1. Breed and swine lymphocyte antigen haplotype differences in agglutination titers following vaccination with B. bronchiseptica.
- Author
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Rothschild MF, Chen HL, Christian LL, Lie WR, Venier L, Cooper M, Briggs C, and Warner CM
- Subjects
- Agglutination Tests veterinary, Analysis of Variance, Animals, Cytotoxicity Tests, Immunologic, Female, Lymphocytes immunology, Male, Models, Genetic, Swine immunology, Vaccination veterinary, Antibodies, Bacterial biosynthesis, Bacterial Vaccines immunology, Bordetella immunology, Major Histocompatibility Complex, Swine genetics
- Abstract
Genetic differences in immune response to B. bronchiseptica after vaccination with a commercial B. bronchiseptica bacterin were investigated in 1,069 8-wk-old pigs. These pigs were from 65 litters born in the spring and 66 litters born in the fall of 1982 and were purebreds from the Chester White (n = 128), Duroc (n = 281), Hampshire (n = 143), Landrace (n = 309) and Yorkshire (n = 208) breeds. Each litter was raised separately. Individual pigs were vaccinated im at 4 and 6 wk of age with 2 ml of B. bronchiseptica bacterin. At 8 wk of age, 8 ml of blood were collected from each animal and serum prepared to determine agglutinating antibody titers against B. bronchiseptica bacterin by a bacterial agglutination method. In addition, lymphocytes were separated from 1 ml of heparinized blood and used to determine Swine Lymphocyte Antigen (SLA) haplotypes by using cytotoxic antibodies against the SLA complex. Antisera for 3 SLA haplotypes were made available by the National Institutes of Health. Results indicated that breed of pig (P less than .01) and dam of pig (P less than .01) affected the immune response of the pig after B. bronchiseptica vaccination. Higher immune response was also associated (P less than .05) with one of the SLA haplotypes tested. Heritability estimates for immune response following vaccination were .10 +/- .12 (half-sib) and .42 +/- .19 (full-sib). Results suggest that the relationship of the SLA complex to immune response in the pig and nonadditive genetic and maternal effects on immune response should be further investigated.
- Published
- 1984
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