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Published in: Reproductive Biology and Endocrinology 1/2020

Open Access 01-12-2020 | Contraception | Research

Sperm impairing microbial factor: potential candidate for male contraception

Authors: Aditi Chauhan, Deepali Thaper, Vijay Prabha

Published in: Reproductive Biology and Endocrinology | Issue 1/2020

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Abstract

Background

Despite significant advances in contraceptive options for women, vasectomy and condoms are the only options available for male contraception. Due to this limitation, the burden of contraception resides on the shoulders of females only. Therefore, there is an urgent need to develop a safe, effective and reversible method of contraception for men. Amongst the alternative approaches, microbial derived products are gaining attention of the scientific world to combat unintended pregnancies. Earlier in our laboratory, sperm impairing microbial factor (Sperm immobilization factor) isolated from Staphylococcus aureus has shown excellent contraceptive efficacy in female mice. Keeping this in mind, the present study was carried out to exploit the sperm immobilization factor (SIF) as potential male contraceptive using vas deferens for administration in mouse model.

Methods

SIF (10, 50, 100 or 200 μg) was inoculated in the lumen of right vas deferens whereas the left vas deferens served as control. The mice were sacrificed at Day 3, 7, 14, 21, 30, 45, 60 and 90 after inoculation and the results in terms of change in body weight, seminal parameters, Tissue somatic indices (TSI), haematological parameters, serum level of testosterone, lipid peroxidation and histology were studied. In order to ratify the SIF induced azoospermia SIF (200 μg) was administered with different doses viz. 100, 200, 300, 400 or 500 μg of SIF binding receptor extracted from mouse spermatozoa.

Results

The weight profile studies of all the experimental groups showed no significant change in the initial and final body weight. In case of seminal parameters, the results revealed that right vas deferens treated with SIF showed azoospermia and with 200 μg of SIF it persisted up to 90 days. TSI of reproductive organs and non-reproductive organs showed no significant change in all the experimental groups. The haematological indices were found to be unaltered throughout the course of investigation however significant decrease in testosterone level was observed in the treated mice. The treatment also affected the oxidative status of the testis. Further, histological studies revealed hypospermatogenesis and late maturation arrest on treated side whereas the left side which served as control showed normal tissue histology. SIF induced azoospermia was ameliorated when administered with 400 μg of SIF binding receptor from mouse spermatozoa.

