| Autor: |
Pralle RS; Department of Animal and Dairy Sciences, University of Wisconsin-Madison, Madison, WI 53706, USA.; School of Agriculture, University of Wisconsin-Platteville, Platteville, WI 53818, USA., Li W; Dairy Forage Research Center, USDA-Agricultural Research Service, Madison, WI 53706, USA., Murphy BN; Dairy Forage Research Center, USDA-Agricultural Research Service, Madison, WI 53706, USA., Holdorf HT; Department of Animal and Dairy Sciences, University of Wisconsin-Madison, Madison, WI 53706, USA., White HM; Department of Animal and Dairy Sciences, University of Wisconsin-Madison, Madison, WI 53706, USA. |
| Abstrakt: |
Lipid-related metabolic disorders (LRMD) are prevalent in early lactation dairy cows, and have detrimental effects on productivity and health. Our objectives were to identify cows resistant or susceptible to LRMD using a ketosis induction protocol (KIP) to discover differentially expressed liver genes and metabolic pathways associated with disposition. Clustering cows based on postpartum lipid metabolite concentrations within dietary treatments identified cows more or less susceptible (MS vs. LS) to LRMD within the control treatment, and more or less resistant (MR vs. LR) within the KIP treatment. Whole-transcriptome RNA sequencing was performed on liver samples (-28, +1, and +14 days relative to calving) to assess differential gene and pathway expression (LS vs. MS; MR vs. LR; n = 3 cows per cluster). Cows within the MS and LR clusters had evidence of greater blood serum β-hydroxybutyrate concentration and liver triglyceride content than the LS and MR clusters, respectively. The inferred metabolism of differentially expressed genes suggested a role of immune response (i.e., interferon-inducible proteins and major histocompatibility complex molecules). Additionally, unique roles for glutathione metabolism and eicosanoid metabolism in modulating susceptibility and resistance, respectively, were implicated. Overall, this research provides novel insight into the role of immunometabolism in LRMD pathology, and suggests the potential for unique control points for LRMD progression and severity. |
