Methicillin-Resistant Staphylococcus aureus Blood Isolates Harboring a Novel Pseudo-staphylococcal Cassette

Eun-Jeong Yoon1, Hyukmin Lee1, Dokyun Kim1

  • 1Department of Laboratory Medicine, Research Institute of Bacterial Resistance, Yonsei University College of Medicine, Seoul, South Korea.

Insights

Researchers identified a novel pseudo-staphylococcal cassette chromosome mec (ΨSCCmec) element in MRSA blood isolates. This element lacks mobility genes, suggesting an evolutionary adaptation in these methicillin-resistant Staphylococcus aureus strains.

Area of Science:

  • Microbiology
  • Genetics
  • Infectious Diseases

Background:

  • Methicillin-resistant Staphylococcus aureus (MRSA) poses a significant threat in both community and healthcare settings.
  • The staphylococcal cassette chromosome mec (SCCmec) element is crucial for MRSA's methicillin resistance.
  • Understanding novel SCCmec variants is vital for tracking MRSA evolution and spread.

Purpose of the Study:

  • To characterize a newly identified pseudo-SCCmec (ΨSCCmec) element in MRSA blood isolates.
  • To investigate the genetic makeup and potential implications of this novel element.
  • To assess the evolutionary significance of ΨSCCmec in MRSA.

Main Methods:

  • Isolation and identification of MRSA from blood specimens.
  • Antimicrobial susceptibility testing using disk diffusion.
  • SCCmec typing via multiplex polymerase chain reaction (PCR).
  • Whole genome sequencing using single molecule real-time (SMRT) technology.

Main Results:

  • Two MRSA isolates (E16SA093 and F17SA003) with sequence type 72 and agr-type I were identified.
  • Both isolates possessed a novel SCCmec IV-like element lacking the cassette chromosome recombinase (ccr) gene complex, termed ΨSCCmec.
  • This ΨSCCmec element resulted from the deletion of the ccr complex and adjacent chromosomal DNA.

Conclusions:

  • The identified ΨSCCmec element, lacking the ccr gene complex, is likely non-mobile, representing a potential evolutionary adaptation.
  • The absence of mobility genes may confer a selective advantage, influencing MRSA's evolutionary trajectory.
  • Close monitoring of MRSA clones carrying this ΨSCCmec element is recommended due to potential dissemination.

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