Competence remodels the pneumococcal cell wall exposing key surface virulence factors that mediate increased host adherence.

Détails

Ressource 1Télécharger: pbio.3001990.pdf (2460.91 [Ko])
Etat: Public
Version: Final published version
Licence: CC BY 4.0
ID Serval
serval:BIB_4DECE69353E7
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Competence remodels the pneumococcal cell wall exposing key surface virulence factors that mediate increased host adherence.
Périodique
PLoS biology
Auteur⸱e⸱s
Minhas V., Domenech A., Synefiaridou D., Straume D., Brendel M., Cebrero G., Liu X., Costa C., Baldry M., Sirard J.C., Perez C., Gisch N., Hammerschmidt S., Håvarstein L.S., Veening J.W.
ISSN
1545-7885 (Electronic)
ISSN-L
1544-9173
Statut éditorial
Publié
Date de publication
01/2023
Peer-reviewed
Oui
Volume
21
Numéro
1
Pages
e3001990
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: epublish
Résumé
Competence development in the human pathogen Streptococcus pneumoniae controls several features such as genetic transformation, biofilm formation, and virulence. Competent bacteria produce so-called "fratricins" such as CbpD that kill noncompetent siblings by cleaving peptidoglycan (PGN). CbpD is a choline-binding protein (CBP) that binds to phosphorylcholine residues found on wall and lipoteichoic acids (WTA and LTA) that together with PGN are major constituents of the pneumococcal cell wall. Competent pneumococci are protected against fratricide by producing the immunity protein ComM. How competence and fratricide contribute to virulence is unknown. Here, using a genome-wide CRISPRi-seq screen, we show that genes involved in teichoic acid (TA) biosynthesis are essential during competence. We demonstrate that LytR is the major enzyme mediating the final step in WTA formation, and that, together with ComM, is essential for immunity against CbpD. Importantly, we show that key virulence factors PspA and PspC become more surface-exposed at midcell during competence, in a CbpD-dependent manner. Together, our work supports a model in which activation of competence is crucial for host adherence by increased surface exposure of its various CBPs.
Mots-clé
Humans, Streptococcus pneumoniae/genetics, Virulence Factors/genetics, Virulence Factors/metabolism, N-Acetylmuramoyl-L-alanine Amidase/chemistry, N-Acetylmuramoyl-L-alanine Amidase/genetics, N-Acetylmuramoyl-L-alanine Amidase/metabolism, Choline/metabolism, Cell Wall/metabolism, Bacterial Proteins/metabolism
Pubmed
Web of science
Open Access
Oui
Création de la notice
07/03/2023 10:21
Dernière modification de la notice
20/04/2023 7:10
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