Publication | Open Access
Activity of NXL104 in Combination with β-Lactams against Genetically Characterized Escherichia coli and Klebsiella pneumoniae Isolates Producing Class A Extended-Spectrum β-Lactamases and Class C β-Lactamases
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Citations
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References
2011
Year
Extended-spectrum β-LactamasesKlebsiella PneumoniaeEscherichia ColiAntimicrobial ChemotherapyClass C β-LactamasesAntibiotic ResistanceBacterial PathogensDrug ResistanceAntimicrobial StewardshipInfection ControlAntimicrobial ResistanceAerobic CulturingHealth SciencesAntimicrobial Drug DiscoveryExtended-spectrum β-LactamaseAntimicrobial PharmacokineticsPharmacologyClinical MicrobiologyAntimicrobial Resistance GeneAntimicrobial SusceptibilityAntibioticsMicrobiologyMedicinePartner Cephalosporins
The novel non-β-lactam β-lactamase inhibitor NXL104, in combination with cefepime, ceftazidime, ceftriaxone, amdinocillin, and meropenem, was tested against 190 extended-spectrum β-lactamase (ESBL)-producing Escherichia coli and Klebsiella pneumoniae isolates, 94 AmpC-hyperproducing E. coli isolates, and 8 AmpC/ESBL-coexpressing E. coli isolates. NXL104 restored 100% susceptibility to the partner cephalosporins for all isolates tested. Amdinocillin and meropenem MICs were modestly improved (2 to 32 times lower) by NXL104. These results suggest that NXL104 may be useful in combination with β-lactams for the treatment of infections caused by ESBL- and AmpC-producing Enterobacteriaceae.
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