量子点标记抗体多重检测大肠杆菌和肠炎沙门氏菌

FAHRIYE CEYDA DUDAK, İSMAİL HAKKI BOYACI
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引用次数: 13

摘要

在这项研究中,我们建立了免疫磁分离(IMS)和量子点(QDs)标记耦合技术同时检测大肠杆菌和肠炎沙门氏菌的方法。具有不同发射波长的量子点与反e共轭。大肠杆菌和抗沙门氏菌抗体使用qd抗体偶联物标记免疫磁分离细菌,并测量两种细菌计数的荧光强度。优化了IMS中使用的一抗浓度、偶联过程中量子点与抗体的比例以及用于标记的量子点抗体偶联物的浓度,以提高检测的灵敏度。用量子点标记细菌后,用十二烷基硫酸钠溶液分离量子点,消除了珠菌复合物与量子点之间的猝灭现象。测定了捕获不同浓度细菌的荧光强度,发现大肠杆菌的工作范围为5 × 102 ~ 5 × 105 cfu/mL,肠炎沙门氏菌的工作范围为4 × 102 ~ 4 × 105 cfu/mL。在本研究中,抗体共轭多色量子点(QDs)用于同时检测大肠杆菌和肠炎沙门氏菌。本研究结果表明,在优化分析条件的情况下,QD标签可用于细菌的多重、快速和选择性检测,其检出限与许多新方法相当。此外,通过使用具有不同发射波长的QD标签,可以修改该检测方法以同时检测两种以上的物种。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MULTIPLEX DETECTION OF ESCHERICHIA COLI AND SALMONELLA ENTERITIDIS BY USING QUANTUM DOT-LABELED ANTIBODIES

ABSTRACT

In this study, we demonstrated the simultaneous detection of Escherichia coli and Salmonella enteritidis, by coupling immunomagnetic separation (IMS) with quantum dots (QDs) labeling. QDs having different emission wavelengths were conjugated with anti-E. coli and anti-Salmonella antibodies. QD–antibody conjugates were used to label immunomagnetically separated bacteria and the fluorescence intensities were measured for enumerations of both species. The concentrations of primary antibodies used in IMS, the ratio of QDs to antibodies during the conjugation and the concentration of QD–antibody conjugates used in labeling were optimized to enhance the sensitivity of the assay. After labeling bacteria with QDs, the quenching observed between bead–bacteria complex and QDs was eliminated by separating QDs from the complex using sodium dodecyl sulfate solution. The fluorescence intensities due to the capturing of different concentrations of bacteria were measured and the working ranges were found to be 5 × 102 to 5 × 105 cfu/mL for E. coli and 4 × 102 to 4 × 105 cfu/mL for S. enteritidis.

PRACTICAL APPLICATIONS

In this study, antibody-conjugated multicolor quantum dots (QDs) were used for simultaneous detection of Escherichia coli and Salmonella enteritidis. The results of this study indicate that QD labels can be used in multiplex, rapid and selective detection of bacteria with detection limits comparable with those of many novel methods in cases where the assay conditions are optimized. Furthermore, the assay can be modified for the simultaneous detection of more than two species through using QD labels having different emission wavelengths.

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来源期刊
Journal of Rapid Methods and Automation in Microbiology
Journal of Rapid Methods and Automation in Microbiology 生物-生物工程与应用微生物
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