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基于多重生物素标记 DNA 探针的金黄色葡萄球菌 16S rRNA 的即时检测。

Point-of-care detection of 16S rRNA of Staphylococcus aureus based on multiple biotin-labeled DNA probes.

机构信息

College of Life Science and Technology, Heilongjiang Bayi Agricultural University, Daqing, 163319, China.

College of Life Science and Technology, Heilongjiang Bayi Agricultural University, Daqing, 163319, China; Institute of Military Veterinary, Academy of Military Medical Sciences, Changchun, 130122, China.

出版信息

Mol Cell Probes. 2019 Oct;47:101427. doi: 10.1016/j.mcp.2019.101427. Epub 2019 Jul 30.

Abstract

A visual method that combines multiple biotin-labeled DNA probes and lateral-flow nucleic acid biosensor was developed to detect Staphylococcus aureus. The 16S rRNA from Staphyloccocus aureus (S. aureus), coupled with multiple biotin-labeled DNA probes, was functionalized in a signal structure for lateral-flow point-of-care detection. The secondary structure of the 16S rRNA was unwound by two specific capture probes modified by Fam and multiple bridge probes, which extended additional sequences for use as initiators. By utilizing the initiators, each target 16S rRNA with multiple DNA probes could tether a number of biotin molecules, so that a large number of streptavidin-labeled gold nanoparticles could be introduced in the lateral flow assay. The images of the lateral flow detection results obtained using a smartphone were transmitted to a computer via Wi-Fi or Bluetooth connection for quantitative processing by ImageJ. The limit of detection was 10 cfu/mL without sample enrichment, and decreased to 0.12 cfu/mL following a 3-h enrichment of samples in growth medium. Notably, this method presented high specificity and applicability for the detection of S. aureus in food samples. In short, the developed visual non-specific operation method is very suitable for point-of-care diagnosis of pathogens in resource-limited countries.

摘要

开发了一种结合多种生物素标记 DNA 探针和侧向流动核酸生物传感器的可视化方法,用于检测金黄色葡萄球菌。金黄色葡萄球菌(S. aureus)的 16S rRNA 与多种生物素标记 DNA 探针偶联,在侧向流动即时检测的信号结构中具有功能。通过两个 Fam 修饰的特异性捕获探针解开 16S rRNA 的二级结构,并延伸多个桥接探针作为引发子,从而扩展了额外的序列。通过利用引发子,每个带有多个 DNA 探针的靶标 16S rRNA 可以连接许多生物素分子,因此在侧向流动测定中可以引入大量链霉亲和素标记的金纳米粒子。使用智能手机获得的侧向流动检测结果的图像通过 Wi-Fi 或蓝牙连接传输到计算机,然后由 ImageJ 进行定量处理。未经样品富集时的检测限为 10 cfu/mL,在生长培养基中富集 3 小时后,检测限降低至 0.12 cfu/mL。值得注意的是,该方法在检测食品样品中的金黄色葡萄球菌时表现出很高的特异性和适用性。总之,开发的可视化非特异性操作方法非常适合资源有限国家的即时现场病原体诊断。

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