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A Rapid Method for Detection of Salmonella in Milk Based on Extraction of mRNA Using Magnetic Capture Probes and RT-qPCR

机译:基于磁性捕获探针和RT-qPCR提取mRNA的快速检测牛奶中沙门氏菌的方法

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摘要

Magnetic separation is an efficient method for target enrichment and elimination of inhibitors in the molecular detection systems for foodborne pathogens. In this study, we prepared magnetic capture probes by modifying oligonucleotides complementary to target sequences on the surface of amino-modified silica-coated magnetic nanoparticles and optimized the conditions and parameters of probe synthesis and hybridization. We innovatively put the complexes of magnetic capture probes and target sequences into qPCR without any need for denaturation and purification steps. This strategy can reduce manual steps and save time. We used the magnetic capture probes to separate invA mRNA from Salmonella in artificially contaminated milk samples. The detection sensitivity was 104 CFU/ml, which could be increased to 10 CFU/ml after a 12 h enrichment step. The developed method is robust enough to detect live bacteria in a complex environmental matrix.
机译:磁分离是用于食源性病原体分子检测系统中靶标富集和消除抑制剂的有效方法。在这项研究中,我们通过修饰与氨基修饰的二氧化硅包覆的磁性纳米粒子表面上的靶序列互补的寡核苷酸,并优化了探针合成和杂交的条件和参数,制备了磁性捕获探针。我们创新地将磁性捕获探针和靶序列的复合物放入qPCR,而无需变性和纯化步骤。此策略可以减少手动步骤并节省时间。我们使用磁性捕获探针从人工污染的牛奶样品中从沙门氏菌中分离出invA mRNA。检测灵敏度为10 4 CFU / ml,经过12 h富集步骤后可提高至10 CFU / ml。所开发的方法足够健壮,可以检测复杂环境基质中的活细菌。

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