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A High Speed Detection Platform Based on Surface-Enhanced Raman Scattering for Monitoring Antibiotic-Induced Chemical Changes in Bacteria Cell Wall

机译:基于表面增强拉曼散射的高速检测平台用于监测抗生素诱导的细菌细胞壁化学变化

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摘要

Rapid and accurate diagnosis for pathogens and their antibiotic susceptibility is critical for controlling bacterial infections. Conventional methods for determining bacterium's sensitivity to antibiotic depend mostly on measuring the change of microbial proliferation in response to the drug. Such “biological assay” inevitably takes time, ranging from days for fast-growing bacteria to weeks for slow-growers. Here, a novel tool has been developed to detect the “chemical features” of bacterial cell wall that enables rapid identification of drug resistant bacteria within hours. The surface-enhanced Raman scattering (SERS) technique based on our newly developed SERS-active substrate was applied to assess the fine structures of the bacterial cell wall. The SERS profiles recorded by such a platform are sensitive and stable, that could readily reflect different bacterial cell walls found in Gram-positive, Gram-negative, or mycobacteria groups. Moreover, characteristic changes in SERS profile were noticed in the drug-sensitive bacteria at the early period (i.e., ∼1 hr) of antibiotic exposure, which could be used to differentiate them from the drug-resistant ones. The SERS-based diagnosis could be applied to a single bacterium. The high-speed SERS detection represents a novel approach for microbial diagnostics. The single-bacterium detection capability of SERS makes possible analyses directly on clinical specimen instead of pure cultured bacteria.
机译:对病原体及其抗生素敏感性的快速准确诊断对于控制细菌感染至关重要。确定细菌对抗生素敏感性的常规方法主要取决于测量响应药物的微生物增殖的变化。这样的“生物学分析”不可避免地要花费时间,从快速生长细菌的天数到慢速生长细菌的天数不等。在这里,已经开发出一种新颖的工具来检测细菌细胞壁的“化学特征”,从而能够在数小时内快速识别出耐药菌。基于我们新开发的SERS活性底物的表面增强拉曼散射(SERS)技术用于评估细菌细胞壁的精细结构。通过这种平台记录的SERS谱是敏感和稳定的,可以很容易地反映出革兰氏阳性,革兰氏阴性或分枝杆菌组中不同的细菌细胞壁。此外,在抗生素暴露的早期(即约1小时),在药物敏感性细菌中发现了SERS谱的特征性变化,可用于将其与耐药菌区分开。基于SERS的诊断可以应用于单个细菌。高速SERS检测代表了一种用于微生物诊断的新颖方法。 SERS的单细菌检测能力使直接在临床标本上进行分析成为可能,而不是纯培养细菌。

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