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Possible beta-lactamase activities detectable in infective clinical specimens
The Journal of Antibiotics
|December 1, 1977
Summary
Biological activities inactivating beta-lactam antibiotics were found in urine and pleural fluid samples. Klebsiella species inactivated ampicillin, while Enterobacter and Pseudomonas species inactivated cephalothin.
Area of Science:
- Microbiology
- Pharmacology
- Clinical Chemistry
Background:
- Beta-lactam antibiotics are crucial in treating bacterial infections.
- Antibiotic resistance, including enzymatic inactivation, is a growing public health concern.
- Detection of antibiotic-inactivating enzymes in clinical samples is important for understanding treatment efficacy.
Purpose of the Study:
- To investigate the presence and nature of biological beta-lactam antibiotic-inactivating activities in clinical specimens.
- To identify specific bacterial species associated with these inactivating activities.
- To determine the spectrum of antibiotic inactivation by different bacterial isolates.
Main Methods:
- Collection and sterilization of clinical specimens (bacteriuria and suppurating pleural fluids) using membrane filtration.
- Quantification of ampicillin and cephalothin inactivation by filtrates from 1 ml of each specimen.
- Identification of bacterial species present in the filtrates, including Klebsiella sp., Enterobacter sp., and Pseudomonas aeruginosa.
Main Results:
- Biological beta-lactam antibiotic-inactivating activities were detected in both bacteriuria and suppurating pleural fluids.
- Filtrates yielding Klebsiella sp. generally showed inactivation activity against ampicillin.
- Filtrates yielding Enterobacter sp. and Pseudomonas aeruginosa demonstrated inactivation activity against cephalothin.
Conclusions:
- Clinical specimens can harbor biological activities capable of inactivating beta-lactam antibiotics.
- Specific bacterial genera are associated with the inactivation of particular beta-lactam antibiotics.
- These findings highlight the potential for in-situ antibiotic inactivation in infections caused by these bacteria.