Highly sensitive detection of high-risk bacterial pathogens using SERS-based lateral flow assay strips

被引:129
作者
Wang, Rui [1 ]
Kim, Kihyun [1 ]
Choi, Namhyun [1 ]
Wang, Xiaokun [1 ]
Lee, Jiyoung [1 ]
Jeon, Jun Ho [2 ]
Rhie, Gi-eun [2 ]
Choo, Jaebum [1 ]
机构
[1] Hanyang Univ, Dept Bionano Technol, Ansan 15588, South Korea
[2] Korea Cts Dis Control & Prevent, Lab Control Infect Dis, Div High Risk Pathogens, Chungju 28159, South Korea
基金
新加坡国家研究基金会;
关键词
Yersinia pestis; Francisella tularensis; Bacillus anthraces; Surface enhanced Raman scattering; Lateral flow assay; YERSINIA-PESTIS; FRANCISELLA-TULARENSIS; GENOME SEQUENCE; RAPID DETECTION; IMMUNOASSAY; PLAGUE; NANOPARTICLES; TRANSMISSION; TULAREMIA; AGENT;
D O I
10.1016/j.snb.2018.04.162
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Bacterial pathogens such as Yersinia pestis, Francisella tularensis, and Bacillus anthraces are classified into the highest rank of potential bioterrorism agents. Colorimetric lateral flow assay (LFA) strips are commercially available but these conventional strips have drawbacks in terms of low sensitivity and limit of quantitative analysis. Therefore, there is an urgent need for a new sensing platform to detect these pathogens in the early contamination stage. In this study, a novel surface-enhanced Raman scattering (SERS)-based LFA strip was developed for sensitive detection of bacterial pathogens. Target-specific SERS nanotags (Raman reporter-labeled gold nanoparticles) were used as an alternative to the gold nanoparticles in conventional LFA strips. Using these SERS nanotags the presence of bacteria could be identified through a simple color change in the test line. Additionally, highly sensitive and accurate quantitative analysis could be performed by monitoring the characteristic Raman peak intensity of SERS nanotags that were captured in the test line. This highly sensitive method required a short assay time (15 min) and a tiny volume of pathogen sample (40 mu L). We believe that the proposed SERS-based LFA technique has great potential as a valuable tool in the early detection of specific bacterial pathogens in the field due to its excellent analytical sensitivity. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:72 / 79
页数:8
相关论文
共 33 条
[1]   A Method for Quantitative Analysis of Standard and High-Throughput qPCR Expression Data Based on Input Sample Quantity [J].
Adamski, Mateusz G. ;
Gumann, Patryk ;
Baird, Alison E. .
PLOS ONE, 2014, 9 (08)
[2]   Bioengineering bacteriophages to enhance the sensitivity of phage amplification-based paper fluidic detection of bacteria [J].
Alcaine, S. D. ;
Law, K. ;
Ho, S. ;
Kinchla, A. J. ;
Sela, D. A. ;
Nugen, S. R. .
BIOSENSORS & BIOELECTRONICS, 2016, 82 :14-19
[3]  
Amoako KK, 2017, METHODS MOL BIOL, V1492, P203, DOI 10.1007/978-1-4939-6442-0_15
[4]   Kinetically Controlled Seeded Growth Synthesis of Citrate-Stabilized Gold Nanoparticles of up to 200 nm: Size Focusing versus Ostwald Ripening [J].
Bastus, Neus G. ;
Comenge, Joan ;
Puntes, Victor .
LANGMUIR, 2011, 27 (17) :11098-11105
[5]   Quantum dot-based lateral flow immunoassay for detection of chloramphenicol in milk [J].
Berlina, Anna N. ;
Taranova, Nadezhda A. ;
Zherdev, Anatoly V. ;
Vengerov, Yuri Y. ;
Dzantiev, Boris B. .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2013, 405 (14) :4997-5000
[6]   DNA hybridization detection in a microfluidic channel using two fluorescently labelled nucleic acid probes [J].
Chen, Lingxin ;
Lee, Sangyeop ;
Lee, Moonkwon ;
Lim, Chaesung ;
Choo, Jaebum ;
Park, Joong Yull ;
Lee, Sanghoon ;
Joo, Sang-Woo ;
Lee, Kyeong-Hee ;
Choi, Young-Wook .
BIOSENSORS & BIOELECTRONICS, 2008, 23 (12) :1878-1882
[7]   Simultaneous Detection of Dual Prostate Specific Antigens Using Surface-Enhanced Raman Scattering-Based Immunoassay for Accurate Diagnosis of Prostate Cancer [J].
Cheng, Ziyi ;
Choi, Namhyun ;
Wang, Rui ;
Lee, Sangyeop ;
Moon, Kyung Chul ;
Yoon, Soo-Young ;
Chen, Lingxin ;
Choo, Jaebum .
ACS NANO, 2017, 11 (05) :4926-4933
[8]   Quantitative analysis of thyroid-stimulating hormone (TSH) using SERS-based lateral flow immunoassay [J].
Choi, Suji ;
Hwang, Joonki ;
Lee, Sangyeop ;
Lim, Dong Woo ;
Joo, Hoodon ;
Choo, Jaebum .
SENSORS AND ACTUATORS B-CHEMICAL, 2017, 240 :358-364
[9]  
Chung HJ, 2013, NAT NANOTECHNOL, V8, P369, DOI [10.1038/NNANO.2013.70, 10.1038/nnano.2013.70]
[10]   Yersinia pestis as a telluric, human ectoparasite-borne organism [J].
Drancourt, M ;
Houhamdi, L ;
Raoult, D .
LANCET INFECTIOUS DISEASES, 2006, 6 (04) :234-241