THE RELATIONSHIP BETWEEN SINGLE RADIAL HEMOLYSIS, HEMAGGLUTINATION INHIBITION, AND VIRUS NEUTRALIZATION ASSAYS USED TO DETECT ANTIBODIES SPECIFIC FOR EQUINE INFLUENZA-VIRUSES

Citation
Ps. Morley et al., THE RELATIONSHIP BETWEEN SINGLE RADIAL HEMOLYSIS, HEMAGGLUTINATION INHIBITION, AND VIRUS NEUTRALIZATION ASSAYS USED TO DETECT ANTIBODIES SPECIFIC FOR EQUINE INFLUENZA-VIRUSES, Veterinary microbiology, 45(1), 1995, pp. 81-92
Citations number
24
Categorie Soggetti
Microbiology,"Veterinary Sciences
Journal title
ISSN journal
03781135
Volume
45
Issue
1
Year of publication
1995
Pages
81 - 92
Database
ISI
SICI code
0378-1135(1995)45:1<81:TRBSRH>2.0.ZU;2-5
Abstract
Antibodies specific for equine influenza viruses are usually quantifie d using single radial hemolysis (SRH), hemagglutination inhibition (HI ) or virus neutralization (VN). Neutralizing antibodies are thought to provide optimum protection to challenged animals. The purpose of this study was to determine the extent to which SRH and HI assays detect a ntibodies which neutralize equine influenza viruses. Acute and convale scent sera from 41 horses were analyzed using VN, SRH and HI assays. T hese horses were present in a population of Thoroughbred racehorses du ring an epidemic of upper respiratory tract disease associated with in fluenza A/equine/Saskatoon/1/91 (H3N8) infections. Concentrations of a ntibodies binding to influenza A/equine/Kentucky/1/81 (H3N8), A/equine / Miami/1/63 (H3N8), and A/equine/Prague/1/56 (H7N7) were determined, Results of the VN assay were compared with results from the SRH and HI assays for acute antibody levels, changes in antibody concentrations between acute and convalescent sampling, and the occurrence of serocon version. The correlation between assays for pre-exposure antibody leve ls ranged from 88% to 96%, The correlation between assays for change i n antibody concentration ranged from 83% to 90% for the H3N8 viruses. This study shows that antibody concentrations specific for equine infl uenza virus, measured using SRH and HI assays, are highly correlated w ith concentrations detected using a VN assay.