4.7 Article

Transcriptome Analysis to Elucidate the Effects of Milk Replacer Feeding Level on Intestinal Function and Development of Early Lambs

Journal

ANIMALS
Volume 13, Issue 11, Pages -

Publisher

MDPI
DOI: 10.3390/ani13111733

Keywords

lambs; intestine; growth performance; transcriptome sequencing

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Although early feeding strategies have an impact on intestinal development, the influence of milk replacer feeding level on intestinal structure and functional development and the underlying regulatory mechanisms are still unclear. In this study, lambs were fed milk replacer at different levels and assessed for growth performance, feed intake, and intestinal functional development. The study identified differentially expressed genes and pathways involved in nutrient metabolism and coagulation cascades. Additionally, intensive milk replacer feeding affected insulin sensitivity, glucose absorption, and lipid and protein degradation in intestinal tissues through the regulation of specific genes.
Although early feeding strategies influence intestinal development, the effects of milk replacer (MR) feeding level on intestinal structure and functional development and underlying regulatory mechanisms remain unclear. In this study, 14 male Hu lambs were fed MR at 2% or 4% of their average body weight and weaned at 35 days of age. The MR was produced by the Institute of Feed Research of the Chinese Academy of Agricultural Sciences, and it contains 96.91% dry matter, 23.22% protein, and 13.20% fat. Jejunal tissues were assessed by RNA-seq for differences in the gene expression of lambs at 49 days of age; regulatory pathways and mechanisms of the effects of early nutrition on intestinal function and development were analyzed, along with growth performance, feed intake, jejunal histomorphology, and digestive enzyme activities. Increasing MR- feeding levels increased dry matter intake and daily gain before weaning, as well as lactase, amylase, lipase, trypsin, and chymotrypsin activities and intestinal villus length and muscular thickness. Overall, 1179 differentially expressed genes were identified, which were enriched in nutrient metabolism, coagulation cascades, and other pathways. Further, intensive MR feeding affected insulin sensitivity to reduce excessive glucose interception by intestinal tissues to ensure adequate absorbed glucose release into the portal circulation and promoted lipid and protein degradation in intestinal tissues to meet the energy demand of intestinal cells by regulating AHSG, IGFBP1, MGAT2, ITIH, and CYP2E1 expression.

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