Conclusion

SIF, when administered via intra vas deferens route, could lead to complete azoospermia. Therefore, it could be considered as a potential male contraceptive.
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Literature
1.
go back to reference Bavel VJ. The world population explosion: causes, backgrounds and projections for the future. Facts Views Vis Obgyn. 2013;5:281–91.PubMedPubMedCentral Bavel VJ. The world population explosion: causes, backgrounds and projections for the future. Facts Views Vis Obgyn. 2013;5:281–91.PubMedPubMedCentral
3.
go back to reference Holmang S, Marin P, Lindstedt G, Hedelin H. Effect of long-term oral testosterone undecanoate treatment on prostate volume and serum prostate-specific antigen concentration in eugonadal middle-aged men. Prostate. 1993;23:99–106.CrossRef Holmang S, Marin P, Lindstedt G, Hedelin H. Effect of long-term oral testosterone undecanoate treatment on prostate volume and serum prostate-specific antigen concentration in eugonadal middle-aged men. Prostate. 1993;23:99–106.CrossRef
5.
go back to reference Moulana M, Lima R, Reckelhoff JF. Metabolic syndrome, androgens, and hypertension. Curr Hypertens Rep. 2011;13:158–62.CrossRef Moulana M, Lima R, Reckelhoff JF. Metabolic syndrome, androgens, and hypertension. Curr Hypertens Rep. 2011;13:158–62.CrossRef
6.
go back to reference Pasqualotto FF, Lucon AM, Pasqualotto EB, Arap S. Trends in male contraception. Rev Hosp Clin. Fac Med S Paulo. 2003;58:275–83. Pasqualotto FF, Lucon AM, Pasqualotto EB, Arap S. Trends in male contraception. Rev Hosp Clin. Fac Med S Paulo. 2003;58:275–83.
7.
go back to reference Lohiya NK, Alam I, Hussain M, Khan SR, Ansari AS. RISUG: an intravasal injectable male contraceptive. Indian J Med Res. 2014;140:63–72. Lohiya NK, Alam I, Hussain M, Khan SR, Ansari AS. RISUG: an intravasal injectable male contraceptive. Indian J Med Res. 2014;140:63–72.
8.
go back to reference Upadhyay SN, Dhawan S, Talwar GP. Antifertility effects of Neem (Azadirachta indica) oil in male rats by single intra-vas administration: an alternate approach to vasectomy. J Androl. 1993;14:275–81.PubMed Upadhyay SN, Dhawan S, Talwar GP. Antifertility effects of Neem (Azadirachta indica) oil in male rats by single intra-vas administration: an alternate approach to vasectomy. J Androl. 1993;14:275–81.PubMed
9.
go back to reference Thaper D, Rahi DK, Prabha V. Ameliortion of sperm immobilization factor-induced infertility by bacterial antigenic determinants crossreacting with spermatozoa. Reprod Fertil Dev. 2018;31:602–12.CrossRef Thaper D, Rahi DK, Prabha V. Ameliortion of sperm immobilization factor-induced infertility by bacterial antigenic determinants crossreacting with spermatozoa. Reprod Fertil Dev. 2018;31:602–12.CrossRef
10.
go back to reference Reitman S, Frankel S. A colorimetric method for determination of serum glutamate oxaloacetate and glutamic pyruvate transaminase. Am J Clin Pathol. 1957;28:56–8.CrossRef Reitman S, Frankel S. A colorimetric method for determination of serum glutamate oxaloacetate and glutamic pyruvate transaminase. Am J Clin Pathol. 1957;28:56–8.CrossRef
11.
go back to reference Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxidation in animal tissues by thiobarbituric acid reaction. Anal Biochem. 1979;95:351–8.CrossRef Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxidation in animal tissues by thiobarbituric acid reaction. Anal Biochem. 1979;95:351–8.CrossRef
12.
go back to reference Thaper D, Rahi DK, Prabha V. Receptor from streptococcus pyogenes as a potential antidote against sperm immobilization factor-induced sperm impairment and infertility. Microb Pathog. 2019;128:55–62.CrossRef Thaper D, Rahi DK, Prabha V. Receptor from streptococcus pyogenes as a potential antidote against sperm immobilization factor-induced sperm impairment and infertility. Microb Pathog. 2019;128:55–62.CrossRef
13.
go back to reference Singh A, Singh SK. Reversible antifertility effect of aqueous leaf extract of Allamanda cathartica L. in male laboratory mice. Andrologia. 2008;40:337–45.CrossRef Singh A, Singh SK. Reversible antifertility effect of aqueous leaf extract of Allamanda cathartica L. in male laboratory mice. Andrologia. 2008;40:337–45.CrossRef
14.
go back to reference Sewani-Rusikea CR, Gundidzab M. Antifertility effects of Oldenlandia affinis in male rats-a preliminary study. Afr J Tradit Complem. 2011;8:424–8. Sewani-Rusikea CR, Gundidzab M. Antifertility effects of Oldenlandia affinis in male rats-a preliminary study. Afr J Tradit Complem. 2011;8:424–8.
15.
go back to reference Reddy KVR, Gupta SM, Aranha CC. Effect of antimicrobial peptide, Nisin, on the reproductive functions of rats. ISRN Vet Sci. 2011;2011:1–8.CrossRef Reddy KVR, Gupta SM, Aranha CC. Effect of antimicrobial peptide, Nisin, on the reproductive functions of rats. ISRN Vet Sci. 2011;2011:1–8.CrossRef
16.
