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Developmental Modulation of Root Cell Wall Architecture Confers Resistance to an Oomycete Pathogen.

Accepted version
Peer-reviewed

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Authors

Rey, Thomas 
Torode, Thomas A 
Toulotte, Justine 
Chatterjee, Abhishek 

Abstract

The cell wall is the primary interface between plant cells and their immediate environment and must balance multiple functionalities, including the regulation of growth, the entry of beneficial microbes, and protection against pathogens. Here, we demonstrate how API, a SCAR2 protein component of the SCAR/WAVE complex, controls the root cell wall architecture important for pathogenic oomycete and symbiotic bacterial interactions in legumes. A mutation in API results in root resistance to the pathogen Phytophthora palmivora and colonization defects by symbiotic rhizobia. Although api mutant plants do not exhibit significant overall growth and development defects, their root cells display delayed actin and endomembrane trafficking dynamics and selectively secrete less of the cell wall polysaccharide xyloglucan. Changes associated with a loss of API establish a cell wall architecture with altered biochemical properties that hinder P. palmivora infection progress. Thus, developmental stage-dependent modifications of the cell wall, driven by SCAR/WAVE, are important in balancing cell wall developmental functions and microbial invasion.

Description

Keywords

Medicago truncatula, Phytophthora, Rhizobia, SCAR/WAVE, cell wall, disease resistance, root endosymbiosis, susceptibility gene, Actins, Cell Wall, Disease Resistance, Gene Expression Regulation, Plant, Host-Pathogen Interactions, Medicago truncatula, Mutation, Phytophthora, Plant Diseases, Plant Proteins, Plant Roots, Plants, Genetically Modified, Rhizobium, Symbiosis

Journal Title

Curr Biol

Conference Name

Journal ISSN

0960-9822
1879-0445

Volume Title

30

Publisher

Elsevier BV
Sponsorship
European Commission (624398)
The Royal Society (uf110073)
Gatsby Charitable Foundation (unknown)
European Research Council (637537)
Gatsby Charitable Foundation (GAT3395/GLD)
Royal Society (UF160413)
The Gatsby Foundation (GAT3395/GLD), European Research Council (ERC-2014-STG, H2020, 637537) Royal Society (UF110073, UF160413). TR was funded by The European Research Council (FP7-PEOPLE-2013-IEF, FP7, 624398). SB was funded by the University of California, Los Angeles (403976-SB-69313), Gatsby Charitable Foundation (GAT3396/PR4), and Biotechnology and Biological Sciences Research Council (BB.L002884.1). JLK was funded by the George and Lillian Schiff Foundation. DR, E-PJ, FD, and FdeCN were funded by TULIP (no. ANR-10-LABX-41). V.C. is a recipient of a Thailand Research Fund grant (MRG6080235) and also supported by Faculty of Science, Mahidol University, Thailand.