Culture-Independent Multiplexed Detection of Drug-Resistant Bacteria Using Surface-Enhanced Raman Scattering

被引:8
|
作者
Dai, Tingting [1 ]
Xiao, Zhen [2 ]
Shan, Dingying [2 ]
Moreno, Angel [3 ]
Li, Hongquan [4 ]
Prakash, Manu [5 ]
Banaei, Niaz [3 ,6 ,7 ]
Rao, Jianghong [1 ,2 ]
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Radiol, Mol Imaging Program Stanford, Sch Med, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Pathol, Sch Med, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Elect Engn, Stanford, CA 94305 USA
[5] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
[6] Stanford Univ, Dept Med, Div Infect Dis & Geog Med, Sch Med, Stanford, CA 94305 USA
[7] Stanford Univ, Clin Microbiol Lab, Med Ctr, Palo Alto, CA 94304 USA
来源
ACS SENSORS | 2023年
基金
美国国家科学基金会;
关键词
extended-spectrum beta-lactamases; bacteria detection; surface-enhanced Raman scattering; gold nanoparticles; activatable Raman probes; SPECTRUM-BETA-LACTAMASE; MOLECULAR-DETECTION; NANOPARTICLES; FUTURE; GENES; SHAPE;
D O I
10.1021/acssensors.3c01345
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The rapid and accurate detection of bacteria resistance to beta-lactam antibiotics is critical to inform optimal treatment and prevent overprescription of potent antibiotics. Here, we present a fast, culture-independent method for the detection of extended-spectrum beta-lactamases (ESBLs) using surface-enhanced Raman scattering (SERS). The method uses Raman probes that release sulfur-based Raman active molecules in the presence of beta-lactamases. The released thiol molecules can be captured by gold nanoparticles, leading to amplified Raman signals. A broadspectrum cephalosporin probe R1G and an ESBL-specific probe R3G are designed to enable duplex detection of bacteria expressing broad-spectrum beta-lactamases or ESBLs with a detection limit of 10(3) cfu/mL in 1 h incubation. Combined with a portable Raman microscope, our culturing-free SERS assay has reduced screening time to 1.5 h without compromising sensitivity and specificity.
引用
收藏
页码:3264 / 3271
页数:8
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