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Dual input control : activation of the Bartonella henselae VirB/D4 type IV secretion system by the stringent sigma factor RpoH1 and the BatR/BatS two-component system
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 2790366
Author(s) Québatte, Maxime; Dick, Mathias S.; Kaever, Volkhard; Schmidt, Alexander; Dehio, Christoph
Author(s) at UniBasel Schmidt, Alexander
Dehio, Christoph
Québatte, Maxime
Dick, Mathias
Year 2013
Year: comment (Nov)
Title Dual input control : activation of the Bartonella henselae VirB/D4 type IV secretion system by the stringent sigma factor RpoH1 and the BatR/BatS two-component system
Journal Molecular microbiology
Volume 90
Number 4
Pages / Article-Number 756-75
Keywords (p)ppGpp, DksA, SpoT, pathogenicity, stringent response (SR)
Mesh terms Bacterial Proteins, metabolism; Bacterial Secretion Systems; Bartonella henselae, pathogenicity; Gene Expression Regulation, Bacterial; Host-Pathogen Interactions; Mutagenesis; Proteomics; Sigma Factor, metabolism; Signal Transduction; Virulence Factors, metabolism
Abstract The co-ordinated expression of virulence factors is a critical process for any bacterial pathogen to colonize its host. Here we investigated the mechanisms of niche adaptation of the zoonotic pathogen Bartonella henselae by combining genetic approaches and shotgun proteomics. We demonstrated that expression of the VirB/D4 type IV secretion system (T4SS) and its secreted effector proteins require the alternative sigma factor RpoH1, which levels are controlled by the stringent response (SR) components DksA and SpoT. The RpoH1-dependent activation requires an active BatR/BatS two-component system (TCS) while BatR expression is controlled by RpoH1 and the SR components. Deletion of spoT results in a strong attenuation of VirB/D4 T4SS expression whereas dksA, rpoH1 or batR deletion fully abolishes its activity. In contrast to their activating effect on the VirB/D4 T4SS, which is critical at the early stage of host infection, SpoT and DksA negatively regulate the Trw T4SS, which mediates host-specific erythrocyte infection at a later stage of the colonization process. Our findings support a model where the SR signalling and the physiological pH-induced BatR/BatS TCS conjointly control the spatiotemporal expression of B. henselae adaptation factors during host infection.
Publisher Blackwell
ISSN/ISBN 0950-382X
edoc-URL http://edoc.unibas.ch/dok/A6328962
Full Text on edoc No
Digital Object Identifier DOI 10.1111/mmi.12396
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/24033511
ISI-Number WOS:000330108000007
Document type (ISI) Journal Article
 
   

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