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Updated: May 14, 2026

A Fluorescence-based Method to Study Bacterial Gene Regulation in Infected Tissues
Published on: February 19, 2019
Virulence gene and expression analysis of community-associated methicillin-resistant Staphylococcus aureus causing
Wei-Chun Hung1, Hiromitsu Mori, Sayaka Tsuji
1Division of Bacteriology, Department of Infectious Disease Control and International Medicine, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Abstract:
Iliopsoas abscesses (IPAs) from methicillin-resistant Staphylococcus aureus (MRSA) are rare; however, IPAs from community-associated MRSA (CA-MRSA) may be increasing. In Japan, we previously described an adolescent athlete case of Panton-Valentine leukocidin (PVL)-positive ST30 CA-MRSA (strain NN12). In this study, we describe an IPA and discitis case from a variant of the successful PVL-negative CA-MRSA clone (ST8 CA-MRSA/J) in Japan. The patient was a 62-year-old man with intractable eczema, who had been diagnosed with IPAs and discitis (L1-L2). CA-MRSA (strain NN55) was isolated from blood, pus, and joint fluid. The invasive infections seemed to have originated in his intractable eczema, and the characteristics of this case, systemic myalgia and marked thrombocytopenia, seemed to have been caused by an exotoxin. Molecular genetic analysis revealed that NN55 possessed genotype ST8/spa606(t1767)/agr1/CoaIII and SCCmecIV of a novel subtype (encoding new cell-wall-anchored surface protein/J [CWASP/J]), exhibited enhanced expression of the cytolytic peptide genes, psmα and hld, and was resistant to gentamicin (caused by aacA-aphD), similar to ST8 CA-MRSA/J; however, NN55 lacked pathogenicity island SaPIj50 [carrying tst, encoding toxic shock syndrome toxin-1 (TSST-1)] of ST8 CA-MRSA/J, suggesting a variant (ST8 CA-MRSA/Jv). Strains NN12 and NN55 both caused bacteremia, IPAs, and adjacent musculoskeletal infections, preceded by intractable skin infections, and possessed high potential for adherence and enhanced expression of psmα and hld. The data suggest the role of a combination of CA-MRSA adhesin/cytolytic peptides (not PVL or TSST-1) in the pathogenesis of IPAs (and perhaps of systemic myalgia and marked thrombocytopenia).
Insights
Community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA) can cause rare iliopsoas abscesses (IPAs). This study identifies a novel CA-MRSA strain variant responsible for IPA and discitis, linked to skin infections and exotoxin-mediated symptoms.
Area of Science:
- Infectious Diseases
- Microbiology
- Genetics
Background:
- Iliopsoas abscesses (IPAs) caused by methicillin-resistant Staphylococcus aureus (MRSA) are uncommon, but community-associated MRSA (CA-MRSA) strains may be emerging as a cause.
- Previous reports in Japan documented CA-MRSA strains in adolescent athletes, highlighting the potential for diverse clinical presentations.
- Intractable skin conditions can serve as a potential entry point for invasive bacterial infections.
Observation:
- A 62-year-old man with severe eczema developed IPAs and discitis (L1-L2).
- CA-MRSA strain NN55 was isolated from blood, pus, and joint fluid, suggesting an origin from the patient's eczema.
- The patient presented with systemic myalgia and severe thrombocytopenia, potentially due to an exotoxin.
Findings:
- Strain NN55, a variant of ST8 CA-MRSA/J (ST8 CA-MRSA/Jv), was identified. It possesses specific genetic markers, including a novel subtype of SCCmecIV encoding CWASP/J.
- NN55 exhibited enhanced expression of cytolytic peptide genes (psmα and hld) and gentamicin resistance.
- Unlike other ST8 strains, NN55 lacked the SaPIj50 island encoding toxic shock syndrome toxin-1 (TSST-1).
Implications:
- The findings suggest that CA-MRSA strains, through adhesins and cytolytic peptides (excluding PVL and TSST-1), play a significant role in the pathogenesis of IPAs.
- This study highlights the potential for CA-MRSA to cause severe musculoskeletal infections originating from skin infections.
- The specific mechanisms causing systemic myalgia and thrombocytopenia in this case warrant further investigation.
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