| Literature DB >> 33020157 |
Claire Amaris Hobson1, Stéphane Bonacorsi1,2, Hervé Jacquier1,3, Alaksh Choudhury1, Mélanie Magnan1, Aurélie Cointe1,2, Béatrice Bercot1,3, Olivier Tenaillon1, André Birgy4,2.
Abstract
To explore the mutational possibilities of insertions and deletions (indels) in the Klebsiella pneumoniae carbapenemase (KPC) beta-lactamase, we selected for ceftazidime-avibactam-resistant mutants. Of 96 screened mutants, we obtained 19 indels (2 to 15 amino acids), all located in the loops surrounding the active site. Three antibiotic susceptibility phenotypes emerged: an extended-spectrum-beta-lactamase-like phenotype, an activity restricted to ceftazidime, and a carbapenem-susceptible KPC-like phenotype. Tolerance for indels reflects the evolvability of KPC beta-lactamase, which could challenge the therapeutic management of patients.Entities:
Keywords: KPC; carbapenemase; ceftazidime-avibactam; deletion; hydrolysis spectrum; insertion; mutation; mutational tolerance; omega loop
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Year: 2020 PMID: 33020157 PMCID: PMC7674030 DOI: 10.1128/AAC.01175-20
Source DB: PubMed Journal: Antimicrob Agents Chemother ISSN: 0066-4804 Impact factor: 5.191