Abstract

We determined the in vitro susceptibility of four aminoglycosides, which are not of the 4,6-disubstituted deoxystreptamine (DOS) subclass against a collection of carbapenem-resistant Enterobacteriaceae (CRE). CRE clinical strains (n = 134) were collected from multiple hospitals in China and carried blaNDM (blaNDM−1, blaNDM−5 or blaNDM−7; n = 66), blaKPC−2 (n = 62) or blaIMP−4 (n = 7; including one carrying blaNDM−1 and blaIMP−4). MICs of neomycin, paromomycin, streptomycin and apramycin as well as three 4,6-disubstituted DOS aminoglycosides (amikacin, gentamicin and tobramycin) were determined using the broth microdilution with breakpoints defined by the Clinical Laboratory Standards Institute (for amikacin, gentamicin and tobramycin), US Food and Drug Administration (streptomycin), the National Antimicrobial Resistance Monitoring System (apramycin) or la Société Française de Microbiologie (neomycin and paromomycin). Apramycin-resistant strains were subjected to whole genome sequencing using Illumina X10 platform. Among CRE strains, 65.7, 64.9, 79.1, and 95.5% were susceptible to neomycin (MIC50/MIC90, 8/256 μg/ml), paromomycin (4/>256 μg/ml), streptomycin (16/256 μg/ml) and apramycin (4/8 μg/ml), respectively, while only 55.2, 28.4, and 35.1% were susceptible to amikacin (32/>256 μg/ml), gentamicin (128/>256 μg/ml) and tobramycin (64/>256 μg/ml), respectively. Six CRE strains including five Escherichia coli of different sequence types and one Klebsiella pneumoniae were resistant to apramycin and the apramycin-resistant gene aac(3)-IVa was detected in all of these strains. In conclusion, neomycin, paromomycin, streptomycin and apramycin retain activity against most CRE strains. Although none of these non-4,6-disubstituted DOS aminoglycosides are suitable for intravenous use in human at present, these agents warrant further investigations to be used against CRE infections.

Highlights

  • Carbapenem-resistant Enterobacteriaceae (CRE) have emerged as a major worldwide challenge for clinical treatment and public health (Temkin et al, 2014; Iovleva and Doi, 2017; Logan and Weinstein, 2017)

  • Aminoglycosides that are commonly used to treat clinical infections caused by bacteria other than Mycobacterium spp. include amikacin, gentamicin and tobramycin, all of which belong to the 4,6-disubstituted deoxystreptamine (DOS) subclass (Mingeot-Leclercq et al, 1999)

  • MICs of aminoglycosides, ciprofloxacin, imipenem, meropenem, piperacillin-tazobactam and trimethoprim-sulfamethoxazole were determined using broth microdilution following the recommendations of the Clinical Laboratory Standards Institute (CLSI) (CLSI, 2017)

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Summary

Introduction

Carbapenem-resistant Enterobacteriaceae (CRE) have emerged as a major worldwide challenge for clinical treatment and public health (Temkin et al, 2014; Iovleva and Doi, 2017; Logan and Weinstein, 2017). Aminoglycosides that are commonly used to treat clinical infections caused by bacteria other than Mycobacterium spp. include amikacin, gentamicin and tobramycin, all of which belong to the 4,6-disubstituted deoxystreptamine (DOS) subclass (Mingeot-Leclercq et al, 1999). These aminoglycosides retain activities against certain CRE strains (Livermore et al, 2011b) and their combination with other agents has been successful for treating some CRE infection cases (Hirsch and Tam, 2010; Falagas et al, 2014; Rafailidis and Falagas, 2014; Shields et al, 2016). We present susceptibility results of four non-4,6-disubstituted DOS aminoglycosides (apramycin, streptomycin, neomycin and paromomycin) against 134 CRE clinical strains that were collected at multiple hospitals in China

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