| Literature DB >> 32450768 |
Ting-Yu Cheng1,2,3, Alexandra Buckley1,2,3, Albert Van Geelen1,2,3, Kelly Lager1,2,3, Alexandra Henao-Díaz1,2,3, Korakrit Poonsuk1,2,3, Pablo Piñeyro1,2,3, David Baum1,2,3, Ju Ji1,2,3, Chong Wang1,2,3, Rodger Main1,2,3, Jeffrey Zimmerman1,2,3, Luis Giménez-Lirola1,2,3.
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.Entities:
Keywords: ELISA; antibody; oral fluid; pseudorabies virus
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Year: 2020 PMID: 32450768 PMCID: PMC7438652 DOI: 10.1177/1040638720924386
Source DB: PubMed Journal: J Vet Diagn Invest ISSN: 1040-6387 Impact factor: 1.279