Author
Listed:
- Xiongqi Ding
(Université Paris Cité, INSERM UMR-S1151, CNRS UMR-S8253, Institut Necker Enfants Malades)
- Catherine Robbe-Masselot
(Université Lille, CNRS, UMR 8576 - UGSF - Unité de Glycobiologie Structurale et Fonctionnelle)
- Xiali Fu
(Université Paris Cité, INSERM UMR-S1151, CNRS UMR-S8253, Institut Necker Enfants Malades)
- Renaud Léonard
(Université Lille, CNRS, UMR 8576 - UGSF - Unité de Glycobiologie Structurale et Fonctionnelle)
- Benjamin Marsac
(Université Lille, CNRS, UMR 8576 - UGSF - Unité de Glycobiologie Structurale et Fonctionnelle)
- Charlene J. G. Dauriat
(INSERM U1016, CNRS UMR8104, Université Paris Cité, Team «Mucosal Microbiota in Chronic Inflammatory Diseases»)
- Agathe Lepissier
(Université Paris Cité, INSERM UMR-S1151, CNRS UMR-S8253, Institut Necker Enfants Malades)
- Héloïse Rytter
(Université Paris Cité, INSERM UMR-S1151, CNRS UMR-S8253, Institut Necker Enfants Malades)
- Elodie Ramond
(Genoscope, UMR8030, Laboratory of Systems & Synthetic Biology (LISSB), Xenome team)
- Marion Dupuis
(Université Paris Cité, INSERM UMR-S1151, CNRS UMR-S8253, Institut Necker Enfants Malades)
- Daniel Euphrasie
(Université Paris Cité, INSERM UMR-S1151, CNRS UMR-S8253, Institut Necker Enfants Malades)
- Iharilalao Dubail
(Université Paris Cité, INSERM UMR-S1151, CNRS UMR-S8253, Institut Necker Enfants Malades)
- Cécile Schimmich
(Physiopathology and epidemiology of equine diseases (PhEED), RD 675)
- Xiaoquan Qin
(Université Paris Cité, Institut de physique du globe de Paris, CNRS)
- Jessica Parraga
(AP-HP Centre Université de Paris Cité)
- Maria Leite-de-Moraes
(Université Paris Cité, INSERM UMR-S1151, CNRS UMR-S8253, Institut Necker Enfants Malades)
- Agnes Ferroni
(AP-HP Centre Université de Paris Cité)
- Benoit Chassaing
(INSERM U1016, CNRS UMR8104, Université Paris Cité, Team «Mucosal Microbiota in Chronic Inflammatory Diseases»)
- Isabelle Sermet-Gaudelus
(Université Paris Cité, INSERM UMR-S1151, CNRS UMR-S8253, Institut Necker Enfants Malades)
- Alain Charbit
(Université Paris Cité, INSERM UMR-S1151, CNRS UMR-S8253, Institut Necker Enfants Malades)
- Mathieu Coureuil
(Université Paris Cité, INSERM UMR-S1151, CNRS UMR-S8253, Institut Necker Enfants Malades)
- Anne Jamet
(Université Paris Cité, INSERM UMR-S1151, CNRS UMR-S8253, Institut Necker Enfants Malades
AP-HP Centre Université de Paris Cité)
Abstract
Staphylococcus aureus is a predominant cause of chronic lung infections. While the airway environment is rich in highly sialylated mucins, the interaction of S. aureus with sialic acid is poorly characterized. Using S. aureus USA300 as well as clinical isolates, we demonstrate that quorum-sensing dysfunction, a hallmark of S. aureus adaptation, correlates with a greater ability to consume free sialic acid, providing a growth advantage in an air-liquid interface model and in vivo. Furthermore, RNA-seq experiment reveals that free sialic acid triggers transcriptional reprogramming promoting S. aureus chronic lifestyle. To support the clinical relevance of our results, we show the co-occurrence of S. aureus, sialidase-producing microbiota and free sialic acid in the airway of patients with cystic fibrosis. Our findings suggest a dual role for sialic acid in S. aureus airway infection, triggering virulence reprogramming and driving S. aureus adaptive strategies through the selection of quorum-sensing dysfunctional strains.
Suggested Citation
Xiongqi Ding & Catherine Robbe-Masselot & Xiali Fu & Renaud Léonard & Benjamin Marsac & Charlene J. G. Dauriat & Agathe Lepissier & Héloïse Rytter & Elodie Ramond & Marion Dupuis & Daniel Euphrasie & , 2023.
"Airway environment drives the selection of quorum sensing mutants and promote Staphylococcus aureus chronic lifestyle,"
Nature Communications, Nature, vol. 14(1), pages 1-13, December.
Handle:
RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-43863-2
DOI: 10.1038/s41467-023-43863-2
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