PCR based identification and discrimination of agents of mucormycosis and aspergillosis in paraffin wax embedded tissue

被引:166
作者
Bialek, R
Konrad, F
Kern, J
Aepinus, C
Cecenas, L
Gonzalez, GM
Just-Nübling, G
Willinger, B
Presterl, E
Lass-Flörl, C
Rickerts, V
机构
[1] Univ Tubingen Hosp, Inst Trop Med, D-72074 Tubingen, Germany
[2] Univ Hosp Rostock, Inst Med Microbiol Virol & Hyg, D-18057 Rostock, Germany
[3] Univ Autonoma Nuevo Leon, Dept Pathol, Monterrey 64460, NL, Mexico
[4] Univ Autonoma Nuevo Leon, Dept Microbiol, Monterrey, NL, Mexico
[5] Univ Hosp, Med Klin 3, D-60590 Frankfurt, Germany
[6] Med Univ Vienna, Inst Hyg & Med Microbiol, A-1090 Vienna, Austria
[7] Dept Med, Div Infect Dis & Hosp Epidemiol, CH-8091 Zurich, Switzerland
[8] Univ Innsbruck, Dept Hyg & Social Med, A-6010 Innsbruck, Austria
关键词
D O I
10.1136/jcp.2004.024703
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Background: Invasive fungal infections are often diagnosed by histopathology without identification of the causative fungi, which show significantly different antifungal susceptibilities. Aims: To establish and evaluate a system of two seminested polymerase chain reaction (PCR) assays to identify and discriminate between agents of aspergillosis and mucormycosis in paraffin wax embedded tissue samples. Methods: DNA of 52 blinded samples from five different centres was extracted and used as a template in two PCR assays targeting the mitochondrial aspergillosis DNA and the 18S ribosomal DNA of zygomycetes. Results: Specific fungal DNA was identified in 27 of 44 samples in accordance with a histopathological diagnosis of zygomycosis or aspergillosis, respectively. Aspergillus fumigatus DNA was amplified from one specimen of zygomycosis ( diagnosed by histopathology). In four of 16 PCR negative samples no human DNA was amplified, possibly as a result of the destruction of DNA before paraffin wax embedding. In addition, eight samples from clinically suspected fungal infections (without histopathological proof) were examined. The two PCR assays detected a concomitant infection with Absidia corymbifera and A fumigatus in one, and infections with Rhizopus arrhizus and A fumigatus in another two cases. Conclusions: The two seminested PCR assays described here can support a histopathological diagnosis of mucormycosis or aspergillosis, and can identify the infective agent, thereby optimising antifungal treatment.
引用
收藏
页码:1180 / 1184
页数:5
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