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Updated: Sep 10, 2025

Subcutaneous Infection of Methicillin Resistant Staphylococcus Aureus MRSA
Published on: February 9, 2011
Panton-Valentine Leukocidin-Producing Community-Acquired Methicillin-Resistant Staphylococcus aureus in Skin and Soft
Ayaka Aoki1,2, Yuko Hatamiya1,2, Hiroko Fukamatsu1,2
1Department of Dermatology, Kawasaki Medical School, Okayama, Japan.
Abstract:
Panton-Valentine leukocidin (PVL) is a toxin generally produced by community-acquired methicillin-resistant Staphylococcus aureus (CA-MRSA) that is cytotoxic to neutrophils. USA300 is a virulent epidemic PVL-producing MRSA clone; it is increasing. Recently, ΨUSA300, a deleted mutant of USA300, has been identified in Japan. However, reports on the clinical and epidemiological characteristics of PVL-producing MRSA strains, including USA300 and ΨUSA300, remain limited. We included 65 patients who visited our dermatology clinic between January 2020 and May 2024 with skin and soft tissue infections in which CA-MRSA was detected. Clinical information, antimicrobial susceptibility, PVL production, and MRSA strains were analyzed.PVL, found in 70.8% of patients with CA-MRSA infection, was more common in younger patients (median age: 34 years) without underlying diseases and was more likely to present with deep-seated pyoderma (DSP), relapse of clinical symptoms, and intra-familial outbreaks, with a sepsis-related complication rate of 4.3%. Patients with PVL-nonproducing MRSA were anemic and had renal dysfunction. USA300 accounted for 54.3% of the PVL-producing CA-MRSA, and 32.0% of USA300 strains were the ΨUSA300 variant. All PVL-producing CA-MRSA strains were susceptible to rifampicin and minocycline, whereas most remained susceptible to sulfamethoxazole trimethoprim and fosfomycin. All USA300 strains, including ΨUSA300 strains, were susceptible to gentamicin, whereas 44.4% of PVL-producing non-USA300 strains were susceptible.PVL-producing CA-MRSA infections commonly present with clinical manifestations of DSP, relapse of clinical symptoms, and intra-familial outbreaks in younger individuals without underlying diseases and, rarely, with sepsis-related complications. The increased incidence of USA300 and ΨUSA300 strains in Japan, without differences in age, sex, clinical characteristics, clinical recurrence, intra-familial outbreaks, and susceptibility to antibiotics, raises concerns regarding the possibility of the global spread of these infections. Given the susceptibility of these strains to gentamicin, nasal application of gentamicin may be a potential strategy to prevent intra-familial outbreaks and the recurrence of USA300 strains, including ΨUSA300.
Insights
Panton-Valentine leukocidin (PVL)-producing community-acquired methicillin-resistant Staphylococcus aureus (CA-MRSA), including USA300 and its ΨUSA300 variant, frequently causes skin infections in younger individuals. Gentamicin shows promise for preventing outbreaks and recurrence of these strains.
Area of Science:
- Microbiology
- Infectious Diseases
- Dermatology
Background:
- Panton-Valentine leukocidin (PVL) is a key virulence factor in community-acquired methicillin-resistant Staphylococcus aureus (CA-MRSA).
- The USA300 clone and its variant ΨUSA300 are emerging CA-MRSA strains with limited clinical and epidemiological data.
- Understanding the characteristics of PVL-producing MRSA is crucial for managing skin and soft tissue infections.
Purpose of the Study:
- To investigate the clinical and epidemiological features of PVL-producing CA-MRSA infections.
- To analyze antimicrobial susceptibility patterns of prevalent MRSA strains, including USA300 and ΨUSA300.
- To identify potential strategies for preventing PVL-producing MRSA outbreaks and recurrence.
Main Methods:
- Retrospective analysis of 65 patients with CA-MRSA skin and soft tissue infections from January 2020 to May 2024.
- Evaluation of clinical information, PVL production, MRSA strain types (USA300, ΨUSA300), and antimicrobial susceptibility.
- Comparison of clinical characteristics and outcomes between PVL-producing and non-producing MRSA infections.
Main Results:
- PVL was detected in 70.8% of CA-MRSA infections, predominantly in younger patients with deep-seated pyoderma and intra-familial outbreaks.
- USA300 strains, including the ΨUSA300 variant (32.0%), constituted 54.3% of PVL-producing CA-MRSA.
- All PVL-producing CA-MRSA strains were susceptible to rifampicin and minocycline; USA300 and ΨUSA300 strains showed universal susceptibility to gentamicin.
Conclusions:
- PVL-producing CA-MRSA, particularly USA300 and ΨUSA300, are associated with specific clinical presentations like deep-seated pyoderma and intra-familial spread in younger populations.
- The increasing prevalence of these strains in Japan warrants concern for potential global dissemination.
- Nasal gentamicin application is proposed as a preventive strategy against intra-familial outbreaks and recurrence due to high susceptibility.
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