Flexible multiplex PCR to detect SARS‐CoV‐2, coronavirus OC43 and influenza A virus in nasopharyngeal swab samples

• Published in: Journal of applied microbiology Vol. 133; no. 6; pp. 3534 - 3545
• Main Authors: Pelegri‐Martinez, Eduardo, Guruceaga, Xabier, Martin‐Souto, Leire, Abad‐Diaz‐de‐Cerio, Ana, Rementeria, Aitor, Dominguez‐Monedero, Alazne, Gallego, Mikel, Martinez, Oscar, Arana‐Arri, Eunate, Aranzamendi, Maitane, Ramirez‐Garcia, Andoni
• Format: Journal Article
• Language: English
• Published: Cambridge Oxford University Press 01.12.2022; John Wiley and Sons Inc
• Subjects: coronavirus; Coronaviruses; Influenza; Influenza A; influenza A virus; multiplex RT‐qPCR; Multiplexing; OC43; Original; Public health; Respiratory diseases; Reverse transcription; Robust control; SARS‐CoV‐2; Severe acute respiratory syndrome; Severe acute respiratory syndrome coronavirus 2; Viral diseases; Viruses
• ISSN: 1364-5072; 1365-2672
• DOI: 10.1111/jam.15788

Introduction Quantitative reverse transcription PCR (RT‐qPCR) is the leading tool to detect severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2). Given that it will almost certainly continue to coexist with other respiratory viruses in the coming years, our study aimed to design a multiplex PCR system not affected by supplier outages and with reduced cost compared to the existing commercially available kits. Methods and results In this study, combinations of four primers/probe sets were used to construct a flexible RT‐qPCR assay which is capable of discriminating between SARS‐CoV‐2 and the seasonal human coronavirus HCoV‐OC43, or even influenza A virus. Additionally, the human RPP30 gene was used as an internal control. To demonstrate the robustness of the assay, it was applied to a collection of 150 clinical samples. The results showed 100% sensitivity and specificity compared to the automatized system used at the hospital and were better when indeterminate samples were analysed. Conclusions This study provides an efficient method for the simultaneous detection of SARS‐CoV‐2, HCoV‐OC43 and influenza A virus, and its efficacy has been tested on clinical samples showing outstanding results. Significance and impact of the study The multiplex RT‐qPCR design offers an accessible and economical alternative to commercial detection kits for hospitals and laboratories with limited economic resources or facing situations of supply shortage.