| Literature DB >> 32660988 |
Punyawee Dulyayangkul1, Edward J A Douglas1, Filip Lastovka1, Matthew B Avison2.
Abstract
Serine β-lactamases are dominant causes of β-lactam resistance in Klebsiella pneumoniae isolates. Recently, this has driven clinical deployment of the β-lactam-β-lactamase inhibitor pairs ceftazidime/avibactam and meropenem/vaborbactam. We show that four steps, i.e., ompK36 and ramR mutation plus carriage of OXA-232 and KPC-3-D178Y variant β-lactamases, confer ceftazidime/avibactam and meropenem/vaborbactam resistance when both pairs are used together. These findings have implications for decision making about sequential and combinatorial use of these β-lactam-β-lactamase inhibitor pairs to treat K. pneumoniae infections.Entities:
Keywords: KPC; OXA-48; porin; β-lactamase
Mesh:
Substances:
Year: 2020 PMID: 32660988 PMCID: PMC7508580 DOI: 10.1128/AAC.00409-20
Source DB: PubMed Journal: Antimicrob Agents Chemother ISSN: 0066-4804 Impact factor: 5.191