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Cross Talk between Type III Secretion and Flagellar Assembly Systems in Pseudomonas aeruginosa
Author(s) -
Chantal Soscia,
Abderrahman Hachani,
Alain Bernadac,
Alain Filloux,
Sophie Bleves
Publication year - 2007
Publication title -
journal of bacteriology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.652
H-Index - 246
eISSN - 1067-8832
pISSN - 0021-9193
DOI - 10.1128/jb.01677-06
Subject(s) - flagellum , biology , effector , type three secretion system , secretion , regulator , pseudomonas aeruginosa , motility , virulence , microbiology and biotechnology , mutant , strain (injury) , gene , bacteria , genetics , biochemistry , anatomy
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 (ΔfliC ) presented a hyperefficient T3SS and a nonmotile strain assembling flagella (ΔmotAB ) did not. More intriguingly, a strain lackingmotCD 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 nonmotileP. 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 agacA 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.

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