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Development of multiple cross displacement amplification label-based gold nanoparticles lateral flow biosensor for detection of Listeria monocytogenes

机译:用于检测单核细胞增生李斯特菌的基于多重交叉位移扩增标记的金纳米颗粒侧流生物传感器的开发

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摘要

Listeria monocytogenes, one of most problematic foodborne pathogens, is responsible for listeriosis in both humans and animals and mainly transmitted through the food chain. In this report, we propose a simple, rapid, and nearly instrument-free molecular technique using multiple cross displacement amplification (MCDA) label-based gold nanoparticles lateral flow biosensor (LFB) for specific, sensitive, and visual detection of L. monocytogenes. The MCDA-LFB method was carried out at a constant temperature (61°C) for only 20 min during the reaction stage, and then the amplification mixtures were directly detected by using LFB, eliminating the use of an electrophoresis instrument, special reagents, or amplicon analysis equipment. The whole procedure, from sample processing to result indicating, was finished within 1 h. The analytical specificity of MCDA-LFB method was successfully determined by distinguishing the target bacterium from other pathogens. The analytical sensitivity of the MCDA-LFB assay was 10 fg of genomic templates per reaction in pure culture, which was in complete accordance with MCDA by gel electrophoresis, real-time turbidity, and colorimetric indicator. The assay was also successfully applied to detecting L. monocytogenes in pork samples. Therefore, the rapidity, simplicity, and nearly equipment-free platform of the MCDA-LFB technique make it possible for food control, clinical diagnosis, and more. The proof-of-concept assay can be reconfigured to detect various target sequences by redesigning the specific MCDA primers.
机译:单核细胞增生李斯特菌是最有问题的食源性病原体之一,可导致人类和动物的李斯特菌病,并主要通过食物链传播。在此报告中,我们提出了一种简单,快速且几乎无需仪器的分子技术,该技术使用基于多重交叉位移放大(MCDA)标签的金纳米颗粒横向流生物传感器(LFB)来对单核细胞增生李斯特菌进行特异性,灵敏和视觉检测。 MCDA-LFB方法在反应阶段在恒定温度(61°C)下仅进行20分钟,然后通过使用LFB直接检测扩增混合物,而无需使用电泳仪,专用试剂或扩增子分析设备。从样品处理到结果指示的整个过程在1小时内完成。通过将目标细菌与其他病原体区分开来,成功确定了MCDA-LFB方法的分析特异性。在纯培养物中,MCDA-LFB测定的分析灵敏度为每个反应10 fg基因组模板,这与通过凝胶电泳,实时浊度和比色指示剂得出的MCDA完全一致。该测定法还成功地用于检测猪肉样品中的单核细胞增生李斯特氏菌。因此,MCDA-LFB技术的快速,简单和几乎无需设备的平台使食品控制,临床诊断等成为可能。通过重新设计特定的MCDA引物,可以将概念验证分析重新配置为检测各种靶序列。

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