Effect of buffalo PDC-109 on caudal epididymal spermatozoa of bubaline species


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Authors

  • S S RAMTEKE ICAR-Indian Veterinary Research Institute, Izatnagar, Uttar Pradesh 243 122 India
  • J S RAJORIYA College of Veterinary and Animal Husbandry, Rewa, Madhya Pradesh
  • A M SHENDE Nagpur Veterinary College, Nagpur, Maharashtra
  • S K GHOSH ICAR-Indian Veterinary Research Institute, Izatnagar, Uttar Pradesh
  • J K PRASAD ICAR-Central Island Agricultural Research Institute, Port Blair, Andaman and Nicobar Islands
  • P PERUMAL ICAR-ICAR Research Complex for NEH Region, Nagaland Centre, Medziphema, Nagaland
  • M SINGH ICAR-Indian Veterinary Research Institute, Izatnagar, Uttar Pradesh 243 122 India

https://doi.org/10.56093/ijans.v90i12.113166

Keywords:

Buffalo, Caudal epididymal spermatozoa, In vitro capacitation, In vitro fertilization, PDC-109

Abstract

A study was conducted to assess the effect of buffalo seminal PDC-109 on its cauda epididymal spermatozoa. PDC-109 protein was purified by applying two-step chromatography procedures and included into epididymal spermatozoa. Epididymal ejaculates were splited into four groups as Gr 1: Control (without PDC), Gr 2: 20 μg/mL PDC-109, Gr 3: 40 μg/mL PDC-109 and Gr 4: 80 μg/mL PDC-109. Semen quality parameters (SQPs) and in vitro fertility assay were evaluated. Significant improvement in post-thaw SQPs was observed in Gr 2 than in Gr 3, however, Gr 1 had significantly higher value than other groups. It is concluded that PDC-109 has dose dependent effect as increased dose causes detrimental effect in buffalo cauda epididymal sperm.

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References

Arangasamy A. 2003. Isolation of buffalo seminal plasma proteins and their effect on in vitro capacitation, acrosome reaction and fertilizing potential of spermatozoa. Ph.D. Thesis, Deemed University, Indian Veterinary Research Institute, Izatnagar, India.

Batova I, Mollova M and Ivanova M. 1993. Involvement of human seminal plasma glycoprotein defined by a peptide specific monoclonal antibody in the process of sperm capacitation and sperm zona interaction. Human Reproduction Supplement 1: 88.

Chauhan M S, Singla S K, Manik R S and Madan M L. 1997. Increased capacitation of buffalo sperm by heparin as confirmed by electron microscopy and in vitro fertilization. Indian Journal of Experimental Biology 35: 1038–43.

Cormier N and Bailey J L. 2003. A differential mechanism involved during heparin and cryopreservation induced capacitation of bovine spermatozoa. Biology of Reproduction 69: 177–185. DOI: https://doi.org/10.1095/biolreprod.102.011056

Desnoyers L and Manjunath P. 1992. Major proteins of bovine seminal plasma exhibit novel interaction with phospholipids. Journal of Biological Chemistry 267: 10149–55. DOI: https://doi.org/10.1016/S0021-9258(19)50212-5

Fazeli A R, Steenweg W, Bevers M M, de Loos F A M, Van den Broek J and Colenbrander B. 1993. Development of sperm zona pellucida binding assay for bull semen. Veterinary Record 132: 14–16. DOI: https://doi.org/10.1136/vr.132.1.14

Florman H M and First N L. 1988. The regulation of acrosomal exocytosis. II. The zona pellucida-induced acrosome reaction of bovine spermatozoa is controlled by extrinsic positive regulatory elements. Developmental Biology 128: 464–73. DOI: https://doi.org/10.1016/0012-1606(88)90308-9

Fraser L R, Abeydeera L R and Niwa K. 1995. Regulating mechanisms that modulate bull sperm capacitation and acrosomal exocytosis as determined by chlortetracycline analysis. Molecular Reproduction and Development 40: 233– 41. DOI: https://doi.org/10.1002/mrd.1080400213

Gasset M, Saiz J I, Laynez J, Sanz L, Gentzel M, Peterson E T and Calvete J J. 1997. Conformational features and thermal stability of bovine seminal plasma protein PDC-109 oligomers and phosphorycholine-bound complexes. European Journal of Biochemistry 250: 735–44. DOI: https://doi.org/10.1111/j.1432-1033.1997.00735.x

Harrison R A P and Vickers S E. 1990. Use of fluorescent probes to assess membrane integrity in mammalian spermatozoa. Journal of Reproduction and Fertility 88: 343–52. DOI: https://doi.org/10.1530/jrf.0.0880343

Harshan H M, Sanker S, Singh L P, Singh M K, Sudharani S, Ansari M R, Singh S K, Majumdar A C and Joshi P. 2009. Identification of PDC-109 like protein(s) in buffalo seminal plasma. Animal Reproduction Science 115: 306–11. DOI: https://doi.org/10.1016/j.anireprosci.2008.11.007

Iborra A, Companyo M, Martinez P and Morros A. 2000. Cholesterol efflux promotes acrosome reaction in goat spermatozoa. Biology of Reproduction 62: 378–83. DOI: https://doi.org/10.1095/biolreprod62.2.378

Jeyendran R S, Vander Ven H H, Parez-Pelaez M, Crabo B G and Zaneweld L J D. 1984. Development of an assay to assess the functional integrity of the human membrane and its relationship to other semen characteristics. Journal of Reproduction and Fertility 70: 219–28. DOI: https://doi.org/10.1530/jrf.0.0700219

Kumar A. 2005. Effect of seminal plasma heparin binding and non-heparin binding proteins on the freezability and in vitro fertility of buffalo cauda spermatozoa. M.V.Sc. Thesis, Deemed University, Indian Veterinary Research Institute, Izatnagar, India.

