Immunogenicity and Efficacy of a Rough Brucella suisVaccine Delivered Orally or Parenterally to Feral Swine

  • Olsen S
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Abstract

Brucella suis strain 353-1 is a stable vaccine strain that is clinically safe, does not cause positive serologic responses on conventional brucellosis surveillance tests, and induces humoral and cellular immunity in swine after vaccination. In this study, we evaluated tissue clearance and immunologic responses after oral or parenteral vaccination of feral swine with 1.9 x 10 10 colony-forming units (CFU) of strain 353-1, and compared efficacy of vaccination and control treatments in protecting against infection after experimental conjunctival challenge with a virulent B. suis strain. Feral swine vaccinated orally or parentally with strain 353-1 had greater (P < 0.05) mean ELISA titers to Brucella at all sampling times after vaccination when compared to non-vaccinated swine. PBMC from swine parentally vaccinated with 353-1 at 12 or 17 weeks, or oral vaccinates at 12 weeks after vaccination, demonstrated greater (P < 0.05) antigen-specific proliferative responses when compared to responses of PBMC from non-vaccinates. At necropsy, 4 weeks after experimental challenge with virulent B. suis, non-vaccinated feral swine had greater standard tube agglutination titers and disseminated infection with higher (P < 0.05) colonization (CFU/gm) in most tissues as compared to oral or parenteral vaccinates. The virulent challenge strain was not recovered from any tissues collected from parenteral vaccinates at 4 weeks after experimental challenge. Although the challenge strain was recovered at low levels from some samples, tissue colonization in most tissues of oral vaccinates did not differ (P > 0.05) from parenteral vaccinates, but was reduced (P < 0.05) when compared to colonization in non-vaccinated swine.

Figures

  • Table 1: Microbiologic Characteristics of Brucella suis strain 353-1.a
  • Figure 2: Proliferative responses to 107 to 109 CFU of γ-irradiated 353- 1 by peripheral blood mononuclear cells from feral swine vaccinated with saline, or after parenteral or oral vaccination with 1.9 x 1010 CFU of strain 353-1. Cells were incubated at 37o C and 5% CO2 for 7 days and pulsed for 18 hrs with [3H]-thymidine. Results are expressed as mean stimulation indices ± SEM. Means within a sampling time with different superscripts are significantly different (P < 0.05).
  • Figure 1: Serologic responses of feral swine to γ-irradiated 353-1 in am ELISA assay after vaccination with saline, or after parenteral or oral vaccination with 1.9 x 1010 CFU of strain 353-1. Responses are presented as mean optical density ± SEM. Means with different superscripts are significantly different (P < 0.05).
  • Table 2: Recovery of B. suis from tissues obtained at necropsy after conjunctival challenge with B. suis strain 3B of feral swine vaccinated with 1010 colony-forming units of B. suis strain 353-1.
  • Table 3: Colonization (colony-forming units/gm) of B. suis in target tissues at 4 weeks after experimental B. suis challenge of feral swine vaccinated with 1010 colony-forming units of B. suis strain 353-1.

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APA

Olsen, S. C. (2017). Immunogenicity and Efficacy of a Rough Brucella suisVaccine Delivered Orally or Parenterally to Feral Swine. International Journal of Vaccine Research, 2(1), 1–6. https://doi.org/10.15226/2473-2176/2/1/00114

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