Loading…

Development of a low-cost paper-based ELISA method for rapid Escherichia coli O157:H7 detection

Escherichia coli O157: H7 (E. coli O157: H7) has become one of the most dangerous foodborne pathogenic bacteria around the world. Currently, because of the tedious, high-cost and stringent laboratory conditions required, the conventional E. coli O157: H7 detection methods, such as culture-based meth...

Full description

Saved in:
Bibliographic Details
Published in:Analytical biochemistry 2018-02, Vol.542, p.58-62
Main Authors: Pang, Bo, Zhao, Chao, Li, Li, Song, Xiuling, Xu, Kun, Wang, Juan, Liu, Yushen, Fu, Kaiyue, Bao, Hao, Song, Dandan, Meng, Xiangjun, Qu, Xiaofeng, Zhang, Zhuping, Li, Juan
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Escherichia coli O157: H7 (E. coli O157: H7) has become one of the most dangerous foodborne pathogenic bacteria around the world. Currently, because of the tedious, high-cost and stringent laboratory conditions required, the conventional E. coli O157: H7 detection methods, such as culture-based methods and polymerase chain reaction (PCR), have much limitation. Thus, we developed a novel paper-based enzyme-linked immunosorbent assay (p-ELISA) with shorter operation duration, lower cost, relatively higher sensitivity and wider application. This method required less than 3 h and 5 μL of sample to complete the detection. The limit of detection (LOD) for E. coli O157: H7 reached 1 × 104 CFU/mL with high specificity. To be more suitable for on-site testing, the readout could be rapidly obtained without any expensive instruments. In this study, we chose E. coli O157:H7 as the representative, and our method could provide a platform for determination of other pathogenic bacteria.
ISSN:0003-2697
1096-0309
DOI:10.1016/j.ab.2017.11.010