Regulatory RNAs and the HptB/RetS signalling pathways fine-tune Pseudomonas aeruginosa pathogenesis

被引:113
作者
Bordi, Christophe [1 ]
Lamy, Marie-Cecile [1 ]
Ventre, Isabelle [1 ]
Termine, Elise [1 ]
Hachani, Abderrahman [1 ,2 ]
Fillet, Sandy [2 ]
Roche, Beatrice [1 ]
Bleves, Sophie [1 ]
Mejean, Vincent [3 ]
Lazdunski, Andree [1 ]
Filloux, Alain [1 ,2 ]
机构
[1] Univ Mediterranee, Lab Ingn Syst Macromol, UPR9027, CNRS,IMM, F-13402 Marseille 20, France
[2] Univ London Imperial Coll Sci Technol & Med, Div Cell & Mol Biol, Ctr Mol Microbiol & Infect, London SW7 2AZ, England
[3] Univ Mediterranee, Lab Chim Bacterienne, UPR9043, CNRS,IMM, F-13402 Marseille 20, France
关键词
MEDIATED MULTISTEP PHOSPHORELAY; VIBRIO-CHOLERAE; 2-COMPONENT SYSTEMS; VIRULENCE FACTORS; BIOFILM FORMATION; III SECRETION; PAO1; GENES; IDENTIFICATION; EXPRESSION;
D O I
10.1111/j.1365-2958.2010.07146.x
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
P>Bacterial pathogenesis often depends on regulatory networks, two-component systems and small RNAs (sRNAs). In Pseudomonas aeruginosa, the RetS sensor pathway downregulates expression of two sRNAs, rsmY and rsmZ. Consequently, biofilm and the Type Six Secretion System (T6SS) are repressed, whereas the Type III Secretion System (T3SS) is activated. We show that the HptB signalling pathway controls biofilm and T3SS, and fine-tunes P. aeruginosa pathogenesis. We demonstrate that RetS and HptB intersect at the GacA response regulator, which directly controls sRNAs production. Importantly, RetS controls both sRNAs, whereas HptB exclusively regulates rsmY expression. We reveal that HptB signalling is a complex regulatory cascade. This cascade involves a response regulator, with an output domain belonging to the phosphatase 2C family, and likely an anti-anti-sigma factor. This reveals that the initial input in the Gac system comes from several signalling pathways, and the final output is adjusted by a differential control on rsmY and rsmZ. This is exemplified by the RetS-dependent but HptB-independent control on T6SS. We also demonstrate a redundant action of the two sRNAs on T3SS gene expression, while the impact on pel gene expression is additive. These features underpin a novel mechanism in the fine-tuned regulation of gene expression.
引用
收藏
页码:1427 / 1443
页数:17
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