Wang Panxue, Pang Shintaro, Chen Juhong, McLandsborough Lynne, Nugen Sam R, Fan Mingtao, He Lili
Department of Food Science, University of Massachusetts, Amherst, MA 01003, USA.
College of Food Science and Engineering, Northwest A&F University, Yangling 712100, Shaanxi, P. R. China.
Analyst. 2016 Feb 21;141(4):1356-62. doi: 10.1039/c5an02175h.
Here we presented a simple, rapid and label-free surface-enhanced Raman spectroscopy (SERS) based mapping method for the detection and discrimination of Salmonella enterica and Escherichia coli on silver dendrites. The sample preparation was first optimized to maximize sensitivity. The mapping method was then used to scan through the bacterial cells adsorbed on the surface of silver dendrites. The intrinsic and distinct SERS signals of bacterial cells were used as the basis for label-free detection and discrimination. The results show the developed method is able to detect single bacterial cells adsorbed on the silver dendrites with a limit of detection as low as 10(4) CFU mL(-1), which is two orders of magnitude lower than the traditional SERS method under the same experimental condition. The time needed for collecting a 225 points map was approximately 24 minutes. Moreover, the developed SERS mapping method can realize simultaneous detection and identification of Salmonella enterica subsp. enterica BAA1045 and Escherichia coli BL21 from a mixture sample using principle component analysis. Our results demonstrate the great potential of the label-free SERS mapping method to detect, identify and quantify bacteria and bacterial mixtures simultaneously.
在此,我们展示了一种基于表面增强拉曼光谱(SERS)的简单、快速且无需标记的映射方法,用于检测和区分银树枝状晶体上的肠炎沙门氏菌和大肠杆菌。首先对样品制备进行了优化,以最大化灵敏度。然后使用该映射方法扫描吸附在银树枝状晶体表面的细菌细胞。细菌细胞固有的独特SERS信号被用作无需标记的检测和区分的基础。结果表明,所开发的方法能够检测吸附在银树枝状晶体上的单个细菌细胞,检测限低至10(4) CFU mL(-1),在相同实验条件下,这比传统SERS方法低两个数量级。收集一幅225个点的图谱所需时间约为24分钟。此外,所开发的SERS映射方法可以使用主成分分析从混合样品中同时检测和鉴定肠炎沙门氏菌亚种肠炎BAA1045和大肠杆菌BL21。我们的结果证明了无需标记的SERS映射方法在同时检测、鉴定和定量细菌及细菌混合物方面具有巨大潜力。