Literature DB >> 4609906

Interrelationship between serum beta-lysin, lysozyme, and the antibody-complement system in killing Escherichia coli.

D M Donaldson, R R Roberts, H S Larsen, J G Tew.   

Abstract

The effects of different serum components alone and in conjunction with each other on Escherichia coli B were investigated. In general, the viability, turbidity, and electron microscope results were compatible with the following conclusions. The most efficient killing and destruction of E. coli B occurred when beta-lysin, lysozyme, and the antibody-complement system functioned in cooperation with each other at the serum concentration in isotonic solutions. The addition of sucrose protected the bacteria from the lethal and lytic action of these agents. Elimination of lysozyme from serum had the least effect on bactericidal activity, even though lysozyme treatment caused the cell wall to separate from the cytoplasmic membrane and caused clear areas to appear in the inner granular layer of the cell wall. Beta-lysin removal had an intermediate effect on the serum bactericidal activity. Beta-lysin treatment caused cell walls to collapse, allowed cytoplasmic contents to leak out of the cells, and stopped the separation of cell wall and cytoplasmic membrane, which normally takes place in 0.5 M sucrose solution. Inactivation of the complement eliminated the serum bactericidal activity against E. coli B. After treatment with antibody and complement, the cell walls became thick and indistinct, a portion of the cytoplasmic contents escaped, and patches of the middle layer of the cell wall appeared in freeze-etch preparations. Beta-lysin damaged the cytoplasmic membrane, lysozyme damaged the inner peptidoglycan layer of the cell wall, and the antibody-complement system damaged both the middle lipopolysaccharide layer of the cell wall and the cytoplasmic membrane.

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Year:  1974        PMID: 4609906      PMCID: PMC423000          DOI: 10.1128/iai.10.3.657-666.1974

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  24 in total

1.  Locus of the lethal event in the serum bactericidal reaction.

Authors:  D S Feingold; J N Goldman; H M Kuritz
Journal:  J Bacteriol       Date:  1968-12       Impact factor: 3.490

2.  Molecular and structural damage to Escherichia coli produced by antibody, complement, and lysozyme systems.

Authors:  L A Wilson; J K Spitznagel
Journal:  J Bacteriol       Date:  1968-10       Impact factor: 3.490

Review 3.  Use of freeze-etching in the study of biological ultrastructure.

Authors:  H Moor
Journal:  Int Rev Exp Pathol       Date:  1966

4.  Alterations in the morphology of Bacillus subtilis after exposure to beta-lysin and ultraviolet light.

Authors:  A Matheson; D M Donaldson
Journal:  J Bacteriol       Date:  1968-05       Impact factor: 3.490

5.  Ultrastructure of the cell wall of Escherichia coli and chemical nature of its constituent layers.

Authors:  S De Petris
Journal:  J Ultrastruct Res       Date:  1967-07

6.  The reactivity of serum against protoplasts and spheroplasts.

Authors:  L H Muschel; J E Jackson
Journal:  J Immunol       Date:  1966-07       Impact factor: 5.422

7.  Locus of the action of serum and the role of lysozyme in the serum bactericidal reaction.

Authors:  D S Feingold; J N Goldman; H M Kuritz
Journal:  J Bacteriol       Date:  1968-12       Impact factor: 3.490

8.  Penetration of red cell membranes by some membrane-associated particles.

Authors:  R S Weinstein; V M Koo
Journal:  Proc Soc Exp Biol Med       Date:  1968-06

9.  A kinetic study of the bacteriolytic and bactericidal action of human serum.

Authors:  A A Glynn; C M Milne
Journal:  Immunology       Date:  1967-06       Impact factor: 7.397

10.  Normal serum cytotoxicity for P32-labeled smooth Enterobacteriaceae. I. Loss of label, death, and ultrastructural damage.

Authors:  J K Spitznagel; L A Wilson
Journal:  J Bacteriol       Date:  1966-01       Impact factor: 3.490

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  25 in total

Review 1.  TraT lipoprotein, a plasmid-specified mediator of interactions between gram-negative bacteria and their environment.

Authors:  S Sukupolvi; C D O'Connor
Journal:  Microbiol Rev       Date:  1990-12

Review 2.  Molecular basis of bacterial outer membrane permeability.

Authors:  H Nikaido; M Vaara
Journal:  Microbiol Rev       Date:  1985-03

3.  Neutralization of human serum lysozyme by sodium polyanethol sulfonate but not by sodium amylosulfate.

Authors:  W H Traub; P I Fukushima
Journal:  J Clin Microbiol       Date:  1978-09       Impact factor: 5.948

4.  Effect of some R factors on the sensitivity of rough Enterobacteriaceae to human serum.

Authors:  A Fietta; E Romero; A G Siccardi
Journal:  Infect Immun       Date:  1977-11       Impact factor: 3.441

5.  Killing of Gram-negative bacteria with normal human serum and normal bovine serum: use of lysozyme and complement proteins in the death of Salmonella strains O48.

Authors:  G Bugla-Płoskońska; A Kiersnowski; B Futoma-Kołoch; W Doroszkiewicz
Journal:  Microb Ecol       Date:  2009-03-18       Impact factor: 4.552

6.  Insect immunity. 11. Simultaneous induction of antibacterial activity and selection synthesis of some hemolymph proteins in diapausing pupae of Hyalophora cecropia and Samia cynthia.

Authors:  I Faye; A Pye; T Rasmuson; H G Boman; I A Boman
Journal:  Infect Immun       Date:  1975-12       Impact factor: 3.441

7.  The bactericidal activity of sera of healthy neonates and of newborns with hyperbilirubinaemia to Escherichia coli.

Authors:  I Miler; J Vondrácek; L Hromádková
Journal:  Folia Microbiol (Praha)       Date:  1979       Impact factor: 2.099

8.  Increased antibacterial activity against Escherichia coli in bovine serum after the induction of endotoxin tolerance.

Authors:  A W Hill; A L Shears; K G Hibbitt
Journal:  Infect Immun       Date:  1976-07       Impact factor: 3.441

9.  Plasmid-mediated resistance to the bactericidal effects of normal rabbit serum.

Authors:  A M Reynard; M E Beck
Journal:  Infect Immun       Date:  1976-09       Impact factor: 3.441

10.  TnphoA-mediated disruption of K54 capsular polysaccharide genes in Escherichia coli confers serum sensitivity.

Authors:  T A Russo; M C Moffitt; C H Hammer; M M Frank
Journal:  Infect Immun       Date:  1993-08       Impact factor: 3.441

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