Fertilization Capacity of Rooster Spermatozoa in Response to the Modification in the Semen Composition
DOI:
https://doi.org/10.3923/ijps.2012.683.688Keywords:
Bacterial plasmid, lipofectin, rooster spermatozoa, semen dilutionAbstract
An experiment was carried out to study the changes in fertilization capacity of rooster sperms in response to the modification in the biochemical composition of the semen. Chickens of two lines (CE2 and CE4) were used. Seven treatments of semen were designed and included the incubation of sperm with the plasmid, with a mixture of the plasmid and lipofectin at 2.5 or 5% concentration and the incubation of spermatozoa with lipofectin and a semen extender (BPSE). The progenies were obtained from the insemination of hens by the semen of different treatments. Sperm motility was greatly influenced by the treatments. Motility was significantly the highest in the control semen and averaged 92.42% and highly significantly declined to 52.08 and 58.75% in the semen samples treated with the plasmid, lipofectin at 2.5 or 5% concentration and diluted with BPSE. The percentage of live sperm was not affected by the addition of the plasmid. The addition of the plasmid and lipofectin or the dilutent BPSE resulted in a significant reduction in the percentage of live sperms. The percentage of live sperms was 59-62% when the plasmid, lipofectin and BPSE were all together added to the semen samples. The percentages of dead and abnormally-shaped sperm reached to 26.88 and 17.13%, respectively, in the semen treated with plasmid, lipofectin 5% and BPSE. Fertility averaged 88.22% in the eggs of hens inseminated with the control semen and significantly decreased to 42.14% when semen was incubated with the plasmid pUC18 and reached to 58.98% when semen was treated with plasmid, lipofectin (5%) and BPSE.
References
Bajpai, P.K. and K.E. Brown, 1964. The effect of different temperatures on the metabolic activity, morphology and fertilizing capacity of turkey semen. Poult. Sci., 43: 1501-1508.
Bayyari, G.R., J.R. Cook, G.C. Harris, L.B. Macy, M.F. Slavik and J.K. Skeeles, 1990. Research note: The evaluation of chicken spermatozoa using fluorescent staining in a 96-well format. Poult. Sci., 69: 1602-1605.
Bilgili, S.F. and J.A. Renden, 1984. Fluorometric determination of avian sperm viability and concentration. Poult. Sci., 63: 2275-2277.
Clarke, R.N., M.R. Bakst and M.A. Ottinger, 1984. Morphological changes in chicken and turkey spermatozoa incubated under various conditions. Poult. Sci., 63: 801-805.
El-Gendy, E.A., 2009. A model for the genetic employment of chickens local to warm climate 1. Crossing with a fast growing strain and growth patterns of the crossbreds. Int. J. Poult. Sci., 8: 299-306.
El-Gendy, E.A., A.Y. Gad and A. Mostageer, 2007. Sperm-mediated gene transfer in poultry 1. The relationship with rooster sperm viability. Arab. J. Biotech., 10: 1-12.
Felgner, P.L., T.R. Gadek, M. Holm, R. Roman and H.W. Chan et al., 1987. Lipofection: A highly efficient, lipid-mediated DNA-transfection procedure. Proc. Natl. Acad. Sci., 84: 7413-7417.
Giesen, A.F. and T.J. Sexton, 1982. Boltsville poultry semen extender: 7. Comparison of commercial diluents for holding turkey semen six hour 15oC. Poult. Sci., 62: 379-381.
Hafez, E.S.E., 1974. Reproduction in Farm Animals. 3rd Edn., Lea and Febiger, Philadelphia, USA, pp: 312-317.
Khoo, HW., L.H. Ang, H.B. Lim and K.Y. Wong, 1992. Sperm cells as vectors for introducing foreign DNA into zebrafish. Aquaculture, 107: 1-19.
Lake, P.E. and W.M. McIndoe, 1959. The glutamic acid and creatine content of cock seminal plasma. Biochem. J., 71: 303-306.
Lake, P.E. and J.M. Stewart, 1978. Preservation of fowl semen in liquid nitrogen-an improved method. Poult. Sci., 19: 187-194.
Morisson, M., A. Bordas, J.M. Petit, C. Jayat-Vignoles, R. Julien and F. Minvielle, 1997. Associated effects of divergent selection for residual feed consumption on reproduction, sperm characteristics and mitochondria of spermatozoa. Poult. Sci., 76: 425-431.
Nakanishi, A. and A. Iritani, 1993. Gene transfer in the chicken by sperm-mediated methods. Mol. Reprod. Dev., 36: 258-261.
Rottmann, O.J., R. Antes, P. Hofer and G. Maierhofer, 1992. Liposome mediated gene transfer via spermatozoa into avian eggs. J. Anim. Breed Genet., 109: 64-70.
SAS, 1999. SAS/STAT User's Guide: Statistics. SAS Institute Inc., Cary, NC, USA.
Sato, F., T. Soh, M. Hattori and N. Fujihara, 2003. Evaluation of deoxyribonuclease activity in seminal plasma of ejaculated chicken semen. Asian J. Androl., 5: 213-216.
Sexton, T.J., 1986. Effects of dietary protein and season on fertility of turkey semen stored 18 hours hours at 58oC. Poult. Sci., 65: 604-606.
Sexton, T.J., 1987. Effect of semen treatments and age of tom on fertility of unstored semen and semen held 18 hours. Poult. Sci., 66: 1721-1726.
Sexton, T.J., 1977. A new poultry semen extender. 1. Effect of extension on the fertility of chicken semen. Poult. Sci., 56: 1443-1446.
Sexton, T.J. and T.A. Fewlass, 1978. A new poultry semen extender 2. Effect of the diluent components on the fertilizing capacity of chicken semen stored at 5°C. Poult. Sci., 57: 277-284.
Sorensen, A.M., 1979. Animal Reproduction: Principles and Practices. McGraw-Hill, New York, USA.
Squires, J.E. and D. Drake, 1993. Liposome‐mediated DNA transfer to chicken sperm cells. Anim. Biotechn., 4: 71-88.
Trefil, P., P. Thoraval, J. Mika, F. Coudert and G. Dambrine, 1996. Intramagnal insemination of hens can eliminate negative influence of lipofectin on fertilising ability of spermatozoa. Br. Poult. Sci., 37: 661-664.
Wishart, G.J. and Y.I. Wilson, 1999. Temperature-dependent inhibition of motility in spermatozoa from different avian species. Anim. Reprod. Sci., 57: 229-235.
Yin, J., J.J. Zhangb, G.G. Shic, S.F. Xied, X.F. Wange and H.L. Wange, 2009. Sperm mediated human coagulation factor VIII gene transfer and expression in transgenic Mice. Swiss Med. Wkly, 139: 364-372.
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