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Segmented continuous-flow multiplex polymerase chain reaction microfluidics for high-throughput and rapid foodborne pathogen detection

机译:分段连续流多重聚合酶链反应微流体,用于高通量和快速食源性病原体检测

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摘要

High-throughput and rapid identification of multiple foodborne bacterial pathogens is vital in global public health and food industry. To fulfill this need, we propose a segmented continuous-flow multiplex polymerase chain reaction (SCF-MPCR) on a spiral-channel microfluidic device. The device consists of a disposable polytetrafluoroethylene (PTFE) capillary microchannel coiled on three isothermal blocks. Within the channel, n segmented flow regimes are sequentially generated, and m-plex PCR is individually performed in each regime when each mixture is driven to pass three temperature zones, thus providing a rapid analysis throughput of m x n. To characterize the performance of the microfluidic device, continuous-flow multiplex PCR in a single segmented flow has been evaluated by investigating the effect of key reaction parameters, including annealing temperatures, flow rates, polymerase concentration and amount of input DNA. With the optimized parameters, the genomic DNAs from Salmonella enterica. Listeria monocytogenes, Escherichia coli O157:H7 and Staphylococcus aureus could be amplified simultaneously in 19min, and the limit of detection was low, down to 10~2 copies μX~(-1). As proof of principle, the spiral-channel SCF-MPCR was applied to sequentially amplify four different bacterial pathogens from banana, milk, and sausage, displaying a throughput of 4 x 3 with no detectable cross-contamination.
机译:高通量和快速鉴定多种食源性细菌病原体对全球公共卫生和食品工业至关重要。为了满足此需求,我们提出了在螺旋通道微流控设备上的分段连续流多重聚合酶链反应(SCF-MPCR)。该设备由缠绕在三个等温块上的一次性聚四氟乙烯(PTFE)毛细管微通道组成。在通道内,顺序生成n个分段的流态,当驱动每种混合物通过三个温度区时,在每种流态中分别执行m-plex PCR,从而提供了m x n的快速分析通量。为了表征微流控设备的性能,已通过研究关键反应参数(包括退火温度,流速,聚合酶浓度和输入DNA量)的影响,对单段流中的连续流多重PCR进行了评估。通过优化的参数,可得到肠沙门氏菌的基因组DNA。单核细胞增生李斯特菌,大肠杆菌O157:H7和金黄色葡萄球菌可在19min内同时扩增,检出限低,低至10〜2拷贝μX〜(-1)。作为原理的证明,螺旋通道SCF-MPCR用于从香蕉,牛奶和香肠中依次扩增四种不同的细菌病原体,显示出4 x 3的通量,没有可检测到的交叉污染。

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