Candida haemulonii complex: species identification and antifungal susceptibility profiles of clinical isolates from Brazil

被引:67
|
作者
Ramos, Livia S. [1 ]
Figueiredo-Carvalho, Maria Helena G. [2 ]
Barbedo, Leonardo S. [2 ]
Ziccardi, Mariangela [1 ,3 ]
Chaves, Alessandra L. S. [4 ]
Zancope-Oliveira, Rosely M. [2 ]
Pinto, Marcia R. [5 ]
Sgarbi, Diana B. G. [5 ]
Dornelas-Ribeiro, Marcos
Branquinha, Marta H. [1 ]
Santos, Andre L. S. [1 ,6 ]
机构
[1] Univ Fed Rio de Janeiro, Inst Microbiol Paulo de Goes, Dept Microbiol Geral, Lab Invest Peptidases, Rio De Janeiro, Brazil
[2] Fundacao Oswaldo Cruz, Inst Nacl Infectol Evandro Chagas, Lab Micol, Rio De Janeiro, Brazil
[3] Fundacao Oswaldo Cruz, Inst Oswaldo Cruz, Lab Interdisciplinar Pesquisas Med, Rio De Janeiro, Brazil
[4] Inst Nacl Canc, Serv Patol Clin, Lab Micol, Rio De Janeiro, Brazil
[5] Univ Fed Fluminense, Inst Biomed, Rio De Janeiro, Brazil
[6] Univ Fed Rio de Janeiro, Inst Quim, Programa Posgrad Bioquim, Rio de Janeiro, Brazil
关键词
Candida haemulonii complex; Brazilian hospitals; resistance; antifungal susceptibility; AMPHOTERICIN-B; SP NOV; CARE; SURVEILLANCE; FLUCONAZOLE; RESISTANCE; PATIENT; YEASTS; BLOOD; INDIA;
D O I
10.1093/jac/dku321
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: 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, five isolates were identified as C. haemulonii, four as C. duobushaemulonii and three as C. 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 were susceptible-dose dependent to itraconazole, while the remaining isolates (75%) were resistant to this antifungal. 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.
引用
收藏
页码:111 / 115
页数:5
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