Development of a multiplex real-time RT-PCR assay for simultaneous detection of 18 respiratory viruses
Разработка мультиплексного ПЦР в реальном времени (RT-qPCR) для одновременного обнаружения 18 респираторных вирусов
2026-01-12
SCID: 54.1/578n3sge
Discuss with AI
18 respiratory viruseslimit of detection (LOD): 5-75 copies/25 μLmultiplex RT-qPCRmultiplex real-time RT-PCRsensitivity 99.81% / specificity 100%
Figures from the paper
Abstract (AI)
Acute respiratory tract infections (ARTIs) are a major global health burden with high morbidity and mortality, mainly affecting children under 5 years old and people over 60 years old. The majority of ARTIs are caused by respiratory viruses, such as influenza virus (IFV), respiratory syncytial virus (RSV), human rhinovirus (HRV), human parainfluenza virus (HPIV), human adenovirus (HAdV), human coronavirus (HCoV), human bocavirus (HBoV) and human metapneumovirus (HMPV). Accurate and sensitive diagnosis of respiratory viruses is crucial for clinical treatment and management of patients with ARTIs. Here, we developed a multiplex RT-qPCR assay for detection of 18 common respiratory viruses. The in-house multiplex RT-qPCR assay possesses high sensitivity (limit of detection [LOD]: 5-75 copies/25 μL) and a good linear correlation between the logarithmic copy number and cycle threshold (Ct value, R²≥0.9944), along with excellent specificity characterized by no cross-reactivity within the 18 viruses and no non-specific amplification for other human pathogens. The in-house assay was assessed using 628 clinical samples and compared with Sansure and Easy Diagnosis kits. The results showed a sensitivity of 99.81%, a specificity of 100%, and an overall consistency rate of 99.84% for six target viruses (IAV, IBV, RSV, HRV, HAdV, and SARS-CoV-2). We also reported high prevalences of IAV, HAdV and HRV in Taizhou, Jiangsu, China, and a high potential of HRV co-infection with other respiratory viruses. The new multiplex RT-qPCR assay offers a sensitive, specific, and cost-effective tool for monitoring 18 common respiratory viruses to mitigate the prevalence of ARTIs.
Key Findings
1
Assay demonstrated high analytical sensitivity with limits of detection of 5–75 copies per 25 μL reaction.
2
Assay exhibited excellent specificity with no cross-reactivity among the 18 viruses and no non-specific amplification for other human pathogens.
3
Assay showed strong linearity between log copy number and Ct value (R² ≥ 0.9944).
4
Clinical evaluation on 628 samples versus Sansure and Easy Diagnosis kits yielded 99.81% sensitivity, 100% specificity, and 99.84% overall consistency for six targets (IAV, IBV, RSV, HRV, HAdV, SARS-CoV-2).
5
Developed a multiplex RT-qPCR assay capable of simultaneous detection of 18 common respiratory viruses.
6
Epidemiological findings in Taizhou, Jiangsu, China: high prevalences of IAV, HAdV, and HRV, and frequent HRV co-infections with other respiratory viruses.
7
The assay is presented as a sensitive, specific, and cost-effective tool for monitoring 18 respiratory viruses to help mitigate ARTIs.
Research Object
In-house multiplex real-time reverse transcription quantitative PCR (RT-qPCR) assay for simultaneous detection of 18 common respiratory viruses
Research Subject
Analytical and diagnostic performance (sensitivity/limit of detection, linearity, specificity/no cross-reactivity, clinical sensitivity/specificity and agreement) of the multiplex RT-qPCR for detecting 18 respiratory viruses in clinical samples
Publication Details
Publication Date
2026-01-12
Journal
Publisher
ISSN
Cited by
1
Open access PDF
Access Type
Author Information
Download PDF
Subscribe to digest