Impairment of Cellulose Synthases Required forArabidopsisSecondary Cell Wall Formation Enhances Disease Resistance
Author(s) -
Camilo Hernández-Blanco,
Dong Xin Feng,
Jian Hu,
Andrea SánchezVallet,
Laurent Deslandes,
Francisco Rubio Llorente,
Marta BerrocalLobo,
Harald Keller,
Xavier Barlet,
Clara SánchezRodríguez,
Lisa K. Anderson,
Shauna Somerville,
Yves Marco,
Antonio Molina
Publication year - 2007
Publication title -
the plant cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.324
H-Index - 341
eISSN - 1532-298X
pISSN - 1040-4651
DOI - 10.1105/tpc.106.048058
Subject(s) - biology , cell wall , arabidopsis , mutant , biochemistry , secondary cell wall , ralstonia solanacearum , powdery mildew , arabidopsis thaliana , abscisic acid , microbiology and biotechnology , gene , pathogen , botany
Cellulose is synthesized by cellulose synthases (CESAs) contained in plasma membrane-localized complexes. In Arabidopsis thaliana, three types of CESA subunits (CESA4/IRREGULAR XYLEM5 [IRX5], CESA7/IRX3, and CESA8/IRX1) are required for secondary cell wall formation. We report that mutations in these proteins conferred enhanced resistance to the soil-borne bacterium Ralstonia solanacearum and the necrotrophic fungus Plectosphaerella cucumerina. By contrast, susceptibility to these pathogens was not altered in cell wall mutants of primary wall CESA subunits (CESA1, CESA3/ISOXABEN RESISTANT1 [IXR1], and CESA6/IXR2) or POWDERY MILDEW-RESISTANT5 (PMR5) and PMR6 genes. Double mutants indicated that irx-mediated resistance was independent of salicylic acid, ethylene, and jasmonate signaling. Comparative transcriptomic analyses identified a set of common irx upregulated genes, including a number of abscisic acid (ABA)-responsive, defense-related genes encoding antibiotic peptides and enzymes involved in the synthesis and activation of antimicrobial secondary metabolites. These data as well as the increased susceptibility of ABA mutants (abi1-1, abi2-1, and aba1-6) to R. solanacearum support a direct role of ABA in resistance to this pathogen. Our results also indicate that alteration of secondary cell wall integrity by inhibiting cellulose synthesis leads to specific activation of novel defense pathways that contribute to the generation of an antimicrobial-enriched environment hostile to pathogens.
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