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Human Sperm Interaction with Staphylococcus aureus: A Molecular Approach

DOI: 10.1155/2012/816536

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Abstract:

Sperm immobilization factor (SIF) causing 100% immobilization of spermatozoa isolated from Staphylococcus aureus when characterized using LC-MS (Liquid chromatography-mass spectrometry) showed that this 20?kDa protein had peptide sequence similarity with hsp-70 protein. It was found to completely (100%) inhibit Mg++ ATPase activity of spermatozoa at concentration of 100?μg?mL?1. Sperm samples treated with SIF also showed reduction in calcium ionophore-induced acrosome reaction as compared to control samples (treated with calcium ionophore alone). Binding studies of FITC labelled SIF with spermatozoa using fluorescent microscopy showed binding of SIF to the surface of spermatozoa indicating the presence of SIF binding receptor. The receptor was extracted by 3M NaCl and purified by gel permeation chromatography. Characterization of the receptor by MALDI-TOF (Matrix-assisted laser desorption ionization-time of flight) indicated that the receptor shared sequence similarity with MHC class II antigen. A calorimetric study showed that the receptor moiety on spermatozoa was specific for the purified ligand as binding of the receptor to ligand was enthalpically (?11.9?kJ?mole?1) as well as entropically (21.53?J?mole?1?K?1) favored resulting in the Gibb's free energy of ?18.57?kJ?mole?1. 1. Introduction Staphylococcus aureus is amongst the most versatile and successful of the human pathogens. It has the ability to cause a variety of infections in numerous ecological niches within the host. It colonizes the nares, axillae, vagina, pharynx, or damaged skin surfaces and causes a variety of suppurative (pus-forming) infections and toxinoses in humans. Besides this, S. aureus is arguably the dominant organism implicated in primary infertility, among males and females alike [1]. S. aureus has been observed as causative organism accounting for 68.2% of seminal fluid infections [2]. This is consistent with that reported by Okon et al., where S. aureus was isolated from 62.5% of the seminal fluids [3]. S. aureus has also been reported to be commonly isolated microorganism from cervical samples [4]. Huwe et al. studied the influence of different uropathogenic microorganisms on human sperm motility parameters by means of CASA and reported that S. aureus retards the sperm motility [5]. Similar studies were done by Liu et al. on the effect of certain uropathogenic microorganisms on human sperm motility parameters and found significant decrease in sperm motility when spermatozoa were coincubated with S. aureus [6]. Some authors have suggested that direct interaction between

