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Clinical Characteristics of Turkish Women with Candida krusei Vaginitis and Antifungal Susceptibility of the C. krusei Isolates

DOI: 10.1155/2013/698736

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Abstract:

Objective. Candida krusei causes approximately 1% of vulvovaginal candidiasis (VVC) cases and is naturally resistant to fluconazole. Antifungal testing may be required if C. krusei vaginitis fails to respond to non-fluconazole therapy, particularly in patients with recurrent infections. Design. We investigated the clinical characteristics and antifungal susceptibility profile of vaginal C. krusei isolates. Between 2009 and 2012, we identified 560 unrelated Candida spp.-positive vaginal cultures, of which 28 (5.0%) were C. krusei. These isolates were analyzed according to host factors and the clinical forms of VVC, and their in vitro susceptibility to 10 antifungal agents was tested using a reference microdilution method. Results. We observed that perineal laceration and increased age (>50 years) were significant predictors of C. krusei in vaginal samples ( ). All isolates were susceptible to amphotericin B, caspofungin, ketoconazole, and miconazole. Additionally, susceptible dose-dependent and resistant rates were found for fluconazole as 42.9% and 57.1%, respectively. Remarkably, only 42.9% and 67.9% of the isolates were susceptible to itraconazole and voriconazole, respectively. Conclusions. Understanding local susceptibility patterns, especially those of non-C. albicans Candida species, can significantly aid in the selection of an effective antifungal agent. The in vivo response of C. krusei vaginitis to various antifungal therapeutics remains unknown and requires further research. 1. Introduction Vulvovaginal candidiasis (VVC) is a common illness attributed to an overgrowth of Candida species, and it is estimated that 75% of all women will experience an episode of VVC in their lifetimes. C. albicans accounts for 80–95% of all episodes of VVC worldwide [1, 2]. The prevalence of VVC due to non-C. albicans Candida species previously ranged from 5 to 20%; however, the number of reported cases has increased sharply over the last two decades, particularly for cases of C. glabrata [3, 4]. Therefore, the possibility of antifungal resistant strains of non-C. albicans Candida species in Candida vaginitis should be considered in clinics. The emergence of resistance may be attributed to the following factors (i) the widespread use of over-the-counter (OTC) medications; (ii) long-term use of suppressive azoles; and (iii) the frequent use of courses of antifungal medications [1, 3] or (iv) the increase use of vaginal cultures for reliable diagnoses [2, 5]. There is no evidence to suggest the followings: (i) certain women may be more susceptible to infection by

References

[1]  J. D. Sobel, “Vulvovaginal candidosis,” The Lancet, vol. 369, no. 9577, pp. 1961–1971, 2007.
[2]  M. Ilkit and A. B. Guzel, “The epidemiology, pathogenesis, and diagnosis of vulvovaginal candidosis: a mycological perspective,” Critical Reviews in Microbiology, vol. 37, no. 3, pp. 250–261, 2011.
[3]  F. Parazzini, E. Di Cintio, V. Chiantera, and S. Guaschino, “Determinants of different Candida species infections of the genital tract in women,” European Journal of Obstetrics Gynecology & Reproductive Biology, vol. 93, no. 2, pp. 141–145, 2000.
[4]  A. B. Guzel, M. Ilkit, T. Akar, R. Burgut, and S. C. Demir, “Evaluation of risk factors in patients with vulvovaginal candidiasis and the value of chromID Candida agar versus CHROMagar Candida for recovery and presumptive identification of vaginal yeast species,” Medical Mycology, vol. 49, no. 1, pp. 16–25, 2010.
[5]  P. Nyirjesy, S. M. Seeney, M. H. T. Grody, C. A. Jordan, and H. R. Buckley, “Chronic fungal vaginitis: the value of cultures,” American Journal of Obstetrics and Gynecology, vol. 173, no. 3, pp. 820–823, 1995.
[6]  S. Singh, J. D. Sobel, P. Bhargava, D. Boikov, and J. A. Vazquez, “Vaginitis due to Candida krusei: epidemiology, clinical aspects, and therapy,” Clinical Infectious Diseases, vol. 35, no. 9, pp. 1066–1070, 2002.
[7]  P. Nyirjesy, A. B. Alexander, and M. V. Weitz, “Vaginal Candida parapsilosis: pathogen or bystander?” Infectious Disease in Obstetrics and Gynecology, vol. 13, no. 1, pp. 37–41, 2005.
[8]  M. A. Pfaller, D. J. Diekema, D. L. Gibbs et al., “Candida krusei, a multidrug-resistant opportunistic fungal pathogen: geographic and temporal trends from the ARTEMIS DISK Antifungal Surveillance Program, 2001 to 2005,” Journal of Clinical Microbiology, vol. 46, no. 2, pp. 515–521, 2008.
[9]  J. D. Sobel, M. Zervos, B. D. Reed et al., “Fluconazole susceptibility of vaginal isolates obtained from women with complicated Candida vaginitis: clinical implications,” Antimicrobial Agents and Chemotherapy, vol. 47, no. 1, pp. 34–38, 2003.
[10]  L. Agatensi, F. Franchi, V. Mondello et al., “Vaginopathic and proteolytic Candida species in outpatients attending a gynaecology clinic,” Journal of Clinical Pathology, vol. 44, no. 10, pp. 826–830, 1991.
[11]  H. R. Buckley, “Identification of yeasts,” in Medical Mycology: A Practical Approach, E. G. V. Evans and M. D. Richardson, Eds., pp. 97–109, IRL Press, Oxford, UK, 1989.
[12]  Clinical Laboratory Standards Institution, Reference Method for Broth Dilution Antifungal Susceptibility Testing of Yeasts. Approved Standard CLSI Document M27-A3, Wayne, Pa, USA, 2008.
[13]  A. Kalkanc?, A. B. Güzel, I. I. J. Khalil, M. Aydin, M. Ilkit, and S. Kustimur, “Yeast vaginitis during pregnancy: susceptibility testing of 13 antifungal drugs and boric acid and the detection of four virulence factors,” Medical Mycology, vol. 50, no. 6, pp. 585–593, 2012.
[14]  M. A. Pfaller, D. Andes, D. J. Diekema, A. Espinel-Ingroff, and D. Sheehan, “Wild-type MIC distributions, epidemiological cutoff values and species-specific clinical breakpoints for fluconazole and Candida: time for harmonization of CLSI and EUCAST broth microdilution methods,” Drug Resistance Updates, vol. 13, no. 6, pp. 180–195, 2010.
[15]  D. Marchaim, L. Lemanek, S. Bheemreddy, K. S. Kaye, and J. D. Sobel, “Fluconazole-resistant Candida albicans vulvovaginitis,” Obstetrics & Gynecology, vol. 120, no. 6, pp. 1407–1414, 2012.
[16]  S. S. Richter, R. P. Galask, S. A. Messer, R. J. Hollis, D. J. Diekema, and M. A. Pfaller, “Antifungal susceptibilities of Candida species causing vulvovaginitis and epidemiology of recurrent cases,” Journal of Clinical Microbiology, vol. 43, no. 5, pp. 2155–2162, 2005.
[17]  G. M. Lyon, S. Karatela, S. Sunay, and Y. Adiri, “Antifungal susceptibility testing of Candida isolates from the Candida surveillance study,” Journal of Clinical Microbiology, vol. 48, no. 4, pp. 1270–1275, 2010.

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