Ausejo-Marcos Raquel, Tejedor María Teresa, Miguel-Jiménez Sara, Gómez-Giménez Belén, Soriano-Úbeda Cristina, Mendoza Noelia, Vicente-Carrillo Alejandro, Hurtado William Fernando, Ávila Holguín Celia, Moreno Bernardino, Falceto María Victoria
Department of Biotechnology R&D, Magapor S.L., 50600 Ejea de los Caballeros, Spain.
Department of Anatomy, Embryology and Genetics, Centro de Investigación Biomédica en Red: Enfermedades Cardiovasculares, Faculty of Veterinary Medicine, University of Zaragoza, 50013 Zaragoza, Spain.
Vet Sci. 2024 Sep 9;11(9):420. doi: 10.3390/vetsci11090420.
Boar semen analysis includes sperm motility, concentration, morphology and other more complex analyses such as membrane integrity, DNA damage and seminal plasma components. This study aims to summarize these numerous data by linear combinations of them, to classify ejaculates in several categories (clusters) and to investigate the potential differences among clusters on fertility and prolificacy. Young Pietrain boars (23 ± 3.6 months) were investigated: ten boars from the Nucléus genetic line (group 1: 90 ejaculates weekly) and five boars from the Batallé genetic line (group 2: 30 ejaculates weekly). Computer-assisted semen analysis (CASA) examined motility. Sperm viability, acrosome reaction, early apoptosis, mitochondrial activity and DNA damage were studied by flow cytometry analysis. SPSS v.26 software was used to perform principal component analysis (PCA) and clustering. Three principal components (PC1: speed; PC2: linear path; PC3: DNA damage) were detected and four clusters identified in both groups. Clusters also differed significantly in several variables not included in these PCs (group 1: beat cross frequency and poly (ADP-ribose) polymerase; group 2: cathepsin B, abnormal forms, mitochondrial activity and high DNA stainability). PCA and clustering achieved adequate description of these ejaculates, but no differences among clusters were found for fertility or prolificacy, probably because the minimum sperm requirements had been met.
公猪精液分析包括精子活力、浓度、形态以及其他更复杂的分析,如膜完整性、DNA损伤和精浆成分。本研究旨在通过对这些众多数据进行线性组合来总结它们,将射精分为几类(簇),并研究簇之间在生育力和繁殖力方面的潜在差异。对年轻的皮特兰公猪(23±3.6个月)进行了研究:10头来自核基因系的公猪(第1组:每周90次射精)和5头来自巴塔列基因系的公猪(第2组:每周30次射精)。通过计算机辅助精液分析(CASA)检测活力。通过流式细胞术分析研究精子活力、顶体反应、早期凋亡、线粒体活性和DNA损伤。使用SPSS v.26软件进行主成分分析(PCA)和聚类。在两组中均检测到三个主成分(PC1:速度;PC2:直线轨迹;PC3:DNA损伤)并识别出四个簇。这些簇在这些主成分未包含的几个变量上也存在显著差异(第1组:拍频交叉频率和聚(ADP-核糖)聚合酶;第2组:组织蛋白酶B、异常形态、线粒体活性和高DNA染色性)。主成分分析和聚类对这些射精进行了充分的描述,但未发现簇之间在生育力或繁殖力方面存在差异,可能是因为已满足最低精子要求。