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. 1991 Jan;55(1):37-41.

Cross protection among Haemophilus parasuis strains in immunized gnotobiotic pigs

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Cross protection among Haemophilus parasuis strains in immunized gnotobiotic pigs

O P Miniats et al. Can J Vet Res. 1991 Jan.

Abstract

In an attempt to establish if cross protection can be induced by different strains of Haemophilus parasuis, three groups of 12 gnotobiotic pigs were immunized each with an aluminum hydroxide adsorbed whole cell bacterin of one of three H. parasuis strains. Two weeks later, four pigs within each vaccinated group were challenged with aerosols of live cultures of each of the three test strains and observed for response. Two virulent strains V1 and V2 protected all the vaccinated pigs, while all nonvaccinated controls succumbed to Glasser's disease when challenged with these strains. Vaccination with strain LV (of low virulence) protected the pigs against challenge with strain V2, but not against strain V1. Strain LV did not cause disease in the immunized animals and only in one of ten nonimmunized pigs upon second challenge. The results suggest that strains may differ in antigenicity and that virulence and immunoprotection are positively related. Strains to be used in commercial vaccines should therefore be selected carefully. Antibodies detected in the sera of vaccinated pigs were to outer membrane proteins of the bacteria, but not to lipopolysaccharides or capsular polysaccharides. This would suggest that for gnotobiotic pigs outer membrane proteins are more immunogenic than lipopolysaccharide or capsular antigens. Further work is needed to determine if outer membrane proteins also contribute protective immunogens.

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References

    1. Can Vet J. 1989 Apr;30(4):339-43 - PubMed
    1. Can J Vet Res. 1991 Jan;55(1):33-6 - PubMed
    1. Can J Vet Res. 1988 Jul;52(3):319-24 - PubMed
    1. Can J Vet Res. 1989 Oct;53(4):390-3 - PubMed
    1. Nord Vet Med. 1975 Jan;27(1):20-5 - PubMed

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