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Hemolytic activity of Serratia marcescens

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Abstract

A cell-bound hemolytic activity was found in several strains of Serratia marcescens. One Serratia cell per ten erythrocytes was sufficient to cause complete lysis of human erythrocytes within 2 h in the liquid assay. The hemolytic activity resided in the membrane fraction and could be inactivated by incubating cells with proteases. The hemolytic activity was greatly enhanced in actively metabolizing Serratia cells and was partially controlled by the iron supply. Hemolysis was accompanied by degradation of erythrocyte membrane proteins (band 3 and 6, glycophorin) and was independent of the blood group. The exoprotease secreted by S. marcescens in large amounts was not involved in hemolysis. Comparison with various hemolytic strains of Escherichia coli showed that hemolysis of erythrocytes was more pronounced with S. marcescens than with E. coli. In contrast to hemolysis by E. coli, lysis of erythrocytes by S. marcescens was not enhanced by Ca2+ ions.

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References

  • Braun V (1983) Regulation of iron uptake in Escherichia coli. In: Schlessinger D (ed) Microbiology — 1983. Am Soc Microbiol, Washington DC, 301–305

    Google Scholar 

  • Braun V, Schmitz G (1980) Excretion of a protease by Serratia marcescens. Arch Microbiol 124:55–61

    Google Scholar 

  • Fairbanks G, Steck TL, Wallach DFH (1971) Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane. Biochemistry 10:2606–2617

    Google Scholar 

  • Goebel W, Hedgepeth J (1982) Cloning and functional characterization to the plasmid-encoded hemolysin determinant of Escherichia coli. J Bacteriol 151:1290–1298

    Google Scholar 

  • Graevenitz A von, Rubin SJ (1980) The genus Serratia. CRC Press. Boca Raton

    Google Scholar 

  • Härtlein M, Schießl S, Wagner W, Rolest U, Kreft J, Goebel W (1983) Transport of hemolysin by Escherichia coli. J Cell Biochem 22:87–97

    Google Scholar 

  • Laemmli KK (1970) Cleavage of structural proteins during the assembly of the bacteriophage T4. Nature 227:680–685

    Google Scholar 

  • Mackman N, Holland IB (1984) Functional characterization of a cloned haemolysin determinant from E. coli of human origin encoding information for the secretion of a 107k polypeptide. Mol Gen Genet 196:129–134

    Google Scholar 

  • Ölschläger T, Schramm E, Braun V (1984) Cloning and expression of the activity and immunity genes of colicins B and M on ColBM plasmids. Mol Gen Genet 196:482–487

    Google Scholar 

  • Pugsley AP, Schwartz M (1984) Colicin E2 release: lysis, leakage or secretion? Possible role of a phospholipase. EMBO J 3:2393–2397

    Google Scholar 

  • Roland FB (1977) Interaction of blood with Enterobacteriaceae. Hemolysis, hemagglutination, fibrino lysis. Am J Clin Pathol 67:260–263

    Google Scholar 

  • Smith HW (1963) The haemolysins of Escherichia coli. J Path Bacteriol 85:197–211

    Google Scholar 

  • Springer W, Goebel W (1980) Synthesis and secretion of hemolysin by Escherichia coli. J Bacteriol 144:53–59

    Google Scholar 

  • Waalwijk C, Mac Laren DM, de Graaff J (1983) In vivo function of hemolysin in the nephropathogenicity of Escherichia coli. Infect Immun 42:245–249

    Google Scholar 

Download references

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Dedicated to Professor Dr. Gerhart Drews on the occasion of his 60th birthday

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Braun, V., Günther, H., Neuß, B. et al. Hemolytic activity of Serratia marcescens . Arch. Microbiol. 141, 371–376 (1985). https://doi.org/10.1007/BF00428852

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  • DOI: https://doi.org/10.1007/BF00428852

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