Agriculture and Food Chemistry

Amplification-free, highly sensitive electrochemical DNA-based sensor for simultaneous detection of stx1 and stx2 genes of Shiga toxin-producing E. coli (STEC)

Authors

Abstract

Shiga toxin-producing E. coli (STEC) is a food-borne pathogen of significant public health concern, due to the severity of the illness it can cause and a low infection dose. The key targets in molecular-based assays to detect STEC are stx1 or stx2 genes, coding for the ability to produce Shiga T Toxin 1 and 2. The most commonly used molecular detection techniques, such as PCR and real-time PCR, are considerably time-consuming and there is an urgent need for a more rapid screening assay which could be used in agri-food settings. In this work, an amplification-free multiplex electrochemical sensor for the simultaneous detection of stx1 and stx2 genes was developed using a silicon-based chip comprising of six interdigitated gold microelectrodes(IDE) sensors. Two probes complementary to stx1 and stx2 genes were immobilised on a single chip allowing for multiplex detection. The selectivity of the multiplex sensor was confirmed using fluorescence and electrochemistry. The developed assay conditions allowed for an improved limit of detection by three orders of magnitude compared to the previous reports achieving a amplification-free limit of detection of 100 zM (10-19 M) for both, stx1 and stx2 genes. The developed sensor was validated using chromosomal DNA extracted from a bacterial culture containing no virulence genes, stx1 gene only, and both stx1 and stx2. Such multiplex sensor, if combined with on-chip DNA extraction, could revolutionise the point-of-use detection of STEC as well as other pathogens for instance on-farm or in the food industry.

Content

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Supplementary material

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Amplification-free, highly sensitive electrochemical DNA-based sensor for simultaneous detection of stx1 and stx2 genes of Shiga toxin-producing E. coli (STEC)_Supp Info
This document provides additional content relating to (I) sensor optimisation and (ii) DNA probe immobilisation volume optimisation. Detailed descriptions and five additional figures are provided