Overexpression of Arabidopsis ACBP3 enhances NPR1-dependent plant resistance to Pseudomonas syringe pv tomato DC3000

Plant Physiol. 2011 Aug;156(4):2069-81. doi: 10.1104/pp.111.176933. Epub 2011 Jun 13.

Abstract

ACBP3 is one of six Arabidopsis (Arabidopsis thaliana) genes, designated ACBP1 to ACBP6, that encode acyl-coenzyme A (CoA)-binding proteins (ACBPs). These ACBPs bind long-chain acyl-CoA esters and phospholipids and are involved in diverse cellular functions, including acyl-CoA homeostasis, development, and stress tolerance. Recombinant ACBP3 binds polyunsaturated acyl-CoA esters and phospholipids in vitro. Here, we show that ACBP3 plays a role in the plant defense response to the bacterial pathogen Pseudomonas syringae pv tomato DC3000. ACBP3 mRNA was up-regulated upon pathogen infection and treatments using pathogen elicitors and defense-related phytohormones. Transgenic Arabidopsis ACBP3 overexpressors (ACBP3-OEs) showed constitutive expression of pathogenesis-related genes (PR1, PR2, and PR5), cell death, and hydrogen peroxide accumulation in leaves. Consequently, ACBP3-OEs displayed enhanced resistance to the bacterial pathogen P. syringae DC3000. In contrast, the acbp3 T-DNA insertional mutant was more susceptible and exhibited lower PR gene transcript levels upon infection. Using the ACBP3 OE-1 line in combination with nonexpressor of PR genes1 (npr1-5) or coronatine-insensitive1 (coi1-2), we concluded that the enhanced PR gene expression and P. syringae DC3000 resistance in the ACBP3-OEs are dependent on the NPR1-mediated, but not the COI1-mediated, signaling pathway. Given that ACBP3-OEs showed greater susceptibility to infection by the necrotrophic fungus Botrytis cinerea while the acbp3 mutant was less susceptible, we suggest that ACBP3 plays a role in the plant defense response against biotrophic pathogens that is distinct from necrotrophic pathogens. ACBP3 function in plant defense was supported further by bioinformatics data showing up-regulation of many biotic and abiotic stress-related genes in ACBP3 OE-1 in comparison with the wild type.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arabidopsis / drug effects
  • Arabidopsis / genetics
  • Arabidopsis / immunology*
  • Arabidopsis / microbiology*
  • Arabidopsis Proteins / genetics
  • Arabidopsis Proteins / metabolism*
  • Arachidonic Acid / pharmacology
  • Botrytis / drug effects
  • Botrytis / physiology
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Cell Death / drug effects
  • Disease Resistance / drug effects
  • Disease Resistance / immunology*
  • Gene Expression Regulation, Plant / drug effects
  • Gene Knockout Techniques
  • Genes, Plant / genetics
  • Green Fluorescent Proteins / metabolism
  • Hydrogen Peroxide / metabolism
  • Intracellular Space / drug effects
  • Intracellular Space / metabolism
  • Oligonucleotide Array Sequence Analysis
  • Phenotype
  • Plant Diseases / immunology*
  • Plant Diseases / microbiology
  • Plant Growth Regulators / pharmacology
  • Pseudomonas syringae / drug effects
  • Pseudomonas syringae / physiology*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Salicylic Acid / metabolism

Substances

  • ACBP3 protein, Arabidopsis
  • Arabidopsis Proteins
  • Carrier Proteins
  • NPR1 protein, Arabidopsis
  • Plant Growth Regulators
  • RNA, Messenger
  • Green Fluorescent Proteins
  • Arachidonic Acid
  • Hydrogen Peroxide
  • Salicylic Acid