单核细胞增生李斯特菌
数字聚合酶链反应
塔克曼
大肠杆菌
检出限
复式(建筑)
荧光
微生物学
聚二甲基硅氧烷
微流控
实时聚合酶链反应
化学
细菌
生物
致病菌
色谱法
聚合酶链反应
纳米技术
材料科学
遗传学
基因
DNA
光学
物理
作者
Xiaojun Bian,Fengxiang Jing,Gang Li,Xiaoyun Fan,Chunping Jia,Hongbo Zhou,Qinghui Jin,Jianlong Zhao
标识
DOI:10.1016/j.bios.2015.07.016
摘要
Sensitive and rapid identification of pathogenic bacterial is extremely important due to the serious threat of pathogens to human health. In this study, we demonstrate the simultaneous and sensitive detection of pathogenic Escherichia coli O157 and Listeria monocytogenes using a novel duplex droplet digital PCR (ddPCR) platform. The ddPCR platform, which uses a mineral oil-saturated polydimethylsiloxane (OSP) chip to overcome the problem of droplet evaporation, integrates the functions of droplet generation, on-chip amplification and end-point fluorescence readout. Simultaneous detection of two kinds of bacterial is achieved by the design of differentially labeled TaqMan-MGB fluorescent probes. Compared with a quantitative real-time PCR approach, the OSP chip-based duplex ddPCR platform exhibits high sensitivity, which is at the level of single molecule resolution without significant cross-assay interference. Moreover, the applicability of the proposed method is also evaluated in artificially contaminated drinking water sample, which displays a low detection limit down to 10 CFU/mL for both pathogenic bacterial within 2 h.
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