Summary
PANDEMIC is an ambitious high-risk/high-gain program to deliver an innovative pathogen-guided strategy for crop disease resistance. The wheat blast pandemic is a clear and present danger to global food security. It is caused by the blast fungus, Magnaporthe oryzae, which, after emerging in Brazil only ~35 years ago, has spread over the last 5 years to Southeast Asia and Africa. We discovered that all isolates of the pandemic wheat blast fungus belong to a single, asexual clonal lineage. These pandemic isolates carry a supernumerary mini-chromosome (mChr) of ~2 Mb, which encodes 19 secreted effector (virulence) proteins and renders the pandemic lineage highly virulent. We propose that this mChr is the Achilles’ heel of the pandemic fungus. In PANDEMIC, my team and I will target the mChr virulence properties by gene editing and engineering of disease resistance genes that target mChr-encoded effectors. The central hypothesis of this project is, that detailed knowledge about the biophysical properties of pathogen effector-host target interactions can guide bioengineering of non-transgenic disease resistance in wheat.
To achieve our goal, we will employ a multi-disciplinary approach combining genetics, structural biology, and gene editing. Specifically, we will pursue the following objectives:
1. GENETICS. Determine the mChr-encoded effectors conferring high virulence on the pandemic wheat blast fungus.
2. BIOPHYSICS. Define the biophysical properties of effector-host target interactions.
3. IMMUNITY. Apply CRISPR/Cas gene editing to deliver innovative, non-transgenic solutions for blast disease management.
At the completion of this project, my team and I will generate a detailed understanding of the biophysical properties of mChr-encoded effector-target protein complexes and deliver novel traits and non-transgenic solutions for developing resistance against the pandemic wheat blast fungus.
To achieve our goal, we will employ a multi-disciplinary approach combining genetics, structural biology, and gene editing. Specifically, we will pursue the following objectives:
1. GENETICS. Determine the mChr-encoded effectors conferring high virulence on the pandemic wheat blast fungus.
2. BIOPHYSICS. Define the biophysical properties of effector-host target interactions.
3. IMMUNITY. Apply CRISPR/Cas gene editing to deliver innovative, non-transgenic solutions for blast disease management.
At the completion of this project, my team and I will generate a detailed understanding of the biophysical properties of mChr-encoded effector-target protein complexes and deliver novel traits and non-transgenic solutions for developing resistance against the pandemic wheat blast fungus.
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More information & hyperlinks
| Web resources: | https://cordis.europa.eu/project/id/101077853 |
| Start date: | 01-10-2023 |
| End date: | 30-09-2028 |
| Total budget - Public funding: | 1 499 999,00 Euro - 1 499 999,00 Euro |
Cordis data
Original description
PANDEMIC is an ambitious high-risk/high-gain program to deliver an innovative pathogen-guided strategy for crop disease resistance. The wheat blast pandemic is a clear and present danger to global food security. It is caused by the blast fungus, Magnaporthe oryzae, which, after emerging in Brazil only ~35 years ago, has spread over the last 5 years to Southeast Asia and Africa. We discovered that all isolates of the pandemic wheat blast fungus belong to a single, asexual clonal lineage. These pandemic isolates carry a supernumerary mini-chromosome (mChr) of ~2 Mb, which encodes 19 secreted effector (virulence) proteins and renders the pandemic lineage highly virulent. We propose that this mChr is the Achilles’ heel of the pandemic fungus. In PANDEMIC, my team and I will target the mChr virulence properties by gene editing and engineering of disease resistance genes that target mChr-encoded effectors. The central hypothesis of this project is, that detailed knowledge about the biophysical properties of pathogen effector-host target interactions can guide bioengineering of non-transgenic disease resistance in wheat.To achieve our goal, we will employ a multi-disciplinary approach combining genetics, structural biology, and gene editing. Specifically, we will pursue the following objectives:
1. GENETICS. Determine the mChr-encoded effectors conferring high virulence on the pandemic wheat blast fungus.
2. BIOPHYSICS. Define the biophysical properties of effector-host target interactions.
3. IMMUNITY. Apply CRISPR/Cas gene editing to deliver innovative, non-transgenic solutions for blast disease management.
At the completion of this project, my team and I will generate a detailed understanding of the biophysical properties of mChr-encoded effector-target protein complexes and deliver novel traits and non-transgenic solutions for developing resistance against the pandemic wheat blast fungus.
Status
SIGNEDCall topic
ERC-2022-STGUpdate Date
31-07-2023
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