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Subcutaneous Infection of Methicillin Resistant Staphylococcus Aureus MRSA
Published on: February 9, 2011
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.
Abstract:
Reports of severe infections caused by Panton-Valentine leukocidin (PVL)-positive community-acquired methicillin-resistant Staphylococcus aureus (CA-MRSA) are increasing. Pediatric infections caused by CA-MRSA, including in children without known risk factors, are on the rise worldwide. In recent years, PVL-producing USA300-related clones and ST22-PT clones producing both PVL and toxic shock syndrome toxin-1 (TSST-1) have been identified, which suggests an emerging threat. We treated 10 pediatric patients with severe or recurrent MRSA infections between 2021 and 2024. These included four cases of recurrent subcutaneous abscesses, two cases of necrotizing pneumonia, and one case each of bacteremia, suppurative osteomyelitis, cellulitis, and infective endocarditis. Four patients had underlying medical conditions. Molecular analysis revealed that all of the isolates carried SCCmec type IV, 50 % were PVL-positive, and 30 % produced TSST-1. Multilocus sequence typing showed that 60 % of isolates belonged to sequence type (ST) 8 clones suspected to be USA300-related variants. Furthermore, one isolate belonged to the ST22-PT clone. These findings revealed that CA-MRSA accounts for the majority of MRSA infections even in pediatric patients, with severe cases caused by PVL or TSST-1 positive strains. CA-MRSA has also spread within healthcare settings and could pose a significant risk to pediatric patients with underlying conditions. Furthermore, the results suggest that severe infections caused by USA300-related clone and ST22-PT could increase in the future. Ongoing molecular surveillance is essential to guide effective treatment and infection-control strategies.
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.
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