College of Animal Science and Technology, Gansu Agricultural University, Lanzhou 730000, P. R. China.
College of Pastoral Agriculture Science and Technology, Lanzhou University, Lanzhou 730000, P. R. China.
Sci Rep. 2016 Aug 31;6:32479. doi: 10.1038/srep32479.
Early consumption of starter feed promotes rumen development in lambs. We examined rumen development in lambs fed starter feed for 5 weeks using histological and biochemical analyses and by performing high-throughput sequencing in rumen tissues. Additionally, rumen contents of starter feed-fed lambs were compared to those of breast milk-fed controls. Our physiological and biochemical findings revealed that early starter consumption facilitated rumen development, changed the pattern of ruminal fermentation, and increased the amylase and carboxymethylcellulase activities of rumen micro-organisms. RNA-seq analysis revealed 225 differentially expressed genes between the rumens of breast milk- and starter feed-fed lambs. These DEGs were involved in many metabolic pathways, particularly lipid and carbohydrate metabolism, and included HMGCL and HMGCS2. Sequencing analysis of 16S rRNA genes revealed that ruminal bacterial communities were more diverse in breast milk-than in starter feed-fed lambs, and each group had a distinct microbiota. We conclude that early starter feeding is beneficial to rumen development and physiological function in lambs. The underlying mechanism may involve the stimulation of ruminal ketogenesis and butanoate metabolism via HMGCL and HMGCS2 combined with changes in the fermentation type induced by ruminal microbiota. Overall, this study provides insights into the molecular mechanisms of rumen development in sheep.
早期食用开食料可促进羔羊瘤胃发育。我们通过组织学和生化分析以及对瘤胃组织进行高通量测序,研究了 5 周龄羔羊食用开食料的瘤胃发育情况。此外,还比较了开食料喂养羔羊的瘤胃液与母乳喂养对照的瘤胃液。我们的生理生化发现,早期食用开食料促进了瘤胃发育,改变了瘤胃发酵模式,增加了瘤胃微生物的淀粉酶和羧甲基纤维素酶活性。RNA-seq 分析显示,母乳和开食料喂养羔羊的瘤胃中有 225 个差异表达基因。这些差异表达基因参与了许多代谢途径,特别是脂质和碳水化合物代谢,包括 HMGCL 和 HMGCS2。16S rRNA 基因测序分析表明,母乳喂养的羔羊瘤胃细菌群落比开食料喂养的羔羊更为多样,每个群体都有独特的微生物群。我们得出结论,早期食用开食料有利于羔羊瘤胃发育和生理功能。其潜在机制可能涉及通过 HMGCL 和 HMGCS2 刺激瘤胃酮体生成和丁酸盐代谢,同时结合瘤胃微生物引起的发酵类型变化。总的来说,本研究为绵羊瘤胃发育的分子机制提供了新见解。