Abstract

BackgroundThis study was aimed to characterize the genetic diversity and expression of three putative resistance-nodulation-cell division (RND)-type efflux systems and their contribution to multidrug efflux in clinical isolates of Acinetobacter baumannii.MethodsAntimicrobial susceptibility testing of 95 A. baumannii isolates was determined by Kirby-Bauer disk diffusion for 18 antibiotics and minimum inhibitory concentration (MIC) of colistin was determined by the broth microdilution method. Moreover, the MIC of five classes of antibiotics was assessed using E-test strips in the presence and absence of phenylalanine-arginine beta-naphthylamide (PAβN). Regulatory genes of the RND efflux pumps (adeRS, adeL, adeN and baeSR) were subjected to sequencing. The relative expression of adeB, adeG and adeJ genes was determined by quantitative real-time PCR (qRT-PCR).ResultsOverall, the majority of isolates (94%) were extensively drug-resistant (XDR). In the phenotypic assay, efflux pump activity was observed in 40% of the isolates against multiple antibiotics mainly tigecycline. However, we found no efflux activity against imipenem. Several amino acid substitutions were detected in the products of regulatory genes; except in AdeN. Of note, G186V mutation in AdeS was found to be associated with overexpression of its efflux pump. No insertion sequences were detected.ConclusionsOur findings outlined the role of RND efflux pumps in resistance of A. baumannii to multiple antibiotics particularly tigecycline, and pointed out the importance of a variety of single mutations in the corresponding regulatory systems. Further studies are required to decipher the precise role of RND efflux pumps in multidrug-resistant clinical isolates of A. baumannii.

Highlights

  • This study was aimed to characterize the genetic diversity and expression of three putative resistancenodulation-cell division (RND)-type efflux systems and their contribution to multidrug efflux in clinical isolates of Acinetobacter baumannii

  • Resistance-nodulation-cell division (RND) superfamily pumps are ubiquitous in Gram-negative bacteria and are remarkable for their ability to be selected after exposure to an antibiotic [7]

  • Antimicrobial susceptibility testing (AST) and efflux pump activity determination Antibiotic susceptibility profile was determined by KirbyBauer disk diffusion for 18 antibiotics (Mast Co., Merseyside, UK) on Mueller–Hinton (MH) agar (Merck, Germany), and minimum inhibitory concentration (MIC) of colistin was determined by broth microdilution method in Mueller–Hinton broth (Merck, Germany), as described by the clinical and laboratory standards institute (CLSI) [25]

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Summary

Introduction

This study was aimed to characterize the genetic diversity and expression of three putative resistancenodulation-cell division (RND)-type efflux systems and their contribution to multidrug efflux in clinical isolates of Acinetobacter baumannii. Genomic plasticity and genetic variabilities; including mutations in endogenous structural or regulatory genes and insertion of mobile genetic elements, can account for the development of various resistance mechanisms in XDR-AB isolates. Intrinsic resistance determinants such as chromosomally encoded carbapenemase genes, decreased membrane permeability, and efflux systems are inherent in A. baumannii. Antibiotic extrusion occurs mainly through overexpression of efflux pumps. Resistance-nodulation-cell division (RND) superfamily pumps are ubiquitous in Gram-negative bacteria and are remarkable for their ability to be selected after exposure to an antibiotic [7]

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