Membrane filtration test for rapid presumptive differentiation of four Candida species

被引:16
作者
Bauters, TG
Peleman, R
Moerman, M
Vermeersch, H
De Looze, D
Noens, L
Nelis, HJ
机构
[1] Univ Ghent, Dept Pharmaceut Anal, Lab Pharmaceut Microbiol, B-9000 Ghent, Belgium
[2] Ghent Univ Hosp, Dept Internal Med, Div Infect Dis, B-9000 Ghent, Belgium
[3] Ghent Univ Hosp, Dept Head & Neck Surg, B-9000 Ghent, Belgium
[4] Ghent Univ Hosp, Dept Gastroenterol, B-9000 Ghent, Belgium
[5] Ghent Univ Hosp, Dept Haematol, B-9000 Ghent, Belgium
关键词
D O I
10.1128/JCM.37.5.1498-1502.1999
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A rapid enzymatic two-step test for the presumptive differentiation of four Candida species commonly occurring in various clinical samples is described. The technique involves membrane filtration of a liquid sample, followed by preincubation of the membrane filter on Sabouraud glucose agar supplemented with ticarcillin-clavulanic acid to yield microcolonies. In a separate assay step, parts of the filter are placed on absorbent pads impregnated;vith fluorogenic 4-methylumbelliferyl ( 4-MU) enzyme substrates (4-MU-N-acetyl-beta-D-galactosaminide, 4-MU-phosphate, 4-MU-pyrophosphate. and 4-MU-beta-D-galactoside) in combination with 0.1% digitonin acting as a membrane permeabilizer. The membrane Biter in contact with the assay medium is incubated to allow cleavage of the enzyme substrate, resulting in fluorescent microcolonies under long-wavelength UV light This approach, tested on 301 clinical samples, is able to presumptively differentiate C. albicans, C. glabrata, C. krusei, and C. tropicalis and to distinguish them from other Candida spp. in about 9 to 11 h. Overall agreement with the conventional methods of 94.4% tone Candida species present in the sample to 83.8% (multiple Candida spp. present) aas obtained, The false-negative rates, with reference to identification by traditional methods were 1.39 (single species) and 3.8% (multiple species).
引用
收藏
页码:1498 / 1502
页数:5
相关论文
共 25 条
[1]   Direct identification and recognition of yeast species from clinical material by using albicans ID and CHROMagar Candida plates [J].
Baumgartner, C ;
Freydiere, AM ;
Gille, Y .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (02) :454-456
[2]   Evaluation of CHROMagar Candida medium for the isolation and presumptive identification of species of Candida of clinical importance [J].
Bernal, S ;
Mazuelos, EM ;
Garcia, M ;
Aller, AI ;
Martinez, MA ;
Gutierrez, MJ .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1996, 24 (04) :201-204
[3]   RAPID DETECTION OF YEAST ENZYMES BY USING 4-METHYLUMBELLIFERYL SUBSTRATES [J].
BOBEY, DG ;
EDERER, GM .
JOURNAL OF CLINICAL MICROBIOLOGY, 1981, 13 (02) :393-394
[4]  
BODEY GP, 1992, CANDIDIASIS PATHOGEN, P371
[5]   PROTEIN DETERMINATION IN PERMEABILIZED YEAST-CELLS USING THE COOMASSIE BRILLIANT BLUE-DYE BINDING ASSAY [J].
CORDEIRO, CAA ;
FREIRE, AP .
ANALYTICAL BIOCHEMISTRY, 1994, 223 (02) :321-323
[7]   PERMEABILIZED CELLS [J].
FELIX, H .
ANALYTICAL BIOCHEMISTRY, 1982, 120 (02) :211-234
[8]   Evaluation of latex reagents for rapid identification of Candida albicans and C-krusei colonies [J].
Freydiere, AM ;
Buchaille, L ;
Guinet, R ;
Gille, Y .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (04) :877-880
[9]   FUTURE-DIRECTIONS OF ANTIFUNGAL CHEMOTHERAPY [J].
GRAYBILL, JR .
CLINICAL INFECTIOUS DISEASES, 1992, 14 :S170-S181
[10]  
*I HYG EP, 1996, NAT PROGR SURV HOSP