Abstract:A pregnant mouse model was developed to follow the course of infection after peroral inoculation with six different strains of Listeria monocytogenes and one strain of Listeria innocua. Tissues were sampled and analyzed by microbiologic and histologic methods for 5 days postinoculation. In gnotobiotic pregnant BALB/c mice, L. monocytogenes Scott A (SA), serotype 4b, colonized the gastrointestinal tract, translocated to the livers and spleens of mice by day 1 postinoculation, and multiplied in these tissues unt… Show more
“…Murine models are useful for the study of several bovine infectious diseases such as, for example, brucellosis (TOBIAS et al, 1993), listeriosis (LAMMERDING et al, 1992), paratuberculosis (CHIODINI and BUERGELT, 1993), and mycosis ( JENSEN and SCHQNHEYDER, 1993). Infections in cattle due to Bacillus licheniformis, a spore-forming facultatively anaerobic bacterium, occur world wide, but most aspects of the infection are unknown.…”
Summary
The pathogenicity of Bacillus licheniformis was assessed in normal and immunodepressed BALB/c mice. The animals were challenged intravenously with 4 times 107 colony forming units of B. licheniformis (ATCC 14580) and both normal and immunodepressed mice were susceptible. However, the infection was more severe in the immunosuppressed animals. In normal mice, lesions were restricted to the liver and kidneys, while lesions also occurred in other organs of immunodepressed mice. By crossed immunoelectrophoresis it was shown that antigens of B. licheniformis are potent immunogens, and the bacteria could be identified in tissue sections by immunostaining. Immunohistochemically, B. licheniformis was demonstrated in hepatic and pulmonic macrophages, and from some animals the bacteria were also reisolated.
“…Murine models are useful for the study of several bovine infectious diseases such as, for example, brucellosis (TOBIAS et al, 1993), listeriosis (LAMMERDING et al, 1992), paratuberculosis (CHIODINI and BUERGELT, 1993), and mycosis ( JENSEN and SCHQNHEYDER, 1993). Infections in cattle due to Bacillus licheniformis, a spore-forming facultatively anaerobic bacterium, occur world wide, but most aspects of the infection are unknown.…”
Summary
The pathogenicity of Bacillus licheniformis was assessed in normal and immunodepressed BALB/c mice. The animals were challenged intravenously with 4 times 107 colony forming units of B. licheniformis (ATCC 14580) and both normal and immunodepressed mice were susceptible. However, the infection was more severe in the immunosuppressed animals. In normal mice, lesions were restricted to the liver and kidneys, while lesions also occurred in other organs of immunodepressed mice. By crossed immunoelectrophoresis it was shown that antigens of B. licheniformis are potent immunogens, and the bacteria could be identified in tissue sections by immunostaining. Immunohistochemically, B. licheniformis was demonstrated in hepatic and pulmonic macrophages, and from some animals the bacteria were also reisolated.
“…There have been relatively few experimental studies of the host response to gastrointestinal infection with L. monocytogenes. Although these have established the importance of cellular immunity, there is little information regarding the roles of specific cell populations and mediators (8,13,(15)(16)(17).…”
mentioning
confidence: 99%
“…Previous reports from several laboratories, including our own, have established that the resistance of mice to gastrointestinal infection with L. monocytogenes is quite high (13,(15)(16)(17). As a result, in our first experiment, we chose to infect mice i.g.…”
Treatment with the antigranulocyte monoclonal antibody (MAb) RB6-8C5 increased the severity of infection in mice intragastrically inoculated with Listeria monocytogenes. Most MAb RB6-8C5-treated mice died when inoculated intragastrically with as few as 4 ؋ 10 4 L. monocytogenes bacteria, whereas most control mice survived intragastric inoculation with 4 ؋ 10 8 L. monocytogenes bacteria. The increased severity of infection in MAb RB6-8C5-treated mice appeared to result from listerial multiplication in the spleen and liver rather than from local proliferation in the intestinal tract or mesenteric lymph nodes.
“…which lack the virulence gene cluster of L. monocytogenes may offer an intriguing alternative approach (69). Several groups have succeeded in expressing L. monocytogenes virulence genes, such as prfA, plcA, hiy, and actA, in recombinant L. innocua (70)(71)(72)(73). Indeed, expression of hly conferred upon L. innocua the ability to escape phagosomes and replicate within the cytosol, while expression of pIcA allowed survival and growth in phagolysosomes (73.…”
Section: Protection Against Crpv-induced Tumorsmentioning
The ability of Listeria monocytogenes (L. monocytogenes) to enter the cytosol of host cells allows secreted proteins to efficiently enter the endogenous antigen-processing pathway leading to presentation by MHC class I molecules. L. monocytogenes has recently been exploited as a live vaccine vehicle for the induction of immunological memory against heterologous antigens. We have established a genetic system for site-specific integration of antigen expression cassettes into the Listeria genome which allows regulated expression and secretion of heterologous proteins. The ability of recombinant strains to stimulate long-term immunological memory and CD8+ T-cell-mediated protective immunity was investigated using the lymphocytic choriomeningitis virus (LCMV) murine infection model. Vaccination of mice with recombinant Listeria strains expressing LCMV antigens induced LCMV-specific CD8+ T cells which protected mice against LCMV challenge. We have also used a cottontail rabbit papillomavirus model to test the ability of recombinant Listeria strains to stimulate protective antitumor immunity in domestic rabbits. These studies have demonstrated the protective efficacy of recombinant L. monocytogenes vaccines and have established an experimental system for systematic analysis of cytotoxic T-cell induction by an intracellular bacterium.
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