Bond A, Mills K M, Ferreira C R, Harford I, Flack B, Long J A, Diehl K
Department of Animal and Avian Sciences, University of Maryland, College Park, MD, United States.
Agricultural Research Service, Beltsville Agricultural Research Center, United States Department of Agriculture, Beltsville, MD, United States.
Front Physiol. 2024 Nov 15;15:1504557. doi: 10.3389/fphys.2024.1504557. eCollection 2024.
Biomarkers indicative of sperm mobility in broiler breeders would provide the ability to screen for fertility potential, with a positive correlation established between sperm mobility and fertilization potential. This study characterized the lipidome of seminal plasma (SP), sperm cell (SC), and whole semen (WS) isolated from broiler breeder roosters with different sperm mobility phenotypes across key timepoints of the semen production cycle.
WS samples were collected from five high mobility roosters and five low mobility roosters during early, mid, and late semen production, with SP separated from SC by centrifugation. Using multiple reaction monitoring (MRM) profiling, a total of 3241 lipid species were identified in rooster semen across ten lipid classes. Metaboanalyst 6.0 was used to analyze the relative ion intensity for each lipid species due to sperm mobility phenotype through a t-test and due to timepoint through a one-way ANOVA, with lipid ontology enrichment analysis performed using LION. Metaboanalyst 6.0 was also used to perform biomarker analysis for the sperm mobility phenotype in WS samples.
Lipid class total abundance differed with sample type, sperm mobility phenotype, and timepoint. A total of 31, 99, and 112 lipid species were found to be different between low and high mobility males across timepoints in the SP, SC, and WS samples, respectively. Lipid ontology enrichment analysis revealed stark contrasts in lipid-based functions key to sperm survival, storage, and productivity between low and high sperm mobility phenotypes. Through biomarker analysis, 8 lipid species were identified as excellent sperm mobility biomarkers that could be detected in early and mid-semen production.
Timepoint based changes in lipid species were unique to each sperm mobility phenotype, with low sperm mobility roosters exhibiting a larger number of lipid species changes over the semen production cycle in the SP and SC when compared to high sperm mobility roosters. This is the first study to characterize poultry semen lipidome using MRM profiling. The lipid species identified between low and high sperm mobility roosters could be utilized in the poultry industry as potential biomarkers of fertility potential, with the ability to screen for the economical trait of fertility potential early in semen production.
能够指示肉种鸡精子活力的生物标志物将有助于筛选其生育潜力,因为精子活力与受精潜力之间存在正相关关系。本研究对在精液生产周期的关键时间点采集的、具有不同精子活力表型的肉种鸡的精浆(SP)、精子细胞(SC)和全精液(WS)的脂质组进行了表征。
在精液生产的早期、中期和晚期,从五只高活力公鸡和五只低活力公鸡采集WS样本,通过离心将SP与SC分离。使用多反应监测(MRM)分析,在公鸡精液中总共鉴定出属于十个脂质类别的3241种脂质。使用Metaboanalyst 6.0通过t检验分析由于精子活力表型导致的每种脂质的相对离子强度,并通过单因素方差分析分析由于时间点导致的相对离子强度,使用LION进行脂质本体富集分析。还使用Metaboanalyst 6.0对WS样本中的精子活力表型进行生物标志物分析。
脂质类别的总丰度因样本类型、精子活力表型和时间点而异。在SP、SC和WS样本中,分别发现低活力和高活力雄性在不同时间点之间共有31、99和112种脂质存在差异。脂质本体富集分析揭示了低精子活力和高精子活力表型在对精子存活、储存和生产力至关重要的基于脂质的功能方面存在明显差异。通过生物标志物分析,鉴定出8种脂质为优秀的精子活力生物标志物,可在精液生产的早期和中期检测到。
基于时间点的脂质种类变化对于每种精子活力表型都是独特的,与高精子活力公鸡相比,低精子活力公鸡在精液生产周期中SP和SC中的脂质种类变化数量更多。这是第一项使用MRM分析表征家禽精液脂质组的研究。在低精子活力和高精子活力公鸡之间鉴定出的脂质种类可在家禽行业中用作生育潜力的潜在生物标志物,从而能够在精液生产早期筛选出生育潜力这一经济性状。