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表面增强拉曼散射法鉴定耐甲氧西林金黄色葡萄球菌使用正电荷的银纳米粒子。

Surface-enhanced Raman scattering method for the identification of methicillin-resistant Staphylococcus aureus using positively charged silver nanoparticles.

机构信息

Department of Laboratory Medicine, Southwest Hospital, Army Medical University (Third Military Medical University), Chongqing, 400038, China.

Institut des Molécules et Matériaux du Mans (IMMM - UMR CNRS 6283), Le Mans Université, Avenue Olivier Messiaen, 72085, Le Mans cedex 9, France.

出版信息

Mikrochim Acta. 2019 Jan 12;186(2):102. doi: 10.1007/s00604-018-3150-6.

DOI:10.1007/s00604-018-3150-6
PMID:30637528
Abstract

The article describes a SERS-based method for diagnosis of bacterial infections. Positively charged silver nanoparticles (AgNPs) were employed for identification of methicillin-resistant Staphylococcus aureus (MRSA). It is found that AgNPs undergo self-assembly on the surface of bacteria via electrostatic aggregation. The assembled AgNPs are excellent SERS substrates. To prove the capability of SERS to differentiate between S. aureus and other microorganisms, six standard strains including S. aureus 29213, S. aureus 25923, C. albicans, B. cereus, E. coli, and P. aeruginosa were tested. To further demonstrate its applicability for the identification of MRSA in clinical samples, 52 methicillin-sensitive S. aureus (MSSA) isolates and 215 MRSA isolates were detected by SERS. The total measurement time (include incubation) is 45 min when using a 3 μL sample. The method gives a strongly enhanced Raman signal (at 730 cm and 1325 cm) with good reproducibility and repeatability. It was successfully applied to the discrimination of the six strain microorganisms. The typical Raman peaks of S. aureus at 730, 1154, 1325, and 1457 cm were observed, which were assigned to the bacterial cell wall components (730 cm- adenine, glycosidic ring mode, 1154 cm- unsaturated fatty acid, 1325 cm- adenine, polyadenine, and 1457 cm for -COO- stretching). S. aureus was completely separated from other species by partial least squares discriminant analysis (PLS-DA). Moreover, 52 MSSA isolates and 215 MRSA isolates from clinical samples were identified by PLS-DA. The accuracy was almost 100% when compared to the standard broth microdilution method. A classification based on latent structure discriminant analysis provided spectral variability directly. Conceivably, the method offers a potent tool for the identification of bacteria and antibiotics resistance, and for studies on antibiotic-resistance in general. Graphical abstract Schematic of the surface-enhanced Raman scattering (SERS) measurements on Staphylococcus aureus (S. aureus) using positively charged silver nanoparticles (AgNPs). AgNPs are adsorbed on the bacterial cell wall by electrostatic attraction. SERS spectra were analyzed by PLS-DA for the identification of Staphylococcus aureus (MRSA) and methicillin-resistant Staphylococcus aureus (MSSA). MRSA isolates were divided into four groups, including R1, R2, R3, and R4. MSSA just includes group S.

摘要

本文描述了一种基于 SERS 的细菌感染诊断方法。带正电荷的银纳米粒子 (AgNPs) 被用于鉴定耐甲氧西林金黄色葡萄球菌 (MRSA)。研究发现,AgNPs 通过静电聚集在细菌表面上自组装。组装后的 AgNPs 是出色的 SERS 基底。为了证明 SERS 能够区分金黄色葡萄球菌和其他微生物的能力,对包括金黄色葡萄球菌 29213、金黄色葡萄球菌 25923、白色念珠菌、蜡样芽孢杆菌、大肠杆菌和铜绿假单胞菌在内的 6 种标准菌株进行了测试。为了进一步证明其在临床样本中鉴定 MRSA 的适用性,使用 SERS 检测了 52 株甲氧西林敏感金黄色葡萄球菌 (MSSA) 分离株和 215 株耐甲氧西林金黄色葡萄球菌 (MRSA) 分离株。使用 3μL 样本时,总测量时间(包括孵育时间)为 45 分钟。该方法得到了具有良好重现性和可重复性的强增强拉曼信号(在 730cm 和 1325cm 处)。它成功应用于六种微生物的区分。观察到金黄色葡萄球菌在 730、1154、1325 和 1457cm 处的典型拉曼峰,其被分配给细菌细胞壁成分(730cm-腺嘌呤,糖苷环模式,1154cm-不饱和脂肪酸,1325cm-腺嘌呤,多腺嘌呤和 1457cm-COO-拉伸)。通过偏最小二乘判别分析(PLS-DA),金黄色葡萄球菌完全与其他物种分离。此外,还通过 PLS-DA 鉴定了来自临床样本的 52 株 MSSA 分离株和 215 株 MRSA 分离株。与标准肉汤微量稀释法相比,准确率几乎达到 100%。基于潜在结构判别分析的分类直接提供了光谱可变性。可以想象,该方法为细菌鉴定和抗生素耐药性提供了有力的工具,也为抗生素耐药性研究提供了有力的工具。

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