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Dissection of Bacterial Wilt on Medicago truncatula Revealed Two Type III Secretion System Effectors Acting on Root Infection Process and Disease Development^[C],[W],[OA]

Université de Toulouse, INPT, Laboratoire Symbiose et Pathologie des Plantes, ENSAT, BP 31607 Auzeville-Tolosane, 31326 Castanet-Tolosan, France (M.T., M.-J.T., F.V., L.G., M.-F.J.); Surfaces Cellulaires et Signalisation chez les Végétaux, UPS-CNRS UMR 5546, 31326 Castanet-Tolosan, France (A.J.); and Laboratoire des Interactions Plantes Microorganismes, INRA/CNRS UMR 441/2594, 31326 Castanet-Tolosan, France (S.G.)

Ralstonia solanacearum is the causal agent of the devastating bacterial wilt disease, which colonizes susceptible Medicago truncatula via the intact root tip. Infection involves four steps: appearance of root tip symptoms, root tip cortical cell invasion, vessel colonization, and foliar wilting. We examined this pathosystem by in vitro inoculation of intact roots of susceptible or resistant M. truncatula with the pathogenic strain GMI1000. The infection process was type III secretion system dependent and required two type III effectors, Gala7 and AvrA, which were shown to be involved at different stages of infection. Both effectors were involved in development of root tip symptoms, and Gala7 was the main determinant for bacterial invasion of cortical cells. Vessel invasion depended on the host genetic background and was never observed in the resistant line. The invasion of the root tip vasculature in the susceptible line caused foliar wilting. The avrA mutant showed reduced aggressiveness in all steps of the infection process, suggesting a global role in R. solanacearum pathogenicity. The roles of these two effectors in subsequent stages were studied using an assay that bypassed the penetration step; with this assay, the avrA mutant showed no effect compared with the GMI1000 strain, indicating that AvrA is important in early stages of infection. However, later disease symptoms were reduced in the gala7 mutant, indicating a key role in later stages of infection.

^[C] Some figures in this article are displayed in color online but in black and white in the print edition.

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www.plantphysiol.org/cgi/doi/10.1104/pp.109.141523

^* Corresponding author; e-mail jardinaud{at}ensat.fr.

Received May 15, 2009; accepted May 28, 2009; published June 3, 2009.