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PVL Staphylococcus aureus osteomyelitis complicating septic arthritis in a UK soldier serving in Iraq
J G Penn-Barwell1, S Finnikin, I Sargeant
1Selly Oak Hospital, Raddlebarn Road, Selly Oak, Birmingham B29 6JD. Jowan@doctors.net.uk
Insights
The first adult case of Panton-Valentine Leukocidin (PVL) secreting Staphylococcus aureus musculoskeletal infection occurred in a soldier. Military clinicians should consider PVL testing for severe S. aureus bone and joint infections.
Area of Science:
- Infectious Diseases
- Orthopedic Surgery
- Microbiology
Background:
- Panton-Valentine Leukocidin (PVL) is a toxin produced by some Staphylococcus aureus strains.
- PVL-producing S. aureus has been linked to musculoskeletal infections in pediatric and adolescent populations.
Observation:
- This report details the first documented adult case of PVL-secreting S. aureus causing musculoskeletal infection.
- A 26-year-old British Army soldier presented with septic arthritis, followed by femoral osteomyelitis.
- The causative S. aureus strain isolated from tissue biopsy was confirmed to encode the PVL gene.
Findings:
- The soldier experienced recurrent, severe musculoskeletal infections requiring surgical intervention and prolonged antibiotic treatment.
- While S. aureus colonization rates may be higher in soldiers, PVL gene prevalence is similar to the general UK population.
- Soldiers possess risk factors that may increase susceptibility to PVL-secreting S. aureus infections.
Implications:
- Military healthcare providers must be aware of the potential for PVL-secreting S. aureus in aggressive musculoskeletal infections.
- A low threshold for specific PVL testing is recommended for military personnel presenting with severe S. aureus bone and joint infections.
- This case highlights the need for vigilance regarding PVL-producing S. aureus in adult military populations.
Abstract:
Musculoskeletal infections caused by Panton-Valentine Leukocidin (PVL) secreting Stapylococcus aureus in children and adolescents have previously been reported. We report the first adult case in a 26 year-old British Army soldier who presented with a S. aureus septic arthritis. He was treated by surgical washout and antibiotics and discharged but was readmitted five months later with an ipsilateral femoral osteomyelitis requiring debridement. The causative S. aureus grown from tissue biopsy taken at time of surgery was found to encode the PVL gene. Whilst there is evidence that soldiers in Iraq have a greater rate of S. aureus colonisation on their skin, the proportion that encode the PVL gene is similar to that observed in the UK. Soldiers are however, subject to the known risk factors that increase vulnerability to PVL secreting S. aureus infection. Military clinicians need to be aware of PVL secreting S. aureus and have a low threshold for requesting specific testing in aggressive musculoskeletal S. aureus infections.
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