1887

Abstract

Mutants of PAC1R (serotype O:3) which were resistant to bacteriophage D were isolated and shown to react with O:5d, O:9 and O:13 antisera as well as O:3. Antisera to the parent strain and to the three polyagglutinating (PA) mutants also showed cross-reactions. The mutants differed from the parent strain in their lipopolysaccharide (LPS) composition. The LPS from two of the three mutants yielded high molecular weight polysaccharide fractions. Although the high molecular weight fraction from one of the mutants contained the amino sugars and other components characteristic of the O:3 serotype strains, its mobility on Sephadex G75 was different from that of the parent strain. The high molecular weight material from the second mutant lacked the O-antigenic determinants but these were present in a semi-rough LPS fraction. The third mutant appeared rough and completely lacked the O-antigenic components. These three mutants were compared with the parent strain and with a non-agglutinating LPS-defective mutant which lacked both O-antigenic side chains and all neutral sugars in the outer core. Agglutination with absorbed sera and haemagglutination using purified LPS and ELISA detection suggested that wall components other than LPS were responsible for some of the cross-reactions observed. The components responsible were detected after SDS-PAGE of crude outer membrane fractions by a combination of Coomassie blue and silver-staining and antigenic components were detected by immunoelectrophoresis and ELISA-linked immunoblotting of the gels. The main antigenic determinants detected by antiserum to the parent strain were in the high molecular weight O-polysaccharide fractions and in the semi-rough fractions of the LPS, with some activity due to the H protein of the outer membrane. O:5d antisera reacted with unidentified high molecular weight polysaccharide fractions. Cross-reactions with the O:9 antiserum appeared to be due mainly to the F porin and, to a lesser extent, to the G and E proteins of the outer membrane. O:13 antiserum reacted with high molecular weight polysaccharide fractions but also with the rough core and F and H protein. Cross-reactivity of the other three mutant antisera could largely be interpreted in terms of the outer membrane components exposed in each strain. One reacted strongly with the F porin and the rough core, while the others reacted with a number of protein and LPS-derived fractions. It is suggested that, in these PA mutants, changes in LPS composition modify their O-antigenicity and also expose other outer membrane components to varying extents. It is these protein and rough core components which are responsible for the cross-reactivity with heterologous O-antisera.

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1984-03-01
2024-04-26
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References