go back to reference Oliveira ECS, Fagundes AKF, Melo CCS, Nery LTB, Revoredo RG, Andrade TFG, et al. Intratesticular injection of a zinc-based solution for contraception of domestic cats: a randomized clinical trial of efficacy and safety. Vet J. 2013;197:307–10.CrossRef Oliveira ECS, Fagundes AKF, Melo CCS, Nery LTB, Revoredo RG, Andrade TFG, et al. Intratesticular injection of a zinc-based solution for contraception of domestic cats: a randomized clinical trial of efficacy and safety. Vet J. 2013;197:307–10.CrossRef
17.
go back to reference Ramya MC, Shivabasavaiah T. Reversible antifertility effect of Opuntia elatior mill. Fruit extract. Int J Reprod Contracept Obstet Gynecol. 2015;4:392–7.CrossRef Ramya MC, Shivabasavaiah T. Reversible antifertility effect of Opuntia elatior mill. Fruit extract. Int J Reprod Contracept Obstet Gynecol. 2015;4:392–7.CrossRef
18.
go back to reference Singh SK, Rath SK. Effect of gossypol tetra acetic acid on the reproductive organs in male mice. In: Singh VK, Govil JN, editors. Recent progress in medicinal plants. Houston: Studium Press LLC; 2008. p. 167–84. Singh SK, Rath SK. Effect of gossypol tetra acetic acid on the reproductive organs in male mice. In: Singh VK, Govil JN, editors. Recent progress in medicinal plants. Houston: Studium Press LLC; 2008. p. 167–84.
19.
go back to reference Mishra RK, Singh SK. Effect of aqueous leaf extract of Azadirachta indica on the reproductive organs in male mice. Indian J Exp Biol. 2005;43:1093–103.PubMed Mishra RK, Singh SK. Effect of aqueous leaf extract of Azadirachta indica on the reproductive organs in male mice. Indian J Exp Biol. 2005;43:1093–103.PubMed
20.
go back to reference Singh A, Singh SK. Reversible antifertility effect of aqueous leaf extract of Allamanda cathartica L. in male laboratory mice. Andrologia. 2008;40:337–45.CrossRef Singh A, Singh SK. Reversible antifertility effect of aqueous leaf extract of Allamanda cathartica L. in male laboratory mice. Andrologia. 2008;40:337–45.CrossRef
21.
go back to reference Ashok P, Meenakshi B. Contraceptive effect of Curcuma longa (L.) in male albino rat. Asian J Androl. 2004;6:71–4.PubMed Ashok P, Meenakshi B. Contraceptive effect of Curcuma longa (L.) in male albino rat. Asian J Androl. 2004;6:71–4.PubMed
22.
go back to reference Verma HP, Singh SK. Effect of aqueous leaf extract of Dalbergia sissoo Roxb. On spermatogenesis and fertility in male mice. Eur J Contracep Repr. 2014;19:475–86.CrossRef Verma HP, Singh SK. Effect of aqueous leaf extract of Dalbergia sissoo Roxb. On spermatogenesis and fertility in male mice. Eur J Contracep Repr. 2014;19:475–86.CrossRef
23.
go back to reference Singh SK, Chakravarty S. Antispermatogenic and antifertility effects of 20, 25-diazacholeastrol dihydrochloride in mice. Reprod Toxicol. 2003;17:37–44.CrossRef Singh SK, Chakravarty S. Antispermatogenic and antifertility effects of 20, 25-diazacholeastrol dihydrochloride in mice. Reprod Toxicol. 2003;17:37–44.CrossRef
24.
go back to reference Verma HP, Singh SK. Antifertility efficacy of Coccinia indica in male mice and its possible mechanisms of action on spermatogenesis. Gen Comp Endocrinol. 2017;241:89–99.CrossRef Verma HP, Singh SK. Antifertility efficacy of Coccinia indica in male mice and its possible mechanisms of action on spermatogenesis. Gen Comp Endocrinol. 2017;241:89–99.CrossRef
25.
go back to reference Sharma N, Jacob D. Assessment of reversible contraceptive efficacy of methanol extract of Mentha arvensis L. leaves in male albino mice. J Ethnopharmacol. 2002;80:9–13.CrossRef Sharma N, Jacob D. Assessment of reversible contraceptive efficacy of methanol extract of Mentha arvensis L. leaves in male albino mice. J Ethnopharmacol. 2002;80:9–13.CrossRef
26.
go back to reference Etim EA, Adebayo YA, Ifeanyi OE. Effect of Achyranthes Aspera leaf extract on hematological parameters of Swiss albino mice. World. 2019;4:96–101. Etim EA, Adebayo YA, Ifeanyi OE. Effect of Achyranthes Aspera leaf extract on hematological parameters of Swiss albino mice. World. 2019;4:96–101.
27.
go back to reference O’Donell L, Meachem SJ, Stanton PG, McLachlan RI. Endocrine regulation of spermatogenesis. In: Knobil, Neill’s, editors. Physiology of reproduction. St Louis: Elsevier Academic Press; 2006. p. 1017–69. O’Donell L, Meachem SJ, Stanton PG, McLachlan RI. Endocrine regulation of spermatogenesis. In: Knobil, Neill’s, editors. Physiology of reproduction. St Louis: Elsevier Academic Press; 2006. p. 1017–69.
28.
go back to reference Smith LB, Walker WH. The regulation of spermatogenesis by androgens. Semin Cell Dev Biol. 2014;30:2–13.CrossRef Smith LB, Walker WH. The regulation of spermatogenesis by androgens. Semin Cell Dev Biol. 2014;30:2–13.CrossRef
29.
go back to reference Bisht S, Faiq M, Tolahunase M, Dada R. Oxidative stress and male infertility. Nat Rev Urol. 2017;14:470–85.CrossRef Bisht S, Faiq M, Tolahunase M, Dada R. Oxidative stress and male infertility. Nat Rev Urol. 2017;14:470–85.CrossRef
Metadata
Title
Sperm impairing microbial factor: potential candidate for male contraception
Authors
Aditi Chauhan
Deepali Thaper
Vijay Prabha
Publication date
01-12-2020
Publisher
BioMed Central
Published in
Reproductive Biology and Endocrinology / Issue 1/2020
Electronic ISSN: 1477-7827
DOI
https://doi.org/10.1186/s12958-020-00654-4

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