State Key Laboratory of Frigid Zone Cardiovascular Diseases (SKLFZCD); Research Center for Innovative Technology of Pharmaceutical Analysis, College of Pharmacy, Harbin Medical University, No. 157 Baojian Road, Nangang District, Harbin City, Heilongjiang Province 150081, China.
Department of Chinese Formulae, Heilongjiang University of Chinese Medicine, No. 24 Heping Road, Xiangfang District, Harbin City, Heilongjiang Province 150081, China.
Anal Chem. 2024 May 28;96(21):8566-8575. doi: 10.1021/acs.analchem.4c00622. Epub 2024 May 15.
Unraveling bacterial identity through Raman scattering techniques has been persistently challenging due to homogeneously amplified Raman signals across a wide variety of bacterial molecules, predominantly protein- or nucleic acid-mediated. In this study, we present an approach involving the use of silver nanoparticles to completely and uniformly "mask" adsorption on the surface of bacterial molecules through sodium borohydride and sodium chloride. This approach enables the acquisition of enhanced surface-enhanced Raman scattering (SERS) signals from all components on the bacterial surface, facilitating rapid, specific, and label-free bacterial identification. For the first time, we have characterized the identity of a bacterium, including its DNA, metabolites, and cell walls, enabling the accurate differentiation of various bacterial strains, even within the same species. In addition, we embarked on an exploration of the origin and variability patterns of the main characteristic peaks of Gram-positive and Gram-negative bacteria. Significantly, the SERS peak ratio was found to determine the inflection point of accelerated bacterial death upon treatment with antimicrobials. We further applied this platform to identify 15 unique clinical antibiotic-resistant bacterial strains, including five strains in human urine, a first for Raman technology. This work has profound implications for prompt and accurate identification of bacteria, particularly antibiotic-resistant strains, thereby significantly enhancing clinical diagnostics and antimicrobial treatment strategies.
通过拉曼散射技术揭示细菌的身份一直具有挑战性,因为在广泛的细菌分子中,蛋白质或核酸介导的拉曼信号均匀地放大。在这项研究中,我们提出了一种方法,涉及使用银纳米粒子通过硼氢化钠和氯化钠完全和均匀地“掩盖”吸附在细菌分子表面上。这种方法能够从细菌表面的所有成分获得增强的表面增强拉曼散射(SERS)信号,从而实现快速、特异和无标记的细菌鉴定。我们首次对细菌的身份进行了表征,包括其 DNA、代谢物和细胞壁,能够准确区分不同的细菌株,即使在同一物种内也是如此。此外,我们还探索了革兰氏阳性菌和革兰氏阴性菌主要特征峰的起源和可变性模式。重要的是,SERS 峰比被发现可以确定在对抗生素治疗时细菌死亡加速的拐点。我们进一步将该平台应用于鉴定 15 种独特的临床抗生素耐药细菌株,包括 5 株来自人尿液的细菌,这是拉曼技术的首次应用。这项工作对于快速准确地鉴定细菌,特别是抗生素耐药菌株具有深远的意义,从而显著增强了临床诊断和抗菌治疗策略。