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PMID: 16557925 Published · ppublish English Journal Article

Effects of serum components on gram-negative bacteria during bactericidal reactions.

Infection and immunity ·Vol. 3 ·No. 1 ·1971-01-00 ·Pages 107-15

Melching L, Vas SI

Abstract

Biochemical changes which occur in a smooth strain of Escherichia coli were investigated with hyperimmune rabbit serum as a source of antibody and fresh normal guinea pig serum as a source of complement. Ribonucleic acid synthesis, as shown by incorporation of (3)H-uridine, was decreased as early as 5 min, and deoxyribonucleic acid synthesis, shown by incorporation of (3)H-thymidine, was decreased after 15 min of reaction. Incorporation of glycerol-2-(3)H into membrane lipid ceased after 25 to 30 min, probably as a result of functional or physical disruption of the membrane, or both. Permeability control (as indicated by loss of (3)H-uridine-labeled compounds and by decrease in optical density) and protein synthesis were subsequently shown to be affected after 30 min. The metabolic state of the bacteria was found to be important in determining the outcome of the reaction. This was shown by the influence of the type of medium on the reaction. A complex nutrient medium decreased susceptibility as compared with a simple medium. The energy sources glycerol and acetate also decreased susceptibility. It is postulated that the ability of the cell to prevent or repair damage to the cell membrane may be involved. Therefore, metabolic conditions which allow retention of vital processes associated with the cytoplasmic membrane and cell surface will mitigate the bactericidal effect. Such conditions may occur in vivo during bactericidal reactions.

Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Melching L
Department of Microbiology and Immunology, McGill University, Montreal, Quebec, Canada.
Vas S I
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Article Info
Journal
Infection and immunity
Abbr.
Infect Immun
ISSN
0019-9567
Published
1971-01-00
Pages
107-15
Language
English
Region
United States
NLM ID
0246127
PMCID
PMC416114
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