Instituto de Ganadería de Montaña (CSIC-Universidad de León), Finca Marzanas, Grulleros, León, Spain.
Institute of Zootechnics, Università Cattolica del Sacro Cuore, Via Emilia Parmense, Piacenza, Italy.
J Anim Sci. 2018 Apr 14;96(4):1495-1507. doi: 10.1093/jas/sky029.
The increasing world population is driving demand for improved efficiency of feed resources of livestock. However, the molecular mechanisms behind various feed efficiency traits and their regulation by nutrition remain poorly understood. Here, we aimed to identify differentially expressed (DE) genes in the liver tissues of fattening Merino lambs and differences in metabolites accumulated in plasma to identify modified metabolic pathways as a consequence of milk restriction during the suckling period. Twenty-four male Merino lambs (4.81 ± 0.256 kg) were divided into 2 groups (n = 12 per dietary treatment). The first group (ad libitum, ADL) was kept permanently with the dams, whereas the other group (restricted, RES) was milk restricted. When they reached 15 kg of live body weight (LBW), all the animals were offered the same complete pelleted diet at the same level (35 g DM/kg LBW per day) to ensure no differences in dry matter intake. All the lambs were harvested when they reached 27 kg of LBW. For transcriptomic analysis, 4 liver samples from each group (8 samples in total) were selected for RNA sequencing (RNA-seq), and plasma samples from all animals (24 samples in total) were used to perform a nontargeted metabolomic analysis on a hybrid quadrupole-time-of-flight mass spectrometer coupled to an ultra-high performance liquid chromatographic system (UHPLC/QTOF-MS). Thirty-eight DE annotated genes were identified by RNA-seq, with 23 DE genes being down-regulated and 15 up-regulated in the liver of RES lambs relative to the ADL group (P < 0.10). Also, the metabolomic assay identified 38 differentially accumulated compounds (P < 0.10). In general, those genes and pathways involved in protein synthesis or protease inhibitors were down-regulated in the RES group, whereas those related to proteolytic degradation were up-regulated, thus suggesting a higher catabolism of proteins in these lambs. RES lambs showed over-expression of xenobiotic metabolism pathways, whereas those genes related to β-oxidation of fatty acids were down-regulated. According to the data obtained, early feed restriction during the suckling period of Merino lambs promoted long-term effects on both the hepatic transcriptomic profile and plasma metabolic profile, which might have modified fatty acids metabolism, catabolism of proteins, and detoxification of xenobiotics, thus reducing feed efficiency during the fattening period.
世界人口的增长推动了提高家畜饲料资源效率的需求。然而,各种饲料效率性状的分子机制及其受营养调节的机制仍知之甚少。在这里,我们旨在鉴定育肥美利奴羔羊肝脏组织中差异表达(DE)的基因,并鉴定血浆中积累的代谢物的差异,以鉴定由于哺乳期限制而导致的代谢途径的改变。24 只雄性美利奴羔羊(4.81 ± 0.256kg)分为 2 组(每组 12 只,每只日粮处理)。第一组(自由采食,ADL)与母羊永久保持在一起,而另一组(限制采食,RES)则限制采食。当它们达到 15kg 活体体重(LBW)时,所有动物都以相同的完全颗粒日粮以相同的水平(每天 35gDM/kgLBW)提供,以确保干物质摄入量没有差异。当所有羔羊达到 27kgLBW 时,所有羔羊都被收获。为了进行转录组分析,从每组中选择 4 个肝脏样本(每组 8 个样本,共 8 个样本)进行 RNA 测序(RNA-seq),并对所有动物的血浆样本(共 24 个样本)进行非靶向代谢组分析,使用混合四极杆-飞行时间质谱仪与超高效液相色谱系统(UHPLC/QTOF-MS)耦合。RNA-seq 鉴定了 38 个差异表达的注释基因,其中 RES 羔羊肝脏中 23 个基因下调,15 个基因上调(P<0.10)。此外,代谢组学分析鉴定了 38 种差异积累的化合物(P<0.10)。一般来说,RES 组中参与蛋白质合成或蛋白酶抑制剂的基因和途径下调,而与蛋白水解降解相关的基因上调,因此表明这些羔羊的蛋白质分解代谢更高。RES 羔羊表现出对外源代谢途径的过度表达,而与脂肪酸β-氧化相关的基因下调。根据获得的数据,早期哺乳期限制对美利奴羔羊的肝转录组谱和血浆代谢谱都产生了长期影响,这可能改变了脂肪酸代谢、蛋白质分解代谢和外源化合物的解毒,从而降低了育肥期的饲料效率。