Quality and freezing qualities of first and second ejaculates collected from endangered Gulf Coast Native rams

被引:17
作者
Nel-Themaat, L.
Harding, G. D.
Chandler, J. E.
Chenevert, J. F.
Damiani, P.
Fernandez, J. M.
Humes, P. E.
Pope, C. E.
Godke, R. A.
机构
[1] Louisiana State Univ, Dept Anim Sci, Ctr Agr, Baton Rouge, LA 70803 USA
[2] Louisiana State Univ, Ctr Agr, Dept Dairy Sci, Baton Rouge, LA 70803 USA
[3] Genex Custom Collect Serv, Baton Rouge, LA 70802 USA
[4] Audubon Ctr Res Endangered Species, New Orleans, LA 70131 USA
关键词
sheep-spennatozoa; electro-ejaculation; freezing; progressive motility; Gulf Coast Native Sheep;
D O I
10.1016/j.anireprosci.2005.09.014
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
The Gulf Coast Native sheep, or Louisiana Native sheep, is an endangered previously feral domestic sheep population of European origin that has been under natural selection pressure for reproductive survival in their transplanted range while roaming in the southern Gulf Coast Region of the United States. This sheep population has an increased natural resistance to internal parasites, breeds year-around and has a greater percentage of live lambs as compared with other breeds of sheep raised in similar environments. To preserve the genetic diversity of this important feral sheep population, semen was collected by electro-ejaculation and subjected to cryopreservation for subsequent storage in a genome resource bank. Unrelated rams (n = 5) were collected 3 days-a-week, allowing at least 2 days of rest between collections. Two ejaculates were obtained from each ram per collection day, with the second collection conducted 10 min after the first ejaculation. Semen was processed using the standard Salamon cryopreservation procedure in a Tris-yolk-glycerol extender, frozen in 0.5 ml plastic straws using liquid nitrogen (LN2) vapor and stored in LN2. Each ejaculate was evaluated for volume, sperm concentration/ml (x 10(9)/ml), number of spermatozoa/ejacul ate (x 10(9)), sperm progressive motility (%) for pre-cooled semen, cooled semen and semen after thawing. For the five rams, each semen variable for the first ejaculate was compared with that of the second ejaculate collected 10 min later. The mean semen volume, sperm concentration and number of spermatozoa per ejaculate obtained from the first ejaculate were significantly greater (P < 0.01) than those of the second ejaculate (comparisons being 1.62 and 1.06; 3.2 and 1.5; 5.4 and 1.8, respectively). Overall, the mean motility of pre-cooled (22 degrees C), cooled (5 degrees C) and frozen (- 196 degrees C) post-thawed spermatozoa was less (P <= 0.01) in the first ejaculate (71.5, 64.8 and 34.1%, respectively) compared with that of the second ejaculate (75, 72.4 and 44.1%, respectively). Conversely, no differences were detected in loss in the percent progressive motility of sperm from cooled sperm to post-thaw sperm from the first and second ejaculates. In summary, our findings suggest sperm collected during the second ejaculate 10 min after the first ejaculate of rams survives thawing with a greater rate of progressive motility than that of the first ejaculate. The ability to collect two consecutive ejaculates in a short period by electro-ejaculation could be valuable for gamete resource banking and preserving genetic diversity of the Gulf Coast Native sheep. (c) 2005 Published by Elsevier B.V.
引用
收藏
页码:251 / 261
页数:11
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