Activity of the Bacillus thuringiensisNprRNprX cellcell communication system is co-ordinated to the physiological stage through a complex transcriptional regulation

被引:27
作者
Dubois, Thomas [1 ,2 ]
Perchat, Stephane [1 ,2 ]
Verplaetse, Emilie [1 ,2 ]
Gominet, Myriam [3 ]
Lemy, Christelle [1 ,2 ]
Aumont-Nicaise, Magali [4 ]
Grenha, Rosa [5 ]
Nessler, Sylvie [4 ,5 ]
Lereclus, Didier [1 ,2 ]
机构
[1] INRA, Micalis UMR1319, F-78280 La Miniere, Guyancourt, France
[2] AgroParisTech, Micalis UMR1319, F-78350 Jouy En Josas, France
[3] Inst Pasteur, CNRS URA2172, Unite Biol Bacteries Pathogenes Gram Positif, F-75015 Paris, France
[4] Univ Paris 11, CNRS UMR8619, Inst Biochim & Biophys Mol & Cellulaire, F-91400 Orsay, France
[5] CNRS, UPR 3082, Lab Enzymol & Biochim Struct, Ctr Rech Gif, F-91198 Gif Sur Yvette, France
关键词
D O I
10.1111/mmi.12168
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
NprR is a quorum sensor of the RNPP family found in bacteria of the Bacillus cereus group. In association with its cognate peptide NprX, NprR controls the expression of genes essential for survival and sporulation of Bacillus thuringiensis during its necrotrophic development in insects. Here, we report that the nprRnprX genes are not autoregulated and are co-transcribed from a sigma A-dependent promoter (PA) located upstream from nprR. The transcription from PA starts at the onset of the stationary phase and is controlled by two transcriptional regulators: CodY and PlcR. The nutritional repressor CodY represses nprRnprX transcription during the exponential growth phase and the quorum sensor PlcR activates nprRnprX transcription at the onset of stationary phase. We show that nprX is also transcribed independently of nprR from two promoters, PH and PE, dependent on the sporulation-specific sigma factors, sigma H and sigma E respectively. Both promoters ensure nprX transcription during late stationary phase while transcription from PA has decreased. These results show that the activity of the NprRNprX quorum sensing system is tightly co-ordinated to the physiological stage throughout the developmental process of the Bacillus.
引用
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页码:48 / 63
页数:16
相关论文
共 76 条
[1]  
Agaisse H., Lereclus D., Structural and functional analysis of the promoter region involved in full expression of the cryIIIA toxin gene of Bacillus thuringiensis, Mol Microbiol, 13, pp. 97-107, (1994)
[2]  
Agaisse H., Gominet M., Okstad O.A., Kolsto A.B., Lereclus D., PlcR is a pleiotropic regulator of extracellular virulence factor gene expression in Bacillus thuringiensis, Mol Microbiol, 32, pp. 1043-1053, (1999)
[3]  
Arantes O., Lereclus D., Construction of cloning vectors for Bacillus thuringiensis, Gene, 108, pp. 115-119, (1991)
[4]  
Auchtung J.M., Lee C.A., Grossman A.D., Modulation of the ComA-dependent quorum response in Bacillus subtilis by multiple Rap proteins and Phr peptides, J Bacteriol, 188, pp. 5273-5285, (2006)
[5]  
Baldus J.M., Green B.D., Youngman P., Moran Jr C.P., Phosphorylation of Bacillus subtilis transcription factor Spo0A stimulates transcription from the spoIIG promoter by enhancing binding to weak 0A boxes, J Bacteriol, 176, pp. 296-306, (1994)
[6]  
Bassler B.L., Losick R., Bacterially speaking, Cell, 125, pp. 237-246, (2006)
[7]  
Belitsky B.R., Sonenshein A.L., Genetic and biochemical analysis of CodY-binding sites in Bacillus subtilis, J Bacteriol, 190, pp. 1224-1236, (2008)
[8]  
Bongiorni C., Stoessel R., Shoemaker D., Perego M., Rap phosphatase of virulence plasmid pXO1 inhibits Bacillus anthracis sporulation, J Bacteriol, 188, pp. 487-498, (2006)
[9]  
Bouillaut L., Perchat S., Arold S., Zorrilla S., Slamti L., Henry C., Et al., Molecular basis for group-specific activation of the virulence regulator PlcR by PapR heptapeptides, Nucleic Acids Res, 36, pp. 3791-3801, (2008)
[10]  
Bravo A., Agaisse H., Salamitou S., Lereclus D., Analysis of cryIAa expression in sigE and sigK mutants of Bacillus thuringiensis, Mol Gen Genet, 250, pp. 734-741, (1996)