Growth of Pasteurella multocida in Vaccinated and Normal Mice

Author:

Collins F. M.1

Affiliation:

1. Trudeau Institute, Saranac Lake, New York 12983

Abstract

Specific pathogen-free CD-1 mice are highly susceptible to infection by Pasteurella multocida strain 5A whether introduced intravenously, intraperitoneally, subcutaneously, or aerogenically. The growth of the challenge organism in the blood, liver, spleen, lung, and peritoneal cavity was quantitated hourly for up to 12 h. Unvaccinated mice died 9 to 12 h after intravenous challenge due to the uncontrolled growth of the organism in all tissues tested. The rate of removal of the bacteria from the blood and of phagocytosis by peritoneal macrophages was extremely slow. In the absence of specific opsonins, more than 90% of the unopsonized challenge inoculum remained in the extracellular growth phase throughout the challenge period. Vaccination of mice with two doses of 10 8 heat-killed (60 C for 60 min) P. multocida given 7 days apart protected the mice against 100 to 1,000 lethal challenge doses. Survival data and growth curves obtained for both actively and passively immunized mice indicated that a humorally mediated immune mechanism was involved. Peak resistance to challenge occurred 21 to 28 days after the mice received the second dose of antigen, and this correlated with an 8- to 16-fold increase in specific agglutinin titers over the same time. Resistance to aerogenic challenge by vaccinated mice was less effective than when other routes of infection were used. The significance of these findings is discussed.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

Reference12 articles.

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2. Bain R. V. S. 1963. Hemorrhagic septacemia. Food Agricultural Organization. Agricultural studies no. 62.

3. Mechanisms of acquired resistance in mouse typhoid;Blanden R. V.;J. Exp. Med.,1966

4. Pasteurellosis: Pasteurella multocida and Pasteurella hemolvtica;Carter G. R.;Advan. Vet. Sci.,1967

5. Mechanisms of antimicrobial immunity;Collins F. M.;J. Reticuloendothel. Soc.,1971

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