肺炎克雷伯菌
量子点
石墨烯
塔克曼
材料科学
纳米技术
肺炎克雷伯菌
聚合酶链反应
生物
细菌
基因
遗传学
大肠杆菌
金黄色葡萄球菌
作者
Lijuan Huang,Bing Du,Xiaohu Cui,Meiqi Liu,Zhoufei Li,Xiaoyun Cui,Ziying Xu,Zihui Yu,Shuo Zhao,Yanling Feng,Hanqing Zhao,Jianhai Long,Jing Yuan
出处
期刊:ACS Sensors
[American Chemical Society]
日期:2025-07-28
卷期号:10 (8): 5633-5643
被引量:2
标识
DOI:10.1021/acssensors.5c00508
摘要
Klebsiella pneumoniae (Kpn) is a common opportunistic pathogen, with hypervirulent strains (hvKpn) posing significant risks even to healthy individuals. Traditional clinical diagnostics often use real-time quantitative polymerase chain reaction (PCR) with TaqMan probes, which are costly and unstable due to their reliance on fluorophore and quencher molecules. This study introduces a novel probe using silicon-doped carbon quantum dots (Si-QDs) and single-layer graphene oxides (GOs), forming the Si-QD-probe-GO. This new probe offers excellent selectivity, sensitivity, stability, low photobleaching, and cost-effectiveness. A sensor array targeting khe, peg-344, and iucA genes is developed to detect Kpn and differentiate between classical Kpn (cKpn) and hvKpn. Using a partial least-squares discriminant analysis (PLS-DA) model, the system achieves 100% accuracy in distinguishing hvKpn from cKpn. The study also employs droplet digital PCR (ddPCR) with microfluidic technology to enhance sensitivity and quantification, achieving a detection limit of 5 CFU/mL. In a mouse pneumonia model, the PLS-DA model accurately identifies hvKpn in lung samples. The ddPCR quantification using Si-QD-probe-GO shows strong correlation with traditional culture methods. This research presents a promising ddPCR system for precise detection and virulence identification of Kpn, offering a new direction for clinical diagnostics.
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