期刊
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY
卷 67, 期 6, 页码 1354-1358出版社
OXFORD UNIV PRESS
DOI: 10.1093/jac/dks079
关键词
-lactamase inhibitors; AmpC -lactamases; CTX-M-15-lactamases; outer membrane proteins
资金
- Cerexa, Inc.
- Forest Research Institute, Inc.
- AstraZeneca
- Dechra
- Eco Animal Health
- GlaxoSmithKline
- Merck
Ceftarolineavibactam (NXL104) is a novel inhibitor combination active against Enterobacteriaceae with class A and C -lactamases. We investigated its risk of mutational resistance. Single- and multi-step mutants were sought and characterized from Enterobacteriaceae with extended-spectrum -lactamases (ESBLs), AmpC -lactamases and KPC -lactamases. Overgrowth occurred on agar with low MIC multiples of ceftarolineavibactam, but frequencies for single-step mutants were 10(9). Most mutants were unstable, with only three remaining resistant on subculture. For one, from an CTX-M-15-positive Escherichia coli, the ceftarolineavibactam MIC was raised, but the organism had reduced resistance to ceftaroline and lost resistance to other oxyimino-cephalosporins, with this profile retained when the mutant bla(CTX-M-15) was cloned into E. coli DH5. Sequencing identified a Lys237Gln substitution in the CTX-M-15 variant. The other two stable single-step mutants were from an AmpC-derepressed Enterobacter cloacae strain; these had unaltered or slightly reduced resistance to other -lactams. Both had amino acids 213226 deleted from the O loop of AmpC. Further stable mutants were obtained from AmpC-inducible and -derepressed E. cloacae in multi-step selection, and these variously had reduced expression of OmpC and OmpF, and/or Asn366His/Ile substitutions in AmpC. Stable resistant mutants were difficult to select. Those from AmpC-derepressed E. cloacae had porin loss or AmpC changes, including O loop deletions. A Lys237Gln substitution in CTX-M-15 conferred resistance, but largely abolished ESBL activity.
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