Evaluating the InSignia IFI27 expression assay for detecting viral respiratory infection compared to a traditional gene normalisation assay.

Publication date: Jul 01, 2025

Host gene expression is crucial for understanding disease progression and developing diagnostic biomarkers. Previously, we identified a novel immune biomarker IFI27, validated with routine RT-qPCR methods employed in a research setting, that discriminates between influenza and bacteria in patients with suspected respiratory infection. This study aimed to assess the InSignia method, which employs a novel gene normalization technique to yield a variable transcript analysis (VITA) index. The VITA index measures gene expression relative to a non-transcribed region of DNA, such that it is independent of sample quality or quantity. We compared IFI27 gene expression measured by the InSignia assay to that of the research assay in blood samples collected from patients with respiratory diseases and SARS-CoV-2 vaccinated individuals. The study found a strong correlation and acceptable agreement between traditional ΔCq methods and InSignia for IFI27 levels in the higher range (log(ΔCq) > 1), but not for IFI27 expression levels below this range, likely due to the different normalization strategies. Notably the InSignia assay was more sensitive in detecting viral infection among hospital patients. These findings suggest that the InSignia assay, which supports high throughput workflows, may be used for the rapid detection of viral infection in patients with respiratory symptoms.

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Concepts Keywords
Biomarker Biomarkers
Blood Biomarkers
Ifi27 COVID-19
Influenza Female
Vaccinated Gene Expression Profiling
Humans
IFI27 protein, human
Male
Membrane Proteins
Membrane Proteins
Middle Aged
Respiratory Tract Infections
SARS-CoV-2

Semantics

Type Source Name
disease IDO assay
disease MESH infection
disease IDO host
disease MESH disease progression
disease MESH influenza
disease IDO bacteria
disease IDO quality
disease IDO blood
disease MESH respiratory diseases
disease MESH viral infection
disease MESH cancers
disease MESH bacterial infections
disease IDO nucleic acid
disease MESH Allergy
drug DRUGBANK Coenzyme M
disease IDO organism
disease IDO susceptibility
disease IDO innate immune response
disease IDO process
disease MESH respiratory infections
disease IDO history
disease MESH sore throat
disease MESH Parainfluenza
disease MESH co infection
disease MESH asthma
pathway KEGG Asthma
disease MESH COPD
disease MESH pneumonia
drug DRUGBANK Edetic Acid
drug DRUGBANK Water
disease IDO pathogen
drug DRUGBANK Phosphate ion
disease MESH COVID-19

Original Article

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