Literature DB >> 22526311

In vitro activity of MK-7655, a novel β-lactamase inhibitor, in combination with imipenem against carbapenem-resistant Gram-negative bacteria.

Elizabeth B Hirsch1, Kimberly R Ledesma, Kai-Tai Chang, Michael S Schwartz, Mary R Motyl, Vincent H Tam.   

Abstract

Carbapenem-resistant bacteria represent a significant treatment challenge due to the lack of active antimicrobials available. MK-7655 is a novel β-lactamase inhibitor under clinical development. We investigated the combined killing activity of imipenem and MK-7655 against four imipenem-resistant bacterial strains, using a mathematical model previously evaluated in our laboratory. Time-kill studies (TKS) were conducted with imipenem and MK-7655 against a KPC-2-producing Klebsiella pneumoniae isolate (KP6339) as well as 3 Pseudomonas aeruginosa isolates (PA24226, PA24227, and PA24228) with OprD porin deletions and overexpression of AmpC. TKS were performed using 25 clinically achievable concentration combinations in a 5-by-5 array. Bacterial burden at 24 h was determined in triplicate by quantitative culture and mathematically modeled using a three-dimensional response surface. Mathematical model assessments were evaluated experimentally using clinically relevant dosing regimens of imipenem, with or without MK-7655, in a hollow-fiber infection model (HFIM). The combination of imipenem and MK-7655 was synergistic for all strains. Interaction indices were as follows: for KP6339, 0.50 (95% confidence interval [CI], 0.42 to 0.58); for PA24226, 0.60 (95% CI, 0.58 to 0.62); for PA24227, 0.70 (95% CI, 0.66 to 0.74); and for PA24228, 0.55 (95% CI, 0.49 to 0.61). In the HFIM, imipenem plus MK-7655 considerably reduced the bacterial burden at 24 h, while failure with imipenem alone was seen against all isolates. Sustained suppression of bacterial growth at 72 h was achieved with simulated doses of 500 mg imipenem plus 500 mg MK-7655 in 2 (KP6339 and PA24227) strains, and it was achieved in an additional strain (PA24228) when the imipenem dose was increased to 1,000 mg. Additional studies are being conducted to determine the optimal dose and combinations to be used in clinical investigations.

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Year:  2012        PMID: 22526311      PMCID: PMC3393460          DOI: 10.1128/AAC.05927-11

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  15 in total

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Authors:  D M Livermore
Journal:  Antimicrob Agents Chemother       Date:  1992-09       Impact factor: 5.191

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3.  Interplay of efflux system, ampC, and oprD expression in carbapenem resistance of Pseudomonas aeruginosa clinical isolates.

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Journal:  Antimicrob Agents Chemother       Date:  2006-05       Impact factor: 5.191

4.  Multiple-dose pharmacokinetics of imipenem-cilastatin.

Authors:  G L Drusano; H C Standiford; C Bustamante; A Forrest; G Rivera; J Leslie; B Tatem; D Delaportas; R R MacGregor; S C Schimpff
Journal:  Antimicrob Agents Chemother       Date:  1984-11       Impact factor: 5.191

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Authors:  Vincent H Tam; Amy N Schilling; Russell E Lewis; David A Melnick; Adam N Boucher
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8.  Impact of AmpC overexpression on outcomes of patients with Pseudomonas aeruginosa bacteremia.

Authors:  Vincent H Tam; Kai-Tai Chang; Amy N Schilling; Mark T LaRocco; Layne O Genty; Kevin W Garey
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10.  Quantitative assessment of combination antimicrobial therapy against multidrug-resistant Acinetobacter baumannii.

Authors:  Tze-Peng Lim; Kimberly R Ledesma; Kai-Tai Chang; Jing-Guo Hou; Andrea L Kwa; Michael Nikolaou; John P Quinn; Randall A Prince; Vincent H Tam
Journal:  Antimicrob Agents Chemother       Date:  2008-05-27       Impact factor: 5.191

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Journal:  Antimicrob Agents Chemother       Date:  2014-03-31       Impact factor: 5.191

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Review 5.  [New antibiotics prior to approval: is this the end of the innovative stagnation?].

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Review 6.  Multidrug-resistant Gram-negative bacteria in solid organ transplant recipients with bacteremias.

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Journal:  Eur J Clin Microbiol Infect Dis       Date:  2014-11-12       Impact factor: 3.267

7.  New Polymyxin B Dosing Strategies To Fortify Old Allies in the War against KPC-2-Producing Klebsiella pneumoniae.

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8.  Pharmacodynamic and response surface analysis of linezolid or vancomycin combined with meropenem against Staphylococcus aureus.

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9.  In Vitro and In Vivo Activities of OP0595, a New Diazabicyclooctane, against CTX-M-15-Positive Escherichia coli and KPC-Positive Klebsiella pneumoniae.

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Journal:  Antimicrob Agents Chemother       Date:  2016-04-22       Impact factor: 5.191

Review 10.  Overcoming resistance to β-lactam antibiotics.

Authors:  Roberta J Worthington; Christian Melander
Journal:  J Org Chem       Date:  2013-03-28       Impact factor: 4.354

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