In vitro activity of antimycotic agents determined by E-test method against vaginal shape Candida species

被引:20
作者
Candido, RC
Toloi, MRT
Franceschini, SA
Garcia, FR
Minto, ECM
机构
[1] Univ Sao Paulo, Fac Ciencias Farmaceut Ribeirao Preto, Dept Anal Clin Toxicol & Bromatol, BR-14040903 Ribeirao Preto, Brazil
[2] SISUSP, Ribeirao Preto, Brazil
关键词
C-albicans; C-krusei; C-parapsilosis; C-tropicalis; E-test; yeasts;
D O I
10.1023/A:1006928628550
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Vaginal candidiasis continues to be a common cause of vaginal discharge, pruritus and other local complaints in women worldwide. Although numerous antimycotic agents are available for the treatment of yeast vaginitis there is little comparative data on the in vitro activity of these drugs. The objectives of this study were to isolate and identify the Candida species in the vagina and anus of patients treated in a gynaecology clinic, as well as determine the susceptibility to azolic compounds measured by the E-test method. Vaginal and rectal swabs were collected from 80 adult non-pregnant patients, seen at a gynaecological clinic, aged 18-59 years, with sexual activity, with and without vaginitis. The swabs were processed by methods routinely used for the detection of pathogenic yeasts. The susceptibility of the isolates to fluconazole, ketoconazole and itraconazole, was measured by the agar diffusion method (E-test), using RPMI 1640 medium with 2% glucose and phosphate buffer. Candida species (33) strains were isolated from 17 patients at similar proportions from both anatomical sites, and 12 patients harboured 24 strains of C. albicans in the vaginal and rectal tracts. Twenty one percent of the strains of C. albicans were resistant to ketoconazole, 54% were resistant to itraconazole and 0% were resistant to fluconazole. The sensitivity of strains isolated from the two sites were similar, indicating that these are strains of the same phenotype.
引用
收藏
页码:15 / 20
页数:6
相关论文
共 31 条
[1]   PERSISTENCE OF THE SAME CANDIDA-ALBICANS STRAIN DESPITE FLUCONAZOLE THERAPY - DOCUMENTATION BY PULSED-FIELD GEL-ELECTROPHORESIS [J].
BLUMBERG, HM ;
HENDERSHOT, EF ;
LOTT, TJ .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1992, 15 (06) :545-547
[2]  
BODEY GP, 1992, CLIN INFECT DIS S1, V14, P161
[3]   INTERFERENCE WITH EFFECTS OF AMPHOTERICIN-B ON CANDIDA-ALBICANS CELLS BY 2-CHLOROETHYL-1-NITROSOUREAS [J].
BRAJTBURG, J ;
ELBERG, S ;
KOBAYASHI, GS ;
MEDOFF, G .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1988, 32 (03) :327-330
[4]  
BRUATTO M, 1992, MYCOSES, V35, P53
[5]   COMPARISON OF E-TEST AND NATIONAL-COMMITTEE-FOR-CLINICAL-LABORATORY-STANDARDS BROTH MACRODILUTION METHOD FOR AZOLE ANTIFUNGAL SUSCEPTIBILITY TESTING [J].
COLOMBO, AL ;
BARCHIESI, F ;
MCGOUGH, DA ;
RINALDI, MG .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (03) :535-540
[6]   INVITRO STUDIES WITH R-51,211 (ITRACONAZOLE) [J].
ESPINELINGROFF, A ;
SHADOMY, S ;
GEBHART, RJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1984, 26 (01) :5-9
[7]   Interlaboratory evaluation of Etest method for testing antifungal susceptibilities of pathogenic yeasts to five antifungal agents by using Casitone agar and solidified RPMI 1640 medium with 2% glucose [J].
EspinelIngroff, A ;
Pfaller, M ;
Erwin, ME ;
Jones, RN .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (04) :848-852
[8]  
Horsburgh C R Jr, 1983, Am J Med, V74, P23, DOI 10.1016/0002-9343(83)90511-9
[9]   EMERGENCE OF AZOLE DRUG-RESISTANCE IN CANDIDA SPECIES FROM HIV-INFECTED PATIENTS RECEIVING PROLONGED FLUCONAZOLE THERAPY FOR ORAL CANDIDOSIS [J].
JOHNSON, EM ;
WARNOCK, DW ;
LUKER, J ;
PORTER, SR ;
SCULLY, C .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1995, 35 (01) :103-114
[10]  
Kreger-van-Rij N. J. W., 1984, YEAST TAXONOMIC STUD