Streptococcus agalactiae Capsule Polymer Length and Attachment Is Determined by the Proteins CpsABCD
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Le résumé fourni par la source
Background: The polysaccharide capsule is a major virulence factor of Streptococcus agalactiae . Results: Mutations of the genes cpsABCD result in aberrant capsule length and localization. Conclusion: The CpsABCD proteins form a system that modulates termination of capsule elongation. Significance: This work proposes a model for the unified action of CpsABCD. The production of capsular polysaccharides (CPS) or secreted exopolysaccharides is ubiquitous in bacteria, and the Wzy pathway constitutes a prototypical mechanism to produce these structures. Despite the differences in polysaccharide composition among species, a group of proteins involved in this pathway is well conserved. Streptococcus agalactiae (group B Streptococcus ; GBS) produces a CPS that represents the main virulence factor of the bacterium and is a prime target in current vaccine development. We used this human pathogen to investigate the roles and potential interdependencies of the conserved proteins CpsABCD encoded in the cps operon, by developing knock-out and functional mutant strains. The mutant strains were examined for CPS quantity, size, and attachment to the cell surface as well as CpsD phosphorylation. We observed that CpsB, -C, and -D compose a phosphoregulatory system where the CpsD autokinase phosphorylates its C-terminal tyrosines in a CpsC-dependent manner. These Tyr residues are also the target of the cognate CpsB phosphatase. An interaction between CpsD and CpsC was observed, and the phosphorylation state of CpsD influenced the subsequent action of CpsC. The CpsC extracellular domain appeared necessary for the production of high molecular weight polysaccharides by influencing CpsA-mediated attachment of the CPS to the bacterial cell surface. In conclusion, although having no impact on cps transcription or the synthesis of the basal repeating unit, we suggest that these proteins are fine-tuning the last steps of CPS biosynthesis ( i.e. the balance between polymerization and attachment to the cell wall).
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Le contrôle bibliographique ouvert
DOI retrouvé dans Crossref DOI retrouvé ; titre concordant.
- Titre Crossref
- Streptococcus agalactiae Capsule Polymer Length and Attachment Is Determined by the Proteins CpsABCD
- Date Crossref
- 01/04/2015
- Éditeur
- Elsevier BV
- Type
- journal-article
Ce recoupement confirme des métadonnées liées au DOI. Il ne confirme ni la méthode ni les conclusions de l’étude, et il ne compte pas comme une seconde source scientifique indépendante.
Où se fait cette recherche
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Novartis (Switzerland) pays non établi dans la noticeEntreprise
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Research Center From Novartis Vaccines and Diagnostics pays non établi dans la noticeStructure de recherche
Novartis (Switzerland) et From Novartis Vaccines and Diagnostics — Research Center.
Une affiliation ne permet pas de déduire la nationalité d’un auteur.