References

[1]  A. R. M. Momoh, B. O. Idonije, E. O. Nwoke et al., “Pathogenic bacteria-a probable cause of primary infertility among couples in Ekpoma,” Journal of Microbiology and Biotechnology Research, vol. 1, pp. 66–71, 2011.
[2]  M. A. Emokpae, P. O. Uadia, and N. M. Sadiq, “Contribution of bacterial infection to male infertility in Nigerians,” Online Journal of Health and Allied Sciences, vol. 8, no. 1, pp. 1–5, 2009.
[3]  K. O. Okon, M. Nwaogwu, S. O. Zailani, and C. Chana, “Pattern of seminal fluid indices among infertile male partners attending the infertility clinic of University of Maiduguri Teaching Hospital, Maiduguri, Nigeria,” Highland Medical Research Journal, vol. 1, pp. 18–23, 2005.
[4]  F. E. Okonofua, K. A. Ako-Nai, and M. D. Dighitoghi, “Lower genital tract infections in infertile Nigerian women compared with controls,” Genitourinary Medicine, vol. 71, no. 3, pp. 163–168, 1995.
[5]  P. Huwe, T. Diemer, M. Ludwig, J. Liu, H. G. Schiefer, and W. Weidner, “Influence of different uropathogenic microorganisms on human sperm motility parameters in an in vitro experiment,” Andrologia, vol. 30, no. 1, pp. 55–59, 1998.
[6]  J. H. Liu, H. Y. Li, Z. G. Cao, Y. F. Duan, Y. Li, and Z. Q. Ye, “Influence of several uropathogenic microorganisms on human sperm motility parameters in vitro,” Asian Journal of Andrology, vol. 4, no. 3, pp. 179–182, 2002.
[7]  T. Diemer, W. Weidner, H. W. Michelmann, H. G. Schiefer, E. Rovan, and F. Mayer, “Influence of Escherichia coli on motility parameters of human spermatozoa in vitro,” International Journal of Andrology, vol. 19, no. 5, pp. 271–277, 1996.
[8]  R. Nú?ez-Calonge, P. Caballero, C. Redondo, F. Baquero, M. Martínez-Ferrer, and M. A. Meseguer, “Ureaplasma urealyticum reduces motility and induces membrane alterations in human spermatozoa,” Human Reproduction, vol. 13, no. 10, pp. 2756–2761, 1998.
[9]  T. Erbengi, “Ultrastructural observations on the entry of Chlamydia trachomatis into human spermatozoa,” Human Reproduction, vol. 8, no. 3, pp. 416–421, 1993.
[10]  J. D. Paulson, “Isolation of a spermatozoal immobilization factor from Escherichia coli filtrates,” Fertility and Sterility, vol. 28, no. 2, pp. 182–185, 1977.
[11]  V. Prabha, T. Gupta, S. Kaur, N. Kaur, S. Kala, and A. Singh, “Isolation of a spermatozoal immobilization factor from Staphylococcus aureus filtrates,” Canadian Journal of Microbiology, vol. 55, no. 7, pp. 874–878, 2009.
[12]  M. F. Nelson, “Wrongful life: impaired infant's cause of action recognized—Curlender v. Bio-Science Laboratories,” Brigham Young University law review, vol. 1980, no. 3, pp. 676–683, 1980.
[13]  A. A. Alcivar, L. E. Hake, C. F. Millette, J. M. Trasler, and N. B. Hecht, “Mitochondrial gene expression in male germ cells of the mouse,” Developmental Biology, vol. 135, no. 2, pp. 263–271, 1989.
[14]  K. Ohashi, F. Saji, M. Kato, T. Tsutsui, T. Tomiyama, and O. Tanizawa, “Acrobeads test: a new diagnostic test for assessment of the fertilizing capacity of human spermatozoa,” Fertility and Sterility, vol. 63, no. 3, pp. 625–630, 1995.
[15]  V. Prabha, N. Chaudhary, and S. Kaur, “Molecular mimicry between bacteria and spermatozoa,” Journal of Urology, vol. 186, no. 6, pp. 2442–2447, 2011.
[16]  World Health Organisation, WHO Laboratory Manual For the Examination and Processing of Human Semen, Cambridge University Press, Cambridge, UK, 2010.
[17]  V. Prabha, Aanam, T. Dhir, and S. Kaur, “Bacteriological study of the cervix of females suffering from unexplained infertility,” American Journal of Biomedical Sciences, vol. 3, pp. 84–89, 2011.
[18]  M. W. Kielley, “Mitochondrial ATPase,” in Methods in Enzymology, S. P. Colowick and N. O. Kaplan, Eds., pp. 593–595, Academic Press, New York,NY, USA, 1955.
[19]  J. B. Chappel, “The effect of alkylguanidines on mitochondrial metabolism,” The Journal of Biological Chemistry, vol. 238, pp. 410–417, 1963.
[20]  A. Boyce, A. Casey, and G. Walsh, “A phytase enzyme-based biochemistry practical particularly suited to students undertaking courses in biotechnology and environmental science,” Biochemistry and Molecular Biology Education, vol. 32, no. 5, pp. 336–340, 2004.
[21]  P. Quinn, J. F. Kerin, and G. M. Warnes, “Improved pregnancy rate in human in vitro fertilization with the use of a medium based on the composition of human tubal fluid,” Fertility and Sterility, vol. 44, no. 4, pp. 493–498, 1985.
[22]  J. Jiang and D. Y. Lu, “Detection of bacteria from semen of infertile males and their seminal parameters,” Chinese Journal of Andrology, vol. 10, pp. 196–198, 1996.
[23]  A. Neuer, S. D. Spandorfer, P. Giraldo, S. Dieterle, Z. Rosenwaks, and S. S. Witkin, “The role of heat shock proteins in reproduction,” Human Reproduction Update, vol. 6, no. 2, pp. 149–159, 2000.
[24]  B. H. Gibbons and I. R. Gibbons, “Flagellar movement and adenosine triphosphatase activity in sea urchin sperm extracted with triton X-100,” Journal of Cell Biology, vol. 54, no. 1, pp. 75–97, 1972.
[25]  R. Henkel, C. Muller, W. Miska, H. Gips, and W. B. Schill, “Determination of the acrosome reaction in human spermatozoa is predictive of fertilization in vitro,” Human Reproduction, vol. 8, no. 12, pp. 2128–2132, 1993.
[26]  B. I. Rose and B. Scott, “Sperm motility, morphology, hyperactivation, and ionophore-induced acrosome reactions after overnight incubation with mycoplasmas,” Fertility and Sterility, vol. 61, no. 2, pp. 341–348, 1994.
[27]  F. M. Kohn, I. Erdmann, T. Oeda, K. F. El-Mulla, H. G. Schiefer, and W. B. Schill, “Influence of urogenital infections on sperm functions,” Andrologia, vol. 30, no. 1, pp. 73–80, 1998.
[28]  K. F. El-Mulla, F. M. K?hn, M. Dandal et al., “In vitro effect of Escherichia coli on human sperm acrosome reaction,” Archives of Andrology, vol. 37, no. 2, pp. 73–78, 1996.
[29]  C. Krausz, L. Bonaccorsi, M. Luconi et al., “Intracellular calcium increase and acrosome reaction in response to progesterone in human spermatozoa are correlated with in-vitro fertilization,” Human Reproduction, vol. 10, no. 1, pp. 120–124, 1995.
[30]  R. I. Morimoto, A. Tissieres, and C. Georgopoulos, “The stress response, function of the proteins, and perspectives,” in Stress Proteins in Biology and Medicine, R. I. Morimoto, A. Tissieres, and C. Georgopoulos, Eds., pp. 1–36, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, USA, 1990.

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