Comparison of standard phenotypic assays with a PCR method to discriminate Candida albicans and C-dubliniensis

被引:37
作者
Mähnss, B
Stehr, F
Schäfer, W
Neuber, K
机构
[1] Univ Hosp Hamburg, Dept Dermatol, D-20246 Hamburg, Germany
[2] Univ Hamburg, Inst Bot, AMPIII, Hamburg, Germany
关键词
Candida dubliniensis; Candida albicans; polymerase chain reaction; Staib agar;
D O I
10.1111/j.1439-0507.2004.01054.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
In 1995, Candida dubliniensis was described as a new species in the genus Candida. Its close relationship to C. albicans has proved problematic in the identification of C. dubliniensis in clinical specimens. The objective of this study was to determine if reproducible differentiation between both species can be obtained by phenotypic assays. Therefore, 100 strains from 86 patients with the ability to produce chlamydospores were examined with different methods including API ID 32 C, colour development on CHROMagar, chlamydospore formation on Staib agar, growth at different temperatures and germ tube formation at 39degreesC. Additionally, polymerase chain reaction (PCR) was used as gold standard. Six of the investigated strains were C. dubliniensis. The results suggest that there is still no single phenotypic method satisfactory to distinguish between C. albicans and C. dubliniensis.
引用
收藏
页码:55 / 61
页数:7
相关论文
共 26 条
[1]   Differentiation of Candida dubliniensis from Candida albicans on Staib agar and caffeic acid-ferric citrate agar [J].
Al Mosaid, A ;
Sullivan, D ;
Salkin, IF ;
Shanley, D ;
Coleman, DC .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (01) :323-327
[2]   Rapid identification of Candida dubliniensis by indirect immunofluorescence based on differential localization of antigens on C-dubliniensis blastospores and Candida albicans germ tubes [J].
Bikandi, J ;
San Millán, R ;
Moragues, MD ;
Cebas, G ;
Clarke, M ;
Coleman, DC ;
Sullivan, DJ ;
Quindós, G ;
Pontón, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (09) :2428-2433
[3]   Phylogenetic analysis and rapid identification of Candida dubliniensis based on analysis of ACT1 intron and exon sequences [J].
Donnelly, SM ;
Sullivan, DJ ;
Shanley, DB ;
Coleman, DC .
MICROBIOLOGY-UK, 1999, 145 :1871-1882
[4]  
Fell Jack W., 1993, Molecular Marine Biology and Biotechnology, V2, P174
[5]   ISOLATION OF THE CANDIDA-ALBICANS GENE FOR OROTIDINE-5'-PHOSPHATE DECARBOXYLASE BY COMPLEMENTATION OF S-CEREVISIAE URA3 AND ESCHERICHIA-COLI PYRF MUTATIONS [J].
GILLUM, AM ;
TSAY, EYH ;
KIRSCH, DR .
MOLECULAR & GENERAL GENETICS, 1984, 198 (01) :179-182
[6]   Phenotypic and genotypic characterization of oral yeasts from Finland and the United States [J].
Hannula, J ;
Saarela, M ;
Alaluusua, S ;
Slots, J ;
Asikainen, S .
ORAL MICROBIOLOGY AND IMMUNOLOGY, 1997, 12 (06) :358-365
[7]  
Jabra-Rizk MA, 2000, J CLIN MICROBIOL, V38, P2423
[8]   Rapid differentiation of Candida albicans from other Candida species using its unique germ tube formation at 39°C [J].
Kim, D ;
Shin, WS ;
Lee, KH ;
Kim, K ;
Park, JY ;
Koh, CM .
YEAST, 2002, 19 (11) :957-962
[9]   Detection of Candida dubliniensis in oropharyngeal samples from human immunodeficiency virus-infected patients in North America by primary CHROMagar Candida screening and susceptibility testing of isolates [J].
Kirkpatrick, WR ;
Revankar, SG ;
McAtee, RK ;
Lopez-Ribot, JL ;
Fothergill, AW ;
McCarthy, DI ;
Sanche, SE ;
Cantu, RA ;
Rinaldi, MG ;
Patterson, TF .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (10) :3007-3012
[10]   Rapid PCR test for discriminating between Candida albicans and Candida dubliniensis isolates using primers derived from the pH-regulated PHR1 and PHR2 genes of C-albicans [J].
Kurzai, O ;
Heinz, WJ ;
Sullivan, DJ ;
Coleman, DC ;
Frosch, M ;
Mühlschegel, FA .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (05) :1587-1590