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Utilization of Ferroproteins by Candida albicans during Candidastasis by Apotransferrin  

Han, Yong-Moon (College of Pharmacy, Dongduk Women's University)
Publication Information
Archives of Pharmacal Research / v.28, no.8, 2005 , pp. 963-969 More about this Journal
Abstract
Many reports have stated that some of the pathogenic bacteria can obtain iron from ferroproteins, such as cytochrome C, ferritin, hemin, hemoglobin, and myoglobin. These reports prompted us to determine if an opportunistic pathogenic fungus, Candida albicans, can utilize ferroproteins to circumvent the iron-regulatory effect of transferrin. The following assays were carried out to measure in vitro growth stimulation by the ferroproteins: as an initial step, C. albicans was cultured in iron-free (pretreated with apotransferrin for 24h) culture medium. Once Candida albicans yeast cell growth reached stasis from iron starvation, individual ferroproteins were added to the culture media. Results showed that hemin, hemoglobin, and myoglobin supported a partial growth recovery. Additional studies with haptoglobin, a serum protein that interacts with the globin moiety of certain ferroproteins, established that C. albicans could obtain iron from the haptoglobin-ferroprotein complexes. These data indicate that the heme part of the ferroproteins is the source of iron. This implies that heme oxygenase, CaHMX1 might be involved in bringing about dissociation of heme-containing protein for iron-acquisition. In addition, anticandidal activity of transferrin takes place not only by the process of iron regulation, but also by direct interaction with the yeast cells.
Keywords
Candida albicans; Transferrin; Ferroproteins; Haptoglobin; Heme;
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1 Caroline, L., Taschdjian, C. L., Kozin, P. J., and Schade, A. L. Reversal of serum fungistasis by addition of iron. J. Invest. Dermatol., 43, 415-419 (1964)   DOI
2 Eaton, J. W., Brandt, P., and Mahoney, J. R. Haptoglobin: a natural bacteriostat. Science, 215, 691-692 (1982)   DOI   PUBMED
3 Esterly, N. B., Bramner, S. R., and Crounse, R. G. Relationship of transferrin and iron to serum inhibition of Candida albicans. J. Invest. Dermatol. 49, 437-442 (1967)   DOI   ScienceOn
4 Fletcher, J. and Huehns, E. R. Function of transferrin. Nature, 218, 1211-1214 (1986)   DOI   ScienceOn
5 Han, Y., Kozel, T. R., Zhang, M. X., MacGill, R. S., Caroll, M. C., and Cutler, J. E. Complement is essential for protection by an IgM and an IgG3 monoclonal antibody against experimental, hematogenously disseminated candidiasis. J. Immunol., 167, 1550-1557 (2001)   DOI
6 Han, Y. and Lee, J. Berberine synergy with amphotericin B against disseminated candidiasis. Biol. Pharm. Bull., 28, 541- 544 (2005a)   DOI   ScienceOn
7 Han, Y. Ginkgo terpene component has an anti-inflammatory effect on Candida albicans-caused arthritic inflammation. Int. Immunopharm., 5, 1049-1056 (2005b)   DOI   PUBMED   ScienceOn
8 Otto, B. R., Sparrius, A. M., Verweis-Van Vught, J. J., and MaClaren, D. M. Iron-regulated outer membrane protein of Bacteroides fragilis. Infect. Immun., 58, 3954-3958 (1990)
9 Perry, R. D. and Brubaker, R. R. Accumulation of iron by Yersiniae. J. Bacteriol. 137, 1290-1298 (1979)
10 Pidock, K. A., Wooten, J. A., Daley, B. A., and Stull, T. L. Iron acquisition by Haemophilus influenza. Infect. Immun., 56, 721-725 (1998)
11 Santos, R., Buisson, N., Knight, S., Dancis, A., Camadro, J. M., and Lesuisse, E. Hemin uptake and use as an iron source by Candida albicans: role of CAHMX1-encoded haem oxygenase. Microbiol., 149, 579-588 (2003)   DOI   ScienceOn
12 Simonson, C., Brener, D., and Devoe, I. W. Expression of a high affinity mechanism for acquisition of transferrin iron by Neisseria meningutudis. Infect. Immun., 36, 107-113 (1982)
