Please use this identifier to cite or link to this item: https://ninho.inca.gov.br/jspui/handle/123456789/6573
Title: Candida haemulonii complex: species identification and antifungal susceptibility profiles of clinical isolates from Brazil
Authors: Ramos, Livia de Souza
Carvalho, Maria Helena Galdino Figueiredo de
Barbedo, Leonardo Silva
Ziccardi, Mariangela
Chaves, Alessandra Leal da Silva
Oliveira, Rosely Maria Zancopé
Silva, Marcia Ribeiro Pinto da
Sgarbi, Diana Bridon da Graça
Ribeiro, Marcos Dornelas
Sá, Marta Helena Branquinha de
Santos, André Luis Souza dos
Keywords: Hospitais
Hospitals
Hospitales
Candida
Farmacorresistência Fúngica Múltipla
Drug Resistance, Multiple, Fungal
Farmacorresistencia Fúngica Múltiple
Suscetibilidade a Doenças
Disease Susceptibility
Susceptibilidad a Enfermedades
Issue Date: 2015
Publisher: Journal Antimicrobial Chemother
Citation: RAMOS, Livia de Souza et al. Candida haemulonii complex: species identification and antifungal susceptibility profiles of clinical isolates from Brazil. Journal Antimicrobial Chemother, v. 70, p. 111 –115, 2015.
Abstract: The emerging fungal pathogens comprising the Candida haemulonii complex (Candida haemulonii, Candida haemulonii var. vulnera and Candida duobushaemulonii) are notable for their antifungal resistance. Twelve isolates with phenotypic similarity to C. haemulonii were recovered from patients in Brazilian hospitals. Here we aimed to identify these isolates by a molecular approach, using the current classification of this fungal complex, and to evaluate their antifungal susceptibility profiles. Methods: The fungal isolates were rechecked to certify their authentication by mycology methodologies and then characterized by ITS1-5.8S-ITS2 gene sequencing. A susceptibility assay was performed using the broth microdilution method published by CLSI (M27-A3/M27-S3). Results: Based on biochemical tests, all Brazilian isolates were identified as C. haemulonii. After employing ITS sequencing,fiveisolateswereidentifiedasC.haemulonii,fourasC.duobushaemuloniiandthreeasC.haemulonii var. vulnera. All 12 clinical isolates were resistant to amphotericin B (MICs ranged from 2 to .16 mg/L) and fluconazole (MICs ≥64 mg/L). One isolate of C. haemulonii var. vulnera and two isolates of C. duobushaemulonii weresusceptible-dose dependent to itraconazole, while the remaining isolates(75%) were resistant to thisantifungal. Eight out of 12 isolates (66.7%) were resistant to voriconazole (MICs ≥16 mg/L), while all isolates were susceptible to caspofungin (MICs≤0.5 mg/L). Conclusions: Our results reinforce the importance of molecular identification in differentiating species of the C. haemulonii complex. Moreover, the antifungal multiresistant profile of clinical isolates of the C. haemulonii complex represents a challenge to the treatment of such infections.
Description: p. 111 –115. : il. p&b.
URI: http://sr-vmlxaph03:8080/jspui/handle/123456789/6573
ISSN: 1460-2091
Appears in Collections:Artigos de Periódicos da área de Farmácia



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