Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/357438
Type: Artigo
Title: Resistance surveillance in candida albicans: a five-year antifungal susceptibility evaluation in a brazilian university hospital
Author: Peron, Isabela Haddad
Reichert-Lima, Franqueline
Busso-Lopes, Ariane Fidelis
Nagasako, Cristiane Kibune
Lyra, Luzia
Moretti, Maria Luiza
Schreiber, Angelica Zaninelli
Abstract: Candida albicans caused 44% of the overall candidemia episodes from 2006 to 2010 in our university tertiary care hospital. As different antifungal agents are used in therapy and also immunocompromised patients receive fluconazole prophylaxis in our institution, this study aimed to perform an antifungal susceptibility surveillance with the C. albicans bloodstream isolates and to characterize the fluconazole resistance in 2 non-blood C. albicans isolates by sequencing ERG11 gene. The study included 147 C. albicans bloodstream samples and 2 fluconazole resistant isolates: one from oral cavity (LIF 12560 fluconazole MIC: 8 mu g/mL) and one from esophageal cavity (LIF-E10 fluconazole MIC: 64 mu g/mL) of two different patients previously treated with oral fluconazole. The in vitro antifungal susceptibility to amphotericin B (AMB), 5-flucytosine (5FC), fluconazole (FLC), itraconazole (ITC), voriconazole (VRC), caspofungin (CASP) was performed by broth microdilution methodology recommended by the Clinical and Laboratory Standards Institute documents (M27-A3 and M27-S4, CLSI). All blood isolates were classified as susceptible according to CLSI guidelines for all evaluated antifungal agents (MIC range: 0,125-1.00 mu g/mL for AMB, <= 0.125-1.00 mu g/mL for 5FC, <= 0.125-0.5 mu g/mL for FLC, <= 0.015-0.125 mu g/mL for ITC, <= 0.015-0.06 mu g/mL for VRC and <= 0.015-0.125 mu g/mL for CASP). In this study, we also amplified and sequenced the ERG11 gene of LIF 12560 and LIF-E10 C. albicans isolates. Six mutations encoding distinct amino acid substitutions were found (E116D, T128K, E266D, A298V, G448V and G464S) and these mutations were previously described as associated with fluconazole resistance. Despite the large consumption of antifungals in our institution, resistant blood isolates were not found over the trial period. Further studies should be conducted, but it may be that the very prolonged direct contact with the oral antifungal agent administered to the patient from which was isolated LIF E-10, may have contributed to the development of resistance
Subject: Guia de prática clínica
Doenças transmissíveis
Candidíase invasiva
Resistência a medicamentos
Country: Estados Unidos
Editor: Public Library of Science
Rights: Aberto
Identifier DOI: 10.1371/journal.pone.0158126
Address: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0158126
Date Issue: 2016
Appears in Collections:FCM - Artigos e Outros Documentos

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