Plasmids in epidermolytic strains of Staphylococcus aureus

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Insights

Staphylococcus aureus plasmids carrying toxin genes were identified. Plasmid elimination revealed type ii toxin and bacteriocin production are plasmid-encoded, while type i toxin is likely chromosomal.

Area of Science:

  • Microbiology
  • Molecular Biology
  • Genetics

Background:

  • Staphylococcus aureus produces various toxins, including epidermolytic toxins (serotypes i and ii).
  • The genetic basis for toxin production, particularly plasmid involvement, requires further elucidation.
  • Bacteriocin production and antibiotic resistance can also be plasmid-mediated in bacteria.

Purpose of the Study:

  • To investigate the role of plasmid DNA in the production of Staphylococcus aureus epidermolytic toxins (serotypes i and ii).
  • To determine the genetic linkage between toxin production, bacteriocin production, and cadmium resistance.
  • To analyze the relatedness of plasmids carrying these determinants.

Main Methods:

  • Screening of Staphylococcus aureus strains for plasmid DNA using gel electrophoresis.
  • Plasmid elimination through curing techniques.
  • Phenotypic analysis of cured strains for toxin and bacteriocin production.
  • Restriction endonuclease analysis (EcoRI and HindIII) of isolated plasmids.

Main Results:

  • All serotype ii toxin-producing strains harbored a 42 kb plasmid, essential for both type ii toxin (Toxii+) and bacteriocin (Bac+) production.
  • Serotype i toxin (Toxi+) production was not consistently eliminated with plasmid loss, suggesting chromosomal linkage.
  • Cadmium resistance was linked to the 42 kb plasmid in some strains.
  • Restriction analysis indicated close relatedness among the 42 kb plasmids from different strains.

Conclusions:

  • Type ii toxin and bacteriocin production in Staphylococcus aureus are plasmid-encoded.
  • Type i toxin production is likely chromosomally determined.
  • The 42 kb plasmid plays a significant role in mediating multiple phenotypes, including toxin and bacteriocin production and potentially cadmium resistance.

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