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RESEARCH ARTICLE

202 Proteomic, metabolomic and fatty acid composition in lactating and non-lactating mares’ uterine fluids

E. Derisoud A , A. Hankele B , L. Jouneau A , C. Dubois C , D. Rousseau-Ralliard A , M. Dahirel A , L. Wimel C , S. Ulbrich B and P. Chavatte-Palmer A
+ Author Affiliations
- Author Affiliations

A UMR BDR, INRA, ENVA, Université Paris Saclay, Jouy en Josas, France;

B Animal Physiology, Institute of Agricultural Sciences, ETH Zürich, Zürich, Switzerland;

C IFCE, Station Experimentale de la Valade, Chamberet, France

Reproduction, Fertility and Development 32(2) 229-230 https://doi.org/10.1071/RDv32n2Ab202
Published: 2 December 2019

Abstract

In the equine industry, horse breeders aim to produce one foal per mare per year. Thus, mares are bred while nursing. In high-yielding dairy cattle, concurrent lactation and conception may affect embryo quality, but effects on uterine fluid (UF) quality are unknown. No data are available in horses. The aim of our study was to analyse the effect of nursing on protein, metabolite and fatty acid (FA) compositions of UF at ~7.5 days post-ovulation. Anglo-Arab mares (multiparous (2.7 ± 0.9 foals), 10.8 ± 2.5 years old) that were either nursing (N; 105 ± 12 days of lactation) or barren (B) were inseminated with the semen of the same stallion at induction of ovulation with human chorionic gonadotrophin. Ovulation was confirmed by ultrasound within 48 h. At 7.4 ± 0.7 days post-ovulation, UF was collected with a human tampon that was left for 10 min in the uterus before embryo collection. Only mares for which no embryo was collected were selected (n = 5 in both groups). Trypsin digestion followed by liquid chromatography-tandem mass spectrometry analysis was used for proteomic analysis, with subsequent characterisation with the PANTHER platform using an overrepresentation test (Fisher's exact type with false discovery rate correction) with the PANTHER pathway database. An untargeted approach based on liquid chromatography-tandem mass spectrometry was performed for metabolomics (normalisation to 50 µg of protein), and data were analysed with the MS Peaks to Pathways tool of the MetaboAnalyst platform, using both the GSEA and mummichog algorithms (cut-off = 0.05). Fatty acid composition (% of total FA) was analysed using gas chromatography. Differences between groups were analysed using a linear model with permutation using R software with the pgirmess package (P = 0.05 for significance). Altogether, 2706 proteins with at least two peptides were identified in mares’ UF, with 164 being differentially expressed. Ubiquitin proteasome, involved in embryo-endometrium interactions, was the most enriched pathway in N mares (fold enrichment = 15.12; P < 0.0001). For metabolomics, ubiquinone biosynthesis [MetaFishNet, P = 0.02; NES (Enrichment Score for the variable)/(mean of all Enrichment Score in all permutations in the dataset) = 1.84] was enriched in N mares. N-Glycans, mainly guanosine diphosphate mannose (Kyoto Encyclopedia of Genes and Genomes, P = 0.04; NES = −1.33) and leukotriene biosynthesis (Biocyc; P = 0.006; NES = −1.31), were enriched in B mares with differentially expressed leukotrienes C4/D4. The proportion of saturated FA was higher in N vs. B mares (38.4 ± 3.6% vs. 33.2 ± 3.6%; P = 0.03), probably due to increased palmitic (P = 0.08) and stearic (P = 0.08) acid proportions. In conclusion, pathways involved in uterine receptivity and inflammation seem to be enriched in B mares. Fatty acids that are readily available in the diet were more present in N mares, possibly because more elaborate FA are exported to the mammary gland for milk production. Nursing could thus modify the inflammatory response in the uterine environment at ~7.5 days post-ovulation and could affect reproductive efficiency in horses.