Prevalence of naturally occurring antisperm antibodies (ASA) in blood serum and seminal plasma, and their relationship with cryopreserved semen quality and fertility of buffalo bulls
201 / 54
Keywords:
Acrosome reaction, Antisperm antibodies, Buffalo bulls, Fertility, Semen qualityAbstract
The present study was undertaken to determine the levels of antisperm antibodies (ASA), sperm-bound immunoglobulins A and G (IgA and IgG) in blood serum and seminal plasma of breeding buffalo bulls, and establish their relationship with quality and fertility of cryopreserved semen. Frozen semen (50 straws/bull) was procured from thirty Murrah buffalo bulls. Additionally, fresh semen of same ejaculate of each bull was also separated for seminal plasma for ASA analysis. Blood samples of all bulls were collected in non-heparinized vials and serum was harvested from them. The ASA, IgA- and IgG-bound spermatozoa were analyzed in blood serum and seminal plasma by immuno-peroxidase assay (IPA) and immunobead-binding assay (IBA). On the basis of per cent ASA, IgA- and IgG-type, all bulls were divided into 2 groups viz. group 1 (< 40% ASA, IgA and IgG in serum; < 20% ASA, IgA and IgG in seminal plasma) and group 2 (> 40% ASA, IgA and IgG in serum; > 20% ASA, IgA and IgG in seminal plasma) for further comparisons. The frozen-thawed semen was also evaluated for percent motility (total and progressive), concentration, viability, abnormality, HOST, acrosome integrity, acrosome reaction, CMPT and first FSCR. The percentage of ASA (37.1±3.8 vs 22.3±1.5), IgA- (44.2±3.1 vs 21.6±2.7) and IgG-bound spermatozoa (35.5±3.0 vs 19.7±4.6) were significantly higher in serum than in seminal plasma. In blood serum, sperm motility, acrosome reaction, CMPT and FSCR were significantly higher in bulls with < 40% ASA as compared to their counterparts. In seminal plasma, bulls with < 20% ASA exhibited significantly higher sperm concentration as compared to their contemporary mates. Sperm concentration (982.2±50.4 vs 874.9±36.3%) in blood serum and acrosome reaction (56.6±2.7 vs 49.9±2.3%) in seminal plasma were the only parameters that were significantly higher in bulls with < 40% and < 20% IgA, respectively than in their counterparts. For IgG-type, sperm concentration and acrosome reaction were significantly higher in bulls with < 40% than in those with > 40% IgG in blood serum. In seminal plasma, acrosome reaction and FSCR were significantly higher in bulls with < 20% IgG than in their contemporary mates. In conclusion, detection of surface-bound ASA was associated with changes in quality and fertility of buffalo bull semen.
Downloads
References
Singh A K, Brar P S and Cheema R S. 2016. Relationship between sperm penetration distance in cervical mucus and frozen semen characteristics vis-à-vis buffalo bull fertility. Indian Journal of Animal Sciences 86(12): 1405–08.
Singh A K, Brar P S and Cheema R S. 2017. Characterization of fertility-associated antigens in seminal fluid and their relationship with vital sperm function tests vis-à-vis fertility of breeding buffalo bulls. Indian Journal of Animal Sciences 87(3): 297–303.
Bronson R. 1999. Antisperm antibodies: A critical evaluation and clinical guidelines. Journal of Reproductive Immunology 45: 159–83. DOI: https://doi.org/10.1016/S0165-0378(99)00044-3
Chamley L W and Clarke G N. 2007. Antisperm antibodies and conception. Seminars in Immunopathology 29: 169–84. DOI: https://doi.org/10.1007/s00281-007-0075-2
Comhaire F H, Mahmoud A M, Depuydt C E, Zalata A A and Christophe A B. 1999. Mechanisms and effects of male genital tract infection on sperm quality and fertilizing potential: The Andrologist’s Viewpoint. Human Reproduction Update 5: 393–98. DOI: https://doi.org/10.1093/humupd/5.5.393
Cui D, Han G, Shang Y, Liu C, Xia L, Li L and Yi S. 2015. Antisperm antibodies in infertile men and their effect on semen parameters. A systematic review and meta-analysis. Clinica Chimica Acta 444: 29–36. DOI: https://doi.org/10.1016/j.cca.2015.01.033
Fayemi O. 2005. Sperm antibodies and reproductive efficiency in the Zebu cattle in South Western Nigeria. Pakistan Veterinary Journal 25: 111–14.
