Title
Development of a duplex Fluorescent Microsphere Immunoassay (FMIA) for the detection of antibody responses to influenza A and newcastle disease viruses
Date Issued
01 January 2014
Access level
open access
Resource Type
journal article
Author(s)
University of Manitoba
Publisher(s)
Elsevier
Abstract
Highly pathogenic avian influenza virus (HPAI) and virulent forms of avian paramyxovirus-1 (APMV-1) cause serious illnesses in domestic poultry, both of which are reportable to the World Organization of Animal Health (OIE). The clinical presentation of avian influenza (AI) and APMV-1 infections are difficult to differentiate, emphasizing the importance of rapid and sensitive serologic assays that are able to distinguish them. Currently, a variety of serological assays are used for the serologic diagnosis of both diseases, but these assays are not used in multiplex formats. In this study, development of a duplex fluorescent microsphere immunoassay (FMIA) based on Luminex xMAP Technology is described. The assay employs MagPlex magnetic microspheres that are covalently coated with recombinant avian influenza virus nucleoprotein and APMV-1 nucleocapsid antigens produced in a baculovirus insect cell expression system. The assay is able to detect AIV antibodies against all existing hemagglutinin (H1-H16) subtypes and simultaneously detect antibodies against APMV-1. In the process of this assay development different bead coupling conditions were compared. The assay has the capability of detecting serum antibodies from chickens and turkeys and optimization was accomplished by using 2462 chicken and 446 turkey field and experimental sera and had a comparable detection capability with currently used assays in the laboratory. Assay threshold values were calculated with Receiver Operating Characteristic Analysis (ROC) in non-parametric analysis due to a highly skewed data distribution; this analysis resulted in AIV nucleoprotein relative diagnostic sensitivity and specificity of 99.7%, and 97.3% respectively. The APMV-1 nucleocapsid relative diagnostic sensitivity and specificity were 95.4%, and 98.5% respectively. © 2014.
Start page
167
End page
177
Volume
405
Language
English
OCDE Knowledge area
Inmunología
Virología
Subjects
Scopus EID
2-s2.0-84897453331
PubMed ID
Source
Journal of Immunological Methods
ISSN of the container
00221759
Sponsor(s)
The project was funded by CFIA (WIN-A-1304), Manitoba Egg Producers and MAFRI (Manitoba Agriculture, Food and Rural Initiatives) . The authors would like to acknowledge Dr. Kathleen Hooper McGreevy and Animal Health Laboratory (AHL), Guelph, ON for providing the field sera used in the studies, Dr. Kurtis Swelka and his animal care staff for helping out with animal experiments, Dr. Andre Broes (Bio-Vet) for his input in assay development, and Dr. Gary Crow for his statistical analysis advice. CSF/Avian staff and Kate Hole for their help in some aspects of the assay validation.
Sources of information:
Directorio de Producción Científica
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