A distinctive dual-channel quorum-sensing system operates in Vibrio anguillarum.

Détails

ID Serval
serval:BIB_056B3A38AC1D
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
A distinctive dual-channel quorum-sensing system operates in Vibrio anguillarum.
Périodique
Molecular microbiology
Auteur⸱e⸱s
Croxatto A., Pride J., Hardman A., Williams P., Cámara M., Milton D.L.
ISSN
0950-382X (Print)
ISSN-L
0950-382X
Statut éditorial
Publié
Date de publication
06/2004
Peer-reviewed
Oui
Volume
52
Numéro
6
Pages
1677-1689
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Résumé
Many bacterial cells communicate using diffusible signal molecules to monitor cell population density via a process termed quorum sensing. In marine Vibrio species, the Vibrio harveyi-type LuxR protein is a key player in a quorum-sensing phosphorelay cascade, which controls the expression of virulence, symbiotic and survival genes. Previously, we characterized Vibrio anguillarum homologues of LuxR (VanT) and LuxMN (VanMN) and, in this study, we have identified homologues of LuxPQ (VanPQ) and LuxOU (VanOU). In contrast to other Vibrio species, vanT was expressed at low cell density and showed no significant induction as the cell number increased. In addition, although the loss of VanO increased vanT expression, the loss of VanU, unexpectedly, decreased it. Both VanN and VanQ were required for repression of vanT even in a vanU mutant, suggesting an alternative route for VanNQ signal transduction other than via VanU. VanT negatively regulated its own expression by binding and repressing the vanT promoter and by binding and activating the vanOU promoter. The signal relay results in a cellular response as expression of the metalloprotease, empA, was altered similar to that of vanT in all the mutants. Consequently, the V. anguillarum quorum-sensing phosphorelay systems work differently from those of V. harveyi and may be used to limit rather than induce vanT expression.
Mots-clé
Bacterial Proteins/genetics, Bacterial Proteins/metabolism, DNA, Bacterial/chemistry, DNA, Bacterial/isolation & purification, Gene Expression Regulation, Bacterial, Genes, Bacterial, Genes, Reporter, Metalloproteases/biosynthesis, Molecular Sequence Data, Mutation, Phosphoproteins/genetics, Phosphotransferases/genetics, RNA, Bacterial/analysis, RNA, Messenger/analysis, Repressor Proteins/genetics, Sequence Analysis, DNA, Sequence Homology, Signal Transduction, Trans-Activators/genetics, Transcription Factors/genetics, Vibrio/genetics, Vibrio/growth & development, Vibrio/physiology, Virulence/genetics, beta-Galactosidase/metabolism
Pubmed
Web of science
Open Access
Oui
Création de la notice
24/03/2019 13:50
Dernière modification de la notice
20/08/2019 13:27
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