Bi Liyan, Wang Xiao, Cao Xiaowei, Liu Luying, Bai Congcong, Zheng Qingyin, Choo Jaebum, Chen Lingxin
Transformative Otology and Neuroscience Center, Binzhou Medical University, Yantai 264003, China.
Transformative Otology and Neuroscience Center, Binzhou Medical University, Yantai 264003, China.
Talanta. 2020 Dec 1;220:121397. doi: 10.1016/j.talanta.2020.121397. Epub 2020 Jul 14.
There is a challenge to obtain an ultrasensitive and rapid approach to detect bacteria and identify resistance. As a powerful bioanalytical tool, surface-enhanced Raman scattering (SERS) in bacterial detection have attracted increasing attentions. Herein, we developed a SERS-active Au@Ag core-shell nanorod (Au@AgNR) tag platform for ultrasensitive bacteria detection and antibiotic-susceptibility testing (AST). The platform established that surface enhanced Raman scattered Rhodamine 6G (R6G) absorption at 1517 cm had a good linearity (RI = 3865 + 193logC; R = 0.97) with logarithm of E. coli concentration over a range of 10-10 CFU (colony forming unit)/mL with limit of detection as low 10 CFU/mL. When E. coli was exposed to ampicillin at minimum inhibitory concentration (MIC, 4 μg/mL), Raman spectroscopy showed the obvious variation between ampicillin-susceptible E. coli (Amp-E. coli) and the ampicillin-resistant E. coli (Amp-E. coli). Combined with principal component analysis (PCA) statistical analysis, the Raman intensity variation mentioned above allows to obtain rapid antibiotic resistance testing (<3.5 h). In addition, E.coli spiked into blood from C57BL/6 mice can be identified clearly, indicating the potential for point-of-care diagnostics.
获得一种超灵敏且快速的方法来检测细菌并鉴定耐药性是一项挑战。作为一种强大的生物分析工具,表面增强拉曼散射(SERS)在细菌检测中已引起越来越多的关注。在此,我们开发了一种用于超灵敏细菌检测和抗生素敏感性测试(AST)的SERS活性金@银核壳纳米棒(Au@AgNR)标记平台。该平台证实,表面增强拉曼散射的罗丹明6G(R6G)在1517 cm处的吸收与大肠杆菌浓度的对数在10-10 CFU(菌落形成单位)/mL范围内具有良好的线性关系(RI = 3865 + 193logC;R = 0.97),检测限低至10 CFU/mL。当大肠杆菌暴露于最低抑菌浓度(MIC,4 μg/mL)的氨苄青霉素时,拉曼光谱显示敏感氨苄青霉素的大肠杆菌(Amp-E. coli)和耐氨苄青霉素的大肠杆菌(Amp-E. coli)之间存在明显差异。结合主成分分析(PCA)统计分析,上述拉曼强度变化能够实现快速抗生素耐药性测试(<3.5小时)。此外,能清晰鉴定出掺入C57BL/6小鼠血液中的大肠杆菌,这表明了即时诊断的潜力。