Effects of early lactation body condition loss in dairy cows on serum lipid profiles and on oocyte and cumulus cell transcriptomes

• Published in: Journal of dairy science Vol. 105; no. 10; pp. 8470 - 8484
• Main Authors: Ruebel, Meghan L, Martins, Lilian Rigatto, Schall, Peter Z, Pursley, J Richard, Latham, Keith E
• Format: Journal Article
• Language: English
• Published: United States Elsevier 01.10.2022
• Subjects: 3-Hydroxybutyric Acid; Animals; body condition loss; Calcium - metabolism; Cattle; Cumulus Cells - metabolism; Diet - veterinary; Fatty Acids - metabolism; Fatty Acids, Nonesterified; Female; Insulins; Lactation - physiology; lipid metabolism; Milk - metabolism; mitochondrial activity; oocyte transcriptome; Oocytes; Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha; Postpartum Period - metabolism; Pregnancy; Reactive Oxygen Species - metabolism; Receptor, Fibroblast Growth Factor, Type 4 - metabolism; Transcriptome; body condition loss; oocyte transcriptome; lipid metabolism; mitochondrial activity
• ISSN: 0022-0302; 1525-3198
• DOI: 10.3168/jds.2022-21919

The objective of this study was to determine the effect of early lactation body condition (BC) loss in multiparous dairy cows on serum lipids and the effect of these changes on oocyte and cumulus cell transcriptomes. Body condition loss in dairy cattle after parturition is associated with reduced fertility and increased pregnancy loss. The complex interplay between BC, nutrition, dry matter intake, milk production, and time of calving has presented a barrier to understanding mechanisms leading to reduced fertility. We identified cows that lost BC (L group; n = 10) or maintained or gained BC (M/G group; n = 8) during the first 27 to 33 d in milk and investigated changes in serum fatty acids and oocyte and cumulus cell transcriptomes at 75 to 81 d in milk. The L group had increased serum levels of nonesterified fatty acids and mead acid, and reduced serum levels of petroselaidic acid and behenic acid. Transcriptome analyses revealed 38 differentially expressed genes (DEG) in oocytes and 71 DEG in cumulus cells of L (n = 3) compared with M/G group (n = 3). Network analysis connected serum fatty acid changes to downstream effects including reduced inflammatory response and mitochondrial membrane depolarization, increased production of reactive oxygen species, and functions related to fatty acid metabolism and cytoplasmic organization in oocytes. These effects were associated with predicted effects on signaling in oocytes through calcium, insulin, O-GlcNAcase (OGA), fibroblast growth factor receptor 4 (FGF4R), peroxisome proliferator activated receptor gamma coactivator 1 α (PPARGC1A), and phospholipase D2 (PLD2) pathways, with a connection to the cumulus cell via calcium signaling. These results connect BC loss following parturition to changes in serum lipid levels, and changes potentially affecting oocyte quality; thus, these results provide new insight into mechanism of reduced fertility.