Molecular epidemiology and pathogenicity analysis of community-acquired MRSA in Japanese children with a severe or

Atsushi Miyake1, Kenji Gotoh1, Hiroyuki Miyazaki1

  • 1The Department of Infection Control and Prevention Kurume University School of Medicine, Japan; The Department of Pediatrics and Child Health Kurume University School of Medicine, Japan.

Insights

Severe infections in children caused by Panton-Valentine leukocidin (PVL)-positive community-acquired methicillin-resistant Staphylococcus aureus (CA-MRSA) are increasing globally. Molecular analysis identified PVL and TSST-1 producing strains, highlighting the need for ongoing surveillance.

Area of Science:

  • Infectious Diseases
  • Microbiology
  • Pediatrics

Background:

  • Reports of severe infections caused by Panton-Valentine leukocidin (PVL)-positive community-acquired methicillin-resistant Staphylococcus aureus (CA-MRSA) are increasing globally.
  • Pediatric infections caused by CA-MRSA are rising worldwide, affecting children with and without known risk factors.
  • Emerging threats include PVL-producing USA300-related clones and ST22-PT clones, which also produce toxic shock syndrome toxin-1 (TSST-1).

Purpose of the Study:

  • To investigate the characteristics of severe or recurrent MRSA infections in pediatric patients.
  • To identify the molecular profiles of CA-MRSA isolates causing severe infections in children.
  • To assess the risk posed by specific CA-MRSA clones in pediatric healthcare settings.

Main Methods:

  • Retrospective analysis of 10 pediatric patients with severe or recurrent MRSA infections treated between 2021 and 2024.
  • Molecular analysis of MRSA isolates, including SCCmec typing, PVL and TSST-1 detection.
  • Multilocus sequence typing (MLST) to determine sequence types (STs) and identify specific clones like USA300 variants and ST22-PT.

Main Results:

  • CA-MRSA accounted for the majority of MRSA infections in the studied pediatric cohort.
  • Severe cases were frequently caused by PVL-positive (50%) or TSST-1-positive (30%) strains.
  • Sixty percent of isolates belonged to ST8 (USA300-related variants), and one isolate was identified as ST22-PT.

Conclusions:

  • CA-MRSA, particularly PVL or TSST-1 positive strains, is a significant cause of severe pediatric infections.
  • CA-MRSA poses a risk in healthcare settings, especially for immunocompromised children.
  • Continued molecular surveillance is crucial for effective treatment and infection control of pediatric MRSA infections, particularly concerning USA300-related and ST22-PT clones.