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. 1984 Jun;44(3):633–636. doi: 10.1128/iai.44.3.633-636.1984

Isotype of protective anti-Salmonella antibodies in experimental mouse salmonellosis.

H Saxén, O Mäkelä, S B Svenson
PMCID: PMC263652  PMID: 6202639

Abstract

Mice and a rabbit were immunized with heat-killed Salmonella typhimurium bacteria or with an O-4,12 antigen-specific octasaccharide-protein conjugate. Immunoglobulin isotypes of the antisera were tested for their capacity to protect mice against experimental salmonellosis. Antibodies of immunoglobulin M + A isotypes were more protective than the immunoglobulin G antibodies in each of the two pools of mouse sera. The same protective pattern was also seen with a rabbit antiserum elicited by the artificial octasaccharide-protein conjugate, i.e., with antibodies with the exclusive specificity for the O-4,12 antigen determinants of S. typhimurium.

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Selected References

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  1. Engvall E., Perlmann P. Enzyme-linked immunosorbent assay, Elisa. 3. Quantitation of specific antibodies by enzyme-labeled anti-immunoglobulin in antigen-coated tubes. J Immunol. 1972 Jul;109(1):129–135. [PubMed] [Google Scholar]
  2. Galanos C., Lüderitz O., Westphal O. A new method for the extraction of R lipopolysaccharides. Eur J Biochem. 1969 Jun;9(2):245–249. doi: 10.1111/j.1432-1033.1969.tb00601.x. [DOI] [PubMed] [Google Scholar]
  3. Karch H., Gmeiner J., Nixdorff K. Alteration of the immunoglobulin G subclass responses in mice to lipopolysaccharide: effects of nonbacterial proteins and bacterial membrane phospholipids or outer membrane proteins of Proteus mirabilis. Infect Immun. 1983 Apr;40(1):157–165. doi: 10.1128/iai.40.1.157-165.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Karjalainen K., Mäkelä O. A mendelian idiotype is demonstrable in the heteroclitic anti-NP antibodies of the mouse. Eur J Immunol. 1978 Feb;8(2):105–111. doi: 10.1002/eji.1830080207. [DOI] [PubMed] [Google Scholar]
  5. Kuusi N., Nurminen M., Saxen H., Valtonen M., Mäkelä P. H. Immunization with major outer membrane proteins in experimental salmonellosis of mice. Infect Immun. 1979 Sep;25(3):857–862. doi: 10.1128/iai.25.3.857-862.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Mackaness G. B., Blanden R. V., Collins F. M. Host-parasite relations in mouse typhoid. J Exp Med. 1966 Oct 1;124(4):573–583. doi: 10.1084/jem.124.4.573. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Metcalf E. S., O'Brien A. D. Characterization of murine antibody response to Salmonella typhimurium by a class-specific solid-phase radioimmunoassay. Infect Immun. 1981 Jan;31(1):33–41. doi: 10.1128/iai.31.1.33-41.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Nikaido H., Levinthal M., Nikaido K., Nakane K. Extended deletions in the histidine-rough-B region of the Salmonella chromosome. Proc Natl Acad Sci U S A. 1967 Jun;57(6):1825–1832. doi: 10.1073/pnas.57.6.1825. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Péterfy F., Kuusela P., Mäkelä O. Affinity requirements for antibody assays mapped by monoclonal antibodies. J Immunol. 1983 Apr;130(4):1809–1813. [PubMed] [Google Scholar]
  10. Reed N. D., Manning J. K., Rudbach J. A. Immunologic responses of mice to lipopolysaccharide from Escherichia coli. J Infect Dis. 1973 Jul;128(Suppl):70–74. doi: 10.1093/infdis/128.supplement_1.s70. [DOI] [PubMed] [Google Scholar]
  11. Reif A. E. Batch preparation of rabbit gammaG globulin with deae-cellulose. Immunochemistry. 1969 Sep;6(5):723–731. doi: 10.1016/0019-2791(67)90136-x. [DOI] [PubMed] [Google Scholar]
  12. Rowley D., Turner K. J. Number of molecules of antibody required to promote phagocytosis of one bacterium. Nature. 1966 Apr 30;210(5035):496–498. doi: 10.1038/210496a0. [DOI] [PubMed] [Google Scholar]
  13. Saxen H., Mäkelä O. The protective capacity of immune sera in experimental mouse salmonellosis is mainly due to IgM antibodies. Immunol Lett. 1982 Nov;5(5):267–272. doi: 10.1016/0165-2478(82)90110-9. [DOI] [PubMed] [Google Scholar]
  14. Seppälä I., Sarvas H., Péterfy F., Mäkelä O. The four subclasses of IgG can be isolated from mouse serum by using Protein A-Sepharose. Scand J Immunol. 1981 Oct;14(4):335–342. doi: 10.1111/j.1365-3083.1981.tb00573.x. [DOI] [PubMed] [Google Scholar]
  15. Svenson S. B., Lindberg A. A. Coupling of acid labile Salmonella specific oligosaccharides to macromolecular carriers. J Immunol Methods. 1979;25(4):323–335. doi: 10.1016/0022-1759(79)90025-5. [DOI] [PubMed] [Google Scholar]
  16. Svenson S. B., Lindberg A. A. Protection against mouse typhoid by artificial Salmonella vaccines. Scand J Infect Dis Suppl. 1980;Suppl 24:210–215. [PubMed] [Google Scholar]
  17. Svenson S. B., Nurminen M., Lindberg A. A. Artificial Salmonella vaccines: O-antigenic oligosaccharide-protein conjugates induce protection against infection with Salmonella typhimurium. Infect Immun. 1979 Sep;25(3):863–872. doi: 10.1128/iai.25.3.863-872.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Valtonen V. V. Mouse virulence of Salmonella strains: the effect of different smooth-type O side-chains. J Gen Microbiol. 1970 Dec;64(3):255–268. doi: 10.1099/00221287-64-3-255. [DOI] [PubMed] [Google Scholar]
  19. Watson J., Riblet R. Genetic control of responses to bacterial lipopolysaccharides in mice. I. Evidence for a single gene that influences mitogenic and immunogenic respones to lipopolysaccharides. J Exp Med. 1974 Nov 1;140(5):1147–1161. doi: 10.1084/jem.140.5.1147. [DOI] [PMC free article] [PubMed] [Google Scholar]

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