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Recovery and Cryopreservation of Epididymal Sperm of Plains Bison ( Bison bison bison ) as a Model for Salvaging the Genetics of Wood Bison ( Bison bison athabascae )
Author(s) -
Aurini LC,
Whiteside DP,
Elkin BT,
Thundathil JC
Publication year - 2009
Publication title -
reproduction in domestic animals
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.546
H-Index - 66
eISSN - 1439-0531
pISSN - 0936-6768
DOI - 10.1111/j.1439-0531.2008.01087.x
Subject(s) - sperm , andrology , biology , semen , cryopreservation , acrosome , epididymis , bison bison , zoology , anatomy , botany , embryo , ecology , genetics , medicine
Contents The objective of this study was to optimize recovery and cryopreservation of epididymal sperm from plains bison, as a model for wood bison. In Phase 1, cauda epididymides were recovered from bison (n = 14) immediately after slaughter, minced and incubated in Sp‐TALPH buffer for 3 h at 36°C. The resulting sperm suspensions were cryopreserved in Triladyl ® , using a protocol for bovine semen. In Phase 2, epididymal sperm were cryopreserved in either Triladyl ® or Andromed ® . The mean (±SD) estimated number of sperm recovered was 468 ± 207 × 10 6 . There was an increase (p < 0.05) in the proportion of sperm with normal morphology between initial recovery and after extension (52.4 ± 4.6 vs 69.7 ± 2.4%), with a concurrent decrease (p < 0.05) in the proportion of sperm with distal droplets. Median values for progressively motile sperm in post‐thaw samples (60%) were lower (p < 0.05) than that after extension or after chilling (70% for both). The mean percentages of viable sperm and of sperm with an intact acrosome were lower (p < 0.05) for frozen‐thawed samples (38.7 ± 2.8 and 85.2 ± 1.1) compared with extended (66.2 ± 2.2 and 92.4 ± 0.9) or chilled (63.7 ± 2.5 and 90.0 ± 1.0) samples. Rates of cleavage, morulae and blastocyst production were not significantly different for chilled (70.9, 38.7 and 8.0%) vs post‐thaw sperm (73.0, 46.0 and 6.3%). There was no significant difference between extenders for most sperm characteristics. In conclusion, we developed a functional protocol for the recovery and cryopreservation of epididymal sperm from plains bison, which may have implications for the genetic preservation of wood bison.

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