Highly conjugative pMG1-like plasmids carrying Tn1546-like transposons that encode vancomycin resistance in

Haruyoshi Tomita1, Koichi Tanimoto, Satoshi Hayakawa

  • 1Department of Bacteriology and Bacterial Infection Control, Gunma University Graduate School of Medicine, Maebashi, Gunma 371-8511, Japan.

Journal of Bacteriology
|November 18, 2003
PubMed

Insights

This study details 12 VanA-type vancomycin-resistant enterococci, including Enterococcus faecium and Enterococcus avium. Researchers identified and characterized three conjugative plasmids responsible for vancomycin resistance transfer between enterococci strains.

Area of Science:

  • Microbiology
  • Molecular Biology
  • Antimicrobial Resistance

Background:

  • Vancomycin-resistant enterococci (VRE) pose a significant threat in healthcare settings.
  • The VanA type is a common mechanism conferring high-level vancomycin resistance.
  • Understanding the genetic elements mediating VRE spread is crucial for infection control.

Purpose of the Study:

  • To characterize VanA-type vancomycin-resistant enterococci isolates.
  • To identify and analyze the conjugative plasmids responsible for vancomycin resistance.
  • To investigate the transfer efficiency and genetic relatedness of these plasmids.

Main Methods:

  • Isolation and identification of vancomycin-resistant enterococci.
  • Plasmid DNA isolation and characterization (size, type).
  • Conjugation experiments to assess transfer efficiency between enterococcal strains.
  • Plasmid homology analysis.

Main Results:

  • Twelve VanA-type VRE isolates were analyzed (10 E. faecium, 2 E. avium).
  • Three conjugative plasmids (pHTalpha, pHTbeta, pHTgamma) were isolated from E. faecium strains.
  • These plasmids demonstrated high-efficiency transfer during broth mating and showed homology to pMG1.

Conclusions:

  • The identified plasmids are key mobile genetic elements mediating vancomycin resistance spread in enterococci.
  • Efficient plasmid transfer highlights the potential for rapid dissemination of VRE.
  • Homology to pMG1 suggests a common origin or shared genetic features among resistance plasmids.

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