4.7 Article

2D nanomaterial sensing array using machine learning for differential profiling of pathogenic microbial taxonomic identification

Journal

MICROCHIMICA ACTA
Volume 189, Issue 8, Pages -

Publisher

SPRINGER WIEN
DOI: 10.1007/s00604-022-05368-5

Keywords

Pathogenic microbial taxonomic; Molecular response differential profiling; Machine learning approach; Accurate recognition

Funding

  1. Abo Akademi University (ABO)
  2. National Key R&D Program of China [2019YFA0905800]
  3. National Science Foundation of China [21705048]
  4. Guangdong Basic and Applied Basic Research Foundation [2021A1515012333]
  5. Natural Science Foundation of Jiangxi Province [20192ACBL20046]
  6. Fundamental Research Funds for the Central Universities [20720200004]
  7. Key Project of College Youth Natural Fund of Fujian Province [JZ160404]
  8. Key Laboratory of Sensing Technology and Biomedical Instruments of Guangdong Province [2020B1212060077]
  9. Qingdao XINO Tech company

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An integrated custom cross-response sensing array combining visible machine learning approach has been developed for rapid and accurate pathogenic microbial taxonomic identification. The array consists of 2D nanomaterial and fluorescently labeled single-stranded DNA as sensing elements, allowing extraction of differential response profiles and visualization of the recognition process. Experimental results demonstrate high accuracy in identifying microorganisms under a smaller dataset, overcoming the dependence on big data in conventional methods. The detection concentration ranges for various microorganisms have also been tested.
An integrated custom cross-response sensing array has been developed combining the algorithm module's visible machine learning approach for rapid and accurate pathogenic microbial taxonomic identification. The diversified cross-response sensing array consists of two-dimensional nanomaterial (2D-n) with fluorescently labeled single-stranded DNA (ssDNA) as sensing elements to extract a set of differential response profiles for each pathogenic microorganism. By altering the 2D-n and different ssDNA with different sequences, we can form multiple sensing elements. While interacting with microorganisms, the competition between ssDNA and 2D-n leads to the release of ssDNA from 2D-n. The signals are generated from binding force driven by the exfoliation of either ssDNA or 2D-n from the microorganisms. Thus, the signal is distinguished from different ssDNA and 2D-n combinations, differentiating the extracted information and visualizing the recognition process. Fluorescent signals collected from each sensing element at the wavelength around 520 nm are applied to generate a fingerprint. As a proof of concept, we demonstrate that a six-sensing array enables rapid and accurate pathogenic microbial taxonomic identification, including the drug-resistant microorganisms, under a data size of n=288. We precisely identify microbial with an overall accuracy of 97.9%, which overcomes the big data dependence for identifying recurrent patterns in conventional methods. For each microorganism, the detection concentration is 10(5) similar to 10(8) CFU/mL for Escherichia coli, 10(2) similar to 10(7) CFU/mL for E. coli beta, 10(3) similar to 10(8) CFU/mL for Staphylococcus aureus, 10(3) similar to 10(7) CFU/mL for MRSA, 10(2) similar to 10(8) CFU/ mL for Pseudomonas aeruginosa, 10(3) similar to 10(8) CFU/mL for Enterococcus faecalis, 10(2) similar to 10(8) CFU/mL for Klebsiella pneumoniae, and 10(3) similar to 10(8) CFU/mL for Candida albicans. Combining the visible machine learning approach, this sensing array provides strategies for precision pathogenic microbial taxonomic identification.

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