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CHERI Report Summary

Project ID: 705631
Funded under: H2020-EU.1.3.2.

Periodic Reporting for period 1 - CHERI (Chromatin targeting and remodelling by bacterial effectors in plant immunity)

Reporting period: 2016-04-01 to 2018-03-31

Summary of the context and overall objectives of the project

In nature, plants are challenged by disease-causing pathogens such as viruses, bacteria and fungi. Understanding mechanisms of plant disease and disease resistance is of fundamental importance to sustainable agriculture and human health. Unlike mammals, plants lack a circulating immune system. Plants instead rely on the innate immune capacity of each cell and systemic signals that disseminate from infection sites. Successful pathogens use effectors to suppress plant immunity and cause disease. Plants have evolved disease resistance genes encoding immune receptors that perceive specific pathogen effectors to mount effector-triggered immunity. In Arabidopsis, a heteromeric pair of intracellular immune receptors forms a functional recognition complex which senses virulence activities of two structurally unrelated bacterial effectors at the nuclear chromatin. Results suggest that effector targeting of histone modifications and chromatin remodelling interferes with host basal immunity and that this is transduced by the receptor pair to activation of defence pathways. The underlying molecular mechanisms remain unclear. We have found that the two bacterial effectors interact with an overlapping set of chromatin-associated proteins and with certain immune receptor domains. We hypothesize that the effectors converge on the same chromatin machinery for promoting disease and that their actions are intercepted by the immune receptor system which is physically connected to basal immunity signalling components. By using the effectors as molecular probes, this proposal aims to elucidate how the chromatin environment is modulated during infection and how effector perturbations are converted to effective immunity.

Work performed from the beginning of the project to the end of the period covered by the report and main results achieved so far

The project was initially divided in 3 objectives. Due to shifted schedules in the experimental plan, the objective 1 and 2 have not been fully completed. However, by initiating a fourth objective, the researcher has anticipated the potential non finalization of the project and generated new data related to the field.

By establishing, designing and using innovative experiment, the project has led to a better understanding of how an immuno-receptor complex can be targeted by a bacterial effector and might modify its conformation at the chromatin level. Exciting data generated by objective 4 have brought new insights about a bacterial effector molecular function and virulence activity never suspected before. This project opens new research guidelines that could be easily followed up within a PhD thesis or postdoc project and lead to high quality scientific outputs and publications.

Progress beyond the state of the art and expected potential impact (including the socio-economic impact and the wider societal implications of the project so far)

This pioneering project which uses the model plant A. thaliana opens a novel research area in the field of plant pathology and constitutes a new research axis in Parker group. Until now, the question of the involvement of chromatin remodeling processes (often referred as “epigenetic” mechanisms) in plant defense was addressed exclusively in the frame of the transcriptional induction of defense genes. Here, the work conducted went in a totally different direction and follow the idea that upon infection a pathogen might modulate host chromatin to circumvent plant defense.
In animals, pathogen-triggered chromatin remodeling is well documented and considered as a very promising area for future research on infectious diseases. However, to date plant pathogen-triggered chromatin remodeling has received very little attention. The CHERI project working model offers the opportunity to evaluate the importance of this process in the plant responses to different pathogens.

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