Antibiotic-induced release of endotoxin from bacteria in vitro
* Departments of Clinical Microbiology Intensive Care, Queen Elizabeth Hospital, Birmingham B15 2TH School of Biological Sciences, University of Birmingham, Birmingham B15 2TT Received December 22, 1992 Surmmary: The ability of cefotaxime, ciprofloxacin, piperacillin and tobramycin to cause release...
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Published in | Journal of medical microbiology Vol. 40; no. 1; pp. 23 - 30 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
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Soc General Microbiol
01.01.1994
Society for General Microbiology |
Subjects | |
Online Access | Get full text |
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Summary: | * Departments of Clinical Microbiology
Intensive Care, Queen Elizabeth Hospital, Birmingham B15 2TH
School of Biological Sciences, University of Birmingham, Birmingham B15 2TT
Received December 22, 1992
Surmmary: The ability of cefotaxime, ciprofloxacin, piperacillin and tobramycin to cause release of endotoxin was examined in vitro with cultures of Enterobacter cloacae and Escherichia coli . Endotoxin was measured by a quantitative limulus amoebocyte lysate assay and its presence was confirmed by silver staining of the lipopolysaccharide moiety following SDS-PAGE. The morphology of the bacteria during antibiotic exposure was examined by scanning electronmicroscopy. Cefotaxime, ciprofloxacin and piperacillin caused significant endotoxin release, correlating with their ability to affect cell-wall morphology, causing filamentation, wall breakage and cell lysis. In contrast, little endotoxin was released when bacteria were exposed to tobramycin and no morphological changes were observed when bacteria were exposed to bactericidal concentrations of this aminoglycoside. Its antimicrobial spectrum and bactericidal activity make tobramycin an appropriate agent for treatment of sepsis caused by gram-negative bacteria and its lack of propensity to elicit excessive release of endotoxin may avoid exacerbation of endotoxin-related shock in sepsis.
* Correspondence should be sent to Dr T. S. J. Elliott. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0022-2615 1473-5644 |
DOI: | 10.1099/00222615-40-1-23 |