首页> 外文期刊>Journal of Clinical Pathology >PCR based identification and discrimination of agents of mucormycosis and aspergillosis in paraffin wax embedded tissue.
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PCR based identification and discrimination of agents of mucormycosis and aspergillosis in paraffin wax embedded tissue.

机译:基于PCR的石蜡蜡包埋组织中毛霉菌病和曲霉病病原的鉴定和鉴别。

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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.
机译:背景:侵袭性真菌感染通常通过组织病理学诊断而未鉴定致病真菌,而致病真菌表现出明显不同的抗真菌药敏性。目的:建立和评估两个半嵌套式聚合酶链反应(PCR)检测系统,以鉴定和区分石蜡包埋的组织样本中的曲霉病和毛霉菌病。方法:从五个不同中心的52个盲样品中提取DNA,并将其用作模板,分别针对线粒体曲霉病DNA和合子菌的18S核糖体DNA进行两次PCR检测。结果:根据组织病理学诊断of合真菌或曲霉病,分别在44个样品中的27个中鉴定出了特定的真菌DNA。从一个合子标本(通过组织病理学诊断)中扩增出烟曲霉DNA。在16个PCR阴性样本中,有四个没有扩增人类DNA,这可能是由于石蜡包埋之前DNA的破坏。此外,还检查了八种来自临床可疑真菌感染的样本(无组织病理学证据)。两种PCR检测方法均发现了同时发生的黑附病和烟曲霉感染,以及另外两例感染了阿育根霉和烟曲霉的感染。结论:本文所述的两种半巢式PCR检测可以支持组织病理学诊断毛霉菌病或曲霉病,并可以鉴定感染因子,从而优化抗真菌治疗。

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