Original Article

Histological Changes of the Ovary in Pregnant Mice Vaginally Exposed to Toxoplasma gondii

Abstract

Background:Congenital toxoplasmosis is one cause of abortion. Infection can disrupt ovarian cycles and because toxoplasmosis is an infectious disease may have a similar effect on the ovaries. The purpose of this study was to investigate the pathological changes in the ovaries due to toxoplasmosis.
 Methods:Tachyzoites of Toxoplasma gondii were harvested from peritoneal fluid of mice, experimentally infected. Two females and one male mouse were housed per cage for mating in the overnight. The pregnant mice were divided into experi-mental and control groups. Experimental group were infected by parasite but the control group received the normal saline. The experimental and control mice were euthanized. Ovaries and uterine horns of animals were removed and prepared for light microscopy.
Results:Ovaries of infected pregnant mice presented gross morphological differ-ences compared to the control groups. In ovaries of experimental groups, changes of corpus luteum were observed. The comparison of experimental and control groups revealed that the number of primary follicles, secondary follicle, atretic pri-mary follicles and atretic secondary follicles had significant differences (P≤0.001).
Conclusion:Toxoplasma gondii alters ovarian follicular growth and development in mice. In addition, it alters number of different phases of follicles and corpus lu-teum in ovaries of mice.

Dubey J. Toxoplasmosis–a waterborne zoonosis. Vet Parasitol. 2004;126:57-72.

Dubey J. The history of Toxoplasma gondii--the first 100 years. J Eukaryot Microbiol. 2008;55:467-75.

Sawardekar KP. Profile of major congenital malformations at nizwa hospital, oman: 10 year review. J Paediatrs Child H . 2005;41:323-30.

Klein S. Hormonal and immunological mechanisms mediating sex differences in parasite infection. Parasite Immunol. 2004;26:247-64.

Care AS, Diener KR, Jasper MJ, Brown HM, Ingman WV, Robertson SA. Macrophages regulate corpus luteum development during embryo implantation in mice. J Clini Invest. 2013;123:3472-87.

Gatkowska J, Wieczorek M, Dziadek B, Dzitko K, Dlugonska H. Sex-dependent neu-rotransmitter level changes in brains of Toxoplasma gondii infected mice. Exp Parasitol. 2013;133:1-7.

Antonios SN, Ismail HI, Essa T. Hypothalamic origin of reproductive failure in chronic experimental toxoplasmosis. J Egypt Soc Parasitol. 2000;30:593-9.

Stahl W, Dias JA, Turek G. Hypothalamic-adenohypophyseal origin of reproductive failure in mice following chronic infection with Toxoplasma gondii. Proc Soc Exp Biol Med. 1985;178:246-9.

Stahl W, Kaneda Y, Noguchi T. Reproductive failure in mice chronically infected with Toxoplasma gondii. Parasitol Res. 1994;80:22-8.

Flegr J, Lindová J, Kodym P. Sex-dependent toxoplasmosis-associated differences in

testosterone concentration in humans. Parasitology. 2008;135:427-31.

Fux B, Ferreira A, Cassali G, Tafuri WL, Vitor RW. Experimental toxoplasmosis in balb/c mice. Prevention of vertical disease transmission by treatment and reproductive failure in chronic infection. Mem Inst Oswaldo Cruz. 2000;95:121-6.

Coutinho LB, Gomes AO, Araújo ECB, Barenco PVC, Santos JL, Caixeta DR, Silva DAO, Cunha-Júnior JP, Ferro EAV, Silva NM. The impaired pregnancy outcome in murine congenital toxoplasmosis is associated with a pro-inflammatory immune response, but not correlated with decidual inducible nitric oxide synthase expression. Int J Parasitol. 2012;42:341-52.

Fallah E, Navazesh R, Majidi J, Kushavar H, Mahdipourzareh N. An epidemiological study of Toxoplasma infection among high- school girls in jolfa. J Reprod Infertil. 2005;6:261-70.

