Fluconazole and voriconazole susceptibility in oral colonization isolates of Candida spp. in HIV patients. / Susceptibilidad a fluconazol y voriconazol en aislados orales de Candida spp. en pacientes con VIH.
Resumen
Abstract.
The identification of Candida species and their antifungal susceptibility is important for the treatment of infected patients. The aim was to determine the susceptibility to fluconazole and voriconazole in isolates from oral colonization of Candida spp. in HIV patients. From the 135 patients studied, 33.3% were females and 66.7% males, with a mean age of 36.6 years and 83.7% of them were under treatment. The identification of the specie was performed by the API20CAUX® test and the antifungal susceptibility was determined by the disc diffusion test. Strains of C. parapsilosis and C. krusei were used as quality controls. The Candida species identificated were: C. parapsilosis complex 52%, C. albicans complex 36% and C. famata 12%. 60% of the isolates were susceptible to fluconazole and 40% were dose-dependent. All were susceptible to voriconazole. In this study, none of the patients had oropharyngeal candidiasis however, 18.5% had Candida spp. colonization, this percentage being below other studies in HIV carriers. We found a high proportion of nonalbicans species but no difference in the CD4+ counts between patients.
Resumen.
Identificar las especies de Candida y la susceptibilidad a los antifúngicos es importante para el tratamiento adecuado de pacientes infectados. El objetivo fue determinar la susceptibilidad a fluconazol y voriconazol de Candida spp. en aislados de colonizaciones orales en pacientes con VIH. La identificación se realizó mediante la prueba API20CAUX® y la prueba de difusión de disco para la sensibilidad a los antifúngicos. Se utilizaron cepas de C. parapsilosis y C. krusei como control de calidad. De los 135 pacientes, el 33,3% eran mujeres y el 66,7% hombres con una edad media de 36,6 años y el 83,7% recibían tratamiento. Las especies de Candida identificadas fueron: complejo C. parapsilosis 52%, complejo C. albicans 36% y C. famata 12%. La susceptibilidad al fluconazol 60% eran susceptibles y 40% dependía de la dosis. Todas eran susceptibles al voriconazol. En este estudio, ninguno tenía candidiasis orofaríngea, sin embargo, el 18.5% tenía colonización por Candida spp., aunque el porcentaje está por debajo de otros estudios en portadores de VIH. Encontramos una alta proporción de especies no-albicans. No hubo diferencias en el recuento de CD4+ entre los pacientes
Descargas
Citas
Nanteza M, Tusiime J, Kalyango J, Kasan- gaki A. Association between oral candidia- sis and low CD4+ count among HIV positive patients in Hoima Regional Referral Hos- pital. BMC Oral Health 2014;14:143. doi: 10.1186/1472-6831-14-143. Li X, Lei L, Tan D, Jiang L, Zeng X, Dan H. Oropharyngeal Candida colonization in human immunodeficiency virus infected patients. APMIS 2013;121(5):375-402. doi: 10.1111/apm.12006.
Patil S, Majumdar B, Sarode SC, Sarode GS, Awan KH. Oropharyngeal candidiasis in HIV-infected patients - An update. Front Microbiol 2018; 15(9):980. doi: 10.3389/ fmicb.2018.00980.
Pfaller M. Antifungal drug resistance: mechanisms, epidemiology, and conse- quences for treatment. Am J Med 2012; 125(1Suppl):S3-13. doi: 10.1016/j.am- jmed.2011.11.001.
UNAIDS. WHO case definitions of HIV for surveillance and revised clinical staging and immunological classification of HIV-related disease in adults and children. 2013;6-16.
Pfaller M, Andes D, Diekema D, Espinel- Ingroff A, Sheehan D. Wild-type MIC dis- tributions, epidemiological cutoff values and species-specific clinical breakpoints for fluconazole and Candida: time for har- monization of CLSI and EUCAST broth microdilution methods. Drug Resist Up- date 2010; 13(6):180-195. doi: 10.1016/j. drup.2010.09.002.
National Committee for Clinical Labora- tory Standards (NCCLS). Method for anti- fungal disk diffusion susceptibility testing of yeast. Approved guideline M44-A. 2004; 24:1-23.
Mushi MF, Bader OB, Taverne-Ghad- walb L, Biic Ch, Großb U, Mshanaa S. Oral candidiasis among African human immunodeficiency virus-infected indi- viduals: 10 years of systematic review and meta-analysis from sub-Saharan Africa. J Oral Microbiol 2017;9(1):1317579. doi: 10.1080/20002297.2017.1317579.
Konaté A, Barro-Kiki PCM, Kassi KF, An- gora KE, Vanga-Bosson H, Djohan V, Bé- dia-Tanoh AV, Miézan AJS, Yavo W, Menan EIH. Oropharyngeal candidiasis prevalence among HIV-infected patients at the teach- ing hospital of Treichville. J Mycolog Med 2017;27(4):549-553. doi: 10.1016/j.myc- med.2017.08.005.
Dos Santos PM, McArthur CP, Africa CW. Multi-drug resistant oral Candida species isolated from HIV-positive patients in South Africa and Cameroon. Diag Microbiol Infect Dis 2014;79(2):222-227.
Nweze EI, Ogbonnaya UL. Oral Candida isolates among HIV-infected subjects in Ni- geria. J Microbiol Immunol Infect 2011;44: 172-177. doi: 10.1016/j.jmii.2011.01.028.
HIV InSite. University of California, San Francisco. Available on: http://hiv- insite.ucsf.edu/global?page=cr05-ve- 00&post=19&cid=VE. (Last date access December 31th 2015).
