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Updated: Jul 20, 2026

Subcutaneous Infection of Methicillin Resistant Staphylococcus Aureus (MRSA)
Published on: February 9, 2011
Community-acquired Staphylococcus aureus infections in term and near-term previously healthy neonates
Regine M Fortunov1, Kristina G Hulten, Wendy A Hammerman
1Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
Insights
Community-acquired methicillin-resistant Staphylococcus aureus (CA-MRSA) is an increasing threat to neonates. USA300 is the predominant CA-MRSA clone causing infections in previously healthy infants.
Area of Science:
- Neonatal infectious diseases
- Molecular epidemiology of bacterial pathogens
- Antimicrobial resistance surveillance
Background:
- Community-acquired Staphylococcus aureus infections are rising in pediatric populations.
- Neonatal S. aureus infections present unique clinical challenges due to the vulnerability of newborns.
Observation:
- A retrospective review identified 89 S. aureus infections in neonates (< or = 30 days old) between 2001 and 2005.
- Methicillin-resistant S. aureus (MRSA) infections significantly increased during the study period.
- The predominant clone identified was USA300, a strain known to carry Panton-Valentine leukocidin (PVL) genes.
Findings:
- 61 of 89 S. aureus infections were MRSA, with a notable increase from 2002 to 2004.
- Skin and soft tissue infections were most common (77/89), with MRSA isolates more frequently requiring drainage.
- Invasive manifestations included shock, musculoskeletal and urinary tract infections, bacteremia, and empyema; one death occurred.
- Concurrent maternal S. aureus infection was associated with 13/61 MRSA cases.
Implications:
- Community-acquired MRSA represents a significant and growing proportion of S. aureus infections in healthy neonates.
- Male infants aged 7-12 days are most commonly affected, suggesting a potential window of susceptibility.
- The prevalence of the USA300 clone highlights the need for targeted surveillance and treatment strategies for neonatal MRSA infections.
Background:
Community-acquired, methicillin-resistant Staphylococcus aureus infections are increasing among children.
Objective:
Our goal is to describe the clinical presentation of neonatal community-acquired S aureus disease and provide molecular analyses of the infecting isolates.
Patients And Methods:
We retrospectively reviewed the demographics and hospital course of term and near-term previously healthy neonates, < or = 30 days of age, with community-acquired S aureus infections presenting after nursery discharge between August 2001 and March 2005 at Texas Children's Hospital. Prospectively collected isolates were characterized by pulsed-field gel electrophoresis, staphylococcal cassette chromosome mec type, and the presence of PVL genes.
Results:
Of 89 S aureus infections, 61 were methicillin-resistant S aureus; S aureus infections increased each year. Methicillin-resistant S aureus infections increased from 10 of 20 to 30 of 36 infections from 2002 to 2004. Most subjects, 65 of 89, were male. Symptoms began at 7 to 12 days of age for 26 of 45 male infants with methicillin-resistant S aureus. Most infections, 77 of 89, involved skin and soft tissue; 28 of 61 methicillin-resistant S aureus versus 7 of 28 methicillin-susceptible S aureus infections required drainage. Invasive manifestations included shock, musculoskeletal and urinary tract infection, perinephric abscess, bacteremia, empyema/lung abscess, and a death. Maternal S aureus or skin-infection history occurred with 13 of 61 methicillin-resistant S aureus versus 1 of 28 methicillin-susceptible S aureus infections. The predominant community clone, USA300 (PVL genes +), accounted for 55 of 57 methicillin-resistant S aureus and 3 of 25 methicillin-susceptible S aureus isolates.
Conclusions:
Community-acquired methicillin-resistant S aureus is a substantial and increasing proportion of S aureus infections in previously healthy neonates. Male infants 7 to 12 days of age are affected most often. Neonatal community-acquired S aureus infection may be associated with concurrent maternal infection. USA300 is the predominant clone among these neonatal isolates in our region.
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