Enhanced defense responses in Arabidopsis induced by the cell wall protein fractions from Pythium oligandrum require SGT1, RAR1, NPR1 and JAR1

Plant Cell Physiol. 2009 May;50(5):924-34. doi: 10.1093/pcp/pcp044. Epub 2009 Mar 20.

Abstract

The cell wall protein fraction (CWP) is purified from the non-pathogenic biocontrol agent Pythium oligandrum and is composed of two glycoproteins (POD-1 and POD-2), which are structurally similar to class III elicitins. In tomato plants treated with CWP, jasmonic acid (JA)- and ethylene (ET)-dependent signaling pathways are activated, and resistance to Ralstonia solanaceraum is enhanced. To dissect CWP-induced defense mechanisms, we investigated defense gene expression and resistance to bacterial pathogens in Arabidopsis thaliana ecotype Col-0 treated with CWP. When the leaves of Col-0 were infiltrated with CWP, neither visible necrosis nor salicylic acid (SA)-responsive gene (PR-1 and PR-5) expression was induced. In contrast, JA-responsive gene (PDF1.2 and JR2) expression was up-regulated and the resistance to R. solanaceraum and Pseudomonas syringae pv. tomato DC3000 was enhanced in response to CWP. Such CWP-induced defense responses were completely compromised in CWP-treated coi1-1 and jar1-1 mutants with an impaired JA signaling pathway. The induction of defense-related gene expression after CWP treatment was partially compromised in ET-insensitive ein2-1 mutants, but not in SA signaling mutants or nahG transgenic plants. Global gene expression analysis using cDNA array also suggested that several other JA- and ET-responsive genes, but not SA-responsive genes, were up-regulated in response to CWP. Further analysis of CWP-induced defense responses using another eight mutants with impaired defense signaling pathways indicated that, interestingly, the induction of JA-responsive gene expression and enhanced resistance to two bacterial pathogens in response to CWP were completely compromised in rar1-1, rar1-21, sgt1a-1, sgt1b (edm1) and npr1-1 mutants. Thus, the CWP-induced defense system appears to be regulated by JA-mediated and SGT1-, RAR1- and NPR1-dependent signaling pathways.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arabidopsis / genetics
  • Arabidopsis / metabolism*
  • Arabidopsis / microbiology
  • Arabidopsis Proteins / genetics
  • Arabidopsis Proteins / metabolism
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism
  • Cell Wall / chemistry*
  • Cyclopentanes / metabolism
  • Cyclopentanes / pharmacology
  • Ethylenes / metabolism
  • Ethylenes / pharmacology
  • Gene Expression Regulation, Plant
  • Genes, Plant
  • Glucosyltransferases / genetics
  • Glucosyltransferases / metabolism
  • Intracellular Signaling Peptides and Proteins
  • Nucleotidyltransferases / genetics
  • Nucleotidyltransferases / metabolism
  • Oligonucleotide Array Sequence Analysis
  • Oxylipins / metabolism
  • Oxylipins / pharmacology
  • Plant Diseases / genetics
  • Plants, Genetically Modified / genetics
  • Plants, Genetically Modified / metabolism
  • Plants, Genetically Modified / microbiology
  • Pseudomonas syringae / pathogenicity
  • Pythium / chemistry*
  • RNA, Plant / metabolism
  • Ralstonia / pathogenicity
  • Salicylic Acid / metabolism
  • Salicylic Acid / pharmacology
  • Signal Transduction*

Substances

  • Arabidopsis Proteins
  • Carrier Proteins
  • Cyclopentanes
  • Ethylenes
  • Intracellular Signaling Peptides and Proteins
  • NPR1 protein, Arabidopsis
  • Oxylipins
  • PBS2 protein, Arabidopsis
  • RNA, Plant
  • jasmonic acid
  • ethylene
  • Glucosyltransferases
  • SGT1 protein, Arabidopsis
  • JAR1 protein, Arabidopsis
  • Nucleotidyltransferases
  • Salicylic Acid