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Superoxide Anion Production by Human Neutrophils Activated by Trichomonas vaginalis

  • Song, Hyun-Ouk (Department of Parasitology, School of Medicine, Catholic University of Daegu) ;
  • Ryu, Jae-Sook (Department of Environmental Biology and Medical Parasitology, Hanyang University College of Medicine)
  • Received : 2013.07.04
  • Accepted : 2013.08.08
  • Published : 2013.08.31

Abstract

Neutrophils are the predominant inflammatory cells found in vaginal discharges of patients infected with Trichomonas vaginalis. In this study, we examined superoxide anion ($O^{\cdot}_{2^-}$) production by neutrophils activated by T. vaginalis. Human neutrophils produced superoxide anions when stimulated with either a lysate of T. vaginalis, its membrane component (MC), or excretory-secretory product (ESP). To assess the role of trichomonad protease in production of superoxide anions by neutrophils, T. vaginalis lysate, ESP, and MC were each pretreated with a protease inhibitor cocktail before incubation with neutrophils. Superoxide anion production was significantly decreased by this treatment. Trichomonad growth was inhibited by preincubation with supernatants of neutrophils incubated for 3 hr with T. vaginalis lysate. Furthermore, myeloperoxidase (MPO) production by neutrophils was stimulated by live trichomonads. These results indicate that the production of superoxide anions and MPO by neutrophils stimulated with T. vaginalis may be a part of defense mechanisms of neutrophils in trichomoniasis.

