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Chronic Staphylococcus aureus Lung Infection Correlates With Proteogenomic and Metabolic Adaptations Leading to an Increased Intracellular Persistence.
Tan, Xin; Coureuil, Mathieu; Ramond, Elodie; Euphrasie, Daniel; Dupuis, Marion; Tros, Fabiola; Meyer, Julie; Nemazanyy, Ivan; Chhuon, Cerina; Guerrera, Ida Chiara; Ferroni, Agnes; Sermet-Gaudelus, Isabelle; Nassif, Xavier; Charbit, Alain; Jamet, Anne.
Afiliación
  • Tan X; Université Paris Descartes, INSERM U1151 - CNRS UMR 8253, Institut Necker-Enfants Malades. Team: Pathogenesis of Systemic Infections, Paris, France.
  • Coureuil M; Université Paris Descartes, INSERM U1151 - CNRS UMR 8253, Institut Necker-Enfants Malades. Team: Pathogenesis of Systemic Infections, Paris, France.
  • Ramond E; Université Paris Descartes, INSERM U1151 - CNRS UMR 8253, Institut Necker-Enfants Malades. Team: Pathogenesis of Systemic Infections, Paris, France.
  • Euphrasie D; Université Paris Descartes, INSERM U1151 - CNRS UMR 8253, Institut Necker-Enfants Malades. Team: Pathogenesis of Systemic Infections, Paris, France.
  • Dupuis M; Université Paris Descartes, INSERM U1151 - CNRS UMR 8253, Institut Necker-Enfants Malades. Team: Pathogenesis of Systemic Infections, Paris, France.
  • Tros F; Université Paris Descartes, INSERM U1151 - CNRS UMR 8253, Institut Necker-Enfants Malades. Team: Pathogenesis of Systemic Infections, Paris, France.
  • Meyer J; Université Paris Descartes, INSERM U1151 - CNRS UMR 8253, Institut Necker-Enfants Malades. Team: Pathogenesis of Systemic Infections, Paris, France.
  • Nemazanyy I; Plateforme d'étude du métabolisme, Structure Fédérative de Recherche INSERM US24/CNRS UMS3633, Paris, France.
  • Chhuon C; Plateforme Protéome Institut Necker-Enfants Malades, PPN, Structure Fédérative de Recherche SFR Necker, University Paris Descartes, Paris, France.
  • Guerrera IC; Proteomics platform 3P5-Necker, Université Paris Descartes - Structure Fédérative de Recherche Necker, INSERM US24/CNRS UMS3633, Paris, France.
  • Ferroni A; Laboratoire de Microbiologie de l'hopital Necker, University Paris Descartes, Paris, France.
  • Sermet-Gaudelus I; Université Paris Descartes, INSERM U1151 - CNRS UMR 8253, Institut Necker-Enfants Malades. Team: Canalopathies épithéliales: la mucoviscidose et autres maladies, Paris, France.
  • Nassif X; Université Paris Descartes, INSERM U1151 - CNRS UMR 8253, Institut Necker-Enfants Malades. Team: Pathogenesis of Systemic Infections, Paris, France.
  • Charbit A; Université Paris Descartes, INSERM U1151 - CNRS UMR 8253, Institut Necker-Enfants Malades. Team: Pathogenesis of Systemic Infections, Paris, France.
  • Jamet A; Université Paris Descartes, INSERM U1151 - CNRS UMR 8253, Institut Necker-Enfants Malades. Team: Pathogenesis of Systemic Infections, Paris, France.
Clin Infect Dis ; 69(11): 1937-1945, 2019 11 13.
Article en En | MEDLINE | ID: mdl-30753350
ABSTRACT

BACKGROUND:

Chronic lung infection in cystic fibrosis (CF) patients by Staphylococcus aureus is a well-established epidemiological fact. Indeed, S. aureus is the most commonly identified pathogen in the lungs of CF patients. Improving our understanding of the mechanisms associated with the persistence of S. aureus is therefore an important issue.

METHODS:

We selected pairs of sequential S. aureus isolates from 3 patients with CF and from 1 patient with non-CF chronic lung disease. We used a combination of genomic, proteomic, and metabolomic approaches with functional assays for in-depth characterization of S. aureus long-term persistence.

RESULTS:

In this study, we show that late S. aureus isolates from CF patients have an increased ability for intracellular survival in CF bronchial epithelial-F508del cells compared to ancestral early isolates. Importantly, the increased ability to persist intracellularly was confirmed for S. aureus isolates within the own-patient F508del epithelial cells. An increased ability to form biofilm was also demonstrated. Furthermore, we identified the underlying genetic modifications that induce altered protein expression profiles and notable metabolic changes. These modifications affect several metabolic pathways and virulence regulators that could constitute therapeutic targets.

CONCLUSIONS:

Our results strongly suggest that the intracellular environment might constitute an important niche of persistence and relapse necessitating adapted antibiotic treatments.
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Texto completo: 1 Colección: 01-internacional Asunto principal: Staphylococcus aureus Límite: Humans Idioma: En Revista: Clin Infect Dis Asunto de la revista: DOENCAS TRANSMISSIVEIS Año: 2019 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Asunto principal: Staphylococcus aureus Límite: Humans Idioma: En Revista: Clin Infect Dis Asunto de la revista: DOENCAS TRANSMISSIVEIS Año: 2019 Tipo del documento: Article País de afiliación: Francia