Genomic evolution of Staphylococcus aureus isolates colonizing the nares and progressing to bacteremia

PLoS One. 2018 May 3;13(5):e0195860. doi: 10.1371/journal.pone.0195860. eCollection 2018.

Abstract

Background: Nasal colonization by Staphylococcus aureus is a key risk factor for bacteremia. The objective of this study is to identify genomic modifications occurring in nasal carriage strains of S. aureus as they progress to bacteremia in a cohort of hospitalized patients.

Methods: Eight patients with S. aureus bacteremia were identified. Genomic sequences of the bloodstream isolates were compared with 57 nasal isolates collected longitudinally prior to the occurrence of bacteremia, which covered a timespan of up to 326 days before bacteremia.

Results: Within each subject, nasal colonizing strains were closely related to bacteremia strains. Within a subject, the number of single nucleotide polymorphisms (SNPs) observed between time points was greater than within a single time point. Co-colonization and strain replacement were observed in one case. In all cases colonization progressed to bacteremia without addition of new virulence genes. In one case, a mutation in the accessory gene regulator gene caused abrogation of agr function.

Conclusion: S. aureus evolves in the human nares at a variable rate. Progression of S. aureus nasal colonization to nosocomial infection is seldom associated with acquisition of new virulence determinants. Mutation in the agr gene with abrogation of function was associated with progression to bacteremia in one case.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Bacteremia / microbiology*
  • Bacteremia / therapy
  • Cohort Studies
  • Evolution, Molecular*
  • Female
  • Genomics*
  • Hospitalization
  • Humans
  • Male
  • Middle Aged
  • Nasal Cavity / microbiology*
  • Risk Factors
  • Staphylococcal Infections / microbiology*
  • Staphylococcal Infections / therapy
  • Staphylococcus aureus / genetics*
  • Staphylococcus aureus / physiology*

Grants and funding

This work was supported by the Department of Veterans Affairs: VA Merit Review Grant I01BX007080 to MTB (https://www.research.va.gov/services/shared_docs/resources.cfm#5). The sponsor had no role in study design; in the collection, analysis and interpretation of data; in the writing of the report; or in the decision to submit the article for publication.