13 Weinberg, E. D. Iron and interaction. Microbiol. Rev., 42, 45-66 (1978)
14 Cowart, R. E. and Foster, B. G. Differential effects of on the growth of Listeria monocytogens: minimum requirements and mechanism if acquistion. J. Bacteriol., 142, 581-587 (1985)
15 Phelps, C. F. and Antonini, E. A study of the kinetics of iron and copper binding to hen ovotrasferrin. J. Biochem., 147, 385- 391 (1975)   DOI
16 Gentry, M. J., Confer, A. W., Weinberg, E. D., and Homer, J. T. Cytotoxin (leukotoxin) production by Pasteurella haemolytica: requirement for as iron-containing compound. Am. J. Vet. Res., 47, 1919-1923 (1986)
17 Howard, D. H. Acqusition, transport, and storage of iron by pathogenic fungi. Clin. Microbiol. Rev., 12, 394-404 (1999)
18 Finkelstein, R. A., Sciortino, C. V., and McIntosh, M. A. Role of iron in microbe-host interactions. Rev. Infect. Dis., 5, S759- S777 (1983)   DOI
19 Valenti, P., Visca, P., Giovani, A., and Oris, N. Interaction between lactoferrin and ovotransferrin and candida cell. FEMS Microbiol. Lett., 33, 271- 275 (1986)   DOI
20 Young, I. G., Cox, G. B., and Gibson, F. 2,3-Dihydroxy-benzoate as bacterial growth factor and its route of biosynthesis. Biochim. Biophys. Acta, 441, 319-331 (1967)
21 Masson, P. J. and Heremans, J. F. Lactoferrin in milk from different species. Comp. Biochem. Physiol., 39B, 119-129 (1971)
22 Bullen, J. J., Rogers, H. J., and Griffiths, E. Role of iron in bacterial infection. Curr. Top. Microbial. Imunol., 80, 1-35 (1978)
23 Cutler, J. E. and Han, Y. Fungal factors implicated in pathogenesis. In The mycota VI: human and animal relationship (Eds: Howard, D. H. and Miller, J). Springer- Verlag, Berlin. pp 1-29 (1996)
24 Bullen, J. J. The significance of iron in infection. Rev. Infec. Dis., 3, 1127-1138 (1981)   DOI
25 Pendrak, M. L., Chao, M. P., Yan, S. S., and Roberts, D. D. Heme oxygenase in Candida albicans is regulated by hemoglobin and is necessary for metabolism of exogenous heme and hemoglobin to -biliverdin. J. Biol. Chem., 279, 3426-3433 (2004)   DOI
26 Griffiths, E. Availability of iron and survival of bacteria in infection. In Medical Microbiology. (Eds. Easmon, C. S. F. et al.). Vol. 3, pp 153-157. Academic press. London, (1983)
27 Masson, P. J., Heremans, J. F., and Dive, C. H. An iron-binding protein common to many external secretions. Clin. Chim. Acta, 14, 729-734 (1966)   DOI   ScienceOn
28 Roth, F. J. Jr. and Goldstein, M. I. Inhibition of growth of pathogenic yeast by human serum. J. Invest. Dermatol., 36, 383-387 (1961)   DOI
29 Graham, G. F. and Bates, G. W. Approaches to the standardization of serum unsaturated iron-binding capacity. J. Lab. Clin. Med., 88, 477-486 (1976)
30 Han, Y., Riesselman, M. H., and Cutler, J. E. Protection against candidiasis by an immunoglobulin G3 monoclonal antibody specific for the same mannotriose as an IgM protective antibody. Infect. Immun., 68, 1649-1654 (2000)   DOI   ScienceOn
31 Weinberg, E. D. Role of iron in host-parasite interaction. J. Infect. Dis., 124, 401-410 (1971)   DOI   ScienceOn
32 Hamaguchi, H., Isomoto, A., Miyake, Y., and Nakajima, H. Some spectra properties of the human hemoglobinhaptoglobin complex. Biochemistry, 10, 1741-1745 (1971)   DOI   ScienceOn
33 Zakaria-Meehan, Z., Massad, G., Simpson, L. M. Travis, J. C., and Oliver, J. D. Ability of Vibrio vulnificus to obtain iron from hemoglobin-haptoglobin. Infect. Immun., 56, 275-277 (1998)
34 Green, I., Kirkpatrick, C. H., and Dale, D. C. Lactoferrin-specific localization in the nuclei of human polymorphonuclear neutrophilic leukocytes. Proc. Soc. Exp. Biol. Med., 137, 1311-1317 (1971)   DOI
35 Garcia-Mendoza, C. and Novales-Lidieu, M. Chitin in the new wall of regenerating protoplasts of Candida utilis. Nature, 220, 1035-1036 (1968)   DOI   ScienceOn
36 Stull, T. Protein sources of heme for Haemophilus influenza. Infect. Immun., 55, 148-153 (1997)