Adaptive change inferred from genomic population analysis of the ST93 epidemic clone of community-associated methicillin-resistant Staphylococcus aureus

Community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA) has emerged as a major public health problem around the world. In Australia, ST93-IV[2B] is the dominant CA-MRSA clone and displays significantly greater virulence than other S. aureus. Here, we have examined the evolution of ST93 via genomic analysis of 12MSSA and 44MRSAST93 isolates, collected from around Australia over a 17-year period. Comparative analysis revealed a core genome of 2.6Mb, sharing greater than 99.7% nucleotide identity. The accessory genome was 0.45Mb and comprised additional mobile DNA elements, harboring resistance to erythromycin, trimethoprim, and tetracycline. Phylogenetic inference revealed amolecular clock and suggested that a single clone of methicillin susceptible, Panton-Valentine leukocidin (PVL) positive, ST93 S. aureus likely spread from North Western Australia in the early 1970s, acquiring methicillin resistance at least twice in the mid 1990s. We also explored associations between genotype and important MRSA phenotypes including oxacillin MIC and production of exotoxins (a-hemolysin [Hla], d-hemolysin [Hld], PSMa3, and PVL). High-level expression of Hla is a signature feature of ST93 and reduced expression in eight isolates was readily explained by mutations in the agr locus. However, subtle but significant decreases in Hldwere also noted over time that coincided with decreasing oxacillin resistance and were independent of agr mutations. The evolutionof ST93 S. aureus is thus associated with a reductionin both exotoxin expression and oxacillin MIC, suggesting MRSA ST93 isolates are under pressure for adaptive change