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Updated: Jan 31, 2026

Subcutaneous Infection of Methicillin Resistant Staphylococcus Aureus MRSA
Published on: February 9, 2011
Regional outbreak of community-associated methicillin-resistant Staphylococcus aureus ST834 in Japanese children
Yuki Uehara1,2,3, Takashi Sasaki4,5, Tadashi Baba4,5
1Department of Infection Control Science, Juntendo University Graduate School of Medicine, 2-1-1, Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan. yuuehara@juntendo.ac.jp.
Background:
Community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA) infection has recently become a challenging problem worldwide and in Japan. We experienced 10 pediatric patients infected with CA-MRSA and hospitalized from 2011 to 2014 in a tertiary care hospital in Saitama, Japan, and assessed the characteristic of the strains using a whole genome sequencing (WGS)-based approach.
Methods:
CA-MRSA strains isolated from infected patients who required hospitalization for treatment were evaluated in this study. Antimicrobial susceptibility tests, molecular typing by PCR and pulse-field gel electrophoresis (PFGE) were performed to characterize MRSA strains. WGS was performed for detailed genetic analysis.
Results:
A total of 582 MRSA strains (35.2%) were identified among 1625 S. aureus strains collected during the study period. Ten MRSA strains (1.7%) were defined as CA-MRSA clinically, and all were isolated from pediatric patients. All strains mainly caused purulent lymphadenitis, were susceptible to fluoroquinolone and tetracycline, exhibited sequence type (ST) 834 or its single-locus variants and contained staphylococcal cassette chromosome mec (SCCmec) type IVc. Phylogenic analysis by PFGE and WGS revealed close relatedness of all strains, with the number of single nucleotide polymorphisms ranging from 35 to 119 by WGS. Out of the ten strains, nine possessed the genomic island SaPISaitama2 containing tst, sec and sel genes. SaPISaitama2 comprises a mosaic of genomic islands SaPIm4 and SaPIm1 harbored by a hospital-associated MRSA strain Mu50.
Conclusions:
This study describes a regional outbreak of ST834-related CA-MRSA in children with a unique pathogenicity island in Japan. Pediatric patient tropism of this clone could be enhanced by susceptibility to fluoroquinolones and tetracyclines, which cannot be prescribed to children.
Insights
Community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA) infections are a growing concern in Japan. This study identified a specific CA-MRSA strain (ST834) predominantly affecting children, characterized by unique genetic features and antibiotic susceptibility.
Area of Science:
- Microbiology
- Genomics
- Infectious Diseases
Background:
- Community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA) presents a significant global and Japanese health challenge.
- This study investigated 10 pediatric CA-MRSA cases hospitalized between 2011 and 2014 in Saitama, Japan.
Purpose of the Study:
- To characterize CA-MRSA strains from hospitalized pediatric patients using whole genome sequencing (WGS).
- To understand the genetic relatedness and unique features of these CA-MRSA strains.
Main Methods:
- Isolation and identification of MRSA strains from hospitalized patients.
- Antimicrobial susceptibility testing, PCR, and PFGE for molecular typing.
- Whole genome sequencing (WGS) for detailed genetic analysis and phylogenetic reconstruction.
Main Results:
- Ten CA-MRSA strains were identified from pediatric patients, primarily causing purulent lymphadenitis.
- All strains belonged to sequence type (ST) 834 or its variants, harbored SCCmec type IVc, and were susceptible to fluoroquinolones and tetracyclines.
- Phylogenetic analysis revealed close relatedness among strains (35-119 SNPs via WGS). Nine strains possessed a unique genomic island, SaPISaitama2, containing virulence genes.
Conclusions:
- A regional outbreak of ST834-related CA-MRSA in children was identified in Japan.
- The unique pathogenicity island (SaPISaitama2) and susceptibility to certain antibiotics may contribute to pediatric tropism.
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