Detection of Candida spp. in blood cultures using nucleic acid sequence-based amplification (NASBA)

被引:31
作者
Borst, A [1 ]
Hall, MALV [1 ]
Verhoef, J [1 ]
Fluit, AC [1 ]
机构
[1] Univ Utrecht, Med Ctr, Eijkman Winkler Inst Microbiol Infect Dis & Infla, Utrecht, Netherlands
关键词
Candida spp; NASBA; BacT/Alert;
D O I
10.1016/S0732-8893(01)00211-5
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Candida spp. are the main causes of fungal infections in immunocompromised patients. It is known, that the routinely used automated blood culture systems may fail to detect yeasts. We therefore investigated, whether Nucleic Acid Sequence-Based Amplification (NASBA) can be used to improve the detection rate of Candida spp. in blood cultures. Culture-positive as well as negative blood cultures from patients with a proven candidaemia were analyzed, and the results of BacT/Alert monitoring were compared with the results of NASBA-based detection of yeast RNA. With the NASBA-assay, the number of positive blood cultures increased from 21% to 34%. The NASBA-assay may confirm the diagnosis and demonstrate the need for prolonged treatment. In addition it may shorten the time to detection. In summary, using NASBA for the detection of yeast RNA in blood cultures, we have shown for the first time that it is possible to improve the detection rate of yeasts in blood cultures by using amplification technology. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:155 / 160
页数:6
相关论文
共 24 条
  • [1] RAPID DETECTION AND IDENTIFICATION OF CANDIDA-ALBICANS AND TORULOPSIS (CANDIDA) GLABRATA IN CLINICAL SPECIMENS BY SPECIES-SPECIFIC NESTED PCR AMPLIFICATION OF A CYTOCHROME-P-450 LANOSTEROL-ALPHA-DEMETHYLASE (L1A1) GENE FRAGMENT
    BURGENERKAIRUZ, P
    ZUBER, JP
    JAUNIN, P
    BUCHMAN, TG
    BILLE, J
    ROSSIER, M
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1994, 32 (08) : 1902 - 1907
  • [2] NUCLEIC-ACID SEQUENCE-BASED AMPLIFICATION
    COMPTON, J
    [J]. NATURE, 1991, 350 (6313) : 91 - 92
  • [3] Rapid detection of Candida albicans in clinical samples by DNA amplification of common regions from C-albicans-secreted aspartic proteinase genes
    Flahaut, M
    Sanglard, D
    Monod, M
    Bille, J
    Rossier, M
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (02) : 395 - 401
  • [4] Antimicrobial susceptibility and frequency of occurrence of clinical blood isolates in Europe from the SENTRY Antimicrobial Surveillance Program, 1997 and 1998
    Fluit, AC
    Jones, ME
    Schmitz, FJ
    Acar, J
    Gupta, R
    Verhoef, J
    [J]. CLINICAL INFECTIOUS DISEASES, 2000, 30 (03) : 454 - 460
  • [5] Use of simulated blood cultures to compare a specific fungal medium with a standard microorganism medium for yeast detection
    Fricker-Hidalgo, H
    Chazot, F
    Lebeau, B
    Pelloux, H
    Ambroise-Thomas, P
    Grillot, R
    [J]. EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1998, 17 (02) : 113 - 116
  • [6] MICROTITRATION PLATE ENZYME-IMMUNOASSAY TO DETECT PCR-AMPLIFIED DNA FROM CANDIDA SPECIES IN BLOOD
    FUJITA, SI
    LASKER, BA
    LOTT, TJ
    REISS, E
    MORRISON, CJ
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (04) : 962 - 967
  • [9] Contaminations occurring in fungal PCR assays
    Loeffler, J
    Hebart, I
    Bialek, R
    Hagmeyer, L
    Schmidt, D
    Serey, FP
    Hartmann, M
    Eucker, J
    Einsele, H
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (04) : 1200 - 1202
  • [10] MAKSYMIUK AW, 1984, AM J MED, V77, P20