Detection of pseudorabies virus antibody in swine oral fluid using a serum whole-virus indirect ELISA
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Published on: December 4, 2015
Ting-Yu Cheng1,2,3, Alexandra Buckley1,2,3, Albert Van Geelen1,2,3
1Department of Veterinary Diagnostic and Production Animal Medicine, College of Veterinary Medicine (Cheng, Henao-Díaz, Poonsuk, Piñeyro, Baum, Main, Zimmerman, Giménez-Lirola), Iowa State University, Ames, IA.
Abstract:
We evaluated the detection of pseudorabies virus (PRV) antibodies in swine oral fluid. Oral fluid and serum samples were obtained from 40 pigs allocated to 4 treatment groups (10 pigs/group): negative control (NC); wild-type PRV inoculation (PRV 3CR Ossabaw; hereafter PRV); PRV vaccination (Ingelvac Aujeszky MLV; Boehringer Ingelheim; hereafter MLV); and PRV vaccination followed by PRV inoculation at 21 d post-vaccination (MLV-PRV). Using a serum PRV whole-virus indirect IgG ELISA (Idexx Laboratories) adapted to the oral fluid matrix, PRV antibody was detected in oral fluid samples from treatment groups PRV, MLV, and MLV-PRV in a pattern similar to serum. Vaccination alone produced a low oral fluid antibody response (groups MLV and MLV-PRV), but a strong anamnestic response was observed following challenge with wild-type virus (group PRV). Analyses of the oral fluid PRV indirect IgG ELISA results showed good binary diagnostic performance (area under ROC curve = 93%) and excellent assay repeatability (intra-class correlation coefficient = 99.3%). The demonstrable presence of PRV antibodies in swine oral fluids suggests the possible use of oral fluids in pseudorabies surveillance.
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