Ferrer M S, George A, Miller L M J, Garcia Flores E O and Wilkerson M J. 2014. Diagnosis of sperm-bound antisperm antibodies by flow cytometry and their association with semen quality. Journal of Equine Veterinary Science 34: 57–63. DOI: https://doi.org/10.1016/j.jevs.2013.10.034
Ferrer M S, Laflin S, Anderson D E, Miesner M D, Wilkerson M J, George A, Miller L M J, Larson R and Garcia Flores E O. 2015. Prevalence of bovine sperm-bound antibodies and their association with semen quality. Theriogenology 84: 94–100. DOI: https://doi.org/10.1016/j.theriogenology.2015.02.017
Fijak M and Meinhardt A. 2006. The testis in immune privilege. Immunological Reviews 213: 66–81. DOI: https://doi.org/10.1111/j.1600-065X.2006.00438.x
Hollinshead F K, Gillan L, O’Brien J K, Evans G and Maxwell W M C. 2003. In vitro and in vivo assessment of functional capacity of flow cytometrically sorted ram spermatozoa after freezing and thawing. Reproduction Fertility and Development 15: 351–59. DOI: https://doi.org/10.1071/RD03060
Kanchev L, Pavlova S and Danev A. 1993. Assessment of circulating agglutinating antisperm antibodies in buffalo cows with unexplained infertility and attempt to identify buffalo sperm isoantigens. American Journal of Reproductive Immunology 29: 62–68. DOI: https://doi.org/10.1111/j.1600-0897.1993.tb00839.x
Lombardo F, Gandini L, Dondero F and Lenzi A. 2001. Immunology and immunopathology of the male genital tract – antisperm immunity in natural and assisted reproduction. Human Reproduction Update 7: 450–56. DOI: https://doi.org/10.1093/humupd/7.5.450
Sarma D K, Baishya N, Sharma D K, Deka B C and Bhuyan D. 2009. Antisperm antibodies in serum and cervical mucus of normal and repeat breeding cows. Indian Journal of Animal Reproduction 30: 54–56.
Wang W H, Abeydeera L R, Fraser L R and Niwa K. 1995. Functional analysis using chlortetracycline fluorescence an in vitro fertilization of frozen-thawed ejaculated boar spermatozoa incubated in a protein-free chemically defined medium. Journal of Reproduction and Fertility 104: 305–13. DOI: https://doi.org/10.1530/jrf.0.1040305
Yanagimachi R. 1994. Mammalian Fertilization. Physiology of Reproduction. 2nd edn, pp. 189–317. (Eds) Knobil E and Neill J D. Raven Press, New York.
Zodinsanga V, Cheema R S and Mavi P S. 2015. Relationship of naturally occurring antisperm antibodies in blood serum and seminal plasma of cattle bulls with sperm function and fertility tests. Open Journal of Animal Sciences 5: 114–23. DOI: https://doi.org/10.4236/ojas.2015.52014
Zraly Z, Bendova J, Diblikova I, Svecova D, Kummer V, Maskova J and Veznik Z. 2002. Antisperm antibodies in blood sera of bulls and correlations with age, breed and ejaculate quality. Acta Veterinaria 71: 303–08. DOI: https://doi.org/10.2754/avb200271030303
Downloads
Submitted
Published
Issue
Section
License
The copyright of the articles published in The Indian Journal of Animal Sciences is vested with the Indian Council of Agricultural Research, which reserves the right to enter into any agreement with any organization in India or abroad, for reprography, photocopying, storage and dissemination of information. The Council has no objection to using the material, provided the information is not being utilized for commercial purposes and wherever the information is being used, proper credit is given to ICAR.