4.8 Article

Cascade signal enhancement by integrating DNA walking and RCA reaction-assisted ?silver-link? crossing electrode for ultrasensitive electrochemical detection of Staphylococcus aureus

Journal

BIOSENSORS & BIOELECTRONICS
Volume 217, Issue -, Pages -

Publisher

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2022.114716

Keywords

Electrochemical sensor; DNA walking; Rolling circle amplification; Crossing electrode; Conductivity; Bacteria detection

Funding

  1. National Natural Science Foundation of China [31972173]
  2. Program for Science & Technology Innovation Platform of Hunan Province [2019TP1029]
  3. Program for Science & Technology of Jiangxi Provincial Department of Education [GJJ200852]
  4. College Students Innovations Special Project [DC2021-012]
  5. Distinguished Professor Program of Jinggang Scholars in Institutions of Higher Learning, Jiangxi Province

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A new electrochemical bacterial sensor that couples DNA walking and rolling circle amplification (RCA) reaction-assisted silver-link crossing electrode is proposed for rapid detection and early diagnosis of diseases caused by bacteria. The sensor demonstrates high efficiency, good stability, and low background signal, and has the potential for food monitoring and clinical diagnosis.
The key factor to control the incidence rate of diseases caused by bacteria is rapid detection and early diagnosis. Herein, we proposed a new electrochemical bacterial sensor by coupling DNA walking and rolling circle amplification (RCA) reaction-assisted silver-link crossing electrode. Staphylococcus aureus (S. aureus) was detected using this proof-of concept strategy. Aptamer/DNA walker and auxiliary sequence (AS)/RCA reaction probe (RP) duplexes were modified on the electrode surface. The binding of S. aureus with its aptamer caused the disintegration of aptamer/DNA walker and released DNA walker. With the help of Exo III, DNA walker moved along the electrode surface and AS in AS/RP duplex was continuously digested to release RP. By introducing phi29 DNA polymerase, RCA reaction was performed using RP as the reaction primer to form long single-strand RCA extension products between the electrodes. The silver-link crossing electrode was formed by metallization of gene-link, significant conductivity was thus acquired for bacteria detection. The limit of detection (LOD) was 10 CFU/mL and detection time was 2 h. The proposed sensor has high efficiency, good stability and low background signal, human serum and milk samples were successfully detected, which emerged a promising potential in the food monitoring and clinical diagnosis.

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