4.6 Article

Molecular Beacon Assay Development for Severe Acute Respiratory Syndrome Coronavirus 2 Detection

Journal

SENSORS
Volume 21, Issue 21, Pages -

Publisher

MDPI
DOI: 10.3390/s21217015

Keywords

RNA viruses; SARS-CoV-2; COVID-19; fluorescence detection; diagnosis

Funding

  1. Fundacao para a Ciencia e a Tecnologia (FCT) [149]
  2. Agencia de Investigacao Clinica e Inovacao Biomedica (AICIB)
  3. FCT/MCT [CICS-UBI UIDB/00709/2020, POCI-01-0145-FEDER-022122]
  4. Portuguese NMR Network [ROTEIRO/0031/2013-PINFRA/22161/2016]
  5. FEDER
  6. FCT [UIDP/00709/2020, SFRH/BD/122953/2016, PD/BD/142851/2018, PD/00065/2013]
  7. FCT-Foundation for Science and Technology [SFRH/BD/145106/2019]
  8. PTNMR project [PINFRA/22161/2016-B4]
  9. C4-Cloud Computing Competence Centre, UBIMedical, Universidade da Beira Interior [UIDP/00709/2020]
  10. [2020.05329.BD]
  11. Fundação para a Ciência e a Tecnologia [SFRH/BD/122953/2016, 2020.05329.BD, SFRH/BD/145106/2019] Funding Source: FCT

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The study aimed to develop a molecular beacon-based detection assay for SARS-CoV-2, focusing on ORF1ab and S gene detection, proposing a two-stage COVID-19 testing strategy. The results showed a correlation between high fluorescence levels and low Ct values, indicating an association between viral load and increased MB fluorescence.
The fast spread of SARS-CoV-2 has led to a global pandemic, calling for fast and accurate assays to allow infection diagnosis and prevention of transmission. We aimed to develop a molecular beacon (MB)-based detection assay for SARS-CoV-2, designed to detect the ORF1ab and S genes, proposing a two-stage COVID-19 testing strategy. The novelty of this work lies in the design and optimization of two MBs for detection of SARS-CoV-2, namely, concentration, fluorescence plateaus of hybridization, reaction temperature and real-time results. We also identify putative G-quadruplex (G4) regions in the genome of SARS-CoV-2. A total of 458 nasopharyngeal and throat swab samples (426 positive and 32 negative) were tested with the MB assay and the fluorescence levels compared with the cycle threshold (Ct) values obtained from a commercial RT-PCR test in terms of test duration, sensitivity, and specificity. Our results show that the samples with higher fluorescence levels correspond to those with low Ct values, suggesting a correlation between viral load and increased MB fluorescence. The proposed assay represents a fast (total duration of 2 h 20 min including amplification and fluorescence reading stages) and simple way of detecting SARS-CoV-2 in clinical samples from the upper respiratory tract.

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