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. 1979 Mar;36(3):439–447.

Reduction of phagocytosis, surface hydrophobicity and charge of Salmonella typhimurium 395 MR10 by reaction with secretory IgA (SIgA).

K E Magnusson, O Stendahl, I Stjernström, L Edebo
PMCID: PMC1457568  PMID: 374252

Abstract

Binding of human colostral secretory IgA (SIgA) to Salmonella typhimurium 395 MR10 decreased the liability to hydrophobic interaction of the bacteria, as analysed by hydrophobic interaction chromatography on Octyl-Sepharose and partition in an aqueous polymer two-phase system consisting of dextran, poly(ethyleneglycol) (PEG) and poly-(ethyleneglycol)-palmitate (P--PEG). SIgA also reduced the negative charge of the bacteria. Treatment of the bacteria with centrifuged but not further fractionated colostrum added positive charge to the bacteria which was removed by treatment with pepsin. Colostral SIgA reduced the in vitro phagocytosis of S. typhimurium MR10 by polymorphonuclear leucocytes. The adhesion of the bacteria to cellulose membrane filters in the absence of phagocytes was also reduced after the interaction with SIgA. It is proposed that the binding of SIgA to bacterial surfaces has hydrophilic and anti-adhesive effects, which may serve to exclude antigen from mucosal surfaces.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Brandtzaeg P. Human secretory component. II. Physicochemical characterization of free secretory component purified from colostrum. Scand J Immunol. 1974;3(6):707–716. doi: 10.1111/j.1365-3083.1974.tb01306.x. [DOI] [PubMed] [Google Scholar]
  2. Chedid L., Parant M., Parant F., Boyer F. A proposed mechanism for natural immunity to enterobacterial pathogens. J Immunol. 1968 Feb;100(2):292–306. [PubMed] [Google Scholar]
  3. Corbeil L. B., Hall C. E., Lein D., Corbeil R. R., Duncan J. R. Immunoglobulin classes in genital secretions of mycoplasma-infected and normal heifers. Infect Immun. 1976 Jun;13(6):1595–1600. doi: 10.1128/iai.13.6.1595-1600.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Cunningham R. K., Söderström T. O., Gillman C. F., van Oss C. J. Phagocytosis as a surface phenomenon. V. Contact angles and phagocytosis of rough and smooth strains of Salmonella typhimurium, and the influence of specific antiserum. Immunol Commun. 1975;4(5):429–442. doi: 10.3109/08820137509057331. [DOI] [PubMed] [Google Scholar]
  5. Eddie D. S., Schulkind M. L., Robbins J. B. The isolation and biologic activities of purified secretory IgA and IgG anti-Salmonella typhimurium "O" antibodies from rabbit intestinal fluid and colostrum. J Immunol. 1971 Jan;106(1):181–190. [PubMed] [Google Scholar]
  6. Edebo L., Lindström F., Sköldstom L., Stendahl O., Tagesson C. On the physical-chemical effect of colostral antibody binding to Escherichia coli O 86. Immunol Commun. 1975;4(6):587–601. doi: 10.3109/08820137509055796. [DOI] [PubMed] [Google Scholar]
  7. Freter R. Parameters affecting the association of vibrios with the intestinal surface in experimental cholera. Infect Immun. 1972 Aug;6(2):134–141. doi: 10.1128/iai.6.2.134-141.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Hill I. R., Porter P. Studies of bactericidal activity to Escherichia coli of porcine serum and colostral immunoglobulins and the role of lysozyme with secretory IgA. Immunology. 1974 Jun;26(6):1239–1250. [PMC free article] [PubMed] [Google Scholar]
  9. Johansson G. Studies on aqueous dextran-poly (ethylene glycol) two-phase systems containing charged poly (ethylene glycol). I. Partition of albumins. Biochim Biophys Acta. 1970 Nov 24;222(2):381–389. doi: 10.1016/0304-4165(70)90127-3. [DOI] [PubMed] [Google Scholar]
  10. Johansson G. The effect of poly(ethyleneglycol) esters on the partition of proteins and fragmented membranes in aqueous biphasic systems. Biochim Biophys Acta. 1976 Dec 21;451(2):517–529. doi: 10.1016/0304-4165(76)90147-1. [DOI] [PubMed] [Google Scholar]
