Kim Yo-Han, Toji Noriyuki, Kizaki Keiichiro, Kushibiki Shiro, Ichijo Toshihiro, Sato Shigeru
United Graduate School of Veterinary Science, Gifu University, Gifu, Japan.
Cooperative Department of Veterinary Medicine, Faculty of Agriculture, Iwate University, Morioka, Iwate, Japan; and.
Physiol Genomics. 2016 Nov 1;48(11):803-809. doi: 10.1152/physiolgenomics.00086.2016. Epub 2016 Sep 23.
We investigated the relationship between ruminal pH and transcriptomic adaptation of the rumen epithelium (RE) of calves fed calf starter with and without forage during the weaning transition. Holstein calves were assigned to groups fed calf starter either with forage (HAY group, n = 3) or without forage (CON group, n = 4). Ruminal pH was measured continuously, and rumen fluid and epithelium were collected 3 wk after weaning. mRNA expression profiles of the RE were examined by one-color microarray. Differentially expressed genes (DEGs) were investigated using the Ingenuity Pathway Analysis (IPA). Mean and maximum ruminal pH were significantly (P < 0.05) higher, and the duration of pH < 5.8 during 1 day was significantly (P < 0.05) shorter, in the HAY group. The proportion of ruminal acetate and the acetate-to-propionate ratio were significantly (P < 0.05) lower in the CON group. DEGs encoding transcription regulators (SREBP1), insulin-like growth factor binding proteins (IGFBP7 and CTGF), ketogenic enzymes (HMGCL, BDH1, and BDH2), and a transporter (SLC16A3) were identified (P < 0.05) between the two groups. A growth factor (TGFB1) and signaling pathway (EGF and EGFR) were activated as upstream regulators. These results suggest that dietary forage alleviates ruminal acidosis, and the decrease in ruminal pH may damage the RE, leading to changes in gene expression to repair the damage. Furthermore, rumen development may be regulated by growth factor (TGFB1) and signaling pathways (EGF and IGFBP) for adaptation to feeding on calf starter with and without forage during the weaning transition.
我们研究了在断奶过渡期,给犊牛饲喂含或不含粗饲料的开食料时,瘤胃pH值与瘤胃上皮(RE)转录组适应性之间的关系。将荷斯坦犊牛分为两组,一组饲喂含粗饲料的开食料(干草组,n = 3),另一组饲喂不含粗饲料的开食料(对照组,n = 4)。连续测量瘤胃pH值,并在断奶后3周收集瘤胃液和瘤胃上皮。通过单色微阵列检测RE的mRNA表达谱。使用 Ingenuity 通路分析(IPA)研究差异表达基因(DEG)。干草组的平均和最大瘤胃pH值显著更高(P < 0.05),且一天中pH < 5.8的持续时间显著更短(P < 0.05)。对照组瘤胃乙酸比例和乙酸与丙酸比值显著更低(P < 0.05)。在两组之间鉴定出编码转录调节因子(SREBP1)、胰岛素样生长因子结合蛋白(IGFBP7和CTGF)、生酮酶(HMGCL、BDH1和BDH2)以及一种转运蛋白(SLC16A3)的DEG(P < 0.05)。一种生长因子(TGFB1)和信号通路(EGF和EGFR)作为上游调节因子被激活。这些结果表明,日粮中的粗饲料可缓解瘤胃酸中毒,瘤胃pH值降低可能会损害RE,导致基因表达发生变化以修复损伤。此外,瘤胃发育可能受生长因子(TGFB1)和信号通路(EGF和IGFBP)调节,以适应断奶过渡期饲喂含或不含粗饲料的开食料。