Complete sequence of pJIE143, a pir-type plasmid carrying ISEcp1-blaCTX-M-15 from an Escherichia coli ST131 isolate

Sally R Partridge1, Justin A Ellem, Sasha G Tetu

  • 1Centre for Infectious Diseases and Microbiology, University of Sydney, Westmead Hospital, Level 3 ICPMR Building, Sydney, New South Wales 2145, Australia. sally.partridge@swahs.health.nsw.gov.au

Insights

A novel plasmid, pJIE143, carrying the bla(CTX-M-15) gene, was identified in Escherichia coli. Its unique IncX-like backbone and inserted transposition unit challenge standard plasmid typing methods.

Area of Science:

  • Microbiology
  • Molecular Biology
  • Genetics

Background:

  • The bla(CTX-M-15) gene confers resistance to extended-spectrum cephalosporins, a significant public health concern.
  • Escherichia coli sequence type 131 (ST131) is a globally disseminated multidrug-resistant pathogen.
  • Standard plasmid typing methods can fail to identify novel or divergent plasmid types.

Purpose of the Study:

  • To characterize the novel plasmid pJIE143 identified in an Escherichia coli ST131 isolate.
  • To elucidate the genetic structure and evolutionary origins of pJIE143.
  • To understand the implications of this novel plasmid for antimicrobial resistance dissemination.

Main Methods:

  • Plasmid DNA extraction and sequencing.
  • Bioinformatic analysis of plasmid backbone and inserted elements.
  • Comparison with known plasmid families and mobile genetic elements.

Main Results:

  • pJIE143 (34 kb) carries the bla(CTX-M-15) gene but is not typable by standard PCR-based replicon typing.
  • Complete sequencing revealed an IncX-like plasmid backbone with a pir-like replication gene and IncX-related iterons.
  • A 2.971-kb ISEcp1-bla(CTX-M-15)-orf477Δ transposition unit, similar to that found in Tn2, is inserted near the pir gene, flanked by direct repeats.

Conclusions:

  • pJIE143 represents a novel IncX-like plasmid carrying the bla(CTX-M-15) gene.
  • The unique genetic architecture of pJIE143 may explain its failure to be typed by standard methods.
  • This finding highlights the need for advanced sequencing techniques to fully characterize antimicrobial resistance plasmids.

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