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The BatR/BatS two-component regulatory system controls the adaptive response of Bartonella henselae during human endothelial cell infection
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 364554
Author(s) Quebatte, Maxime; Dehio, Michaela; Tropel, David; Basler, Andrea; Toller, Isabella; Raddatz, Guenter; Engel, Philipp; Huser, Sonja; Schein, Hermine; Lindroos, Hillevi L.; Andersson, Siv G. E.; Dehio, Christoph
Author(s) at UniBasel Dehio, Christoph
Québatte, Maxime
Engel, Philipp
Year 2010
Title The BatR/BatS two-component regulatory system controls the adaptive response of Bartonella henselae during human endothelial cell infection
Journal Journal of bacteriology
Volume 192
Number 13
Pages / Article-Number 3352-3367
Abstract Here, we report the first comprehensive study of Bartonella henselae gene expression during infection of human endothelial cells. Expression of the main cluster of upregulated genes, comprising the VirB type IV secretion system and its secreted protein substrates, is shown to be under the positive control of the transcriptional regulator BatR. We demonstrate binding of BatR to the promoters of the virB operon and a substrate-encoding gene and provide biochemical evidence that BatR and BatS constitute a functional two-component regulatory system. Moreover, in contrast to the acid-inducible (pH 5.5) homologs ChvG/ChvI of Agrobacterium tumefaciens, BatR/BatS are optimally activated at the physiological pH of blood (pH 7.4). By conservation analysis of the BatR regulon, we show that BatR/BatS are uniquely adapted to upregulate a genus-specific virulence regulon during hemotropic infection in mammals. Thus, we propose that BatR/BatS two-component system homologs represent vertically inherited pH sensors that control the expression of horizontally transmitted gene sets critical for the diverse host-associated life styles of the alphaproteobacteria.
Publisher American Society for Microbiology
ISSN/ISBN 1098-5530
edoc-URL http://edoc.unibas.ch/dok/A5839843
Full Text on edoc Available
Digital Object Identifier DOI 10.1128/JB.01676-09
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/20418395
ISI-Number WOS:000278806100015
Document type (ISI) Article
 
   

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