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Azithromycin resistance levels and mechanisms in Escherichia coli

  • Cláudia Gomes
    ,
  • Lidia Ruiz-Roldán
    ,
  • Judit Mateu
    ,
  • Theresa J. Ochoa
    ,
  • Joaquim Ruiz(corresponding author)
*Corresponding author for this work
  • Universitat de Barcelona
    ,
  • CIBIR
    ,
  • Universidad Peruana Cayetano Heredia
    ,
  • School of Public Health, University of Texas
    ,
Research Output:
Contribution to journal
Article
Peer-review

Open access

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Article number

6089

Journal (Volume, Issue Number)

Scientific Reports (Volume 9, Issue 1)

Publication milestones

  • Published - 01/12/2019

Publication status

Published - 01/12/2019

Publication IDs

  • Scopus: 85064429874
  • PubMed: 30988366

Abstract

Despite azithromycin being used in some countries to treat infections caused by Gram-negative pathogens, no resistance breakpoint for Escherichia coli exists. The aim of this study was to analyse the levels and mechanisms of azithromycin resistance in E. coli. The presence of chromosomal (rplD, rplV and 23S rRNA) mutations, 10 macrolide resistance genes (MRGs) and efflux pump overexpression was determined in 343 E. coli isolates. Overall, 89 (25.9%) isolates had MICs ≥ 32 mg/L to azithromycin, decreasing to 42 (12.2%) when assayed in the presence of Phe-Arg-β-Napthylamide, with 35 of these 42 possessing at least one MRG. Efflux pumps played a role in azithromycin resistance affecting the Minimal Inhibitory Concentration (MIC) levels of 91.2% isolates whereas chromosomal alterations seem to have a minimal role. At least one MRG was found in 22.7% of the isolates with mph(A) being the most commonly found gene. The mph(A) gene plays the main role in the development of azithromycin resistance and 93% of the mph(A)-carrying isolates showed a MIC of 32 mg/L. In the absence of a specific resistance breakpoint our results suggest a MIC of 32 mg/L to be considered in order to detect isolates carrying mechanisms able to confer azithromycin resistance.

Funding Details

JR was supported by program I3, of the ISCIII (grant number: CES11/012). We want to thank Dr. Virve I. Enne for kindly providing the P286 10–99C3, P126 11–99C1 and P473 10–99C3 strains with the mef(B) gene; Dr. Ferran Navarro for kindly providing the P0008 (erm(B)), P0037 (erm(A)) and P00 (mef(A)) strains; Dr. Yolanda Saénz for kindly providing the 2381 (erm(B)), 1920 (erm(C)), 1576 (erm(C) and msr(A)) and 2929 (msr(A)) strains. We also thank Dr. J. Calvo Montes (Hospital Marqués de Valdecilla, Santander, Spain) and Mar Olga Perez-Moreno (Hospital Verge de la Cinta, Tortosa, Spain) for kindly providing E. coli J53-AzR. The authors thank Donna Pringle for editorial assistance. “ISGlobal is a member of the CERCA Programme, Generalitat de Catalunya”.
FundersFunding numbers
Instituto de Salud Carlos III
CES11/012