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Mutations in bla KPC-3 That Confer Ceftazidime-Avibactam Resistance Encode Novel KPC-3 Variants That Function as Extended-Spectrum β-Lactamases
- Source :
- Antimicrobial Agents and Chemotherapy. 61
- Publication Year :
- 2017
- Publisher :
- American Society for Microbiology, 2017.
-
Abstract
- We identified four bla KPC-3 mutations in ceftazidime-avibactam-resistant clinical Klebsiella pneumoniae isolates, corresponding to D179Y, T243M, D179Y/T243M, and EL165-166 KPC-3 variants. Using site-directed mutagenesis and transforming vectors into Escherichia coli , we conclusively demonstrated that mutant bla KPC-3 encoded enzymes that functioned as extended-spectrum β-lactamases; mutations directly conferred higher MICs of ceftazidime-avibactam and decreased the MICs of carbapenems and other β-lactams. Impact was strongest for the D179Y mutant, highlighting the importance of the KPC Ω-loop.
- Subjects :
- 0301 basic medicine
Pharmacology
Genetics
biology
medicine.drug_class
Klebsiella pneumoniae
030106 microbiology
Cephalosporin
Mutant
Mutagenesis (molecular biology technique)
Ceftazidime
biochemical phenomena, metabolism, and nutrition
bacterial infections and mycoses
biology.organism_classification
medicine.disease_cause
Ceftazidime/avibactam
03 medical and health sciences
Infectious Diseases
polycyclic compounds
medicine
Pharmacology (medical)
Site-directed mutagenesis
Escherichia coli
medicine.drug
Subjects
Details
- ISSN :
- 10986596 and 00664804
- Volume :
- 61
- Database :
- OpenAIRE
- Journal :
- Antimicrobial Agents and Chemotherapy
- Accession number :
- edsair.doi...........c3ffd0e3676b99184537d79fbf9a3fac
- Full Text :
- https://doi.org/10.1128/aac.02534-16