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ARS Home » Plains Area » Clay Center, Nebraska » U.S. Meat Animal Research Center » Livestock Bio-Systems » Research » Publications at this Location » Publication #391367

Research Project: Improving Livestock Production by Developing Reproductive and Precision Management Technologies

Location: Livestock Bio-Systems

Title: Proteomic analysis of epididymal and ejaculated sperm and respective fluids

Author
item MENEGATTI ZOCA, SAULO - South Dakota State University
item NORTHROP-ALBRECHT, EMMALEE - South Dakota State University
item WALKER, JULIE - South Dakota State University
item Cushman, Robert - Bob
item PERRY, GEORGE - Texas A&M University

Submitted to: Extension Reports
Publication Type: Experiment Station
Publication Acceptance Date: 2/1/2022
Publication Date: 2/5/2022
Citation: Menegatti Zoca, S., Northrop-Albrecht, E.J., Walker, J.A., Cushman, R.A., Perry, G.A. 2022. Proteomic analysis of epididymal and ejaculated sperm and respective fluids. South Dakota State University Beef Day 2022 Summary Publication. 86-99.

Interpretive Summary:

Technical Abstract: Ejaculated and epididymal semen was collected from mature Angus bulls (n = 9), and then centrifuged to separate sperm and fluid. Fluids were collected and sperm pellets were resuspended in a high ionic solution and vortexed to remove loosely attached proteins. Sperm samples were centrifuged, and the supernatant was collected. Samples collected for protein analysis were snap frozen in liquid nitrogen and stored at -80 ºC. Protein analysis was performed by liquid chromatography with tandem mass spectrometry (LCMS/MS). Yearling Angus cross bulls (n = 40) were used for sperm cultures. Ejaculated (n = 20) and epididymal (n = 20) sperm were collected, diluted and cultured in a commercial media at pH 5.8, 6.8 and 7.3, at 4 ºC and evaluated for motility and viability every 24 h until motility was below 20%. There was an effect of pH, time and pH by time interaction for motility and viability for both ejaculated and epididymal sperm (P = 0.05). At 216 h of incubation epididymal sperm at pH 7.3 and ejaculated sperm at pH 6.8 dropped below 20% motility. Overall, in all samples, a total of 458 unique proteins were identified. It was identified that ejaculated fluid and ejaculated sperm had 178 and 298 proteins, respectively. Also, it was identified that epididymal fluid and epididymal sperm had 311 and 344 proteins, respectively. There were Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways significantly enriched (FDR < 0.05) for ejaculated fluid (n = 8), epididymal fluid (n = 24), ejaculated sperm (n = 10), and epididymal sperm (n = 18). The most important KEGG pathway identified was the metabolic pathway. Within the metabolic pathway the glycolysis/gluconeogenesis, pentose phosphate, and glutathione metabolism pathways were significantly enriched among proteins only present in epididymal samples. Other proteins identified that may be related to epididymal sperm’s increased longevity were peroxidases and glutathione peroxidases for their antioxidant properties.