Meropenem-Vaborbactam Resistance Selection, Resistance Prevention, and Molecular Mechanisms in Mutants of KPC-Producing Klebsiella pneumoniae

被引:2
|
作者
Sun, Dongxu [1 ]
Rubio-Aparicio, Debora [1 ]
Nelson, Kirk [1 ]
Dudley, Michael N. [1 ]
Lomovskaya, Olga [1 ]
机构
[1] Med Co, San Diego, CA 07054 USA
关键词
vaborbactam; Klebsiella pneumoniae carbapenemases; KPC; resistance development; single-step mutants; BETA-LACTAMASE INHIBITOR; SEQUENCE TYPE 258; CARBAPENEM RESISTANCE; CEFTAZIDIME-AVIBACTAM; ENTEROBACTERIACEAE; RPX7009; SUSCEPTIBILITY; GENE; MUTATIONS; STRAINS;
D O I
10.1128/AAC.01694-17
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Vaborbactam (formerly RPX7009) is a new beta-lactamase inhibitor based on a cyclic boronic acid pharmacophore with potent inhibitory activity against Klebsiella pneumoniae carbapenemases (KPC). It has been developed in combination with meropenem. The objective of these studies was to identify the concentrations of both agents associated with the selection or prevention of single-step mutations leading to reduced sensitivity to the combination and to characterize the selected mutations. Eighteen strains of KPC-producing Klebsiella pneumoniae with various degrees of sensitivity to meropenem (MICs, 8 to 512 mu g/ml) and meropenem-vaborbactam (MICs, <= 0.06 to 32 mu g/ml) and preexisting resistance mechanisms were selected from a worldwide collection of isolates recovered from surveillance studies, emphasizing strains for which MICs were in the upper range of the meropenem-vaborbactam MIC distribution. Meropenem and vabor-bactam at 8 mu g/ml each suppressed the drug resistance mutation frequency to <1 X 10(-8) in 77.8% (14/18) of strains, and all strains were inhibited when the meropenem concentration was increased to 16 mu g/ml. Mutants selected at lower drug concentrations showed phenotypes associated with previously described carbapenem resistance mechanisms, including ompK36 inactivation in mutants selected from OmpK36-proficient strains and an increased bla(KPC) gene copy number in strains with partially functional ompK36. No mutations in the coding region of bla(KPC) were identified. These data indicate that the selection of mutants with reduced sensitivity to meropenem-vaborbactam from KPC-producing Klebsiella pneumoniae strains is associated with previously described mechanisms involving porin mutations and the increase in the bla(KPC) gene copy number and not changes in the KPC enzyme and can be prevented by the drug concentrations achieved with optimal dosing of the combination.
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页数:14
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