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Updated: Jun 19, 2026

Genotyping of Staphylococcus aureus by Ribosomal Spacer PCR (RS-PCR)
Published on: November 4, 2016
USA300 is the predominant genotype causing Staphylococcus aureus septic arthritis in children
Maria A Carrillo-Marquez1, Kristina G Hulten, Wendy Hammerman
1Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA. mamarque@bcm.edu
Background:
Staphylococcus aureus is the most common cause of septic arthritis (SA) in children. USA300 is the predominant community methicillin-resistant (MRSA) clone. Panton-Valentine leukocidin genes (pvl) have been associated with severe disease.
Methods:
Patients with S. aureus SA were identified from the Texas Children's Hospital surveillance study. Pulsed field gel electrophoresis and pvl polymerase chain reaction were performed on isolates.
Results:
Forty-five patients with S. aureus SA were identified between August 2001 and October 2008. Median age was 5.5 years (0.3-17.9 years); 69% were previously healthy. The most common joints affected were hip (40%) followed by knee (36%). Associated infection sites were osteomyelitis (n = 14), pyomyositis/myositis (n = 13), and cellulitis (n = 9). Bacteremia for 1 to 5 days occurred in 31% of the patients. Patients with associated osteomyelitis were more likely to be bacteremic (P = 0.001), have fever >2 days (P = 0.03), and to have C-reactive protein (CRP) > or = 10 mg/dL (P = 0.01). Of 44 available isolates, 16 were MRSA; 13 of 16 were USA300 and 14 of 16 were pvl+. Twenty-eight isolates were MSSA; 8 of 28 were USA300 and 13 of 28 were pvl+. Infections caused by USA300 isolates were associated with longer duration of fever than non-USA300 isolates (median, [range]: 4 [0-15] days vs 1 [0-8] days) (P = 0.03). Overall, 61% of the isolates were pvl+. CRP > or = 10 mg/dL was more likely in pvl+ infections than in pvl- infections (P = 0.05).
Conclusions:
S. aureus SA caused by USA300 isolates is associated with longer duration of fever. Empirical treatment of SA should include MRSA. CRP levels > or = 10 mg/dL, fever >2 days, and bacteremia should raise suspicion for associated osteomyelitis.
Insights
Staphylococcus aureus septic arthritis in children is often caused by the USA300 MRSA clone, leading to prolonged fever. Empirical treatment should cover MRSA, and elevated CRP suggests osteomyelitis.
Area of Science:
- Pediatric Infectious Diseases
- Bacterial Pathogenesis
- Molecular Epidemiology
Background:
- Staphylococcus aureus is a leading cause of pediatric septic arthritis (SA).
- The USA300 strain is the dominant community-associated methicillin-resistant Staphylococcus aureus (MRSA) clone.
- Panton-Valentine leukocidin (pvl) genes are linked to severe S. aureus infections.
Purpose of the Study:
- To investigate the characteristics of S. aureus septic arthritis in children.
- To determine the prevalence and impact of specific S. aureus clones, including USA300 and pvl-positive strains.
- To identify clinical predictors of associated complications like osteomyelitis.
Main Methods:
- Retrospective review of pediatric patients with S. aureus SA at Texas Children's Hospital.
- Molecular typing of S. aureus isolates using pulsed-field gel electrophoresis.
- Detection of Panton-Valentine leukocidin genes via polymerase chain reaction.
Main Results:
- Forty-five cases of S. aureus SA were identified; hip and knee were most commonly affected.
- USA300 strains, particularly pvl-positive ones, were prevalent among MRSA and MSSA isolates.
- Infections caused by USA300 isolates were associated with a longer duration of fever (P=0.03).
- Elevated C-reactive protein (CRP) levels were more common in pvl-positive infections (P=0.05).
Conclusions:
- Pediatric S. aureus SA caused by the USA300 clone is linked to prolonged fever.
- Empirical treatment for SA should include coverage for MRSA.
- Clinical signs such as fever >2 days, elevated CRP, and bacteremia warrant suspicion for concurrent osteomyelitis.
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