Occurrence of blaNDM-7 within IncX3-type plasmid of Escherichia coli from India

J Infect Chemother. 2017 Apr;23(4):206-210. doi: 10.1016/j.jiac.2016.12.009. Epub 2017 Jan 26.

Abstract

Background: New-Delhi metallo-β-lactamase-7 with higher hydrolytic activity than its ancestor NDM-1 is emerging across the globe including India. In this study, we have investigated the genetic context of blaNDM-7 and alteration in plasmid copy number under concentration gradient carbapenem stress.

Materials and methods: Six blaNDM-7 producing Escherichia coli isolates were obtained from Silchar Medical College and Hospital and the co-existence of other β-lactamases and transferability of this resistant determinant was determined by transformation and conjugation assay followed by typing of the plasmid by PBRT method. Genetic context and plasmid stability of blaNDM-7 was also determined. The change in copy number of transconjugable plasmid carrying blaNDM-7 under exposure of different carbapenem antibiotics was determined by quantitative Real Time PCR.

Results: All the six isolates carrying blaNDM-7 were conjugatively transferable through an IncX3-type plasmid and were also found to co-harbor blaCTX-M-15. Genetic analysis of blaNDM-7 showed an association of ISAba125, IS5 and a truncated portion of ISAba125 in the upstream region and bleMBL gene in the downstream region of blaNDM-7. Complete loss of the plasmids carrying blaNDM-7 was observed between 85th to 90th serial passages when antibiotic pressure was withdrawn. After analyzing the relative copy number it was observed that the copy number of the blaNDM-7 encoding plasmid was highly affected by the concentration of ertapenem.

Conclusion: The present study has first demonstrated presence of IncX3-type plasmid encoding blaNDM-7 within nosocomial isolates of E. coli. Measures must be taken to prevent or atleast slowdown the emergence of this resistance determinant in this country.

Keywords: Carbapenemase; Escherichia coli; IncX3; bla(NDM-7).

MeSH terms

  • Bacterial Proteins / genetics*
  • Carbapenems / pharmacology
  • Conjugation, Genetic / genetics
  • Ertapenem
  • Escherichia coli / drug effects
  • Escherichia coli / genetics*
  • Escherichia coli Infections / microbiology
  • Humans
  • India
  • Plasmids / drug effects
  • Plasmids / genetics*
  • beta-Lactamases / genetics
  • beta-Lactams / pharmacology

Substances

  • Bacterial Proteins
  • Carbapenems
  • beta-Lactams
  • beta-Lactamases
  • Ertapenem