Abstract

The incidence of extended-spectrum β-lactamases (ESBLs) has been increasing worldwide, but screening criteria for detection of ESBLs are not standardized for AmpC-producing Enterobacteriaceae such as Enterobacter species. In this study, we investigated the prevalence of ESBLs and/or AmpC β-lactamases in Japanese clinical isolates of Enterobacter spp. and the association of plasmid-mediated quinolone resistance (PMQR) determinants with ESBL producers. A total of 364 clinical isolates of Enterobacter spp. collected throughout Japan between November 2009 and January 2010 were studied. ESBL-producing strains were assessed by the CLSI confirmatory test and the boronic acid disk test. PCR and sequencing were performed to detect CTX-M, TEM, and SHV type ESBLs and PMQR determinants. For ESBL-producing Enterobacter spp., pulsed-field gel electrophoresis (PFGE) was performed using XbaI restriction enzyme. Of the 364 isolates, 22 (6.0%) were ESBL producers. Seven isolates of Enterobacter cloacae produced CTX-M-3, followed by two isolates producing SHV-12. Two isolates of Enterobacter aerogenes produced CTX-M-2. Of the 22 ESBL producers, 21 had the AmpC enzyme, and six met the criteria for ESBL production in the boronic acid test. We found a significant association of qnrS with CTX-M-3-producing E. cloacae. The 11 ESBL-producing Enterobacter spp. possessing bla CTX-M, bla SHV, or bla TEM were divided into six unique PFGE types. This is the first report about the prevalence of qnr determinants among ESBL-producing Enterobacter spp. from Japan. Our results suggest that ESBL-producing Enterobacter spp. with qnr determinants are spreading in Japan.

Highlights

  • Enterobacter species are an important opportunistic pathogen that can cause nosocomial outbreaks and invasive infections such as bloodstream infections [1,2,3]

  • We investigated the prevalence of extended-spectrum b-lactamases (ESBLs) and/or AmpC b-lactamases in clinical isolates of Enterobacter spp. from Japan and the association of plasmid-mediated quinolone resistance (PMQR) determinants with ESBLproducing isolates

  • We evaluated the usefulness of the boronic acid disk test for detecting production of ESBLs by Enterobacter spp

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Summary

Introduction

Enterobacter species are an important opportunistic pathogen that can cause nosocomial outbreaks and invasive infections such as bloodstream infections [1,2,3]. The prevalence of ESBLs and/or AmpC b-lactamases in clinical isolates of Enterobacter spp. from Japan is unknown. It has been reported that 3-aminophenylboronic acid (BA) is an inhibitor of AmpC [6], and it is possible to detect ESBLs in AmpC-producing strains by the boronic acid disk test [7].

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