Although seminal plasma extracellular vesicles (SPEVs)
play important
roles in sperm function, little is known about their metabolite compositions
and roles in sperm motility. Here, we performed metabolomics and proteomics
analysis of boar SPEVs with high or low sperm motility to investigate
specific biomarkers affecting sperm motility. In total, 140 proteins
and 32 metabolites were obtained through differentially expressed
analysis and weighted gene coexpression network analysis (WGCNA).
Seven differentially expressed proteins (DEPs) (ADIRF, EPS8L1, PRCP,
CD81, PTPRD, CSK, LOC100736569) and six differentially expressed metabolites
(DEMs) (adenosine, beclomethasone, 1,2-benzenedicarboxylic acid, urea,
1-methyl-l-histidine, and palmitic acid) were also identified
in WGCNA significant modules. Joint pathway analysis revealed that
three DEPs (GART, ADCY7, and NTPCR) and two DEMs (urea and adenosine)
were involved in purine metabolism. Our results suggested that there
was significant correlation between proteins and metabolites, such
as IL4I1 and urea (r = 0.86). Furthermore, we detected
the expression level of GART, ADCY7, and CDC42 in sperm of two groups,
which further verified the experimental results. This study revealed
that several proteins and metabolites in SPEVs play important roles
in sperm motility. Our results offered new insights into the complex
mechanism of sperm motility and identified potential biomarkers for
male reproductive diseases.