Daigneault B W, McNamara K A, Purdy P H, Krisher R L, Knox R V, Rodriguez-Zas S L, Miller D J
Department of Animal Sciences, University of Illinois, Urbana-Champaign, IL, USA.
USDA-ARS-NCGRP-NAGP, Fort Collins, CO, USA.
Andrology. 2015 May;3(3):558-68. doi: 10.1111/andr.12035. Epub 2015 Apr 24.
Due to reduced fertility, cryopreserved semen is seldom used for commercial porcine artificial insemination (AI). Predicting the fertility of individual frozen ejaculates for selection of higher quality semen prior to AI would increase overall success. Our objective was to test novel and traditional laboratory analyses to identify characteristics of cryopreserved spermatozoa that are related to boar fertility. Traditional post-thaw analyses of motility, viability, and acrosome integrity were performed on each ejaculate. In vitro fertilization, cleavage, and blastocyst development were also determined. Finally, spermatozoa-oviduct binding and competitive zona-binding assays were applied to assess sperm adhesion to these two matrices. Fertility of the same ejaculates subjected to laboratory assays was determined for each boar by multi-sire AI and defined as (i) the mean percentage of the litter sired and (ii) the mean number of piglets sired in each litter. Means of each laboratory evaluation were calculated for each boar and those values were applied to multiple linear regression analyses to determine which sperm traits could collectively estimate fertility in the simplest model. The regression model to predict the percent of litter sired by each boar was highly effective (p < 0.001, r(2) = 0.87) and included five traits; acrosome-compromised spermatozoa, percent live spermatozoa (0 and 60 min post-thaw), percent total motility, and the number of zona-bound spermatozoa. A second model to predict the number of piglets sired by boar was also effective (p < 0.05, r(2) = 0.57). These models indicate that the fertility of cryopreserved boar spermatozoa can be predicted effectively by including traditional and novel laboratory assays that consider functions of spermatozoa.
由于生育力降低,冷冻保存的精液很少用于商业猪人工授精(AI)。在人工授精前预测单个冷冻射精的生育力以选择更高质量的精液将提高总体成功率。我们的目标是测试新颖和传统的实验室分析方法,以确定与公猪生育力相关的冷冻精子特征。对每个射精进行传统的解冻后活力、生存力和顶体完整性分析。还测定了体外受精、卵裂和囊胚发育情况。最后,应用精子-输卵管结合和竞争性透明带结合试验来评估精子与这两种基质的粘附情况。通过多父本人工授精确定每头公猪接受实验室检测的相同射精的生育力,并定义为(i)所产仔猪的平均百分比和(ii)每窝所产仔猪的平均数量。计算每头公猪每项实验室评估的平均值,并将这些值应用于多元线性回归分析,以确定在最简单的模型中哪些精子特征可以共同估计生育力。预测每头公猪所产仔猪百分比的回归模型非常有效(p < 0.001,r(2) = 0.87),包括五个特征;顶体受损精子、活精子百分比(解冻后0和60分钟)、总活力百分比和与透明带结合的精子数量。预测公猪所产仔猪数量的第二个模型也有效(p < 0.05,r(2) = 0.57)。这些模型表明,通过纳入考虑精子功能的传统和新颖实验室检测方法,可以有效地预测冷冻公猪精子的生育力。