Design and performance of a real-time RT-PCR assay for detection of influenza C viruses

TL;DR

This paper describes a new real-time PCR test for detecting influenza C viruses, which are underreported due to limited diagnostic tools.

Contribution

The novel contribution is a highly sensitive and specific real-time RT-PCR assay targeting a conserved region of influenza C viruses.

Findings

The assay can detect as few as five RNA copies per PCR reaction.

The assay does not cross-react with influenza A, B, or other common respiratory viruses.

The assay shows high sensitivity and specificity in clinical specimens.

Abstract

Influenza C virus (ICV) usually causes a mild upper respiratory tract infection in children and those infected are frequently co-infected with other respiratory viruses. However, there have only been a few hundred documented cases of ICV infection in humans as of the end of 2024. To better understand the epidemiology and clinical impact of ICVs, we developed an influenza C real-time RT-PCR (InfC rRT-PCR) assay that targets a highly conserved region of the matrix gene segment of ICVs. The analytical sensitivity evaluation demonstrated that the InfC rRT-PCR assay was highly sensitive, as it was able to detect as few as five RNA copies per PCR reaction and had robust reactivity over a range of viral RNAs from historical and recent ICVs. The analytical specificity evaluation confirmed the assay did not cross-react with any influenza A or B viruses tested, including several animal-origin viruses, or other common non-influenza respiratory viruses. The performance evaluation on clinical specimens demonstrated the assay was highly sensitive and specific for the detection of ICVs.

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