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High-throughput detection of food-borne pathogenic bacteria using oligonucleotide microarray with quantum dots as fluorescent labels

机译:使用以量子点为荧光标记的寡核苷酸微阵列高通量检测食源性致病菌

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Bacterial pathogens are mostly responsible for food-borne diseases, and there is still substantial room for improvement in the effective detection of these organisms. In the present study, we explored a new method to detect target pathogens easily and rapidly with high sensitivity and specificity. This method uses an oligonucleotide microarray combined with quantum dots as fluorescent labels. Oligonucleotide probes targeting the 16SrRNA gene were synthesized to create an oligonucleotide microarray. The PCR products labeled with biotin were subsequently hybridized using an oligonucleotide microarray. Following incubation with CdSe/ZnS quantum dots coated with streptavidin, fluorescent signals were detected with a PerkinElmer Gx Microarray Scanner. The results clearly showed specific hybridization profiles corresponding to the bacterial species assessed. Two hundred and sixteen strains of food-borne bacterial pathogens, including standard strains and isolated strains from food samples, were used to test the specificity, stability, and sensitivity of the microarray system. We found that the oligonucleotide microarray combined with quantum dots used as fluorescent labels can successfully discriminate the bacterial organisms at the genera or species level, with high specificity and stability as well as a sensitivity of 10 colony forming units (CFU)/mL of pure culture. We further tested 105 mock-contaminated food samples and achieved consistent results as those obtained from traditional biochemical methods. Together, these results indicate that the quantum dot-based oligonucleotide microarray has the potential to be a powerful tool in the detection and identification of pathogenic bacteria in foods
机译:细菌病原体主要是由食源性疾病引起的,在有效检测这些生物方面仍有很大的改进空间。在本研究中,我们探索了一种以高灵敏度和特异性轻松快速地检测目标病原体的新方法。该方法使用结合了量子点的寡核苷酸微阵列作为荧光标记。合成靶向16SrRNA基因的寡核苷酸探针以创建寡核苷酸微阵列。随后用寡核苷酸微阵列杂交标记有生物素的PCR产物。与涂有链霉亲和素的CdSe / ZnS量子点孵育后,用PerkinElmer Gx微阵列扫描仪检测荧光信号。结果清楚地显示了对应于所评估细菌种类的特异性杂交谱。 216种食品传播细菌病原体菌株,包括标准菌株和从食品样品中分离出的菌株,被用于测试微阵列系统的特异性,稳定性和敏感性。我们发现,寡核苷酸微阵列结合用作荧光标记的量子点可以成功地区分属或种水平的细菌,具有高的特异性和稳定性以及对纯培养物的10个菌落形成单位(CFU)/ mL的敏感性。我们进一步测试了105个被模拟污染的食品样品,并获得了与传统生化方法相一致的结果。总之,这些结果表明,基于量子点的寡核苷酸微阵列有可能成为检测和鉴定食品中致病菌的有力工具。

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