首页> 外文期刊>The Journal of molecular diagnostics: JMD >Application of Nuclear Magnetic Resonance to Detect Toxigenic Clostridium difficile from Stool Specimens A Proof of Concept
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Application of Nuclear Magnetic Resonance to Detect Toxigenic Clostridium difficile from Stool Specimens A Proof of Concept

机译:核磁共振检测核磁共振检测从粪便标本检测Toxigenic Clostidion型概念证明

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We evaluated the performance of an early prototype core molecular mirroring nuclear magnetic resonance detection platform (Mentor-100) to detect toxigenic Clostridium difficile from stool. This technology uses customized nanoparticles bound to target specific oligonucleotide probes that form binaries in the presence of nucleic acid from the target microorganism. Liquid patient stool specimens were seeded with C. difficile or other Clostridium species to determine the analytical sensitivity and specificity. Samples underwent nucleic acid extraction and target amplification with probes conjugated with iron nanoparticles. Signal from nuclear magnetic resonance spin spin relaxation time was measured to detect the presence or absence of toxigenic C. difficile. The Limit of detection was <180 colony forming units per reaction of toxigenic C. difficile. No cross-reactivity was observed with nontoxigenic C. difficile, Clostridium sordellii, Clostridium perfringens, Bacillus subtilis, or Paenibacillus polymyxa at 108 colony forming units/mL. Correlation studies using frozen stool samples yielded a sensitivity of 88.4% (61 of 69) and a specificity of 87.0% (40 of 46) as compared with a commercial PCR assay for C. difficile. The area under the curve in the receiver operating characteristic curve analysis was 0.922. The prototype molecular mirroring platform showed promising performance for pathogen detection from clinical specimens. The platform design has the potential to offer a novel, low-cost alternative to currently available nucleic acid based tests.
机译:我们评估了早期原型核心分子镜像核磁共振检测平台(MENTOR-100)的性能,以检测从粪便中脱氧梭菌差异。该技术使用定制的纳米颗粒,其靶向特异性寡核苷酸探针,其在靶微生物存在核酸存在下形成二进制蛋白。液体患者粪便样品用C.艰难梭菌或其他梭菌物种接种,以确定分析敏感性和特异性。样品接受核酸提取和用铁纳米粒子缀合的探针靶扩增。测量来自核磁共振的信号旋转旋转舒适时间以检测毒性偶胆梭菌的存在或不存在。检测限<180个毒性C.艰难梭菌的菌落形成单位。在108个菌落形成单位/ ml下,用呋喃尼酸核酸胺C.艰难梭菌,梭菌,枯草芽孢杆菌,枯草芽孢杆菌或Paenibacillus polymyxa的梭菌差异无叉反应性。使用冷冻粪便样品的相关性研究产生88.4%(61个69个)的敏感性,与C.艰难梭菌的商业PCR测定相比,87.0%(40%)的特异性。接收器操作特征曲线分析的曲线下的区域为0.922。原型分子镜像平台对来自临床标本的病原体检测表现出有希望的性能。平台设计有可能提供新颖的低成本替代目前可用的基于核酸的测试。

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