Theill L, Dudiuk C, Morano C, Gamarra S, Nardin ME, Méndez E, Garcia-Effron G. Prevalence and antifungal susceptibil- ity of Candida albicans and its related spe- cies Candida dubliniensis and Candida af- ricana isolated from vulvovaginal samples in a hospital of Argentina. Rev Argent Mi- crobiol 2016;48(1):43-49. doi: 10.1016/j. ram.2015.10.003.
Terças AL, Marques SG, Moffa EB, Alves MB, de Azevedo MP, Siqueira WL, Mon- teiro CA. Antifungal drug susceptibil- ity of Candida species isolated from HIV- positive patients recruited at a Public Hospital in São Luís, Maranhão, Brazil. Front Microbiol 2017;8:298. doi: 10.3389/ fmicb.2017.00298.
Junqueira J, Vilela S, Rossoni R, Barbosa J, Costa A, Rasteiro V, Suleiman J, Jorge O. Oral colonization by yeasts in HIV-pos- itive patients in Brazil. Rev Inst Med Trop 2012;54(1):17-24. doi: 10.1590/s0036-46652012000100004.
Kaur R, Dhakad M, Goyal R, Bhalla P, Dewan R. Spectrum of opportunistic fun- gal infections in HIV/AIDS patients in ter- tiary care hospital in India. Can J Infect Dis Med Microbiol 2016: 2373424. doi: 10.1155/2016/2373424. Epub 2016 Jun 20.
Thanyasrisung P, Kesakomol P, Pipat- tanagovit P, Youngnak-Piboonratanakit P, Pitiphat W, Matangkasombut O. Oral Can- dida carriage and immune status in Thai human immunodeficiency virus-infected in- dividuals. J Med Microbiol 2014;63(5):753- 759. doi: 10.1099/jmm.0.069773-0
Berberi A, Noujeim Z, Aoun G. Epidemio- logy of oropharyngeal candidiasis in human immunodeficiency virus/acquired immune deficiency syndrome patients and CD4+ Counts. J Int Oral Health 2015;7(3):20-23. PMID: 25878473; PMCID: PMC4385720.
Enwuru CA, Ogunledun A, Idika N. En- wuru NV, Ogbonna F, Aniedobe M, Adeiga Fluconazole resistant opportunistic oro- pharyngeal candida and non-candida yeast- like isolates from HIV infected patients attending ARV clinics in Lagos, Nigeria. Af- rican Health Sciences 2008; 8(3):142-148.
Fothergill AW, Sutton DA, McCarthy DI, Wiederhold NP. Impact of new anti- fungal breakpoints on antifungal resis- tance in Candida species. J Clin Micro- biol 2014;52(3):994-997. doi: 10.1128/ JCM.03044-13.
Nucci M, Queiroz-Telles F, Alvarado-Mat- ute T, Tiraboschi IN, Cortes J, Zurita J, Guzman-Blanco M, Santolaya M, Thomp- son L, Sifuentes-Osornio J, Echevarria J, Colombo A. Epidemiology of candi- demia in Latin America: a laboratory-based survey. PLoS ONE 2013; 8(3): e59373. doi: 10.1371/journal.pone.0059373.
Osaigbovo I, Lofor P, Oladele R. Flucon- azole resistance among oral Candida iso- lates from people living with HIV/AIDS in a Nigerian Tertiary Hospital. J Fungi (Basel). 2017;3(4):E69. doi: 10.3390/jof3040069.
Trofa D, Gácser A, Nosanchuk JD. Candi- da parapsilosis, an emerging fungal patho- gen. Clin Microbiol Rev 2008;21(4):606- 625. doi: 10.1128/CMR.00013-08.
Saúl-García Y, Humbría-García L, Hernán- dez-Valles R. Species distribution and anti- fungal susceptibility of Candida spp. caus- ing superficial mycosis. Coro, Falcon state, Venezuela. Invest Clin 2015; 56(3): 276 –283. PMID:26710542
Moreno X, Reviakina V, Panizo MM, Fe- rrara G, García N, Alarcón V, Garcés MF, Dolande M. Identificación molecular y sensibilidad a los antifúngicos de aisla- mientos de sangre del complejo Candida parapsilosis en Venezuela. Rev Iberoam Micol 2017. http://dx.doi.org/10.1016/j. riam.2016.11.005.
Ngouana T, Krasteva D, Drakulovski P, To- ghueo R, Kouanfack C, Ambe A, Reynes J, Delaporte E, Boyom F, Malli M, Bertout S. Investigation of minor species Candida africana, Candida stellatoidea and Candida dubliniensis in the Candida albicans com- plex among Yaoundé (Cameroon) HIV-in- fected patients. Mycoses. 2015; 58: 33–39. doi: 10.1111/myc.12266.
Saúl García Y, Hernández Valles R. Aisla- miento de Candida spp. en ambiente y per- sonal que labora en una unidad de cuidados intensivos. Rev Soc Ven Microbiol 2014; 34:27-32.
Perozo A, Calvo B, Mesa L, Pineda M. Sus- ceptibilidad a fluconazol y voriconazol por el método de difusión, de cepas de Candi- da, aisladas de hemocultivos en Maracaibo, Venezuela. Kasmera 2011;38(2):114-122.
Calvo B, Mesa L, Perozo A, Pineda M, Bel- trán-Luengo H. Cambios en la distribución de especies de Candida aisladas de hemo- cultivos, en pacientes del Servicio Autóno- mo Hospital Universitario de Maracaibo, Venezuela. Kasmera 2010;38(2):106-117.