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Emergence of clinical isolates of Escherichia coli producing TEM-1 derivatives or an OXA-1 beta-lactamase conferring resistance to beta-lactamase inhibitors.
- Source :
-
Antimicrobial agents and chemotherapy [Antimicrob Agents Chemother] 1994 May; Vol. 38 (5), pp. 1085-9. - Publication Year :
- 1994
-
Abstract
- Sixteen Escherichia coli clinical isolates which were resistant to ampicillin and amoxicillin-clavulanate but susceptible to cephalothin were studied. Eight strains showed the presence of a beta-lactamase which comigrates with reference OXA-1 enzyme. The eight other strains produced different TEM-1 derivatives which had in common a higher Km for penicillins and a higher 50% inhibitory concentration for the beta-lactamase inhibitors. By oligotyping and sequencing of PCR products, it was shown that Ser (AGC) (TEM-30; also called TRI-1) in three strains and Cys (TGC) (TEM-31; also called TRI-2) in one strain were substituted for Arg-241 (CGC), that Leu (CTG) (TEM-33) and Val (GTG) (TEM-34) in one strain each were substituted for Met-67 (ATG), and that in other mutants the two latter substitutions occurred together with the substitution of Asp (GAT) (TEM-35 and TEM-36) for Asn-272 (AAT). Therefore, different sets of amino acid substitutions of TEM-1 can be found in clinical isolates and lead to resistance to beta-lactamase inhibitors.
- Subjects :
- Amoxicillin pharmacology
Base Sequence
Cephalothin pharmacology
Clavulanic Acid
Clavulanic Acids pharmacology
Escherichia coli drug effects
Escherichia coli genetics
Humans
Kinetics
Microbial Sensitivity Tests
Molecular Sequence Data
Point Mutation
Polymerase Chain Reaction
beta-Lactamase Inhibitors
Escherichia coli enzymology
Escherichia coli Infections microbiology
beta-Lactamases biosynthesis
Subjects
Details
- Language :
- English
- ISSN :
- 0066-4804
- Volume :
- 38
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Antimicrobial agents and chemotherapy
- Publication Type :
- Academic Journal
- Accession number :
- 8067742
- Full Text :
- https://doi.org/10.1128/AAC.38.5.1085