Function of BriC peptide in the pneumococcal competence and virulence portfolio.

Détails

Ressource 1Télécharger: journal.ppat.1007328.pdf (6790.95 [Ko])
Etat: Public
Version: de l'auteur⸱e
ID Serval
serval:BIB_977A8BEECDD5
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Function of BriC peptide in the pneumococcal competence and virulence portfolio.
Périodique
PLoS pathogens
Auteur⸱e⸱s
Aggarwal S.D., Eutsey R., West-Roberts J., Domenech A., Xu W., Abdullah I.T., Mitchell A.P., Veening J.W., Yesilkaya H., Hiller N.L.
ISSN
1553-7374 (Electronic)
ISSN-L
1553-7366
Statut éditorial
Publié
Date de publication
10/2018
Peer-reviewed
Oui
Volume
14
Numéro
10
Pages
e1007328
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
Publication Status: epublish
Résumé
Streptococcus pneumoniae (pneumococcus) is an opportunistic pathogen that causes otitis media, sinusitis, pneumonia, meningitis and sepsis. The progression to this pathogenic lifestyle is preceded by asymptomatic colonization of the nasopharynx. This colonization is associated with biofilm formation; the competence pathway influences the structure and stability of biofilms. However, the molecules that link the competence pathway to biofilm formation are unknown. Here, we describe a new competence-induced gene, called briC, and demonstrate that its product promotes biofilm development and stimulates colonization in a murine model. We show that expression of briC is induced by the master regulator of competence, ComE. Whereas briC does not substantially influence early biofilm development on abiotic surfaces, it significantly impacts later stages of biofilm development. Specifically, briC expression leads to increases in biofilm biomass and thickness at 72h. Consistent with the role of biofilms in colonization, briC promotes nasopharyngeal colonization in the murine model. The function of BriC appears to be conserved across pneumococci, as comparative genomics reveal that briC is widespread across isolates. Surprisingly, many isolates, including strains from clinically important PMEN1 and PMEN14 lineages, which are widely associated with colonization, encode a long briC promoter. This long form captures an instance of genomic plasticity and functions as a competence-independent expression enhancer that may serve as a precocious point of entry into this otherwise competence-regulated pathway. Moreover, overexpression of briC by the long promoter fully rescues the comE-deletion induced biofilm defect in vitro, and partially in vivo. These findings indicate that BriC may bypass the influence of competence in biofilm development and that such a pathway may be active in a subset of pneumococcal lineages. In conclusion, BriC is a part of the complex molecular network that connects signaling of the competence pathway to biofilm development and colonization.
Mots-clé
Amino Acid Sequence, Animals, Bacterial Proteins/metabolism, Biofilms/growth & development, Chinchilla, Female, Mice, Peptide Fragments/metabolism, Pneumococcal Infections/genetics, Pneumococcal Infections/metabolism, Pneumococcal Infections/microbiology, Promoter Regions, Genetic, Sequence Homology, Streptococcus pneumoniae/genetics, Streptococcus pneumoniae/growth & development, Streptococcus pneumoniae/metabolism, Virulence
Pubmed
Web of science
Open Access
Oui
Création de la notice
17/10/2018 10:38
Dernière modification de la notice
21/11/2022 9:15
Données d'usage