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

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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Publication Details

Journal
Journal of Clinical Virology
Published
2025-09-27
DOI
https://doi.org/10.1016/j.jcv.2025.105874
Primary Topic
Influenza Virus Research Studies
Type
article
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article

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

Jimma Liddell, William G. Davis, Anna K. Strain, Jaime Christensen et al.
Journal of Clinical Virology
Influenza Virus Research Studies
article

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

Jimma Liddell, William G. Davis, Anna K. Strain, Jaime Christensen, Brian Lynch, Phili Wong, Todd Davis, Christine Warnes, Bo Shu, Nicholas J. Burnett, Sarah Bistodeau, Marie K. Kirby, Beth K Thielen, Ji Liu
article en

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.

Journal of Clinical VirologyVol. 181
Centers for Disease Control and Prevention (US), National Center for Immunization and Respiratory Diseases (US), University of Minnesota Medical Center (US), Minnesota Department of Health (US)
Openalex Percentile: Top 64%
Influenza Virus Research Studies
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Design and performance of a real-time RT-PCR assay for detection of influenza C viruses — Jimma Liddell, William G. Davis, et al. · Journal of Clinical Virology (2025) | TGRS Research Map | TGRS