Laemmli V K. 1970. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227: 660– 85. DOI: https://doi.org/10.1038/227680a0

Manjunath P, Bergeron A, Lefebvre J and Ton J. 2008. Seminal plasma proteins: function and interaction with protective agents during semen preservation. Biochemica et Biophyica Acta 1784: 891–99. DOI: https://doi.org/10.1016/j.bbapap.2008.03.002

Marquez B and Suarez S S. 2007. Bovine sperm hyperactivation is promoted by alkaline-stimulated Ca2+ influx. Biology of Reproduction 76: 660–65. DOI: https://doi.org/10.1095/biolreprod.106.055038

Miller D J, Winer M A and Ax R L. 1990. Heparin binding proteins from seminal plasma bind to bovine spermatozoa and modulate capacitation by heparin. Biology of Reproduction 42: 899– 915. Muller P, Greube A, Topfer-Petersen E and Herrmann A. 2002. Influence of the bovine seminal plasma protein PDC-109 on cholesterol in the presence of phospholipids. European Biophysics Journal 31: 438–47. DOI: https://doi.org/10.1095/biolreprod42.6.899

Rajoriya J S, Prasad J K, Ramteke S S, Perumal P, De A K, Ghosh S K, Raje A, Singh M, Anuj K and Kumaresan A. 2020. Exogenous cholesterol prevents cryocapacitation like changes, membrane fluidity and enhances in vitro fertility in buffalo. Reproduction in Domestic Animals 55(6): 726–36. DOI: https://doi.org/10.1111/rda.13674

Roncoletta M, Morani E S C, Esper C R, Barnabe V H and Franceschini P H. 2006. Fertility-associated proteins in Nellore bull sperm membranes. Animal Reproduction Science 91(1– 2): 77–87. DOI: https://doi.org/10.1016/j.anireprosci.2005.03.014

Salisbury G W, VanDemark N L and Lodge J R. 1985. Physiology of reproduction and artificial insemination of cattle. 2nd ed. W. H. Freeman and Company.

Singh M, Ghosh S K, Prasad J K, Anuj K, Tripathi R P, Bhure S K and Srivastava N. 2014. Seminal PDC-109 protein vis-àvis cholesterol content and freezability of buffalo Spermatozoa. Animal Reproduction Science 144: 22– 9. DOI: https://doi.org/10.1016/j.anireprosci.2013.10.016

Srivastava N, Srivastava S K, Ghosh S K, Singh L P, Prasad J K, Kumar A, Perumal P, Jerome A and Thamizharasan A. 2012. Sequestration of PDC-109 protein improves freezability of crossbred bull spermatozoa. Animal Reproduction Science 131: 54–62. DOI: https://doi.org/10.1016/j.anireprosci.2012.02.003

Srivastava N, Srivastava S K, Ghosh S K, Jerome A, Das G K and Mehrotra S. 2013. Sequestration of PDC-109 protein by specific antibodies and egg yolk cryoprotects bull spermatozoa. Reproduction in Domestic Animals 48: 724–31. DOI: https://doi.org/10.1111/rda.12151

Sukardi S, Curry M R and Watson P F. 1997. Simultaneous detection of the acrosomal status and viability of incubated ram spermatozoa using fluorescent markers. Animal Reproduction Science 46: 89–96. DOI: https://doi.org/10.1016/S0378-4320(96)01599-0

Thérien I, Moreau R and Manjunath P. 1998. Major proteins of bovine seminal plasma and high-density lipoprotein induce cholesterol efflux from epididymal sperm. Biology of Reproduction 59: 768–76. DOI: https://doi.org/10.1095/biolreprod59.4.768

Therien I, Souberyrand S and Manjunath P. 1997. Major proteins of bovine seminal plasma modulate sperm capacitation by high-density lipoprotein. Biology of Reproduction 57: 1080– 88. DOI: https://doi.org/10.1095/biolreprod57.5.1080

Towbin H, Staehelin T and Gordon J. 1979. Electrophoretic transfer of protein from polyacrylaminde gels to nitrocellulose sheets: Procedure and some applications. Proceedings of National Academy of Sciences of United States of America 76: 4350–54. DOI: https://doi.org/10.1073/pnas.76.9.4350

Way A L, Griel L C Jr and Killian G. 2000. Effects of accessory sex gland fluid on viability, capacitation and acrosome reaction of cauda epididymal spermatozoa. Journal of Andrology 21: 213–19.

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2021-07-27

Published

2021-07-28

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How to Cite

RAMTEKE, S. S., RAJORIYA, J. S., SHENDE, A. M., GHOSH, S. K., PRASAD, J. K., PERUMAL, P., & SINGH, M. (2021). Effect of buffalo PDC-109 on caudal epididymal spermatozoa of bubaline species. The Indian Journal of Animal Sciences, 90(12), 1584-1588. https://doi.org/10.56093/ijans.v90i12.113166
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