Species identification of medically important fungi by use of real-time LightCycler PCR

被引:72
作者
Hsu, MC
Chen, KW
Lo, HJ
Chen, YC
Liao, MH
Lin, YH
Li, SY [1 ]
机构
[1] Ctr Dis Control, Div Lab Res & Dev, Lab Mycopathogen Chiamydia & Mycoplasma, Taipei, Taiwan
[2] Natl Hlth Res Inst, Div Clin Res, Taipei, Taiwan
[3] Natl Taiwan Univ Hosp, Dept Internal Med, Taipei 100, Taiwan
关键词
D O I
10.1099/jmm.0.05302-0
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学]; 100705 [微生物与生化药学];
摘要
Invasive fungal infection has become a major cause of morbidity and mortality in immunocompromised patients. Rapid identification of pathogenic fungi to species level is critical for disease treatment. A real-time LightCycler assay aiming at rapid detection and species identification of pathogenic fungi from clinical isolates was developed. Template DNAs of different species were amplified and detected in real time by employing SYBR Green fluorescent dye. The target sequences for species-level detection were located between the 18S and 28S rDNA. Seven fungal species encountered frequently in the clinical setting, Candida albicans, Candida glabrata, Candida krusei, Candida parapsilosis, Candida tropicalis, Candida guilliermondii and Cryptococcus neoformans, could be discriminated by species-specific primers and confirmed by melting-curve analyses. The range of linearity was from 1 ng to 1 pg (mul(-1) water) and the sensitivity was 1 pg fungal DNA mul(-1). Identification by this real-time PCR method matched biochemical identification for all 58 clinical strains. Therefore, the method is simple, rapid and sensitive enough for detection and identification of several fungal species.
引用
收藏
页码:1071 / 1076
页数:6
相关论文
共 37 条
[1]
Detection of Cryptococcus neoformans DNA in tissue samples by nested and real-time PCR assays [J].
Bialek, R ;
Weiss, M ;
Bekure-Nemariam, K ;
Najvar, LK ;
Alberdi, MB ;
Graybill, JR ;
Reischl, U .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2002, 9 (02) :461-469
[2]
Chen YC, 1997, INFECT CONT HOSP EP, V18, P369, DOI 10.1086/647628
[3]
Polymorphic internal transcribed spacer region 1 DNA sequences identify medically important yeasts [J].
Chen, YC ;
Eisner, JD ;
Kattar, MM ;
Rassoulian-Barrett, SL ;
Lafe, K ;
Bui, U ;
Limaye, AP ;
Cookson, BT .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (11) :4042-4051
[4]
Real-time PCR coupled with automated DNA extraction and detection of galactomannan antigen in serum by enzyme-linked immunosorbent assay for diagnosis of invasive aspergillosis [J].
Costa, C ;
Costa, JM ;
Desterke, C ;
Botterel, F ;
Cordonnier, C ;
Bretagne, S .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (06) :2224-2227
[5]
Burden of aspergillosis-related hospitalizations in the United States [J].
Dasbach, EJ ;
Davies, GM ;
Teutsch, SM .
CLINICAL INFECTIOUS DISEASES, 2000, 31 (06) :1524-1528
[6]
Identification of cultured isolates of clinically important yeast species using fluorescent fragment length analysis of the amplified internally transcribed rRNA spacer 2 region [J].
De Baere, Thierry ;
Claeys, Geert ;
Swinne, Danielle ;
Massonet, Caroline ;
Verschraegen, Gerda ;
Muylaert, An ;
Vaneechoutte, Mario .
BMC MICROBIOLOGY, 2002, 2 (1) :1-8
[7]
Invasive aspergillosis [J].
Denning, DW .
CLINICAL INFECTIOUS DISEASES, 1998, 26 (04) :781-803
[8]
Rapid identification of Candida species with species-specific DNA probes [J].
Elie, CM ;
Lott, TJ ;
Reiss, E ;
Morrison, CJ .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (11) :3260-3265
[9]
Fungal endocarditis: Evidence in the world literature, 1965-1995 [J].
Ellis, ME ;
Al-Abdely, H ;
Sandridge, A ;
Greer, W ;
Ventura, W .
CLINICAL INFECTIOUS DISEASES, 2001, 32 (01) :50-62
[10]
Comparison of RapID yeast plus system with API 20C system for identification of common, new, and emerging yeast pathogens [J].
Espinel-Ingroff, A ;
Stockman, L ;
Roberts, G ;
Pincus, D ;
Pollack, J ;
Marler, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (04) :883-886