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IS257-mediated cointegration in the evolution of a family of staphylococcal trimethoprim resistance plasmids

A Leelaporn1, N Firth, I T Paulsen

  • 1School of Biological Sciences, University of Sydney, New South Wales, Australia.

Journal of Bacteriology
|October 1, 1996
PubMed

Insights

Two Staphylococcus epidermidis plasmids, pSK697 and pSK818, show cointegration likely mediated by the IS257 element. This finding offers insights into the mechanism of cointegrate plasmid formation in bacteria.

Area of Science:

  • Microbiology
  • Molecular Biology
  • Genetics

Background:

  • Staphylococcus epidermidis is a significant pathogen, often carrying antibiotic resistance plasmids.
  • Understanding plasmid structure and mobility is crucial for combating bacterial infections.

Purpose of the Study:

  • To analyze the structure of Staphylococcus epidermidis plasmids pSK697 and pSK818.
  • To investigate the role of the IS257 element in the formation of cointegrate plasmids.

Main Methods:

  • Plasmid DNA analysis
  • Sequence analysis of IS257 elements
  • Comparative genomics

Main Results:

  • Plasmids pSK697 and pSK818 are related to known trimethoprim and multidrug resistance plasmids.
  • Both plasmids contain cointegrated elements flanked by IS257.
  • IS257 is implicated in the formation of these cointegrate plasmids via nonresolved replicative transposition.

Conclusions:

  • The IS257 insertion sequence plays a key role in the formation of cointegrate plasmids in Staphylococcus epidermidis.
  • The mechanism involves nonresolved replicative transposition of IS257.
  • This study enhances understanding of plasmid evolution and antibiotic resistance dissemination.

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