Niche-specific genome degradation and convergent evolution shaping <i>Staphylococcus aureus</i> adaptation during severe infections.

Abstract

During severe infections, <i>Staphylococcus aureus</i> moves from its colonising sites to blood and tissues and is exposed to new selective pressures, thus, potentially driving adaptive evolution. Previous studies have shown the key role of the <i>agr</i> locus in <i>S. aureus</i> pathoadaptation; however, a more comprehensive characterisation of genetic signatures of bacterial adaptation may enable prediction of clinical outcomes and reveal new targets for treatment and prevention of these infections. Here, we measured adaptation using within-host evolution analysis of 2590 <i>S</i>. <i>aureus</i> genomes from 396 independent episodes of infection. By capturing a comprehensive repertoire of single nucleotide and structural genome variations, we found evidence of a distinctive evolutionary pattern within the infecting populations compared to colonising bacteria. These invasive strains had up to 20-fold enrichments for genome degradation signatures and displayed significantly convergent mutations in a distinctive set of genes, linked to antibiotic response and pathogenesis. In addition to <i>agr</i>-mediated adaptation, we identified non-canonical, genome-wide significant loci including <i>sucA-sucB</i> and <i>stp1</i>. The prevalence of adaptive changes increased with infection extent, emphasising the clinical significance of these signatures. These findings provide a high-resolution picture of the molecular changes when <i>S. aureus</i> transitions from colonisation to severe infection and may inform correlation of infection outcomes with adaptation signatures.