Feminization and reduction of testicular weight in mouse sparganosis

  • Yang, Hyun-Jong (Department of Parasitology and Ewha Medical Research Center, College of Medicine, Ewha Womans University)
  • Published : 2006.06.01

Abstract

After infection of male mice with the plerocercoids (spargana) of Spirometra mansoni, serum levels of estrogen and testicular weight were analyzed by enzyme-linked immunosorbent assay (ELISA) and weighing machine, respectively. The serum level of estrogen increased progressively in infected mice compared with normal controls, whereas the testicular weight of infected mice decreased significantly (P < 0.05). These results suggest that certain substances from spargana change the steroid hormone metabolisms in the host by unknown pathways, and chronic infection may contribute to change of the function of steroid hormone target organ, i.e., testis, in male mice.

Keywords

References

  1. Cho SY, Bae J, Seo BS, Lee SH (1975) Some aspects of human sparganosis. Korean J Parasitol 13: 60-77 https://doi.org/10.3347/kjp.1975.13.1.60
  2. Carter V, Pierce R, Dufour S, Arme C, Hoole D (2005) The tapeworm Ligula intestinalis (Cestoda: Pseudophyllidea) inhibits LH expression and puberty in its teleost host, Rutilus rutilus. Reproduction 130: 939-945 https://doi.org/10.1530/rep.1.00742
  3. Kong Y, Chung YB, Cho SY, Choi SH, Kang SY (1994) Characterization of three proteases of Spirometra mansoni plerocercoid. Parasitology 108: 359-368 https://doi.org/10.1017/S0031182000076204
  4. Kong Y, Kang SY, Cho SY (1991) Single step purification of potent antigenic protein from sparganum by gelatinaffinity chromatography. Korean J Parasitol 29: 1-7 https://doi.org/10.3347/kjp.1991.29.1.1
  5. Kong Y, Kang SY, Kim SH, Chung YB, Cho SY (1997) A neutral cysteine protease of Spirometra mansoni plerocercoid invoking an IgE response. Parasitology 114: 263-271 https://doi.org/10.1017/S0031182096008529
  6. Larralde C, Morales J, Terrazas I, Govezensky T, Romano MC (1995) Sex hormone changes induced by the parasite lead to feminization of the male host in murine Taenia crassiceps cysticercosis. J Steroid Biochem Mol Biol 52: 575-580 https://doi.org/10.1016/0960-0760(95)00062-5
  7. Lin YC, Rikihisa Y, Kono H, Gu Y (1990) Effects of larval tapeworm (Taenia taeniaeformis) on reproductive functions in male and female host rats. Exp Parasitol 70: 344-352 https://doi.org/10.1016/0014-4894(90)90116-T
  8. Mueller JF (1963) Parasite-induced weight gain in mice. Ann New York Acad Sci 113: 217-233 https://doi.org/10.1111/j.1749-6632.1963.tb40667.x
  9. Morales J, Larralde C, Arteaga M, Govezensky T, Romano Me, Morali G (1996) Inhibition of sexual behavior in male mice infected with Taenia crassiceps cysticerci. J Parasitol 82: 689-693 https://doi.org/10.2307/3283875
  10. Rikihisa Y, Lin YCH, Fukaya T (1985) Taenia taeniaeformis: inhibition of rat testosterone production by excretorysecretory product of the cultured metacestode. Exp Parasitol 59: 390-397 https://doi.org/10.1016/0014-4894(85)90094-3
  11. Sciutto EG, Fragoso M, Diaz L, Valdez F, Lomeli C, Govezensky T, Montoya RM, Larralde C (1991) Murine Taenia crassiceps cysticercosis: H2 complex and sex influence on susceptibility. Parasitol Res 77: 243-246 https://doi.org/10.1007/BF00930866
  12. Shiwaku K, Hirai K, Torii M (1982) Growth-promoting effect of Spirometra erinacei (Rudolphi, 1819) plerocercoids in mature mice: relationship between number of infected plerocercoids and growth-promoting effect. Jap J Parasitol 31: 353-360
  13. Terrazas LI, Bojalil R, Govezensky T, Larralde C (1994) A role for 17-beta-estradiol in immunoendocrine regulation of murine cysticercosis (Taenia crassiceps). J Parasitol 80: 563-568 https://doi.org/10.2307/3283192