤维素降解有关(p < 0.01)。藏羊的糖异生相关基因、葡萄糖-6-磷酸酶催化亚基1 (G6PC1)和磷酸烯醇丙酮酸羧激酶1 (PCK1)以及磷酸烯醇丙酮酸羧激酶(PEPCK)和果糖-1,6-二磷酸酶(FBPase)活性显著高于湖羊(p < 0.01)。线粒体功能相关基因Mitofusin-1 (Mfn1)、Mitofusin-2 (Mfn2)、ATP合成酶亚基6 (ATP6)、细胞色素b (Cytb)等在藏羊中的表达也显著升高(p < 0.01)。柠檬酸(CA)、丙酮酸(PA)、葡萄糖(Glu)等含量差异不显著(p < 0.05)。相关分析表明,瘤胃菌群与肝脏糖异生关键酶活性、基因表达及线粒体功能存在不同程度的相关性。综上所述,藏羊具有较强的纤维降解能力、糖异生中间体的高效利用能力和线粒体氧化磷酸化(OXPHOS)能力,形成了对高海拔环境的适应策略。相比之下,湖羊表现出高效的蛋白质和淀粉降解能力,从而增加了糖异生前体的供应。综上所述,在高海拔地区引入湖羊时,可通过饲粮干预来调节瘤胃微生物,如增加纤维分解菌或增强线粒体氧化能力,以抵消缺氧引起的代谢限制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Study on the Differences in Rumen Microbiota-Liver Gluconeogenesis-Mitochondrial Interaction Between Tibetan Sheep and Hu Sheep in the Qinghai-Tibet Plateau.

As high-quality sheep germplasm resources in China, Hu sheep are characterized by fast growth and development, high fecundity, and tolerance to drought and cold. Tibetan sheep, adapted to high-altitude environments, have developed strong environmental adaptability. To explore the differences in the interaction among rumen microbial flora, hepatic gluconeogenesis, and mitochondrial function between Tibetan sheep and Hu sheep in the Qinghai-Tibet Plateau, this study systematically compared and analyzed the rumen flora density, key enzyme activities related to hepatic gluconeogenesis and mitochondrial function, and the expression levels of related genes in Tibetan sheep and Hu sheep under identical feeding management conditions, followed by correlation analysis. The results showed that Hu sheep had significantly higher densities of Ruminobacteramylophilus (Ram) and Fibrobacter succinogenes (Fs) associated with starch and protein degradation (p < 0.01). The expression levels of Forkhead box O1 (FOXO1), pyruvate carboxylase (PC) activity, and adenosine triphosphate (ATP) content were also significantly higher than those in Tibetan sheep (p < 0.01). In contrast, Tibetan sheep had higher densities of Butyrivibrio fibrisolvens (Bf), Ruminococcus albus (Ra), Ruminococcus flavefaciens (Rf), etc., related to cellulose degradation (p < 0.01). The gluconeogenesis-related genes, Glucose-6-phosphatase catalytic subunit 1 (G6PC1) and phosphoenolpyruvate carboxykinase1 (PCK1), and the activities of phosphoenolpyruvate carboxykinase (PEPCK) and fructose-1,6-bisphosphatase (FBPase) were significantly higher in Tibetan sheep than in Hu sheep (p < 0.01). Mitochondrial function-related genes Mitofusin-1 (Mfn1), Mitofusin-2 (Mfn2), subunit 6 of ATP synthase (ATP6), cytochrome b (Cytb), etc., also showed significantly higher expression in Tibetan sheep (p < 0.01). While no significant differences were observed in the contents of citric acid (CA), pyruvic acid (PA), glucose (Glu), etc. (p > 0.05). Correlation analysis indicated that rumen flora was associated with the key enzyme activities and gene expressions of hepatic gluconeogenesis and mitochondrial function to varying degrees. In summary, Tibetan sheep exhibit strong fiber degradation capacity, the efficient utilization of gluconeogenic intermediates, and mitochondrial oxidative phosphorylation (OXPHOS) ability, forming adaptive strategies for high-altitude environments. By contrast, Hu sheep show efficient protein and starch degradation capacity, thereby enhancing the supply of gluconeogenic precursors. It is indicated that when introducing Hu sheep to high-altitude areas, dietary intervention can be used to regulate rumen microorganisms, such as increasing fiber-decomposing bacteria or enhancing mitochondrial oxidative capacity, to counteract metabolic limitations induced by hypoxia.

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来源期刊
Animals
Animals Agricultural and Biological Sciences-Animal Science and Zoology
CiteScore
4.90
自引率
16.70%
发文量
3015
审稿时长
20.52 days
期刊介绍: Animals (ISSN 2076-2615) is an international and interdisciplinary scholarly open access journal. It publishes original research articles, reviews, communications, and short notes that are relevant to any field of study that involves animals, including zoology, ethnozoology, animal science, animal ethics and animal welfare. However, preference will be given to those articles that provide an understanding of animals within a larger context (i.e., the animals'' interactions with the outside world, including humans). There is no restriction on the length of the papers. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible. Full experimental details and/or method of study, must be provided for research articles. Articles submitted that involve subjecting animals to unnecessary pain or suffering will not be accepted, and all articles must be submitted with the necessary ethical approval (please refer to the Ethical Guidelines for more information).
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