Emergence of AcrAB-mediated tigecycline resistance in a clinical isolate of Enterobacter cloacae during ciprofloxacin treatment

Hornsey, Michael, Ellington, Matthew J, Doumith, Michel, Scott, Geoff, Livermore, David M ORCID: https://orcid.org/0000-0002-9856-3703 and Woodford, Neil (2010) Emergence of AcrAB-mediated tigecycline resistance in a clinical isolate of Enterobacter cloacae during ciprofloxacin treatment. International Journal of Antimicrobial Agents, 35 (5). pp. 478-81. ISSN 1872-7913

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Abstract

Tigecycline resistance remains rare amongst Enterobacteriaceae in the UK, as elsewhere, but has been associated with upregulation of the AcrAB efflux system. Using isolates of an Enterobacter cloacae strain that developed tigecycline resistance in vivo during ciprofloxacin therapy as well as laboratory-selected mutants, we investigated the role of this pump and the global regulator RamA in tigecycline resistance. Laboratory mutants were selected from a susceptible clinical isolate in vitro by exposure to increasing concentrations of tigecycline. Expression of the acrAB operon and the ramA gene was monitored by real-time reverse-transcription polymerase chain reaction (RT-PCR). Overexpression of ramA was achieved using the pBAD expression vector, whilst insertional inactivation of acrB with a gentamicin resistance cassette was achieved with the bacteriophage lambda Red recombination system. Increased tigecycline minimum inhibitory concentrations in the clinical isolate and a laboratory mutant were associated with increases in acrAB and ramA transcripts. Induction of increased ramA expression resulted in increased acrAB expression, whilst insertional inactivation of acrB restored full susceptibility to tigecycline. Treatment with ciprofloxacin, a substrate of AcrAB in E. cloacae, possibly selected for cross-resistance to tigecycline as a result of RamA-mediated AcrAB upregulation.

Item Type: Article
Additional Information: Copyright 2010 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.
Uncontrolled Keywords: anti-bacterial agents,bacterial proteins,bacterial typing techniques,bacteriophage lambda,ciprofloxacin,dna fingerprinting,dna, bacterial,drug resistance, bacterial,electrophoresis, gel, pulsed-field,enterobacter cloacae,enterobacteriaceae infections,gene expression profiling,great britain,humans,male,membrane transport proteins,microbial sensitivity tests,minocycline,molecular sequence data,mutagenesis, insertional,mutation,reverse transcriptase polymerase chain reaction,selection, genetic,sequence analysis, dna
Faculty \ School: Faculty of Medicine and Health Sciences > Norwich Medical School
UEA Research Groups: Faculty of Medicine and Health Sciences > Research Groups > Epidemiology and Public Health
Faculty of Medicine and Health Sciences > Research Groups > Public Health and Health Services Research (former - to 2023)
Depositing User: Pure Connector
Date Deposited: 24 Jan 2014 12:28
Last Modified: 24 Oct 2022 05:45
URI: https://ueaeprints.uea.ac.uk/id/eprint/46683
DOI: 10.1016/j.ijantimicag.2010.01.011

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