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Novel Cassette Assay To Quantify the Outer Membrane Permeability of Five β-Lactams Simultaneously in Carbapenem-ResistantKlebsiella pneumoniaeandEnterobacter cloacae
Author(s) -
Tae Hwan Kim,
Xun Tao,
Bartolomé Moyá,
Yuanyuan Jiao,
Kari B. Basso,
Jieqiang Zhou,
Yinzhi Lang,
Dhruvitkumar S. Sutaria,
Alexandre Prehn Zavascki,
Afonso Luís Barth,
Stephanie M. Reeve,
Herbert P. Schweizer,
Deanna Deveson Lucas,
John D. Boyce,
Robert A. Bonomo,
Richard Lee,
Beom Soo Shin,
Arnold Louie,
George L. Drusano,
Jürgen B. Bulitta
Publication year - 2020
Publication title -
mbio
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.562
H-Index - 121
eISSN - 2161-2129
pISSN - 2150-7511
DOI - 10.1128/mbio.03189-19
Subject(s) - enterobacter cloacae , klebsiella pneumoniae , microbiology and biotechnology , antibiotics , bacterial outer membrane , gram negative bacteria , carbapenem , bacteria , klebsiella , enterobacter , enterobacteriaceae , biology , escherichia coli , biochemistry , gene , genetics
Antimicrobial resistance is causing a global human health crisis and is affecting all antibiotic classes. While β-lactams have been commonly used against susceptible isolates ofKlebsiella pneumoniae andEnterobacter cloacae , carbapenem-resistant isolates are spreading worldwide and pose substantial clinical challenges. Rapid penetration of β-lactams leads to high drug concentrations at their periplasmic target sites, allowing β-lactams to more completely inactivate their target receptors. Despite this, there are limited tangible data on the permeability of β-lactams through the outer membranes of many Gram-negative pathogens. This study presents a novel, cassette assay, which can simultaneously characterize the permeability of five β-lactams in multidrug-resistant clinical isolates. We show that carbapenems, and especially imipenem, penetrate the outer membrane ofK. pneumoniae andE. cloacae substantially faster than noncarbapenem β-lactams. The ability to efficiently characterize the outer membrane permeability is critical to optimize the use of β-lactams and combat carbapenem-resistant isolates.

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