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Title Understanding host plant susceptibility and resistance by indexing and deploying obligate pathogen effectors
   
Acronym Effectoromics
   
Duration 1 June 2007 - 1 June 2010
   
Project leader Jim Beynon, HRI University of Warwick, UK
   

Other project participants

Jane Parker, Max Planck Institute for Plant Breeding Research, Germany
Guido van den Ackerveken, Utrecht University, The Netherlands
Jonathan Jones, John Innes Centre, United Kingdom

  
Funding The German Research Foundation (DFG), Germany
  Netherlands Genomics Initiative / Netherlands Organisation for Scientific Research (NGI/NWO), The Netherlands
  Biotechnological and Biological Sciences Research Council (BBSRC), United Kingdom
   
Total granted budget  € 1,295,221
   
Abstract  

Plant pathogens cause huge crop losses worldwide and cause much human suffering. Recent studies on plant pathogen interactions have revealed that pathogens introduce proteins (pathogenicity effectors) into the host plant to suppress host immune responses. These effectors allow the pathogen to grow and damage the plant. Analysis of the genomes of a group of very important pathogens called the oomycetes, which includes Phyptophthora infestans the causal agent of potato blight, has revealed that they contain massive arsenals of these effector proteins. We have identified and isolated 100 such effector genes from Hyaloperonospora arabidopsidis (Hpat) which infects the model plant Arabidopsis. By delivering these one at a time to the plant we have shown that more than 50% are capable of altering the hosts ability to defend against pathogens. We are now selecting a small number of these with which to identify the host targets to understand how they allow pathogen growth and developement on the host plant. The long term goal of the project would be to develop novel methods to block pathogen growth.

   
 
 
Figure 1 Arabidopsis thaliana ecotype Col-0 infected with Pseudomonas syringae DC3000-LUX delivering a Hyaloperonospora arabidopsidis effector. This oomycete effector suppresses plant defenses increasing the natural virulence of the bacterial pathogen. The bacterial growth is measured via the increase in the Luminescence of the bacteria in planta.