Suppr超能文献

用于检测与脓毒症相关病原体的单管、LATE-PCR、多重终点分析方法的设计与构建,该方法采用开/关型探针

Design and Construction of a Single-Tube, LATE-PCR, Multiplex Endpoint Assay with Lights-On/Lights-Off Probes for the Detection of Pathogens Associated with Sepsis.

作者信息

Carver-Brown Rachel K, Reis Arthur H, Rice Lisa M, Czajka John W, Wangh Lawrence J

机构信息

Department of Biology, Brandeis University, Waltham, MA 02453-2728, USA.

出版信息

J Pathog. 2012;2012:424808. doi: 10.1155/2012/424808. Epub 2012 Dec 26.

Abstract

Aims. The goal of this study was to construct a single tube molecular diagnostic multiplex assay for the detection of microbial pathogens commonly associated with septicemia, using LATE-PCR and Lights-On/Lights-Off probe technology. Methods and Results. The assay described here identified pathogens associated with sepsis by amplification and analysis of the 16S ribosomal DNA gene sequence for bacteria and specific gene sequences for fungi. A sequence from an unidentified gene in Lactococcus lactis subsp. cremoris served as a positive control for assay function. LATE-PCR was used to generate single-stranded amplicons that were then analyzed at endpoint over a wide temperature range in a specific fluorescent color. Each bacterial target was identified by its pattern of hybridization to Lights-On/Lights-Off probes derived from molecular beacons. Complex mixtures of targets were also detected. Conclusions. All microbial targets were identified in samples containing low starting copy numbers of pathogen genomic DNA, both as individual targets and in complex mixtures. Significance and Impact of the Study. This assay uses new technology to achieve an advance in the field of molecular diagnostics: a single-tube multiplex assay for identification of pathogens commonly associated with sepsis.

摘要

目的。本研究的目标是利用滞后聚合酶链反应(LATE-PCR)和“开/关”探针技术构建一种单管分子诊断多重检测方法,用于检测通常与败血症相关的微生物病原体。方法与结果。本文所述的检测方法通过扩增和分析细菌的16S核糖体DNA基因序列以及真菌的特定基因序列来鉴定与败血症相关的病原体。乳酸乳球菌亚种cremoris中一个未鉴定基因的序列用作检测功能的阳性对照。LATE-PCR用于生成单链扩增子,然后在特定荧光颜色的宽温度范围内进行终点分析。每个细菌靶点通过其与源自分子信标的“开/关”探针的杂交模式来鉴定。还检测到了复杂的靶点混合物。结论。在含有低起始拷贝数病原体基因组DNA的样本中,所有微生物靶点均被鉴定出来,无论是作为单个靶点还是在复杂混合物中。研究的意义与影响。该检测方法利用新技术在分子诊断领域取得了进展:一种用于鉴定通常与败血症相关病原体的单管多重检测方法。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验