Abstract

BackgroundTo investigate the presence of metallo-β-lactamase (MBL) genes and the genetic environment of the New Delhi metallo-β-lactamase gene bla NDM-1 in bacteria of food animal origin.Methodology/Principal FindingsGram-negative bacteria with low susceptibility to imipenem (MIC>8 µg/mL) were isolated from swab samples collected from 15 animal farms and one slaughterhouse in eastern China. These bacteria were selected for phenotypic and molecular detection of known MBL genes and antimicrobial susceptibility testing. For the bla NDM-1 positive isolate, conjugation and transformation experiments were carried out to assess plasmid transfer. Southern blotting was conducted to localize the bla NDM-1 genes, and DNA sequencing was performed to determine the sequences of bla NDM-1 and the flanking genes. In total, nine Gram-negative bacteria of four different species presented a MBL phenotype. bla NDM-1 was identified on a mobile plasmid named pAL-01 in an Acinetobacter lwoffii isolate of chicken origin. Transfer of pAL-01 from this isolate to E. coli J53 and JM109 resulted in resistance to multiple β-lactams. Sequence analysis revealed that the bla NDM-1 gene is attached to an intact insertion element ISAba125, whose right inverted repeat (IR-R) overlaps with the promoter sequence of bla NDM-1. Thus, insertion of ISAba125 likely enhances the expression of bla NDM-1.ConclusionThe identification of a bla NDM-1- carrying strain of A. lwoffii in chickens suggests the potential for zoonotic transmission of bla NDM-1 and has important implications for food safety.

Highlights

  • Metallo-b-lactamases (MBLs) in clinical Gram-negative organisms are an important threat to public health

  • The identification of a blaNDM-1- carrying strain of A. lwoffii in chickens suggests the potential for zoonotic transmission of blaNDM-1 and has important implications for food safety

  • In 2009, a novel MBL enzyme, named New Delhi metallo-b-lactamase (NDM-1, encoded by blaNDM-1), was identified in plasmids from Klebsiella pneumoniae and Escherichia coli isolates recovered from a Swedish patient previously hospitalized in India [2]

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Summary

Introduction

Metallo-b-lactamases (MBLs) in clinical Gram-negative organisms are an important threat to public health. In 2009, a novel MBL enzyme, named New Delhi metallo-b-lactamase (NDM-1, encoded by blaNDM-1), was identified in plasmids from Klebsiella pneumoniae and Escherichia coli isolates recovered from a Swedish patient previously hospitalized in India [2]. BlaNDM-1-harboring strains of Enterobacteriaceae have been identified worldwide, with most reports indicating that the isolates originated from the Indian subcontinent with hospital or community acquisition [3] or from the Balkan countries [4]. Coexistence of blaNDM-1 with the class D carbapenemase gene blaOXA-23 in clinical isolates of Acinetobacter baumannii was first detected in India [6]. To investigate the presence of metallo-b-lactamase (MBL) genes and the genetic environment of the New Delhi metallo-b-lactamase gene blaNDM-1 in bacteria of food animal origin

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