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The BDSF quorum sensing receptor RpfR regulates Bep exopolysaccharide synthesis in Burkholderia cenocepacia via interaction with the transcriptional regulator BerB
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 4662849
Author(s) Steiner, Elisabeth; Shilling, Rebecca E.; Richter, Anja M.; Schmid, Nadine; Fazli, Mustafa; Kaever, Volkhard; Jenal, Urs; Tolker-Nielsen, Tim; Eberl, Leo
Author(s) at UniBasel Jenal, Urs
Year 2022
Title The BDSF quorum sensing receptor RpfR regulates Bep exopolysaccharide synthesis in Burkholderia cenocepacia via interaction with the transcriptional regulator BerB
Journal NPJ biofilms and microbiomes
Volume 8
Number 1
Pages / Article-Number 93
Mesh terms Burkholderia cenocepacia, genetics, metabolism; Quorum Sensing, genetics; Burkholderia; Phosphoric Diester Hydrolases
Abstract The polysaccharide Bep is essential for in vitro biofilm formation of the opportunistic pathogen Burkholderia cenocepacia. We found that the Burkholderia diffusible signaling factor (BDSF) quorum sensing receptor RpfR is a negative regulator of the bep gene cluster in B. cenocepacia. An rpfR mutant formed wrinkled colonies, whereas additional mutations in the bep genes or known bep regulators like berA and berB restored the wild-type smooth colony morphology. We found that there is a good correlation between intracellular c-di-GMP levels and bep expression when the c-di-GMP level is increased or decreased through ectopic expression of a diguanylate cyclase or a c-di-GMP phosphodiesterase, respectively. However, when the intracellular c-di-GMP level is changed by site directed mutagenesis of the EAL or GGDEF domain of RpfR there is no correlation between intracellular c-di-GMP levels and bep expression. Except for rpfR, deletion mutants of all 25 c-di-GMP phosphodiesterase and diguanylate cyclase genes encoded by B. cenocepacia showed no change to berA and bep gene expression. Moreover, bacterial two-hybrid assays provided evidence that RpfR and BerB physically interact and give specificity to the regulation of the bep genes. We suggest a model where RpfR binds BerB at low c-di-GMP levels to sequester this RpoN-dependent activator to an RpfR/RpfF complex. If the c-di-GMP levels rise, possibly by the enzymatic action of RpfR, BerB binds c-di-GMP and is released from the RpfR/RpfF complex and associates with RpoN to activate transcription of berA, and the BerA protein subsequently activates transcription of the bep genes.
Publisher Nature Research
ISSN/ISBN 2055-5008
edoc-URL https://edoc.unibas.ch/93699/
Full Text on edoc Available
Digital Object Identifier DOI 10.1038/s41522-022-00356-2
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/36418316
ISI-Number WOS:000886968000001
Document type (ISI) Journal Article
 
   

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