The Pseudomonas syringae type III effector HopD1 suppresses effector-triggered immunity, localizes to the endoplasmic reticulum, and targets the Arabidopsis transcription factor NTL9

New Phytol. 2014 Mar;201(4):1358-1370. doi: 10.1111/nph.12626. Epub 2013 Dec 12.

Abstract

• Pseudomonas syringae type III effectors are known to suppress plant immunity to promote bacterial virulence. However, the activities and targets of these effectors are not well understood. • We used genetic, molecular, and cell biology methods to characterize the activities, localization, and target of the HopD1 type III effector in Arabidopsis. • HopD1 contributes to P. syringae virulence in Arabidopsis and reduces effector-triggered immunity (ETI) responses but not pathogen-associated molecular pattern-triggered immunity (PTI) responses. Plants expressing HopD1 supported increased growth of ETI-inducing P. syringae strains compared with wild-type Arabidopsis. We show that HopD1 interacts with the membrane-tethered Arabidopsis transcription factor NTL9 and demonstrate that this interaction occurs at the endoplasmic reticulum (ER). A P. syringae hopD1 mutant and ETI-inducing P. syringae strains exhibited enhanced growth on Arabidopsis ntl9 mutant plants. Conversely, growth of P. syringae strains was reduced in plants expressing a constitutively active NTL9 derivative, indicating that NTL9 is a positive regulator of plant immunity. Furthermore, HopD1 inhibited the induction of NTL9-regulated genes during ETI but not PTI. • HopD1 contributes to P. syringae virulence in part by targeting NTL9, resulting in the suppression of ETI responses but not PTI responses and the promotion of plant pathogenicity.

Keywords: bacterial pathogens; plant defense; plant disease; plant immunity; type III effector.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Arabidopsis / genetics
  • Arabidopsis / immunology*
  • Arabidopsis / microbiology*
  • Arabidopsis Proteins / metabolism*
  • Bacterial Proteins / metabolism*
  • Bacterial Secretion Systems*
  • Cell Membrane / metabolism
  • Endoplasmic Reticulum / metabolism*
  • Gene Expression Regulation, Plant
  • Genes, Plant
  • Glucans / metabolism
  • Immunity, Innate
  • Plant Immunity*
  • Protein Binding
  • Protein Transport
  • Pseudomonas syringae / growth & development
  • Pseudomonas syringae / pathogenicity*
  • Receptors, Pattern Recognition / metabolism
  • Respiratory Burst
  • Transcription Factors / metabolism*
  • Virulence

Substances

  • Arabidopsis Proteins
  • Bacterial Proteins
  • Bacterial Secretion Systems
  • Glucans
  • NTL9 protein, Arabidopsis
  • Receptors, Pattern Recognition
  • Transcription Factors
  • callose