Keywords

References

  1. Fouts AC, Kraus SJ. Trichomonas vaginalis: reevaluation and its clinical presentation and laboratory diagnosis. J Infect Dis 1993; 141: 137-143.
  2. World Health Organization. Prevalence and incidence of selected sexually transmitted infections, Chlamydia trachomatis, Neisseria gonorrhoeae, syphilis, and Trichomonas vaginalis: methods and results used by the WHO to generate 2005 estimates. WHO, 2011.
  3. Choi KS, Kwon JY, Uh Y, Koo JS, Cha DS, Kim MC. Prevalence of vaginal Trichomanas vaginalis in Kangwon area. Korean J Obstet Gynecol 1996; 39: 1273-1278.
  4. Ryu JS, Chung HL, Min DY, Cho YH, Ro YS, Kim SR. Diagnosis of trichomoniasis by polymerase chain reaction. Yonsei Medical J 1999; 40: 56-60. https://doi.org/10.3349/ymj.1999.40.1.56
  5. Bar Chama N, Fisch H. Infection and pyospermia in male infertility. World J Urol 1993; 11: 76-81.
  6. Lee JJ, Moon HS, Lee TY, Hwang HS, Ahn MH, Ryu JS. PCR for diagnosis of male Trichomonas vaginalis infection with chronic prostatitis and urethritis. Korean J Parasitol 2012; 50: 157-159. https://doi.org/10.3347/kjp.2012.50.2.157
  7. Rein MF, Sullivan JA, Mandell GL. Trichomonacidal activity of human polymorphonuclear neutrophils: killing by disruption and fragmentation. J Infect Dis 1980 142: 575-585. https://doi.org/10.1093/infdis/142.4.575
  8. Davies MJ. Myeloperoxidase-derived oxidation: mechanisms of biological damage and its prevention. J Clin Biochem Nutr 2011; 48: 8-19.
  9. Ryu JS, Choi HK, Min DY, Ha SE, Ahn MH. Effect of iron on the virulence of Trichomonas vaginalis. J Parasitol 2001; 87: 457-460.
  10. Diamond LS. The establishment of various trichomonads of animals and man in axenic cultures. J Parasitol 1957; 43: 488-490.
  11. Min DY, Ryu JS, Park SY, Shin MH, Cho WY. Degradation of human immunoglobulins and cytotoxicity on HeLa cells by live Trichomonas vaginalis. Korean J Parasitol 1997; 35: 39-46. https://doi.org/10.3347/kjp.1997.35.1.39
  12. Shaio MF, Lin PR, Liu JY, Yang KD. Generation of interleukin-8 from human monocytes in response to Trichomonas vaginalis stimulation. Infect Immun 1995; 63: 3864-3870.
  13. Shin MH. Excretory-secretory product of Paragonimus westermani newly excysted metacercariae inhibits superoxide production of granulocytes stimulated with IgG. Korean J Parasitol 2000; 38: 103-106. https://doi.org/10.3347/kjp.2000.38.2.103
  14. Li PF, Dietz R, von Harsdorf R. Reactive oxygen species induce apoptosis of vascular smooth muscle cell. FEBS Lett 1997; 404: 249-252. https://doi.org/10.1016/S0014-5793(97)00093-8
  15. Schreck R, Rieber P, Baeuerle PA. Reactive oxygen intermediates as apparently widely used messengers in the activation of the NF-kappa B transcription factor and HIV-1. EMBO J 1991; 10: 2247-2258.
  16. Chaible LM, Alba-Loureiro TC, Maia AA, Pugine SM, Valle CR, Pithon-Curi TC, Curi R, De Melo MP. Effect of cysticercus cellulosae on neutrophil function and death. Vet Parasitol 2005; 127: 121-129. https://doi.org/10.1016/j.vetpar.2004.09.023
  17. Leoratti FM, Trevelin SC, Cunha FQ, Rocha BC, Costa PA, Gravina HD, Tada MS, Pereira DB, Golenbock DT, Antonelli LR, Gazzinelli RT. Neutrophil paralysis in Plasmodium vivax malaria. PLoS Negl Trop Dis 2012; 6:e1710. https://doi.org/10.1371/journal.pntd.0001710
  18. McQuaid KE, Keenan AK. Endothelial barrier dysfunction and oxidative stress: roles for nitric oxide? Exp Physiol 1997; 82: 369- 376.
  19. Candeias LP, Patel KB, Stratford MR, Wardman P. Free hydroxyl radicals are formed on reaction between the neutrophil-derived species superoxide anion and hypochlorous acid. FEBS Lett 1993; 333: 151-153. https://doi.org/10.1016/0014-5793(93)80394-A
  20. Zhu L, Gunn C, Beckman JS. Bactericidal activity of peroxynitrite. Arch Biochem Biophys 1992; 298: 452-457. https://doi.org/10.1016/0003-9861(92)90434-X
  21. Kettle AJ, Winterbourn CC. Superoxide enhances hypochlorous acid production by stimulated human neutrophils. Biochem Biophys Acta 1990; 1052: 379-385. https://doi.org/10.1016/0167-4889(90)90146-5
  22. Winterbourn CC. Biological reactivity and biomarkers of the neutrophil oxidant, hypochlorous acid. Toxicology 2002; 181 & 182: 223-227.
  23. Styrt B, Sugarman B, Mummaw N, White JC. Chemorepulsion of trichomonads by products of neutrophil oxidative metabolism. J Infect Dis 1991; 163: 176-179. https://doi.org/10.1093/infdis/163.1.176
  24. Park KJ, Ryu JS, DY Min, Lee KT. Leukocyte chemotaxis to Trichomonas vaginalis. Yonsei J Med Sci 1984; 17: 77-87.
  25. Coombs GH, North MJ. An analysis of the proteinases of Trichomonas vaginalis by polyacrylamide gel electrophoresis. Parasitology 1983; 86 (pt. 1): 1-6.
  26. Arroyo R, Alderete JF. Trichomonas vaginalis surface proteinase activity is necessary for parasite adherence to epithelial cells. Infect Immun 1989; 57: 2991-2997.
  27. Ryu JS, Kang JH, Jung SY, Shin MH, Kim JM, Park H, Min DY. Production of interleukin-8 by human neutrophils stimulated with Trichomonas vaginalis. Infect Immun 2004; 72: 1326-1332. https://doi.org/10.1128/IAI.72.3.1326-1332.2004
  28. Nguyen C, Katner HP. Myeloperoxidase deficiency manifesting as pustular candida dermatitis. Clin Infect Dis 1997; 24: 258-260. https://doi.org/10.1093/clinids/24.2.258
  29. Aratani Y, Koyama H, Nyui SI, Suzuki K, Kura F, Maeda N. Severe impairment in early host defense against Candida albicans in mice deficient in myeloperoxidase. Infect Immun 1999; 67: 1828-1836.
  30. Pacheco-Yepez J, Rivera-Aguilar V, Barbosa-Cabrera E, Rojas Hernandez S, Jarillo-Luna. Myeloperoxidase binds to and kills Entamoeba histolytica trophozoites. Parasite Immunol 2011; 33: 255-264. https://doi.org/10.1111/j.1365-3024.2010.01275.x
  31. Hampton MB, Kettle AJ, Winterbourn CC. Involvement of superoxide and myeloperoxidase in oxygen-dependent killing of Staphylococcus aureus by neutrophils. Infect Immun 1996; 64: 3512-3517.
  32. Kutter D, Devaquet P, Vanderstocken G, Paulus JM, Marchal V, Gothot A. Consequences of total and subtotal myeloperoxidase deficiency: risk or benefit? Acta Haematol 2000; 104: 10-15. https://doi.org/10.1159/000041062

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