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利用实时 PCR 对未经纯化的耐甲氧西林金黄色葡萄球菌 (MRSA) DNA 进行微型芯片检测。

Miniature on-chip detection of unpurified methicillin-resistant Staphylococcus aureus (MRSA) DNA using real-time PCR.

机构信息

Mechanical Engineering Department, Vanderbilt University, 2301 Vanderbilt Place, VU Station B 351592, Nashville, TN 37235, United States.

出版信息

J Biotechnol. 2010 Apr 1;146(3):93-9. doi: 10.1016/j.jbiotec.2009.12.013. Epub 2010 Feb 10.

Abstract

This paper evaluates the ability to detect three forms of methicillin-resistant Staphylococcus aureus (MRSA) in a microfluidic system. The MRSA was prepared off-chip by varying levels of sample preparation: one containing purified genomic DNA, another containing the supernatant of a crude preparation using simple reagents, and a third through boiled culture preparation without any additional reagents. Polydimethylsiloxane (PDMS) microfluidic chips were fabricated using soft lithography and then bonded to a 22mmx22mmx0.1mm glass cover slip. A lid fabricated in a similar manner was used during compression to prevent bubble formation and evaporation in the stationary well-based chip. A miniature thermal cycler based on a resistive heater and a small fan were used to cycle through desired temperatures for polymerase chain reaction and fluorescent intensity measurements were taken at each cycle. Each form of template provided positive results utilizing the developed micro-PCR system (verified with gel electrophoresis). A serial dilution of the purified genomic DNA provided a standard curve with an efficiency of 1.77. The lowest concentration that provided clear positive results came from a 3microL sample containing 11.2pg of DNA. The ability to detect MRSA in a sample having undergone minimal sample preparation is a necessary step in the development of a point-of-care detection system capable of identifying infectious organisms.

摘要

本文评估了在微流控系统中检测三种形式的耐甲氧西林金黄色葡萄球菌(MRSA)的能力。通过改变样品制备水平,在离片芯片上制备 MRSA:一种含有纯化的基因组 DNA,另一种含有使用简单试剂的粗制上清液,第三种是通过煮沸培养制备,不添加任何额外的试剂。聚二甲基硅氧烷(PDMS)微流控芯片采用软光刻技术制造,然后与 22mmx22mmx0.1mm 的玻璃盖玻片键合。使用类似的方法制造盖子,在压缩过程中防止固定井基芯片中形成气泡和蒸发。基于电阻加热器和小风扇的微型热循环仪用于循环到所需的聚合酶链反应温度,并在每个循环中进行荧光强度测量。利用开发的微 PCR 系统对每种模板均提供了阳性结果(通过凝胶电泳验证)。经纯化的基因组 DNA 的系列稀释提供了一条效率为 1.77 的标准曲线。提供清晰阳性结果的最低浓度来自包含 11.2pg DNA 的 3μL 样品。在经过最小样品制备的样品中检测 MRSA 的能力是开发能够识别感染性生物的即时检测系统的必要步骤。

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