4.7 Article

Polyclonality, Shared Strains, and Convergent Evolution in Chronic Cystic Fibrosis Staphylococcus aureus Airway Infection

Journal

Publisher

AMER THORACIC SOC
DOI: 10.1164/rccm.202003-0735OC

Keywords

cystic fibrosis; Staphylococcus aureus; whole-genome sequencing; molecular epidemiology; infection

Funding

  1. NIH/National Institute of General Medical Sciences [T32 GM086270-11]
  2. Cystic Fibrosis Foundation [HOFFMA16G0, SINGH19R0, SINGH15R0]
  3. NIH/National Institute of Diabetes and Digestive and Kidney Diseases [P30DK089507]
  4. NIH/NHLBI grant [K24HL141669]

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This study characterized the molecular epidemiology and genetic adaptation of Staphylococcus aureus in chronic CF airway infection, revealing that patients often carry multiple, genetically distinct S. aureus lineages with adaptations in persistence and antimicrobial resistance genes. Limited strain-sharing was identified among patients, and S. aureus genetic diversity was found to be unconstrained, suggesting the need for novel diagnostic and therapeutic approaches in the future.
Rationale: Staphylococcus aureus is the most common respiratory pathogen isolated from patients with cystic fibrosis (CF) in the United States. Although modes of acquisition and genetic adaptation have been described for Pseudomonas aeruginosa, resulting in improved diagnosis and treatment, these features remain more poorly defined for S. aureus. Objectives: Tocharacterize the molecular epidemiology and genetic adaptation of S. aureus during chronic CF airway infection and in response to antibiotic therapy. Methods: We performed whole-genome sequencing of 1,382 S. aureus isolates collected longitudinally over a mean 2.2 years from 246 children with CF at five U.S. centers between 2008 and 2017. Results were integrated with clinical and demographic data to characterize bacterial population dynamics and identify common genetic targets of in vivo adaptation. Measurements and Main Results: Results showed that 455% of patients carried multiple, coexisting S. aureus lineages, often having different antibiotic susceptibility profiles. Adaptation during the course of infection commonly occurred in a set of genes related to persistence and antimicrobial resistance. Individual sequence types demonstrated wide geographic distribution, and we identified limited strain-sharing among children linked by common household or clinical exposures. Unlike P. aeruginosa, S. aureus genetic diversity was unconstrained, with an ongoing flow of new genetic elements into the population of isolates from children with CF. Conclusions: CF airways are frequently coinfected by multiple, genetically distinct S. aureus lineages, indicating that current clinical procedures for sampling isolates and selecting antibiotics are likely inadequate. Strains can be shared by patients in close domestic or clinical contact and can undergo convergent evolution in key persistence and antimicrobial-resistance genes, suggesting novel diagnostic and therapeutic approaches for future study.

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