Fallah M, Rabiee S, Matini M, Taherkhani H. Seroepidemiology of toxoplasmosis in primigravida women in hamadan, islamic republic of iran, 2004. East Mediterr Health J. 2008;14:163-71.

Bayat PD, Eslamirad Z, Shojaee S. Toxoplasmosis: Experimental vaginal infection in NMRI mice and its effect on uterin, placenta and fetus tissues.Iran Red Crescent Med J. 2013;15:595-9.

Fischer AH, Jacobson KA, Rose J, Zeller R. Hematoxylin and eosin staining of tissue and cell sections. CSH Protoc. 2008;2008:pdb prot4986.

Jolly PD, Smith PR, Heath DA, Hudson NL, Lun S, Still LA, Watts CH, McNatty KP. Morphological evidence of apoptosis and the prevalence of apoptotic versus mitotic cells in the membrana granulosa of ovarian follicles during spontaneous and induced atresia in ewes. Biol Reprod. 1997;56:837-46.

Fortune JE. The early stages of follicular development: Activation of primordial follicles and growth of preantral follicles. Anim Reprod Sci. 2003;78:135-63.

Quirk SM, Cowan RG, Harman RM, Hu CL, Porter DA. Ovarian follicular growth and atresia: The relationship between cell proliferation and survival. J Anim Sci. 2004;82 E-Suppl:E40-52.

Bernal AB, Vickers MH, Hampton MB, Poynton RA, Sloboda DM. Maternal undernutrition significantly impacts ovarian follicle number and increases ovarian oxidative stress in adult rat offspring. PLoS One. 2010;5(12):e15558.

Johnson GA, Burghardt RC, Joyce MM, Spencer TE, Bazer FW, Pfarrer C, Gray CA. Osteopontin expression in uterine stroma indicates a decidualization-like differentiation during ovine pregnancy. Biol Reprod. 2003;68:1951-8.

Miller KP, Gupta RK, Greenfeld CR, Babus JK, Flaws JA. Methoxychlor directly affects ovarian antral follicle growth and atresia through bcl-2-and bax-mediated pathways. Toxicol Sci. 2005;88:213-21.

Robertson SA. Regulatory t cells in the corpus luteum—new players in fertility control? Biol Reprod. 2012;86:26, 21-4.

Wu R, Van der Hoek KH, Ryan NK, Norman RJ, Robker RL. Macrophage contributions to ovarian function. Hum Reprod Update. 2004;10:119-33.

Van der Hoek KH, Maddocks S, Woodhouse CM, van Rooijen N, Robertson SA, Norman

RJ. Intrabursal injection of clodronate liposomes causes macrophage depletion and inhibits ovulation in the mouse ovary. Biol Reprod. 2000;62:1059-66.

Turner EC, Hughes J, Wilson H, Clay M, Mylonas KJ, Kipari T, Duncan WC, Fraser HM. Conditional ablation of macrophages disrupts ovarian vasculature. Reproduction. 2011;141:821-31.

Brannstrom M, Pascoe V, Norman R, McClure N. Localization of leukocyte subsets in the follicle wall and in the corpus luteum throughout the human menstrual cycle. Fertil Steril. 1994;61:488-95.

Herbison AE, Porteous R, Pape J-R, Mora JM, Hurst PR. Gonadotropin-releasing hormone neuron requirements for puberty, ovulation, and fertility. Endocrinology. 2008;149:597-604.

Nelson S, McLean M, Jayatilak P, Gibori G. Isolation, characterization, and culture of cell subpopulations forming the pregnant rat corpus luteum. Endocrinology. 1992;130:954-66.

Terranova P, Rice VM. Review: Cytokine involvement in ovarian processes. Am J Reprod Immunol. 1997;37:50-63.

Files
IssueVol 10 No 2 (2015) QRcode
SectionOriginal Article(s)
Keywords
Corpus luteum Histology Ovarian follicles Toxoplasma gondii

Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
How to Cite
1.
Eslamirad Z, Bayat PD, Babaei S. Histological Changes of the Ovary in Pregnant Mice Vaginally Exposed to Toxoplasma gondii. Iran J Parasitol. 1;10(2):273-279.