Exopolyphosphatase of Pseudomonas aeruginosa is essential for the production of virulence factors, and its expression is controlled by NtrC and PhoB acting at two interspaced promoters

被引:21
作者
Gallarato, Lucas A. [1 ]
Sanchez, Diego G. [1 ]
Olvera, Leticia [2 ]
Primo, Emiliano D. [1 ]
Garrido, Monica N. [1 ]
Beassoni, Paola R. [1 ]
Morett, Enrique [2 ]
Lisa, Angela T. [1 ]
机构
[1] Univ Nacl Rio Cuarto, FCEFQyN, Dept Biol Mol, RA-5800 Rio Cuarto, Cordoba, Argentina
[2] Univ Nacl Autonoma Mexico, Inst Biotecnol, Dept Ingn Celular & Biocatalisis, Cuernavaca 62210, Morelos, Mexico
来源
MICROBIOLOGY-SGM | 2014年 / 160卷
关键词
INORGANIC POLYPHOSPHATE; ESCHERICHIA-COLI; PHOSPHORYLCHOLINE PHOSPHATASE; FLUORESCENS PF0-1; PHOSPHOLIPASE-C; GENE; KINASE; TRANSCRIPTION; REGULATOR; SIGMA(54);
D O I
10.1099/mic.0.074773-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The exopolyphosphatase (Ppx) of Pseudomonas aeruginosa is encoded by the PA5241 gene (ppx). Ppx catalyses the hydrolysis of inorganic polyphosphates to orthophosphate (P-i). In the present work, we identified and characterized the promoter region of ppx and its regulation under environmental stress conditions. The role of Ppx in the production of several virulence factors was demonstrated through studies performed on a ppx null mutant. We found that ppx is under the control of two interspaced promoters, dually regulated by nitrogen and phosphate limitation. Under nitrogen-limiting conditions, its expression was controlled from a sigma(54)-dependent promoter activated by the response regulator NtrC. However, under P-i limitation, the expression was controlled from a sigma(70) promoter, activated by PhoB. Results obtained from the ppx null mutant demonstrated that Ppx is involved in the production of virulence factors associated with both acute infection (e.g. motility-promoting factors, blue/green pigment production, C6-C12 quorum-sensing homoserine lactones) and chronic infection (e.g. rhamnolipids, biofilm formation). Molecular and physiological approaches used in this study indicated that P. aeruginosa maintains consistently proper levels of Ppx regardless of environmental conditions. The precise control of ppx expression appeared to be essential for the survival of P. aeruginosa and the occurrence of either acute or chronic infection in the host.
引用
收藏
页码:406 / 417
页数:12
相关论文
共 58 条
[1]   Polyphosphate - an ancient energy source and active metabolic regulator [J].
Achbergerova, Lucia ;
Nahalka, Jozef .
MICROBIAL CELL FACTORIES, 2011, 10
[2]  
AKIYAMA M, 1993, J BIOL CHEM, V268, P633
[3]  
[Anonymous], 2012, Molecular Cloning: A Laboratory Manual
[4]  
Ault-Riché D, 1998, J BACTERIOL, V180, P1841
[5]   Compilation and analysis of σ54-dependent promoter sequences [J].
Barrios, H ;
Valderrama, B ;
Morett, E .
NUCLEIC ACIDS RESEARCH, 1999, 27 (22) :4305-4313
[6]   Using a molecular model and kinetic experiments in the presence of divalent cations to study the active site and catalysis of Pseudomonas aeruginosa phosphorylcholine phosphatase [J].
Beassoni, Paola R. ;
Otero, Lisandro H. ;
Lisa, Angela T. ;
Domenech, Carlos E. .
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS, 2008, 1784 (12) :2038-2044
[7]   The structure of a transcription activation subcomplex reveals how σ70 is recruited to PhoB promoters [J].
Blanco, Alexandre G. ;
Canals, Albert ;
Bernues, Jordi ;
Sola, Maria ;
Coll, Miquel .
EMBO JOURNAL, 2011, 30 (18) :3776-3785
[8]   Rhamnolipids modulate swarming motility patterns of Pseudomonas aeruginosa [J].
Caiazza, NC ;
Shanks, RMQ ;
O'Toole, GA .
JOURNAL OF BACTERIOLOGY, 2005, 187 (21) :7351-7361
[9]   Production of acyl-homoserine lactone quorum-sensing signals by gram-negative plant-associated bacteria [J].
Cha, C ;
Gao, P ;
Chen, YC ;
Shaw, PD ;
Farrand, SK .
MOLECULAR PLANT-MICROBE INTERACTIONS, 1998, 11 (11) :1119-1129
[10]   An improved method for rapid generation of unmarked Pseudomonas aeruginosa deletion mutants -: art. no. 30 [J].
Choi, KH ;
Schweizer, HP .
BMC MICROBIOLOGY, 2005, 5 (1)