4.8 Article

Niche-specific genome degradation and convergent evolution shaping Staphylococcus aureus adaptation during severe infections

Journal

ELIFE
Volume 11, Issue -, Pages -

Publisher

eLIFE SCIENCES PUBL LTD
DOI: 10.7554/eLife.77195

Keywords

within-host evolution; adaptation; Staphylococcus aureus; genomics; Other

Categories

Funding

  1. National Health and Medical Research Council [GNT1105525, GNT1196103]

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This study provides a comprehensive analysis of the genetic variations and evolutionary patterns of Staphylococcus aureus during severe infections. The findings reveal distinct evolutionary signatures and convergent mutations in genes related to antibiotic response and pathogenesis, highlighting the clinical significance of these adaptations. Non-canonical loci associated with adaptation were also identified. These results contribute to a better understanding of the molecular changes when S. aureus transitions from colonization to severe infection and may have implications for predicting clinical outcomes and developing new treatment and prevention strategies.
During severe infections, Staphylococcus aureus 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 agr locus in S. aureus 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 S. aureus 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 agr-mediated adaptation, we identified non-canonical, genome-wide significant loci including sucA-sucB and stp1. 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 S. aureus transitions from colonisation to severe infection and may inform correlation of infection outcomes with adaptation signatures.

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