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

• Published in: Animal reproduction science 2006-10, Vol.95 (3), p.251-261
• Main Authors: 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.
• Format: Article
• Language: English
• Subjects: animal genetic resources; Animals; Conservation of Natural Resources; cryopreservation; Cryopreservation - veterinary; Ejaculation; Electric Stimulation; Electro-ejaculation; fecundity; Freezing; freezing quality; Gulf Coast Native sheep; Hot Temperature; lambs; Louisiana; Male; natural selection; pest resistance; Progressive motility; rams; rare breeds; semen; Semen - physiology; Semen Preservation - veterinary; Sheep - physiology; sheep breeds; Sheep-spermatozoa; Sperm Count; Sperm Motility; spermatozoa; Spermatozoa - abnormalities; Time Factors; volume
• ISSN: 0378-4320; 1873-2232
• DOI: 10.1016/j.anireprosci.2005.09.014

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 (LN 2) vapor and stored in LN 2. Each ejaculate was evaluated for volume, sperm concentration/ml (×10 9/ml), number of spermatozoa/ejaculate (×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 °C), cooled (5 °C) and frozen (−196 °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-