Colorimetric and electrochemical analysis of DNAzyme-LAMP amplicons for the detection of Escherichia coli in food matrices

Foodborne bacteria like Escherichia coli threaten global food security, necessitating affordable, on-site detection methods, especially in resource-limited settings. This study optimized loop-mediated isothermal amplification (LAMP) integrated with peroxidase-mimicking G-quadruplex DNA structures (DNAzyme), termed DNAzyme-LAMP which was designed to incorporate two different catalytic DNAzymes per amplification unit, enabling colorimetric detection of E. coli in leafy vegetables and milk samples. Additionally, we introduce a novel electrochemical method that enhances analytical sensitivity. The optimized DNAzyme-LAMP achieved a detection limit below 6.3 CFU per reaction or 0.1 aM gene copies. This system lays the groundwork for the development of on-site biosensors and can be adapted for detecting other foodborne pathogens.

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Publication Details

Journal
Scientific Reports
Published
2024-11-22
DOI
https://doi.org/10.1038/s41598-024-80392-4
Citations
8
Primary Topic
Biosensors and Analytical Detection
Type
article
Field-Weighted Citation Impact
1.48

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article

Colorimetric and electrochemical analysis of DNAzyme-LAMP amplicons for the detection of Escherichia coli in food matrices

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8 citations
Scientific Reports
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article

Colorimetric and electrochemical analysis of DNAzyme-LAMP amplicons for the detection of Escherichia coli in food matrices

Doris H. D’Souza, Oudessa Kerro Dego, Juan José Ramos Antón, Shigetoshi Eda, Benti Deresa Gelalcha, Brian A. Morgan, Jie Wu, Alaa H. Sewid, Haley C. Dylewski
article en
8 citations

Abstract

Foodborne bacteria like Escherichia coli threaten global food security, necessitating affordable, on-site detection methods, especially in resource-limited settings. This study optimized loop-mediated isothermal amplification (LAMP) integrated with peroxidase-mimicking G-quadruplex DNA structures (DNAzyme), termed DNAzyme-LAMP which was designed to incorporate two different catalytic DNAzymes per amplification unit, enabling colorimetric detection of E. coli in leafy vegetables and milk samples. Additionally, we introduce a novel electrochemical method that enhances analytical sensitivity. The optimized DNAzyme-LAMP achieved a detection limit below 6.3 CFU per reaction or 0.1 aM gene copies. This system lays the groundwork for the development of on-site biosensors and can be adapted for detecting other foodborne pathogens.

Scientific ReportsVol. 14(1)
Zagazig University (EG), University of Tennessee at Knoxville (US)
National Science Foundation
Zero hunger
Openalex Percentile: Top 19%
Biosensors and Analytical Detection
1.48
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