Conjugative transfer of high-level mupirocin resistance and the mobilization of non-conjugative plasmids in

E E Udo1, L E Jacob

  • 1Department of Microbiology, Faculty of Medicine, Kuwait University, Safat.

Microbial Drug Resistance (Larchmont, N.Y.)
|November 18, 1998
PubMed

Insights

A novel conjugative plasmid, pXU12, from Staphylococcus aureus confers mupirocin resistance. This plasmid efficiently mobilizes other resistance plasmids, aiding in the study of antibiotic resistance mechanisms.

Area of Science:

  • Microbiology
  • Molecular Biology
  • Genetics

Background:

  • Antibiotic resistance in Staphylococcus aureus is a growing public health concern.
  • Mupirocin resistance is often mediated by plasmid-borne genes like mupA.
  • Conjugative plasmids play a significant role in the dissemination of antibiotic resistance.

Purpose of the Study:

  • To characterize a novel conjugative plasmid, pXU12, encoding mupirocin resistance.
  • To investigate the mobilization capabilities of pXU12 for other plasmids.
  • To evaluate the utility of pXU12 for transferring non-conjugative plasmids in laboratory settings.

Main Methods:

  • Isolation and characterization of the conjugative plasmid pXU12 from Staphylococcus aureus MB494.
  • Conjugation experiments to assess plasmid transfer frequency and kinetics.
  • Mobilization assays to determine pXU12's ability to transfer other plasmids, including pXU13.

Main Results:

  • The 31-kb conjugative plasmid pXU12 confers high-level mupirocin resistance via the mupA gene.
  • pXU12 demonstrated rapid transfer in conjugation experiments (transconjugants within 15 min).
  • pXU12 efficiently mobilized the erythromycin resistance plasmid pXU13 and 11 other nonconjugative plasmids.

Conclusions:

  • pXU12 is a highly efficient conjugative plasmid capable of mobilizing various non-conjugative plasmids.
  • The findings suggest pXU12 can be a valuable tool for transferring and isolating non-conjugative plasmids from resistant Staphylococcus aureus strains.
  • This research contributes to understanding plasmid-mediated antibiotic resistance and provides a potential laboratory method for plasmid manipulation.

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