Antibiotic-induced release of endotoxin from bacteria in vitro.

Abstract

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.

• Authors: H A Crosby, J F Bion, C W Penn, T S Elliott
• Journal: Journal of medical microbiology (J Med Microbiol) Vol. 40 Issue 1 Pg. 23-30 (Jan 1994) ISSN: 0022-2615 [Print] England
• PMID: 8289210 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Anti-Bacterial Agents
• Endotoxins
• Lipopolysaccharides
• Ciprofloxacin
• Cefotaxime
• Tobramycin
• Piperacillin

Topics

• Anti-Bacterial Agents (pharmacology)
• Cefotaxime (pharmacology)
• Ciprofloxacin (pharmacology)
• Colony Count, Microbial
• Endotoxins (metabolism)
• Enterobacter cloacae (drug effects, metabolism, ultrastructure)
• Escherichia coli (drug effects, metabolism, ultrastructure)
• Humans
• Limulus Test
• Lipopolysaccharides (analysis)
• Microscopy, Electron, Scanning
• Piperacillin (pharmacology)
• Silver Staining
• Tobramycin (pharmacology)