Characterization of SCCmec Instability in Methicillin-Resistant Staphylococcus aureus Affecting Adjacent Chromosomal

C R Scharn1, I A Tickler2, F C Tenover2

  • 1Department of Medical Microbiology and Immunology, Creighton University School of Medicine, Omaha, Nebraska, USA.

Insights

Staphylococcal cassette chromosome mec (SCCmec) stability in MRSA strains was investigated. SCCmec rearrangements, including precise excision and internal deletions, occurred over 3 months, influenced by mobile elements and host cell environment.

Area of Science:

  • Microbiology
  • Genetics
  • Molecular Biology

Background:

  • Staphylococcal cassette chromosome mec (SCCmec) is crucial in staphylococci, containing the mecA gene for methicillin resistance.
  • SCCmec elements can be unstable, with internal mobile elements and recombinases causing rearrangements.
  • SCCmec alterations may impact adjacent chromosomal sequences, such as the staphylococcal protein A (spa) gene.

Purpose of the Study:

  • To investigate the stability of SCCmec in methicillin-resistant Staphylococcus aureus (MRSA) strains.
  • To determine the impact of culturing without antimicrobial selection on SCCmec integrity.
  • To identify factors influencing SCCmec stability, including mobile elements and host cell environment.

Main Methods:

  • MRSA strains with four different SCCmec types were cultured without antimicrobial selection for 3 months.
  • Cefoxitin susceptibility was monitored as an indicator of SCCmec rearrangements.
  • Sequence analysis was performed to characterize SCCmec alterations and adjacent chromosomal changes.

Main Results:

  • SCCmec rearrangements were detected in cefoxitin-susceptible variants after 2 months.
  • The most common rearrangement was precise excision of the entire SCCmec element.
  • Internal SCCmec deletions, some involving loss of the spa gene, were observed after 3 months.
  • No loss of only the mecA gene (empty cassettes) was detected.

Conclusions:

  • SCCmec stability is influenced by internal mobile elements like IS431 and the host cell environment.
  • SCCmec rearrangements, including precise excision and deletions, can occur even without antibiotic pressure.
  • These findings highlight the dynamic nature of SCCmec and its potential impact on the staphylococcal genome.