Induction of immunity with avirulent Listeria monocytogenes 19113 depends on bacterial replication

Author:

Baldridge J R1,Thomashow M F1,Hinrichs D J1

Affiliation:

1. Department of Microbiology, Washington State University, Pullman 99164.

Abstract

Events necessary for triggering the cell-mediated response to intracellular parasites are poorly understood. Here we show that extremely high doses of avirulent Listeria monocytogenes 19113 (greater than 10(9] induce a modest and short-lived state of resistance in BALB/c mice. Induction of this protective state could not be achieved with nonviable bacteria and was blocked by inhibiting replication of viable L. monocytogenes 19113 through antibiotic treatment. The immune response was antigen specific and could be adoptively transferred with lymphoid cells. However, unlike the prototypic acquired cellular resistance induced by virulent Listeria strains, the protective response induced by L. monocytogenes 19113 was extremely short-lived, lasting less than 2 weeks, with a precipitous decline in the activity of the immune cells involved. An intervening in vitro culture period with concanavalin A greatly enhanced the activity of the adoptively transferred immune cells.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

Reference23 articles.

1. Experimental infection of mice with Listeria monocytogenes and L. innocua;Audurier A.;Ann. Microbiol.,1980

2. Enhanced adoptive transfer of immunity to Listeria monocytogenes after in vitro culture of murine spleen cells with concanavalin A;Barry R. A.;Infect. Immun.,1982

3. Intracellular growth of Listeria monocytogenes as a prerequisite for in vivo induction of T cell-mediated immunity;Berche P.;J. Immunol.,1987

4. Adoptive transfer of immunity to Listeria monocytogenes: the influence of in vitro stimulation on Iymphocyte subset requirements;Bishop D. K.;J. Immunol.,1987

5. Effective protection against Listeria monocytogenes and delayed-type hypersensitivity to listerial antigens depend on cooperation between specific L3T4+ and Lyt 2+ T cells;Kaufmann S. H. E.;Infect. Immun.,1985

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