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Proliferation of Toxoplasma gondii in human neutrophils in vitro

Published online by Cambridge University Press:  06 April 2009

M. Nakao
Affiliation:
Department of Medical Zoology, Kobe University School of Medicine, Kobe 650, Japan
E. Konishi
Affiliation:
Department of Medical Zoology, Kobe University School of Medicine, Kobe 650, Japan

Extract

Human neutrophils were infected with tachyzoites of Toxoplasma gondii in vitro. Infection rates after 1 h of incubation were 38·6–52·0% and 16·0–25·8% in the presence or absence of specific antibody respectively. Apparently, neutrophils killed tachyzoites 18 h after infection in the presence of antibody, whereas tachyzoites proliferated in 25·0–35·0% of infected neutrophils in the absence of antibody. Total tachyzoite counts 18 h after infection were approximately 4 times as high as those 1 h after infection in the absence of antibody and complement. Complement also enhanced phagocytosis and killing of tachyzoites by neutrophils, but the effects were less than that of antibody. Superoxide anion was produced intensively within 1 h after infection, depending on the presence of antibody or complement. Neutrophils seem to be responsible for dissemination of tachyzoites in the host during the initial phase of Toxoplasma infection until antibody is produced.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1991

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References

Anderson, S. E. & Remington, J. S. (1974). Effect of text-abstract and activated human macrophages on Toxoplasma gondii. Journal of Experimental Medicine 139, 1154–74.CrossRefGoogle Scholar
Catterall, J. R., Black, C. M., Leventhal, J. P., Rizk, N. W., Wachtel, J. S. & Remington, J. S. (1987). Nonoxidative microbicidal activity in text-abstract human alveolar and peritoneal macrophages. Infection and Immunity 55, 1635–40.CrossRefGoogle Scholar
Flesch, I. & Kaufmann, S. H. E. (1987). Mycobacterial growth inhibition by interferon-γ activated bone marrow macrophages and differential susceptibility among strains of Mycobacterium tuberculosis. Journal of Immunology 138, 4408–13.CrossRefGoogle ScholarPubMed
Holland, P. & Sleamaker, K. (1970). Motile phagocytic defense against protozoa and fungi. Journal of the Reticuloendothelial Society 7, 635.Google Scholar
Jones, T. C. & Hirsch, J. (1972). The interaction between Toxoplasma gondii and mammalian cells. II. The absence of lysosomal fusion with phagocytic vacuoles containing living parasites. Journal of Experimental Medicine 136, 1173–94.CrossRefGoogle ScholarPubMed
Konishi, E. & Takahashi, J. (1983). Reproducible enzyme-linked immunosorbent assay with a magnetic processing system for diagnosis of toxoplasmosis. Journal of Clinical Microbiology 17, 225–31.CrossRefGoogle ScholarPubMed
Kweider, M., Lemesre, J. L., Darcy, F., Kusnierz, J. P., Capron, A. & Santro, F. (1987). Infectivity of Leishmania brasiliensis is dependent on the increasing expression of a 65,000-dalton surface antigen. Journal of Immunology 138, 299305.CrossRefGoogle ScholarPubMed
Locksley, R. M., Wilson, C. B. & Klebanoff, S. J. (1982). Role for endogenous and acquired peroxidase in the toxoplasmacidal activity of murine and human mononuclear phagocytes. Journal of Clinical Investigation 69, 1099–111.CrossRefGoogle ScholarPubMed
Mantovani, B. (1975). Different roles of IgG and complement receptors in phagocytosis by polymorphonuclear leukocytes. Journal of Immunology 115, 1517.CrossRefGoogle ScholarPubMed
McLeod, R., Estes, R., Mack, D. G. & McLeod, E. G. (1983). Effects of human alveolar macrophages and peripheral blood monocytes on Toxoplasma gondii. Journal of Infectious Diseases 147, 957.CrossRefGoogle ScholarPubMed
Mor, N., Goren, M. B. & Pabst, M. J. (1988). Mycobacterium lepraemurium activated macrophages but fails to trigger release of superoxide anion. Journal of Immunology 140, 3956–61.CrossRefGoogle ScholarPubMed
Murray, H. W., Juangbhanich, C. F., Nathan, C. F. & Cohn, Z. A. (1979). Macrophage oxygen-dependent antimicrobial activity. II. The role of oxygen-intermediates. Journal of Experimental Medicine 150, 950–64.CrossRefGoogle ScholarPubMed
Nakao, M. & Konishi, E. (1991). Neutrophil chemotactic factors secreted from Toxoplasma gondii. Parasitology 103, 2934.CrossRefGoogle ScholarPubMed
Payne, N. R. & Horwitz, M. A. (1987). Phagocytosis of Legionella pneumophila is mediated by human monocyte complement receptors. Journal of Experimental Medicine 166, 1377–89.CrossRefGoogle ScholarPubMed
Pick, E. & Mizel, D. (1981). Rapid microassays for the measurement of superoxide and hydrogen peroxide production by macrophages in culture using an automatic enzyme immunoassay reader. Journal of Immunological Methods 46, 211–26.CrossRefGoogle ScholarPubMed
Wilson, C. B. & Remington, J. S. (1979). Activity of human blood leukocytes against Toxoplasma gondii. Journal of Infectious Diseases 140, 890–5.CrossRefGoogle ScholarPubMed
Wilson, C. B., Tsai, V. & Remington, J. S. (1980). Failure to trigger the oxidative metabolic burst by text-abstract macrophages. Possible mechanism for survival of intracellular pathogens. Journal of Experimental Medicine 151, 328–46.CrossRefGoogle Scholar