丁酸钠通过抑制炎症、平衡营养代谢和优化微生物群落功能促进断奶前小牛胃肠道发育

IF 6.3 Animal Nutrition Pub Date : 2023-09-01 DOI:10.1016/j.aninu.2023.04.004
Huiyue Zhong , Wenjing Yu , Min Wang , Bo Lin , Xuezhao Sun , Nan Zheng , Jiaqi Wang , Shengguo Zhao
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引用次数: 2

摘要

丁酸盐能促进小牛的生长和胃肠道发育。但是,它对胃肠道和瘤胃微生物组的信号通路产生影响的机制尚不清楚。本研究旨在揭示喂食高纤维发酵剂的小牛胃肠道上皮和微生物群落对丁酸盐补充的反应的转录组学途径。14头荷斯坦公牛(39.9±3.7 kg,14日龄)分为2组(丁酸钠组,SB;对照组,Ctrl)。SB组补充0.5%的SB。在第51天,屠宰小牛以获得用于分析瘤胃和空肠上皮转录组以及瘤胃微生物宏基因组的样本。补充丁酸钠可提高空肠和瘤胃乳头的平均日增重和发育性能。在瘤胃和空肠上皮中,SB下调与炎症相关的途径,包括NF-κB(PPKCB、CXCL8、CXCL12)、白细胞介素17(IL17A、IL17B、MMP9)和趋化因子(CXCL12、CCL4、CCL8),并上调免疫途径,包括免疫球蛋白A(IgA)产生的肠道免疫网络(CD28)。同时,在空肠上皮中,SB调节与营养代谢相关的途径,包括氮代谢(CA1、CA2、CA3)、酮体的合成和降解(HMGCS2、BDH1、LOC100295719)、脂肪消化和吸收(PLA2G2F、APOA1、APOA4)和PPAR信号通路(FABP4、FABP6、CYP4A11)。宏基因组分析表明,SB显著提高了枯草芽孢杆菌和真杆菌的相对丰度,激活了瘤胃微生物的碳水化合物代谢途径,增加了碳水化合物水解酶的丰度。总之,丁酸盐通过抑制炎症、增强免疫力和能量收集以及激活微生物碳水化合物代谢,对生长和胃肠道发育具有促进作用。这些发现为丁酸盐对小牛营养有益作用背后的潜在机制提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Sodium butyrate promotes gastrointestinal development of preweaning bull calves via inhibiting inflammation, balancing nutrient metabolism, and optimizing microbial community functions

Butyrate promotes the growth and gastrointestinal development of calves. But, the mechanisms behind its effects on signaling pathways of the gastrointestinal tract and rumen microbiome is unclear. This study aimed to reveal transcriptomic pathways of gastrointestinal epithelium and microbial community in response to butyrate supplementation in calves fed a high fiber starter. Fourteen Holstein bull calves (39.9 ± 3.7 kg, 14 d of age) were assigned to 2 groups (sodium butyrate group, SB; control group, Ctrl). The SB group received 0.5% SB supplementation. At d 51, the calves were slaughtered to obtain samples for analysis of the transcriptome of the rumen and jejunum epithelium as well as ruminal microbial metagenome. Sodium butyrate supplementation resulted in a higher performance in average daily gain and development of jejunum and rumen papillae. In both the rumen and jejunum epithelium, SB down-regulated pathways related to inflammation including NF-κB (PPKCB, CXCL8, CXCL12), interleukin-17 (IL17A, IL17B, MMP9), and chemokine (CXCL12, CCL4, CCL8) and up-regulated immune pathways including the intestinal immune network for immunoglobulin A (IgA) production (CD28). Meanwhile, in the jejunum epithelium, SB regulated pathways related to nutritional metabolism including nitrogen metabolism (CA1, CA2, CA3), synthesis and degradation of ketone bodies (HMGCS2, BDH1, LOC100295719), fat digestion and absorption (PLA2G2F, APOA1, APOA4), and the PPAR signaling pathway (FABP4, FABP6, CYP4A11). The metagenome showed that SB greatly increased the relative abundance of Bacillus subtilis and Eubacterium limosum, activated ruminal microbial carbohydrate metabolism pathways and increased the abundance of carbohydrate hydrolysis enzymes. In conclusion, butyrate exhibited promoting effects on growth and gastrointestinal development by inhibiting inflammation, enhancing immunity and energy harvesting, and activating microbial carbohydrate metabolism. These findings provide new insights into the potential mechanisms behind the beneficial effects of butyrate in calf nutrition.

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来源期刊
Animal Nutrition
Animal Nutrition Animal Science and Zoology
CiteScore
9.70
自引率
0.00%
发文量
542
审稿时长
65 days
期刊介绍: Animal Nutrition encompasses the full gamut of animal nutritional sciences and reviews including, but not limited to, fundamental aspects of animal nutrition such as nutritional requirements, metabolic studies, body composition, energetics, immunology, neuroscience, microbiology, genetics and molecular and cell biology related to primarily to the nutrition of farm animals and aquatic species. More applied aspects of animal nutrition, such as the evaluation of novel ingredients, feed additives and feed safety will also be considered but it is expected that such studies will have a strong nutritional focus. Animal Nutrition is indexed in SCIE, PubMed Central, Scopus, DOAJ, etc.
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