Cell interactions of Listeria monocytogenes L forms and peritoneal exudative cells in rats.

Listeria monocytogenes 4b and its forms without cell walls (L forms of a protoplastic type) were used to study in vivo interactions with host cells. Samples of peritoneal lavage fluid were obtained from rats intraperitoneally inoculated at intervals between 1 and 15 days after challenge, for scanning electron microscopic, bacteriological, biochemical, and cytometrical investigations. Scanning electron microscopic examination revealed continuous adhesion of L forms on the macrophage surface up to 15 days after inoculation. The persistence of the L forms within the peritoneal cavity was also shown bacteriologically at all sample times, while the parental bacterial forms were isolated from the peritoneal cavity up to 7 days after challenge. The total count of peritoneal exudative cells determined by automated flow peroxidase cytometry peaked on the 15th day in animals infected with parental forms, while in animals infected with L forms the peak was lower and the macrophage population was predominant. The glycolytic and acid phosphatase activity of peritoneal exudative cells was two times higher in rats infected with L form as compared with rats infected with the L. monocytogenes parental forms on the 3rd day after challenge. An understanding of the nature of the interactions between L forms of L. monocytogenes and peritoneal exudative cells found in vivo could be used to establish the influence of L forms on host cellular defense mechanisms.

[1]  B. Austin,et al.  The role of cell-wall deficient bacteria (L-forms; sphaeroplasts) in fish diseases. , 1991, Society for Applied Bacteriology symposium series.

[2]  D. Morrison The case for specific lipopolysaccharide receptors expressed on mammalian cells. , 1989, Microbial pathogenesis.

[3]  H. Michna The human macrophage system: activity and functional morphology. , 1988, Bibliotheca anatomica.

[4]  B Drewinko,et al.  The technicon H*1--an automated hematology analyzer for today and tomorrow. Complete blood count parameters. , 1987, American journal of clinical pathology.

[5]  E. Goldstein,et al.  Modulation of lysosomal protease-esterase and lysozyme in Kupffer cells and peritoneal macrophages infected with Nocardia asteroides , 1986, Infection and immunity.

[6]  L. Michailova,et al.  Adhesion and phagocytosis of Staphylococcus aureus L‐forms , 1986, Journal of basic microbiology.

[7]  P. Kongshavn Genetic control of resistance to Listeria infection. , 1986, Current topics in microbiology and immunology.

[8]  S. Kaufmann Acquired resistance to facultative intracellular bacteria: relationship between persistence, cross-reactivity at the T-cell level, and capacity to stimulate cellular immunity of different Listeria strains , 1984, Infection and immunity.

[9]  S. Holt,et al.  The in vitro effect of Actinobacillus actinomycetemcomitans strain Y4 lipopolysaccharide on murine peritoneal macrophages. , 1983, Canadian journal of microbiology.

[10]  R. Bally,et al.  Tetracycline-resistant L-forms isolated from an antibiotic-susceptible strain of Listeria monocytogenes , 1982, Antimicrobial Agents and Chemotherapy.

[11]  G. Domingue Cell wall-deficient bacteria : basic principles and clinical significance , 1982 .

[12]  E. Beachey,et al.  Bacterial adherence: adhesin-receptor interactions mediating the attachment of bacteria to mucosal surface. , 1981, The Journal of infectious diseases.

[13]  B. Beaman Induction of L-phase variants of Nocardia caviae within intact murine lungs , 1980, Infection and immunity.

[14]  B. Beaman,et al.  Probable L-Forms of Nocardia asteroides Induced in Cultured Mouse Peritoneal Macrophages , 1974, Infection and immunity.