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首页> 外文期刊>Journal of Clinical Microbiology >Quantitative Multiprobe PCR Assay for Simultaneous Detection and Identification to Species Level of Bacterial Pathogens
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Quantitative Multiprobe PCR Assay for Simultaneous Detection and Identification to Species Level of Bacterial Pathogens

机译:同时检测和鉴定细菌病原体物种水平的定量多探针PCR分析

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We describe a novel adaptation of the TaqMan PCR assay which potentially allows for highly sensitive detection of any eubacterial species with simultaneous species identification. Our system relies on a unique multiprobe design in which a single set of highly conserved sequences encoded by the 16S rRNA gene serves as the primer pair and is used in combination with both an internal highly conserved sequence, the universal probe, and an internal variable region, the species-specific probe. A pre-PCR ultrafiltration step effectively decontaminates or removes background DNA. The TaqMan system described reliabAly detected 14 common bacterial species with a detection limit of 50 fg. Further, highly sensitive and specific pathogen detection was demonstrated with a prototype species-specific probe designed to detect Staphylococcus aureus. This assay has broad potential in the clinical arena for rapid and specific diagnosis of infectious diseases.
机译:我们描述了TaqMan PCR分析的一种新型改编,它潜在地允许对任何真细菌物种进行高度灵敏的检测,同时进行物种鉴定。我们的系统依赖于独特的多探针设计,其中由16S rRNA基因编码的一组高度保守的序列用作引物对,并与内部高度保守的序列,通用探针和内部可变区结合使用,是物种特异性探针。 PCR前超滤步骤可以有效地净化或去除背景DNA。 TaqMan系统描述了可靠地检测到14种常见细菌,检测限为50 fg。此外,通过原型金黄色葡萄球菌的原型特异性探针证明了高灵敏度和特异性的病原体检测。该测定法在临床领域具有广泛的潜力,可以快速,特异性地诊断传染病。

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