High-Resolution Disease Phenotyping Reveals Distinct Resistance Mechanisms of Tomato Crop Wild Relatives against Sclerotinia sclerotiorum

Author:

Einspanier Severin1ORCID,Tominello-Ramirez Christopher1ORCID,Hasler Mario2,Barbacci Adelin3ORCID,Raffaele Sylvain3ORCID,Stam Remco1ORCID

Affiliation:

1. Department of Phytopathology and Crop Protection, Institute of Phytopathology, Faculty of Agricultural and Nutritional Sciences, Christian-Albrechts-University, 24118 Kiel, Germany.

2. Lehrfach Variationsstatistik, Faculty of Agricultural and Nutritional Sciences, Christian-Albrechts-University, Kiel, 24118 Kiel, Germany.

3. Laboratoire des Interactions Plantes Microorganismes Environnement (LIPME), INRAE, CNRS, Castanet Tolosan Cedex, France.

Abstract

Besides the well-understood qualitative disease resistance, plants possess a more complex quantitative form of resistance: quantitative disease resistance (QDR). QDR is commonly defined as a partial but more durable form of resistance and, therefore, might display a valuable target for resistance breeding. The characterization of QDR phenotypes, especially of wild crop relatives, displays a bottleneck in deciphering QDR’s genomic and regulatory background. Moreover, the relationship between QDR parameters, such as infection frequency, lag-phase duration, and lesion growth rate, remains elusive. High hurdles for applying modern phenotyping technology, such as the low availability of phenotyping facilities or complex data analysis, further dampen progress in understanding QDR. Here, we applied a low-cost (<1.000 €) phenotyping system to measure lesion growth dynamics of wild tomato species (e.g., Solanum pennellii or Solanum pimpinellifolium ). We provide insight into QDR diversity of wild populations and derive specific QDR mechanisms and their cross-talk . We show how temporally continuous observations are required to dissect end-point severity into functional resistance mechanisms. The results of our study show how QDR can be maintained by facilitating different defense mechanisms during host–parasite interaction and that the capacity of the QDR toolbox highly depends on the host’s genetic context. We anticipate that the present findings display a valuable resource for more targeted functional characterization of the processes involved in QDR. Moreover, we show how modest phenotyping technology can be leveraged to help answer highly relevant biological questions.

Funder

Deutsche Forschungsgemeinschaft

Agence Nationale de la Recherche

Partenariat Hubert Curien programm

Deutscher Akademischer Austauschdienst France

Publisher

American Association for the Advancement of Science (AAAS)

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