Root-knot nematodes induce pattern-triggered immunity in Arabidopsis thaliana roots

New Phytol. 2016 Jul;211(1):276-87. doi: 10.1111/nph.13893. Epub 2016 Feb 19.

Abstract

Root-knot nematodes (RKNs; Meloidogyne spp.) are plant parasites with a broad host range causing great losses worldwide. To parasitize their hosts, RKNs establish feeding sites in roots known as giant cells. The majority of work studying plant-RKN interactions in susceptible hosts addresses establishment of the giant cells and there is limited information on the early defense responses. Here we characterized early defense or pattern-triggered immunity (PTI) against RKNs in Arabidopsis thaliana. To address PTI, we evaluated known canonical PTI signaling mutants with RKNs and investigated the expression of PTI marker genes after RKN infection using both quantitative PCR and β-glucuronidase reporter transgenic lines. We showed that PTI-compromised plants have enhanced susceptibility to RKNs, including the bak1-5 mutant. BAK1 is a common partner of distinct receptors of microbe- and damage-associated molecular patterns. Furthermore, our data indicated that nematode recognition leading to PTI responses involves camalexin and glucosinolate biosynthesis. While the RKN-induced glucosinolate biosynthetic pathway was BAK1-dependent, the camalexin biosynthetic pathway was only partially dependent on BAK1. Combined, our results indicate the presence of BAK1-dependent and -independent PTI against RKNs in A. thaliana, suggesting the existence of diverse nematode recognition mechanisms.

Keywords: Arabidopsis thaliana; BAK1; Meloidogyne incognita; WRKY11; camalexin; glucosinolate; pattern-triggered immunity; root-knot nematodes (RKNs).

MeSH terms

  • Animals
  • Arabidopsis / genetics
  • Arabidopsis / immunology*
  • Arabidopsis / parasitology*
  • Arabidopsis Proteins / genetics
  • Arabidopsis Proteins / immunology
  • Arabidopsis Proteins / metabolism
  • Gene Expression Regulation, Plant
  • Glucosinolates / metabolism
  • Host-Parasite Interactions / immunology
  • Indoles / metabolism
  • Mutation
  • Pathogen-Associated Molecular Pattern Molecules / immunology*
  • Plant Immunity
  • Plant Roots / parasitology
  • Plants, Genetically Modified
  • Protein Kinases / immunology
  • Protein Kinases / metabolism
  • Protein Serine-Threonine Kinases / genetics
  • Thiazoles / metabolism
  • Transcription Factors / genetics
  • Tylenchoidea / pathogenicity*
  • Tylenchoidea / physiology

Substances

  • Arabidopsis Proteins
  • Atmyb5 protein, Arabidopsis
  • Glucosinolates
  • Indoles
  • Pathogen-Associated Molecular Pattern Molecules
  • Thiazoles
  • Transcription Factors
  • WRKY11 protein, Arabidopsis
  • camalexin
  • LecRK-I.9 protein, Arabidopsis
  • Protein Kinases
  • BAK1 protein, Arabidopsis
  • FLS2 protein, Arabidopsis
  • Protein Serine-Threonine Kinases