Development of multiplex RT‐ddPCR assays for detection of SARS‐CoV‐2 and other common respiratory virus infections

• Published in: Influenza and other respiratory viruses 2023-01, Vol.17 (1), p.e13084-n/a
• Main Authors: Leong, Nathaniel K. C., Gu, Haogao, Ng, Daisy Y. M., Chang, Lydia D. J., Krishnan, Pavithra, Cheng, Samuel S. M., Peiris, Malik, Poon, Leo L. M.
• Format: Article
• Language: English
• Subjects: Assaying; Coinfection - diagnosis; Coinfection - epidemiology; Coronaviruses; COVID-19; COVID-19 - diagnosis; co‐infection; Disease control; Disease transmission; human respiratory viruses; Humans; Infections; Influenza; Multiplexing; Original; Plasmids; Polymerase chain reaction; Real-Time Polymerase Chain Reaction - methods; Reproducibility of Results; Respiratory diseases; Respiratory syncytial virus; Reverse Transcription; RT‐ddPCR; SARS-CoV-2; Severe acute respiratory syndrome coronavirus 2; Target detection; Viral diseases; Viral infections; Viruses
• ISSN: 1750-2640; 1750-2659
• DOI: 10.1111/irv.13084

Background Measures for mitigation of Coronavirus Disease 2019 (COVID‐19) were set to reduce the spread of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS‐CoV‐2). SARS‐CoV‐2 and other respiratory viruses share similar transmission routes and some common clinical manifestations. Co‐circulation of SARS‐CoV‐2 and other common respiratory viruses is imminent. Therefore, development of multiplex assays for detecting these respiratory viruses is essential for being prepared for future outbreaks of respiratory viruses. Methods A panel of three reverse transcription droplet digital PCR (RT‐ddPCR) assays were developed to detect 15 different human respiratory viruses. Evaluations of its performance were demonstrated. A total of 100 local and 98 imported COVID‐19 cases in Hong Kong were screened for co‐infection with other common respiratory viruses. Results All detected viral targets showed distinct signal clusters using the multiplex RT‐ddPCR assays. These assays have a broad range of linearity and good intra‐/inter‐assay reproducibility for each target. The lower limits of quantification for all targets were ≤46 copies per reaction. Six imported cases of COVID‐19 were found to be co‐infected with other respiratory viruses, whereas no local case of co‐infection was observed. Conclusions The multiplex RT‐ddPCR assays were demonstrated to be useful for screening of respiratory virus co‐infections. The strict preventive measures applied in Hong Kong may be effective in limiting the circulation of other human respiratory viruses. The multiplex assays developed in this study can achieve a robust detection method for clinical and research purposes.