Department of Biomedical Engineering, Texas A&M University, College Station, Texas, United States of America.
Department of Plant Pathology and Microbiology, Texas A&M University, College Station, Texas, United States of America.
PLoS One. 2013 Dec 12;8(12):e82704. doi: 10.1371/journal.pone.0082704. eCollection 2013.
Rapid and accurate detection of plant pathogens in the field is crucial to prevent the proliferation of infected crops. Polymerase chain reaction (PCR) process is the most reliable and accepted method for plant pathogen diagnosis, however current conventional PCR machines are not portable and require additional post-processing steps to detect the amplified DNA (amplicon) of pathogens. Real-time PCR can directly quantify the amplicon during the DNA amplification without the need for post processing, thus more suitable for field operations, however still takes time and require large instruments that are costly and not portable. Microchip PCR systems have emerged in the past decade to miniaturize conventional PCR systems and to reduce operation time and cost. Real-time microchip PCR systems have also emerged, but unfortunately all reported portable real-time microchip PCR systems require various auxiliary instruments. Here we present a stand-alone real-time microchip PCR system composed of a PCR reaction chamber microchip with integrated thin-film heater, a compact fluorescence detector to detect amplified DNA, a microcontroller to control the entire thermocycling operation with data acquisition capability, and a battery. The entire system is 25 × 16 × 8 cm(3) in size and 843 g in weight. The disposable microchip requires only 8-µl sample volume and a single PCR run consumes 110 mAh of power. A DNA extraction protocol, notably without the use of liquid nitrogen, chemicals, and other large lab equipment, was developed for field operations. The developed real-time microchip PCR system and the DNA extraction protocol were used to successfully detect six different fungal and bacterial plant pathogens with 100% success rate to a detection limit of 5 ng/8 µl sample.
现场快速准确地检测植物病原体对于防止受感染作物的传播至关重要。聚合酶链反应(PCR)是植物病原体诊断最可靠和被广泛接受的方法,然而,目前的常规 PCR 仪器不具备便携性,并且需要额外的后处理步骤来检测病原体的扩增 DNA(扩增子)。实时 PCR 可以在 DNA 扩增过程中直接定量扩增子,而无需进行后处理,因此更适合现场操作,但仍需要时间,并且需要昂贵且不便于携带的大型仪器。微芯片 PCR 系统在过去十年中出现,以实现常规 PCR 系统的小型化,并减少操作时间和成本。实时微芯片 PCR 系统也已经出现,但不幸的是,所有报道的便携式实时微芯片 PCR 系统都需要各种辅助仪器。在这里,我们提出了一种独立的实时微芯片 PCR 系统,它由一个带有集成薄膜加热器的 PCR 反应室微芯片、一个用于检测扩增 DNA 的紧凑型荧光探测器、一个微控制器(用于控制整个热循环操作并具有数据采集能力)和一个电池组成。整个系统的尺寸为 25×16×8 cm(3),重量为 843 克。一次性微芯片仅需要 8-µl 样品量,单次 PCR 运行消耗 110 mAh 的电量。开发了一种 DNA 提取方案,特别是无需使用液氮、化学品和其他大型实验室设备,用于现场操作。所开发的实时微芯片 PCR 系统和 DNA 提取方案成功地以 100%的成功率检测到六种不同的真菌和细菌植物病原体,检测限为 5ng/8µl 样品。