Literature DB >> 19555458

The PhyR-sigma(EcfG) signalling cascade is involved in stress response and symbiotic efficiency in Bradyrhizobium japonicum.

Benjamin Gourion1, Sandra Sulser, Julia Frunzke, Anne Francez-Charlot, Philipp Stiefel, Gabriella Pessi, Julia A Vorholt, Hans-Martin Fischer.   

Abstract

PhyR is an unusual type of response regulator consisting of a receiver domain and an extracytoplasmic function (ECF) sigma factor-like domain. It was recently described as a master regulator of general stress response in Methylobacterium extorquens. Orthologues of this regulator are present in essentially all free-living Alphaproteobacteria. In most of them, phyR is genetically closely linked to a gene encoding an ECF sigma factor. Here, we investigate the role of these two regulators in the soybean symbiont Bradyrhizobium japonicum USDA110. Using deletion mutants and phenotypic assays, we showed that PhyR and the ECF sigma factor sigma(EcfG) are involved in heat shock and desiccation resistance upon carbon starvation. Both mutants had symbiotic defects on the plant hosts Glycine max (soybean) and Vigna radiata (mungbean). They induced fewer nodules than the wild type and these nodules were smaller, less pigmented, and their specific nitrogenase activity was drastically reduced 2 or 3 weeks after inoculation. Four weeks after infection, soybean nodule development caught up to a large extent whereas most mungbean nodules remained defective even 5 weeks after infection. Remarkably, both mutants triggered aberrant nodules on the different host plants with ectopically emerging roots. Microarray analysis revealed that PhyR and sigma(EcfG) control congruent regulons suggesting both regulators are part of the same signalling cascade. This finding was further substantiated by in vitro protein-protein interaction studies which are in line with a partner-switching mechanism controlling gene regulation triggered by phosphorylation of PhyR. The large number of genes of unknown function present in the PhyR/sigma(EcfG) regulon and the conspicuous symbiotic phenotype suggest that these regulators are involved in the Bradyrhizobium-legume interaction via yet undisclosed mechanisms.

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Year:  2009        PMID: 19555458     DOI: 10.1111/j.1365-2958.2009.06769.x

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  45 in total

1.  The LovK-LovR two-component system is a regulator of the general stress pathway in Caulobacter crescentus.

Authors:  Robert Foreman; Aretha Fiebig; Sean Crosson
Journal:  J Bacteriol       Date:  2012-03-09       Impact factor: 3.490

2.  Stressed by a Lov triangle.

Authors:  Silvia Ardissone; Patrick H Viollier
Journal:  J Bacteriol       Date:  2012-03-23       Impact factor: 3.490

3.  Structural basis of a protein partner switch that regulates the general stress response of α-proteobacteria.

Authors:  Julien Herrou; Grant Rotskoff; Yun Luo; Benoît Roux; Sean Crosson
Journal:  Proc Natl Acad Sci U S A       Date:  2012-05-01       Impact factor: 11.205

4.  Genetic divergence of bradyrhizobium strains nodulating soybeans as revealed by multilocus sequence analysis of genes inside and outside the symbiosis island.

Authors:  Xing Xing Zhang; Hui Juan Guo; Rui Wang; Xin Hua Sui; Yan Ming Zhang; En Tao Wang; Chang Fu Tian; Wen Xin Chen
Journal:  Appl Environ Microbiol       Date:  2014-03-14       Impact factor: 4.792

5.  The Brucella abortus virulence regulator, LovhK, is a sensor kinase in the general stress response signalling pathway.

Authors:  Hye-Sook Kim; Jonathan W Willett; Neeta Jain-Gupta; Aretha Fiebig; Sean Crosson
Journal:  Mol Microbiol       Date:  2014-10-19       Impact factor: 3.501

6.  Role of Sphingomonas sp. strain Fr1 PhyR-NepR-σEcfG cascade in general stress response and identification of a negative regulator of PhyR.

Authors:  Andreas Kaczmarczyk; Sébastien Campagne; Francesco Danza; Lisa C Metzger; Julia A Vorholt; Anne Francez-Charlot
Journal:  J Bacteriol       Date:  2011-09-23       Impact factor: 3.490

7.  Regulation of the Erythrobacter litoralis DSM 8509 general stress response by visible light.

Authors:  Aretha Fiebig; Lydia M Varesio; Xiomarie Alejandro Navarreto; Sean Crosson
Journal:  Mol Microbiol       Date:  2019-06-07       Impact factor: 3.501

8.  From Intracellular Bacteria to Differentiated Bacteroids: Transcriptome and Metabolome Analysis in Aeschynomene Nodules Using the Bradyrhizobium sp. Strain ORS285 bclA Mutant.

Authors:  Florian Lamouche; Anaïs Chaumeret; Ibtissem Guefrachi; Quentin Barrière; Olivier Pierre; Florence Guérard; Françoise Gilard; Eric Giraud; Yves Dessaux; Bertrand Gakière; Tatiana Timchenko; Attila Kereszt; Peter Mergaert; Benoit Alunni
Journal:  J Bacteriol       Date:  2019-08-08       Impact factor: 3.490

9.  Complex two-component signaling regulates the general stress response in Alphaproteobacteria.

Authors:  Andreas Kaczmarczyk; Ramon Hochstrasser; Julia A Vorholt; Anne Francez-Charlot
Journal:  Proc Natl Acad Sci U S A       Date:  2014-11-17       Impact factor: 11.205

10.  The general stress response factor EcfG regulates expression of the C-2 hopanoid methylase HpnP in Rhodopseudomonas palustris TIE-1.

Authors:  Gargi Kulkarni; Chia-Hung Wu; Dianne K Newman
Journal:  J Bacteriol       Date:  2013-03-22       Impact factor: 3.490

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