  1. Chester I. R., Meadow P. M., Pitt T. L. 1973; The relationship between the O-antigenic lipopolysaccharides and serological specificity in Pseudomonas aeruginosa of different O-serotypes. Journal of General Microbiology 78:305–318
    [Google Scholar]
  2. Chester I. R., Meadow P. M. 1975; Heterogeneity of the lipopolysaccharide from Pseudomonas aeruginosa . European Journal of Biochemistry 58:273–282
    [Google Scholar]
  3. Converse C. A., Papermaster D. S. 1975; Membrane protein analysis by two dimensional electrophoresis. Science 189:469–472
    [Google Scholar]
  4. Dankert J., Hofstra H. 1978; Antibodies against outer membrane proteins in rabbit antisera prepared against Escherichia coli . Journal of General Microbiology 104:311–320
    [Google Scholar]
  5. Habs I. 1957; Untersuchungen fiber die OAntigene von Pseudomonas aeruginosa . Zetishrift für Hygiene und Infektkmskrankheiten 144:218–228
    [Google Scholar]
  6. Hammerling U., Westphal O. 1967; Synthesis and use of O-stearoyl polysaccharides in passive haemagglutination and haemolysis. European Journal of Biochemistry 1:46–50
    [Google Scholar]
  7. Hancock R.E.W., Carby A. M. 1979; Outer membrane of Pseudomonas aeruginosa: heat and 2-mercaptoethanol-modifiable proteins. Journal of Bacteriology 140:902–910
    [Google Scholar]
  8. Hancock R.E.W., Poole K., Benz R. 1982a; Outer membrane protein P of Pseudomonas aeruginosa: regulation by phosphate deficiency and formation of small anion-specific channels in lipid bilayer membranes. Journal of Bacteriology 150:730–738
    [Google Scholar]
  9. Hancock R.E.W., Wieczorek A. A., Mutharia L. M., Poole K. 1982b; Monoclonal antibodies against Pseudomonas aeruginosa outer membrane antigens: isolation and characterization. Infection and Immunity 37:166–171
    [Google Scholar]
  10. Hawkes R., Niday E., Gordon J. 1982; A dot immunoblotting assay for monoclonal and other antibodies. Analytical Biochemistry 119:142–147
    [Google Scholar]
  11. Hofstra H., Dankert J. 1980a; Preparation and quantitative determination of antibodies against major outer membrane proteins of E. coli 026 K60. Journal of General Microbiology 117:437–447
    [Google Scholar]
  12. Hofstra H., Dankert J. 1980b; Major outer membrane proteins: common antigens in Enterobacteriaceae species. Journal of General Microbiology 119:123–131
    [Google Scholar]
  13. Holby N. 1982; Microbiology of lung infections in cystic fibrosis patients. Acta paediatrica scandinavica suppl. 301:33–54
    [Google Scholar]
  14. Koval S. F., Meadow P. M. 1977; The isolation and characterization of lipopolysaccharide-defective mutants of Pseudomonas aeruginosa PAC1. Journal of General Microbiology 90:387–398
    [Google Scholar]
  15. Kromnski A. M., Kuzio J., Angus B. L., Hancock R.E.W. 1982; Chemical and chromatographic analysis of lipopolysaccharide from an antibiotic-supersusceptible mutant of Pseudomonas aeruginosa . Antimicrobial Agents and Chemotherapy 21:310–319
    [Google Scholar]
  16. Lambert P. A., Booth B. R. 1982; Exposure of outer membrane proteins on the surface of Pseudomonas aeruginosa PAOl revealed by labelling with [125I]-lactoperoxidase. FEMS Microbiology Letters 14:43–45
    [Google Scholar]
  17. Lanyi B., Bergan T. 1978; Serological characterization of Pseudomonas aeruginosa . Methods in Microbiology 10:93–168
    [Google Scholar]
  18. Meadow P. M., Wells P. L. 1978; Receptor sites for R-type pyocins and bacteriophage E79 in the core part of the lipopolysaccharide of Pseudomonas aeruginosa PAC1. Journal of General Microbiology 106:339–343
    [Google Scholar]
  19. Mizuno T., Kageyama M. 1978; Separation and characterization of the outer membrane of Pseudomonas aeruginosa . Journal of Biochemistry 84:179–191
    [Google Scholar]
  20. Nikaido H. 1979; Non-specific transport through the outer membrane. In Bacteria! Outer Membranes pp. 361–407 Inouye M. Edited by New York:: John Wiley.;
    [Google Scholar]
  21. Ouchterlony D. 1949; Antigen-antibody reactions in gel. Acta pathologia et microbiologia scandinavica 26:507
    [Google Scholar]
  22. Pitt T. L., Erdman Y. T. 1977; The specificity of agglutination reactions with O-antisera of Pseudomonas aeruginosa . Journal of Medical Microbiology 11:15–23
    [Google Scholar]
  23. Rowe P. S. N., Meadow P. M. 1983; Structure of the core oligosaccharide from the lipopolysaccharide of Pseudomonas aeruginosa PAC1R and its defective mutants. European Journal of Biochemistry 132:329–337
    [Google Scholar]
  24. Tahara Y., Wilkinson S. G. 1983; The lipopolysaccharide from Pseudomonas aeruginosa NCTC 8505. Structure of the O-specific polysaccharide. European Journal of Biochemistry 134:299–304
    [Google Scholar]
  25. Towbin H., Staehlin T., Gordon J. 1979; Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proceedings of the National Academy of Sciences of the United States of America 76:4350–4354
    [Google Scholar]
  26. Tsai C.-M., Frasch C. E. 1982; A sensitive method for detecting lipopolysaccharides in polyacrylamide gels. Analytical Biochemistry 119:115–119
    [Google Scholar]
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