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Journal of Bacteriology, April 2007, p. 3124-3132, Vol. 189, No. 8
0021-9193/07/$08.00+0     doi:10.1128/JB.01677-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Cross Talk between Type III Secretion and Flagellar Assembly Systems in Pseudomonas aeruginosa{triangledown}

Chantal Soscia, Abderrahman Hachani, Alain Bernadac, Alain Filloux, and Sophie Bleves*

Laboratoire d'Ingénierie des Systèmes Macromoléculaires (LISM), CNRS-IBSM-UPR9027, 31 Chemin Joseph Aiguier, 13402 Marseille Cedex 20, France

Received 30 October 2006/ Accepted 31 January 2007

Pseudomonas aeruginosa cytotoxicity is linked to a type III secretion system (T3SS) that delivers effectors into the host cell. We show here that a negative cross-control exists between T3SS and flagellar assembly. We observed that, in a strain lacking flagella, T3SS gene expression, effector secretion, and cytotoxicity were increased. Conversely, we revealed that flagellar-gene expression and motility were decreased in a strain overproducing ExsA, the T3SS master regulator. Interestingly, a nonmotile strain lacking the flagellar filament ({Delta}fliC) presented a hyperefficient T3SS and a nonmotile strain assembling flagella ({Delta}motAB) did not. More intriguingly, a strain lacking motCD genes is a flagellated strain with a slight defect in swimming. However, in this strain, T3SS gene expression was up-regulated. These results suggest that flagellar assembly and/or mobility antagonizes the T3SS and that a negative cross talk exists between these two systems. An illustration of this is the visualization by electron microscopy of T3SS needles in a nonmotile P. aeruginosa strain, needles which otherwise are not detected. The molecular basis of the cross talk is complex and remains to be elucidated, but proteins like MotCD might have a crucial role in signaling between the two processes. In addition, we found that the GacA response regulator negatively affects the T3SS. In a gacA mutant, the T3SS effector ExoS is hypersecreted. Strikingly, GacA was previously reported as a positive regulator for motility. Globally, our data document the idea that some virulence factors are coordinately but inversely regulated, depending on the bacterial colonization phase and infection types.


* Corresponding author. Mailing address: Laboratoire d'Ingénierie des Systèmes Macromoléculaires (LISM), CNRS-IBSM-UPR9027, 31 Chemin Joseph Aiguier, 13402 Marseille Cedex 20, France. Phone: 33491164126. Fax: 33491712124. E-mail: bleves{at}ibsm.cnrs-mrs.fr

{triangledown} Published ahead of print on 16 February 2007.


Journal of Bacteriology, April 2007, p. 3124-3132, Vol. 189, No. 8
0021-9193/07/$08.00+0     doi:10.1128/JB.01677-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.




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