Sensitive detection of Escherichia coli O157:H7 using Pt-Au bimetal nanoparticles with peroxidase-like amplification

被引:137
作者
Jiang, Tao [1 ,3 ]
Song, Yang [1 ]
Wei, Tianxiang [1 ]
Li, He [1 ]
Du, Dan [1 ,4 ]
Zhu, Mei-Jun [2 ]
Lin, Yuehe [1 ,4 ]
机构
[1] Washington State Univ, Sch Mech & Mat Engn, Pullman, WA 99164 USA
[2] Washington State Univ, Sch Food Sci, Pullman, WA 99164 USA
[3] Chinese Acad Agr Sci, Lanzhou Vet Res Inst, State Key Lab Vet Etiol Biol, Key Lab Anim Virol,Minist Agr, Lanzhou 730046, Gansu, Peoples R China
[4] Washington State Univ, Paul G Allen Sch Global Anim Hlth, Pullman, WA 99164 USA
关键词
Immunochromatographic assay; Pathogens detection; Pt-Au nanoparticles; Peroxidase; E. coli O157:H7; LATERAL FLOW TEST; MEDIATED ISOTHERMAL AMPLIFICATION; IMMUNOCHROMATOGRAPHIC ASSAY; COLLOIDAL GOLD; MULTISTATE OUTBREAK; RAPID DETECTION; QUANTUM DOTS; TEST STRIP; BIOSENSOR; NANOSTRUCTURES;
D O I
10.1016/j.bios.2015.10.017
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Escherichia coli O157:H7 is one of the most notorious foodborne pathogens causing serious disease at low infectious dose. To protect consumers from deadly foodborne E. coli O157:H7 infection, it is vital to develop a simple, reliable, sensitive and rapid method which can detect low level E. coli O157:H7 in foods at real-time. We have successfully developed a novel immunochromatographic assay (ICA) with enhanced sensitivity for the visual and quantitative detection of E. coli O157:H7. Sandwich-type immunoreactions were performed on the ICA, and Pt-Au bimetal nanoparticles (NPs) were accumulated on the test zone. The signal amplification is based on Pt-Au bimetal NPs possessing high peroxidase activity toward 3,3',5,5'-tetramethylbenzidine, which can produce characteristic colored bands and thus, enable visual detection of E. coli O157:H7 without instrumentation. The innovative aspect of this approach lies in the visualization and quantification of target pathogen through the detection of color intensity. Due to the excellent peroxidase activity of Pt-Au NPs, they emit strong visible color intensity in less than 1 min for visual observation even in low concentration range of E. cali O157:H7. Quantification was performed using a commercial assay meter. The sensitivity was improved more than 1000-folds compared to the conventional test strip based on colored gold-colloids. Although the feasibility was demonstrated using E. coli O157:H7 as a model analyte, this approach could be easily developed to be a universal signal amplification technique and applied to detection of a wide variety of foodborne pathogens and protein biomarkers. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:687 / 694
页数:8
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