Impact of Lysine to Methionine Ratios on Antioxidant Capacity and Immune Function in the Rumen of Tibetan Sheep: An RNA-Seq Analysis.

IF 1.8 3区 农林科学 Q2 VETERINARY SCIENCES
Fengshuo Zhang, Quyangangmao Su, Zhanhong Gao, Zhenling Wu, Qiurong Ji, Tingli He, Kaina Zhu, Xuan Chen, Yu Zhang, Shengzhen Hou, Linsheng Gui
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引用次数: 0

Abstract

With global protein prices on the rise, lowering protein levels in animal feed, together with balancing diet composition and reducing nitrogen emissions, can both reduce the environmental impact of agriculture and save on feed costs. However, the formulation of an ideal amino acid (AA) composition is crucial for better protein utilization by livestock. This study aimed to investigate the effects of different lysine to methionine ratios on the antioxidant capacity and immune function of the rumen in Tibetan sheep. Ninety male Tibetan sheep, weaned at 2 months of age, were randomly divided into three groups (1:1, 2:1 and 3:1 lysine ratios) and subjected to a 100-day feeding trial. RNA sequencing (RNA-seq) was utilized to analyse the impact of different AA ratios on gene expression in rumen tissue, whereas the levels of antioxidant enzymes (total antioxidant capacity [T-AOC], superoxide dismutase [SOD], glutathione peroxidase [GSH-Px] and catalase [CAT]) and immunoglobulins (immunoglobulin A [IgA], immunoglobulin G [IgG] and immunoglobulin M [IgM]) were evaluated. The results indicated that the 1:1 group significantly upregulated the expression of PTGS2, PLA2G12A and PLA2G4 genes, enhancing antioxidant enzyme activity, reducing free radical production and modulating systemic immune responses. COL16A1 and KCNK5 were highly expressed in the protein digestion and absorption pathway, maintaining the structural integrity and function of the rumen epithelium. BMP4 and TGFBR2 were significantly enriched in the cytokine-cytokine receptor interaction pathway and positively correlated with CAT and T-AOC. ITGA8 was upregulated in the 1:1 group, participating in the regulation of various cellular signalling pathways. ATP2B1 was enriched in the cyclic guanosine monophosphate (cGMP)- protein kinase G (PKG) signalling and mineral absorption pathways, primarily influencing oxidative stress and immune responses by regulating intracellular calcium ion concentration. This study demonstrates that a 1:1 lysine to methionine ratio is most beneficial for enhancing the antioxidant capacity and immune function of the rumen in Tibetan sheep.

赖氨酸/蛋氨酸比例对藏羊瘤胃抗氧化能力和免疫功能影响的RNA-Seq分析
随着全球蛋白质价格的上涨,降低动物饲料中的蛋白质水平,同时平衡日粮成分和减少氮排放,既可以减少农业对环境的影响,又可以节省饲料成本。然而,理想氨基酸(AA)组成的配方对于牲畜更好地利用蛋白质至关重要。本试验旨在研究不同赖氨酸/蛋氨酸比例对藏羊瘤胃抗氧化能力和免疫功能的影响。选取2月龄断奶的公藏羊90只,随机分为赖氨酸比例为1:1、2:1和3:1的3组,进行100 d饲养试验。采用RNA测序(RNA-seq)技术分析不同AA比例对瘤胃组织基因表达的影响,同时测定抗氧化酶(总抗氧化能力[T-AOC]、超氧化物歧化酶[SOD]、谷胱甘肽过氧化物酶[GSH-Px]和过氧化氢酶[CAT])和免疫球蛋白(免疫球蛋白A [IgA]、免疫球蛋白G [IgG]和免疫球蛋白M [IgM])水平。结果表明,1:1组显著上调PTGS2、PLA2G12A和PLA2G4基因的表达,增强抗氧化酶活性,减少自由基产生,调节全身免疫反应。COL16A1和KCNK5在蛋白质消化吸收途径中高表达,维持了瘤胃上皮的结构完整性和功能。BMP4和TGFBR2在细胞因子-细胞因子受体相互作用通路中显著富集,且与CAT和T-AOC呈正相关。ITGA8在1:1组上调,参与多种细胞信号通路的调控。ATP2B1富集于环鸟苷单磷酸(cGMP)-蛋白激酶G (PKG)信号通路和矿物质吸收途径,主要通过调节细胞内钙离子浓度影响氧化应激和免疫反应。由此可见,以1:1的赖氨酸/蛋氨酸比例最有利于提高藏羊瘤胃的抗氧化能力和免疫功能。
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来源期刊
Veterinary Medicine and Science
Veterinary Medicine and Science Veterinary-General Veterinary
CiteScore
3.00
自引率
0.00%
发文量
296
期刊介绍: Veterinary Medicine and Science is the peer-reviewed journal for rapid dissemination of research in all areas of veterinary medicine and science. The journal aims to serve the research community by providing a vehicle for authors wishing to publish interesting and high quality work in both fundamental and clinical veterinary medicine and science. Veterinary Medicine and Science publishes original research articles, systematic reviews, meta-analyses, and research methods papers, along with invited editorials and commentaries. Original research papers must report well-conducted research with conclusions supported by the data presented in the paper. We aim to be a truly global forum for high-quality research in veterinary medicine and science, and believe that the best research should be published and made widely accessible as quickly as possible. Veterinary Medicine and Science publishes papers submitted directly to the journal and those referred from a select group of prestigious journals published by Wiley-Blackwell. Veterinary Medicine and Science is a Wiley Open Access journal, one of a new series of peer-reviewed titles publishing quality research with speed and efficiency. For further information visit the Wiley Open Access website.
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