  11. Kaltreider H. B., Chan M. K. The class-specific immunoglobulin composition of fluids obtained from various levels of the canine respiratory tract. J Immunol. 1976 Feb;116(2):423–429. [PubMed] [Google Scholar]
  12. Kobayashi K. Studies on human secretory IgA comparative studies of the IgA-bound secretory piece and the free secretory piece protein. Immunochemistry. 1971 Sep;8(9):785–800. doi: 10.1016/0019-2791(71)90446-0. [DOI] [PubMed] [Google Scholar]
  13. Lizana J., Hellsing K. Polymer enhancement of automated immunological nephelometric analysis, as illustrated by determination of urinary albumin. Clin Chem. 1974 Apr;20(4):415–420. [PubMed] [Google Scholar]
  14. Magnusson K. E., Stendahl O., Stjernström I., Edebo L. The effect of colostrum and colostral antibody SIgA on the physico-chemical properties and phagocytosis of Escherichia coli o86. Acta Pathol Microbiol Scand B. 1978 Apr;86(2):113–120. doi: 10.1111/j.1699-0463.1978.tb00018.x. [DOI] [PubMed] [Google Scholar]
  15. Magnusson K. E., Stendahl O., Tagesson C., Edebo L., Johansson G. The tendency of smooth and rough Salmonella typhimurium bacteria and lipopolysaccharide to hydrophobic and ionic interaction, as studied in aqueous polymer two-phase systems. Acta Pathol Microbiol Scand B. 1977 Jun;85(3):212–218. doi: 10.1111/j.1699-0463.1977.tb01698.x. [DOI] [PubMed] [Google Scholar]
  16. Reed W. P., Cushing A. H. Role of immunoglobulins in protection against Shigella-induced keratoconjunctives. Infect Immun. 1975 Jun;11(6):1265–1268. doi: 10.1128/iai.11.6.1265-1268.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Stendahl O., Edebo L. Phagocytosis of mutants of Salmonella typhimurium by rabbit polymorphonuclear cells. Acta Pathol Microbiol Scand B Microbiol Immunol. 1972;80(4):481–488. doi: 10.1111/j.1699-0463.1972.tb00169.x. [DOI] [PubMed] [Google Scholar]
  18. Stendahl O., Tagesson C., Edebo M. Partition of Salmonella typhimurium in a two-polymer acqueous phase system in relation to liability to phagocytosis. Infect Immun. 1973 Jul;8(1):36–41. doi: 10.1128/iai.8.1.36-41.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Stjernström I., Magnusson K. E., Stendahl O., Tagesson C. Liability to hydrophobic and charge interaction of smooth Salmonella typhimurium 395 MS sensitized with anti-MS immunoglobulin G and complement. Infect Immun. 1977 Nov;18(2):261–265. doi: 10.1128/iai.18.2.261-265.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Tagesson C., Magnusson K. E., Stendahl O. Physicochemical consequences of opsonization: perturbation of liposomal membranes by Salmonella typhimurium 395 MS opsonized with IgG antibodies. J Immunol. 1977 Aug;119(2):609–613. [PubMed] [Google Scholar]
  21. Van Oss C. J., Gillman C. F. Phagocytosis as a surface phenomenon. II. Contact angles and phagocytosis of encapsulated bacteria before and after opsonization by specific antiserum and complement. J Reticuloendothel Soc. 1972 Nov;12(5):497–502. [PubMed] [Google Scholar]
  22. Van Oss C. J., Stinson M. W. Immunoglobulins as aspecific opsonins. I. The influence of polyclonal and monoclonal immunoglobulins on the in vitro phagocytosis of latex particles and Staphylococci by human neutrophils. J Reticuloendothel Soc. 1970 Nov;8(5):397–406. [PubMed] [Google Scholar]
  23. Williams R. C., Gibbons R. J. Inhibition of bacterial adherence by secretory immunoglobulin A: a mechanism of antigen disposal. Science. 1972 Aug 25;177(4050):697–699. doi: 10.1126/science.177.4050.697. [DOI] [PubMed] [Google Scholar]
  24. Zigmond S. H., Hirsch J. G. Effects of cytochalasin B on polymorphonuclear leucocyte locomotion, phagocytosis and glycolysis. Exp Cell Res. 1972 Aug;73(2):383–393. doi: 10.1016/0014-4827(72)90062-6. [DOI] [PubMed] [Google Scholar]
  25. Zipursky A., Brown E. J., Bienenstock J. Lack of opsonization potential of 11S human secretory A. Proc Soc Exp Biol Med. 1973 Jan;142(1):181–184. doi: 10.3181/00379727-142-36983. [DOI] [PubMed] [Google Scholar]

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