4.8 Article

Integrating programmable DNAzymes with electrical readout for rapid and culture-free bacterial detection using a handheld platform

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NATURE CHEMISTRY
卷 13, 期 9, 页码 895-+

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NATURE PORTFOLIO
DOI: 10.1038/s41557-021-00718-x

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  1. Natural Science and Engineering Research Council (NSERC) of Canada
  2. Canada Research Chair programme
  3. NSERC
  4. McMaster University

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This study presents an electrical assay that uses electroactive RNA-cleaving DNAzymes to identify specific bacterial targets and release a DNA barcode for rapid clinical analysis with high sensitivity and specificity. The assay demonstrates high selectivity for Escherichia coli and can accurately diagnose bacterial infections in a short amount of time.
The detection and identification of bacteria currently rely on enrichment steps such as bacterial culture and nucleic acid amplification to increase the concentration of target analytes. These steps increase assay time, cost and complexity, making it difficult to realize a truly rapid point-of-care test. Here we report the development of an electrical assay that uses electroactive RNA-cleaving DNAzymes (e-RCDs) to identify specific bacterial targets and subsequently release a DNA barcode for transducing a signal onto an electrical chip. Integrating e-RCDs into a two-channel electrical chip with nanostructured electrodes provides the analytical sensitivity and specificity needed for clinical analysis. The e-RCD assay is capable of detecting 10 CFU (equivalent to 1,000 CFU ml(-1)) of Escherichia coli selectively from a panel containing multiple non-specific bacterial species. Clinical evaluation of this assay using 41 patient urine samples demonstrated a diagnostic sensitivity of 100% and specificity of 78% at an analysis time of less than one hour compared with the several hours needed for currently used culture-based methods.

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