Evaluation of Directigen Flu A assay for detection of influenza antigen in nasal secretions of horses.
Abstract: The Directigen Flu A assay (Becton Dickinson, Microbiology Systems, Mississauga, Ontario, Canada) is a commercially available immunoassay designed for rapid in vitro recognition of influenza A nucleoprotein. The purpose of this study was to evaluate this assay for detection of influenza virus in nasal secretions of naturally infected horses. The assay was shown to react with representative strains of influenza virus which cause disease in horses and did not react with nasal secretions from uninfected horses kept in isolation. Between 33% and 45% of nasal secretions specimens obtained from clinically diseased horses during influenza epidemics reacted positively in the assay and 95% to 98% of horses not showing signs of disease during influenza epidemics tested negative. In contrast, influenza virus was isolated from only 7% of diseased horses using conventional techniques. Diseased horses which were positive in the Directigen assay had lower pre-exposure influenza antibody concentrations and showed more clinical signs than diseased Directigen-negative horses. This evaluation demonstrates that the Directigen Flu A assay detects influenza virus in nasal secretions of infected horses and is more sensitive than virus isolation.
Publication Date: 1995-03-01 PubMed ID: 7607146DOI: 10.1111/j.2042-3306.1995.tb03049.xGoogle Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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This research investigated the effectiveness of the Directigen Flu A assay in detecting influenza virus in horses. It found that the test was more sensitive than traditional methods, successfully identifying the virus in between 33% and 45% of diseased horses during influenza outbreaks, compared to a 7% detection rate with conventional techniques.
Study Purpose and Method
- This study set out to evaluate the efficacy of the Directigen Flu A assay, a readily available immunoassay, for detecting influenza A nucleoprotein in horses.
- The study specifically addressed its use in identifying the virus in nasal secretions of horses naturally infected with the virus.
Study Findings
- The Directigen Flu A assay reacted with types of influenza virus known to inflict horses with disease, but it didn’t react with secretions from uninfected horses kept separate from the others.
- Between 33% and 45% of nasal secretion samples from horses showing signs of disease during influenza outbreaks responded positively to the assay. This shows a significant level of effectiveness in disease detection.
- On the flip side, the assay ruled out influenza infection in 95% to 98% of horses not showing signs of the disease during flu outbreaks. This suggests high specificity of the test, minimizing false-positive results.
Comparison with Traditional Techniques
- The assay’s performance was compared to conventional techniques used to isolate the influenza virus; the traditional methods detected the virus in only 7% of diseased horses. This outcome underlines the higher sensitivity of the Directigen Flu A assay relative to traditional screening methods.
Correlation with Clinical Symptoms and Pre-Exposure Antibody Levels
- Diseased horses that tested positive in the Directigen assay demonstrated more clinical symptoms and had lower pre-exposure influenza antibody concentrations than horses that tested negative. This highlighted an association between severity of clinical manifestations, antibody levels, and detection results of the assay.
Conclusion
- Overall, the research concluded that the Directigen Flu A assay significantly improves the detection of influenza virus in horses’ nasal secretions, outperforming conventional virus isolation techniques with its greater sensitivity.
Cite This Article
APA
Morley PS, Bogdan JR, Townsend HG, Haines DM.
(1995).
Evaluation of Directigen Flu A assay for detection of influenza antigen in nasal secretions of horses.
Equine Vet J, 27(2), 131-134.
https://doi.org/10.1111/j.2042-3306.1995.tb03049.x Publication
Researcher Affiliations
- Department of Veterinary Internal Medicine, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, Canada.
MeSH Terms
- Animals
- Antigens, Viral / analysis
- Evaluation Studies as Topic
- Hemolysis / immunology
- Horse Diseases / diagnosis
- Horse Diseases / immunology
- Horse Diseases / virology
- Horses
- Immunoassay / veterinary
- Influenza A virus / immunology
- Influenza A virus / isolation & purification
- Nasal Mucosa / immunology
- Nasal Mucosa / metabolism
- Nucleoproteins / analysis
- Orthomyxoviridae Infections / diagnosis
- Orthomyxoviridae Infections / immunology
- Orthomyxoviridae Infections / veterinary
- Reagent Kits, Diagnostic / veterinary
- Sensitivity and Specificity
Citations
This article has been cited 6 times.- Galvin P, Gildea S, Nelly M, Quinlivan M, Arkins S, Walsh C, Cullinane A. The evaluation of three diagnostic tests for the detection of equine influenza nucleoprotein in nasal swabs. Influenza Other Respir Viruses 2014 May;8(3):376-83.
- Bountouri M, Fragkiadaki E, Ntafis V, Kanellos T, Xylouri E. Phylogenetic and molecular characterization of equine H3N8 influenza viruses from Greece (2003 and 2007): evidence for reassortment between evolutionary lineages. Virol J 2011 Jul 14;8:350.
- Diaz-Mendez A, Viel L, Hewson J, Doig P, Carman S, Chambers T, Tiwari A, Dewey C. Surveillance of equine respiratory viruses in Ontario. Can J Vet Res 2010 Oct;74(4):271-8.
- Quinlivan M, Dempsey E, Ryan F, Arkins S, Cullinane A. Real-time reverse transcription PCR for detection and quantitative analysis of equine influenza virus. J Clin Microbiol 2005 Oct;43(10):5055-7.
- Quinlivan M, Cullinane A, Nelly M, Van Maanen K, Heldens J, Arkins S. Comparison of sensitivities of virus isolation, antigen detection, and nucleic acid amplification for detection of equine influenza virus. J Clin Microbiol 2004 Feb;42(2):759-63.
- Sutton GA, Viel L, Carman PS, Boag BL. Study of the duration and distribution of equine influenza virus subtype 2 (H3N8) antigens in experimentally infected ponies in vivo. Can J Vet Res 1997 Apr;61(2):113-20.
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