Abstract
The next-generation aminoglycoside plazomicin, in development for infections due to multidrug-resistant (MDR) Enterobacteriaceae, was evaluated alongside comparators for bactericidal activity in minimum bactericidal concentration (MBC) and time-kill (TK) assays against MDR Enterobacteriaceae isolates with characterized aminoglycoside and β-lactam resistance mechanisms. Overall, plazomicin and colistin were the most potent, with plazomicin demonstrating an MBC50/90 of 0.5/4 μg/ml and sustained 3-log10 kill against MDR Escherichia coli, Klebsiella pneumoniae, and Enterobacter spp.
Keywords:
Enterobacteriaceae; bactericidal; bactericidal activity; multidrug resistance; plazomicin.
Copyright © 2018 Thwaites et al.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Aminoglycosides / pharmacology
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Anti-Bacterial Agents / pharmacology*
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Carbapenems / pharmacology
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Drug Resistance, Multiple, Bacterial / drug effects*
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Drug Resistance, Multiple, Bacterial / genetics
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Enterobacter / drug effects*
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Enterobacter / genetics
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Enterobacter / growth & development
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Escherichia coli / drug effects*
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Escherichia coli / genetics
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Escherichia coli / growth & development
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Fluoroquinolones / pharmacology
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Klebsiella pneumoniae / drug effects*
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Klebsiella pneumoniae / genetics
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Klebsiella pneumoniae / growth & development
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Microbial Sensitivity Tests
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Polymyxins / pharmacology
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Sisomicin / analogs & derivatives*
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Sisomicin / pharmacology
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Tetracyclines / pharmacology
Substances
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Aminoglycosides
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Anti-Bacterial Agents
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Carbapenems
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Fluoroquinolones
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Polymyxins
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Tetracyclines
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plazomicin
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Sisomicin