Affiliations 

  • 1 School of Energy and Power Engineering, Jiangsu University, Zhenjiang, 212013, Jiangsu, China
  • 2 School of Chemistry and Physics, Queensland University of Technology (QUT), Brisbane, 4000, Australia. shahrooz.rahmati@hdr.qut.edu.au
  • 3 Food Safety and Food Integrity (FOSFI), Institute of Tropical Agriculture and Food Security, Universiti Putra Malaysia, 43400, Serdang, Selangor, Malaysia
  • 4 Research Center for Cancer Screening and Epidemiology, AJA University of Medical Sciences, Tehran, 14117-18541, Iran
  • 5 New Technologies Research Center, Amirkabir University of Technology, Tehran, 15916-34311, Iran
  • 6 Applied Microbiology Research Center, Systems Biology and Poisonings Institute, Baqiyatallah University of Medical Sciences, Tehran, 14359-16471, Iran
  • 7 School of Energy and Power Engineering, Jiangsu University, Zhenjiang, 212013, Jiangsu, China. Alexjuven@ujs.edu.cn
  • 8 Department of Molecular Medicine, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, 55469-14177, Iran. g-Tavoosi@tums.ac.ir
  • 9 Centre for Agriculture and the Bioeconomy, Queensland University of Technology (QUT), Brisbane, 4000, Australia
  • 10 School of Chemistry and Physics, Queensland University of Technology (QUT), Brisbane, 4000, Australia
Sci Rep, 2022 Nov 12;12(1):19416.
PMID: 36371566 DOI: 10.1038/s41598-022-23996-y

Abstract

The current COVID-19 pandemic outbreak poses a serious threat to public health, demonstrating the critical need for the development of effective and reproducible detection tests. Since the RT-qPCR primers are highly specific and can only be designed based on the known sequence, mutation sensitivity is its limitation. Moreover, the mutations in the severe acute respiratory syndrome β-coronavirus (SARS-CoV-2) genome led to new highly transmissible variants such as Delta and Omicron variants. In the case of mutation, RT-qPCR primers cannot recognize and attach to the target sequence. This research presents an accurate dual-platform DNA biosensor based on the colorimetric assay of gold nanoparticles and the surface-enhanced Raman scattering (SERS) technique. It simultaneously targets four different regions of the viral genome for detection of SARS-CoV-2 and its new variants prior to any sequencing. Hence, in the case of mutation in one of the target sequences, the other three probes could detect the SARS-CoV-2 genome. The method is based on visible biosensor color shift and a locally enhanced electromagnetic field and significantly amplified SERS signal due to the proximity of Sulfo-Cyanine 3 (Cy3) and AuNPs intensity peak at 1468 cm-1. The dual-platform DNA/GO/AuNP biosensor exhibits high sensitivity toward the viral genome with a LOD of 0.16 ng/µL. This is a safe point-of-care, naked-eye, equipment-free, and rapid (10 min) detection biosensor for diagnosing COVID-19 cases at home using a nasopharyngeal sample.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.