Development of Multiplex Real-Time RT-qPCR Assays for the Detection of SARS-CoV-2, Influenza A/B, and MERS-CoV.


Journal

Journal of visualized experiments : JoVE
ISSN: 1940-087X
Titre abrégé: J Vis Exp
Pays: United States
ID NLM: 101313252

Informations de publication

Date de publication:
10 Nov 2023
Historique:
medline: 29 11 2023
pubmed: 27 11 2023
entrez: 27 11 2023
Statut: epublish

Résumé

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that causes Coronavirus disease 2019 (COVID-19) is a serious threat to the general public's health. During influenza seasons, the spread of SARS-CoV-2 and other respiratory viruses may cause a population-wide burden of respiratory disease that is difficult to manage. For that, the respiratory viruses SARS-CoV-2, Influenza A, Influenza B, and Middle East respiratory syndrome (MERS-CoV) will need to be carefully watched over in the upcoming fall and winter seasons, particularly in the case of SARS-CoV-2, Influenza A, and Influenza B, which share similar epidemiological factors like susceptible populations, mode of transmission, and clinical syndromes. Without target-specific assays, it can be challenging to differentiate among cases of these viruses owing to their similarities. Accordingly, a sensitive and targeted multiplex assay that can easily differentiate between these viral targets will be useful for healthcare practitioners. In this study, we developed a real-time reverse transcriptase-PCR-based assay utilizing an in-house developed R3T one-step RT-qPCR kit for simultaneous detection of SARS-CoV-2, Influenza A, Influenza B, and SARS-CoV-2, MERS-CoV. With as few as 10 copies of their synthetic RNAs, we can successfully identify SARS-CoV-2, Influenza A, Influenza B, and MERS-CoV targets simultaneously with 100% specificity. This assay is found to be accurate, reliable, simple, sensitive, and specific. The developed method can be used as an optimized SARS-CoV-2, Influenza A, Influenza B, and SARS-CoV-2, MERS-CoV diagnostic assay in hospitals, medical centers, and diagnostic laboratories as well as for research purposes.

Identifiants

pubmed: 38009723
doi: 10.3791/65822
doi:

Substances chimiques

RNA 63231-63-0

Types de publication

Journal Article Video-Audio Media

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Atheer Althobaiti (A)

Biological and Environmental Sciences and Engineering Division (BESE), King Abdullah University of Science and Technology (KAUST).

Kareem Hamdan (K)

Biological and Environmental Sciences and Engineering Division (BESE), King Abdullah University of Science and Technology (KAUST).

Mohamed A Sobhy (MA)

Biological and Environmental Sciences and Engineering Division (BESE), King Abdullah University of Science and Technology (KAUST).

Renad Rawas (R)

Biological and Environmental Sciences and Engineering Division (BESE), King Abdullah University of Science and Technology (KAUST).

Masateru Takahashi (M)

Biological and Environmental Sciences and Engineering Division (BESE), King Abdullah University of Science and Technology (KAUST).

Olga Artyukh (O)

Biological and Environmental Sciences and Engineering Division (BESE), King Abdullah University of Science and Technology (KAUST).

Muhammad Tehseen (M)

Biological and Environmental Sciences and Engineering Division (BESE), King Abdullah University of Science and Technology (KAUST); muhammad.tehseen@kaust.edu.sa.

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