1887

Abstract

Mice pre-treated with Concanavalin-A largely survived an intra-peritoneal inoculum of 2 X 107 , whereas all control mice died within 15 h of inoculation. A subpopulation of peritoneal macrophages from Con-A pre-treated mice was able to phagocytose the bacteria (6.7 SEM 1.2% phagocytosing cells) and (16.9 SEM 2.1%), whereas control phagocytes did not phagocytose . The survival of Con-A pre-treated mice allowed their immunisation with living bacteria, and the antiserum thus produced increased the phagocytosis of . Control mice largely survived an inoculum of suspended in 50% immune serum, although the bacteria were resistant to the bactericidal activity of that serum. These results suggest that, in contrast to the delayed humoral protection afforded by immunisation, phagocytosis by phagocytes activated by Con-A conferred early protection to mice against experimental infection by .

Loading

Article metrics loading...

/content/journal/jmm/10.1099/00222615-46-3-251
1997-03-01
2024-04-16
Loading full text...

Full text loading...

/deliver/fulltext/jmm/46/3/medmicro-46-3-251.html?itemId=/content/journal/jmm/10.1099/00222615-46-3-251&mimeType=html&fmt=ahah

References

  1. Jessop H. L., Lambert P. A. The role of surface polysaccharide in determining the resistance of Serratia marcescens to serum killing. J Gen Microbiol 1986; 132:2505–2514
    [Google Scholar]
  2. Joiner K. A., Schmetz M. A., Goldman R. C., Leive L., Frank M. M. Mechanism of bacterial resistance to complement-mediated killing: inserted C5b-9 correlates with killing for Escherichia coli 0111B4 varying in O-antigen capsule and O-polysaccharide coverage of lipid A core oligosaccharide. Infect Immun 1984; 45:113–117
    [Google Scholar]
  3. Taylor P. W. Bacterial and bacteriolytic activity of serum against gram-negative bacteria. Microbiol Rev 1983; 47:46–83
    [Google Scholar]
  4. Muschel L. H., Larsen L. J. The sensitivity of smooth and rough gram-negative bacteria to the immune bactericidal reaction. Proc Soc Exp Biol Med 1970; 133:345–348
    [Google Scholar]
  5. Domenico P., Salo R. J., Cross A. S., Cunha B. A. Polysaccharide capsule-mediated resistance to opsonophagocytosis in Klebsiella pneumoniae . Infect Immun 1994; 62:4495–4499
    [Google Scholar]
  6. Allen P. M., Fisher D., Saunders J. R., Hart C. A. The role of capsular polysaccharide K21b of Klebsiella and of the structurally related colanic-acid polysaccharide of Escherichia coli in resistance to phagocytosis and serum killing. J Med Microbiol 1987; 24:363–370
    [Google Scholar]
  7. Lee C-J. Bacterial capsular polysaccharides – biochemistry, immunity and vaccine. Mol Immunol 1987; 24:1005–1019
    [Google Scholar]
  8. Jessop H. L., Lambert P. A. Immunochemical characterization of the outer membrane complex of Serratia marcescens and identification of the antigens accessible to antibodies on the cell surface. J Gen Microbiol 1985; 131:2343–2348
    [Google Scholar]
  9. Vuopio-Varkila J., Mäkelä P. H. Killing of Escherichia coli in the peritoneal cavity of convalescent mice; role of specific and non-specific immune mechanisms. J Med Microbiol 1988; 25:205–211
    [Google Scholar]
  10. Kumagai Y., Okada K., Ishimaru T., Sawae Y., Kuroiwa A., Nomoto K. Effects of vaccination against systemic Serratia infection. J Clin Lab Immunol 1989; 29:125–132
    [Google Scholar]
  11. Kumagai Y., Okada K., Sawae Y. The effect of humoral and cell-mediated immunity in resistance to systemic Serratia infection. J Med Microbiol 1992; 36:245–249
    [Google Scholar]
  12. Felipe I., Bim S., Somensi C. C. Increased clearance of Candida albicans from the peritoneal cavity of mice pretreated with concanavalin A or jacalin. Braz J Med Biol Res 1995; 28:477–483
    [Google Scholar]
  13. Vaudaux P., Waldvogel F. A. Gentamicin antibacterial activity in the presence of human polymorphonuclear leukocytes. Anti-microb Agents Chemother 1979; 16:743–749
    [Google Scholar]
  14. Tabrizi S. N., Robins-Browne R. M. Elimination of extracellular bacteria by antibiotics in quantitative assays of bacterial ingestion and killing by phagocytes. J Immunol Methods 1993; 158:201–206
    [Google Scholar]
  15. Felipe I., Bim S., Loyola W. Participation of mannose receptor on the surface of stimulated macrophages in the phagocytosis of glutaraldehyde-fixed Candida albicans, in vitro . Braz J Med Biol Res 1989; 22:1251–1254
    [Google Scholar]
  16. Pacheco-Soares C., Gaziri L. C. J., Loyola W., Felipe I. Phagocytosis of enteropathogenic Escherichia coli and Candida albicans by lectin-like receptors. Braz J Med Biol Res 1993; 25:1015–1024
    [Google Scholar]
  17. Edwards P. R., Ewing W. H. Identification of Enterobacteriaceae. 3rd edn Minneapolis: Burgess; 1972311–316
    [Google Scholar]
  18. Pelkonen S., Fine J. A. Rapid turbidimetric assay for the study of serum sensitivity of Escherichia coli . FEMS Microbiol Lett 1987; 42:53–57
    [Google Scholar]
  19. Ferrante A., Staugas R. E., Rowan-Kelly B. Production of tumor necrosis factor alpha and beta by human mononuclear leukocytes stimulated with mitogens, bacteria, and malarial parasites. Infect Immun 1990; 58:3996–4003
    [Google Scholar]
  20. Moscardi-Bacchi M., Brummer E., Stevens D. A. Support of Paracoccidioides brasiliensis multiplication by human monocytes or macrophages: inhibition by activated phagocytes. J Med Microbiol 1994; 40:159–164
    [Google Scholar]
  21. Furriel R. P. M., Lucisano Y. M., Mantovani B. Precipitated immune complexes of IgM as well as of IgG can bind to rabbit polymorphonuclear leucocytes but only the immune complexes of IgG are readily phagocytosed. Immunology 1992; 75:528–534
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/jmm/10.1099/00222615-46-3-251
Loading
/content/journal/jmm/10.1099/00222615-46-3-251
Loading

Data & Media loading...

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error