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Subcutaneous Infection of Methicillin Resistant Staphylococcus Aureus (MRSA)
Published on: February 9, 2011
Pulmonary manifestations in children with invasive community-acquired Staphylococcus aureus infection
Blanca E Gonzalez1, Kristina G Hulten, Megan K Dishop
1Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
Insights
Invasive Staphylococcus aureus infections in children frequently involve the lungs. Panton-Valentine leukocidin (PVL) gene presence strongly correlates with severe pneumonia and metastatic lung disease in these patients.
Area of Science:
- Infectious Diseases
- Pulmonology
- Microbiology
Background:
- Invasive community-acquired Staphylococcus aureus infections are increasingly associated with pulmonary complications.
- Texas Children's Hospital has observed a rise in primary pneumonia and metastatic pulmonary infections.
- Understanding the factors contributing to lung involvement is crucial for patient outcomes.
Purpose of the Study:
- To characterize pulmonary involvement in pediatric invasive community-acquired S. aureus infections.
- To investigate the correlation between Panton-Valentine leukocidin (PVL) and collagen adhesin (cna) genes and pulmonary manifestations.
- To differentiate between primary and metastatic pulmonary disease in affected children.
Main Methods:
- Retrospective review of pediatric patients with invasive S. aureus infections admitted between 2001 and 2004.
- Analysis of chest imaging and postmortem examination reports for pulmonary findings.
- PCR testing of S. aureus isolates for the presence of PVL and cna genes.
Main Results:
- A significant association was found between community-acquired methicillin-resistant S. aureus (MRSA) and abnormal pulmonary imaging (47/70) compared to methicillin-susceptible S. aureus (MSSA) (12/43).
- Panton-Valentine leukocidin (PVL)-positive isolates were highly correlated with abnormal chest imaging findings (51/80) versus PVL-negative isolates (2/23).
- PVL gene presence was independently associated with abnormal chest imaging in patients with secondary pneumonia (P = .03).
Conclusions:
- Pulmonary involvement is a common complication of invasive community-acquired S. aureus infections in children.
- Community-acquired MRSA can lead to both primary pneumonia and metastatic lung disease.
- The presence of genes encoding PVL is a significant risk factor for pulmonary involvement in S. aureus infections.
Background:
Primary pneumonia and metastatic pulmonary infection have become more common in patients with invasive community-acquired Staphylococcus aureus disease at Texas Children's Hospital (TCH; Houston).
Methods:
In this study, we sought to describe pulmonary involvement in children with community-acquired S. aureus invasive infection and to determine whether the presence of genes encoding Panton-Valentine leukocidin (PVL) (luk-S-PV and luk-F-PV) and collagen adhesin (cna) is correlated with pulmonary manifestations. Patients with invasive staphylococcal infections admitted to TCH between 1 August 2001 and 30 June 2004 were studied. Chest imaging and postmortem examination reports were reviewed. Isolates were tested for the presence of genes encoding PVL and collagen adhesin by PCR.
Results:
A total of 47 of 70 patients with community-acquired methicillin-resistant S. aureus (MRSA) infection had abnormal pulmonary imaging findings, compared with 12 of 43 patients with community-acquired methicillin-susceptible S. aureus (MSSA) infection (P < .001). Pneumonia and/or empyema, in addition to septic emboli, were the most common findings. Metastatic pulmonary disease occurred more frequently among patients with osteomyelitis. Severe necrotizing pneumonia was present in 3 children coinfected with influenza and parainfluenza virus. The presence of genes encoding PVL was investigated in 67 MRSA and 36 MSSA isolates. Abnormal chest imaging findings were observed for 51 of 80 patients with PVL-positive isolates, compared with 2 of 23 patients with PVL-negative isolates (P < .001). Only 2 isolates (both of which were MSSA) from patients with abnormal chest radiograph findings carried cna. PVL remained independently associated with abnormal chest imaging findings in patients with secondary pneumonia in a multivariate analysis (P = .03).
Conclusions:
Pulmonary involvement is commonly observed in patients with invasive community-acquired S. aureus infections. Community-acquired MRSA may cause primary community-acquired pneumonia, as well as metastatic pulmonary disease. The presence of genes encoding PVL is highly associated with pulmonary involvement by S. aureus.
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