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基于 DNA 的可扩展磁性纳米粒子聚集检测法用于患者样本中的细菌检测。

Scalable DNA-Based Magnetic Nanoparticle Agglutination Assay for Bacterial Detection in Patient Samples.

机构信息

†Science for Life Laboratory, Department of Biochemistry and Biophysics, Stockholm University, 11418 Stockholm, Sweden.

‡DTU Nanotech, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark.

出版信息

ACS Nano. 2015 Jul 28;9(7):7374-82. doi: 10.1021/acsnano.5b02379. Epub 2015 Jul 16.

DOI:10.1021/acsnano.5b02379
PMID:26166357
Abstract

We demonstrate a nanoparticle-based assay for the detection of bacteria causing urinary tract infections in patient samples with a total assay time of 4 h. This time is significantly shorter than the current gold standard, plate culture, which can take several days depending on the pathogen. The assay is based on padlock probe recognition followed by two cycles of rolling circle amplification (RCA) to form DNA coils corresponding to the target bacterial DNA. The readout of the RCA products is based on optomagnetic measurements of the specific agglutination of DNA-bound magnetic nanoparticles (MNPs) using low-cost optoelectronic components from Blu-ray drives. We implement a detection approach, which relies on the monomerization of the RCA products, the use of the monomers to link and agglutinate two populations of MNPs functionalized with universal nontarget specific detection probes and on the introduction of a magnetic incubation scheme. This enables multiplex detection of Escherichia coli, Proteus mirabilis and Pseudomonas aeruginosa at clinically relevant concentrations, demonstrating a factor of 30 improvement in sensitivity compared to previous MNP-based detection schemes. Thanks to the universal probes, the same set of functionalized MNPs can be used to read out products from a multitude of RCA targets, making the approach truly scalable for parallel detection of multiple bacteria in a future integrated point of care molecular diagnostics system.

摘要

我们展示了一种基于纳米颗粒的检测方法,用于检测引起尿路感染的细菌,总检测时间为 4 小时。这一时间明显短于当前的金标准——平板培养法,平板培养法根据病原体的不同,可能需要数天时间。该检测方法基于发夹探针识别,随后进行两轮滚环扩增(RCA),以形成与目标细菌 DNA 相对应的 DNA 线圈。RCA 产物的读出基于使用 Blu-ray 驱动器的低成本光电元件对 DNA 结合磁性纳米颗粒(MNP)的特异性聚集进行光磁测量。我们采用了一种检测方法,该方法依赖于 RCA 产物的单体化、使用单体将两种功能化的 MNP 连接和聚集,这两种 MNP 带有通用非靶特异性检测探针,并引入了一种磁性孵育方案。这使得能够以临床相关浓度同时检测大肠埃希菌、奇异变形杆菌和铜绿假单胞菌,与以前基于 MNP 的检测方案相比,灵敏度提高了 30 倍。由于使用了通用探针,同一组功能化的 MNP 可以用于读取来自多个 RCA 靶标的产物,这使得该方法在未来的集成即时分子诊断系统中真正能够实现对多种细菌的并行检测。

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