The nematode effector Mj-NEROSs interacts with Rieske's iron-sulfur protein influencing plastid ROS production to suppress plant immunity

New Phytol. 2024 Jun;242(6):2787-2802. doi: 10.1111/nph.19781. Epub 2024 May 1.

Abstract

Root-knot nematodes (RKN; Meloidogyne species) are plant pathogens that introduce several effectors in their hosts to facilitate infection. The actual targets and functioning mechanism of these effectors largely remain unexplored. This study illuminates the role and interplay of the Meloidogyne javanica nematode effector ROS suppressor (Mj-NEROSs) within the host plant environment. Mj-NEROSs suppresses INF1-induced cell death as well as flg22-induced callose deposition and reactive oxygen species (ROS) production. A transcriptome analysis highlighted the downregulation of ROS-related genes upon Mj-NEROSs expression. NEROSs interacts with the plant Rieske's iron-sulfur protein (ISP) as shown by yeast-two-hybrid and bimolecular fluorescence complementation. Secreted from the subventral pharyngeal glands into giant cells, Mj-NEROSs localizes in the plastids where it interacts with ISP, subsequently altering electron transport rates and ROS production. Moreover, our results demonstrate that isp Arabidopsis thaliana mutants exhibit increased susceptibility to M. javanica, indicating ISP importance for plant immunity. The interaction of a nematode effector with a plastid protein highlights the possible role of root plastids in plant defense, prompting many questions on the details of this process.

Keywords: ISP; ROS; effector; plant defense; protein–protein interaction; root plastids.

MeSH terms

  • Animals
  • Arabidopsis Proteins / genetics
  • Arabidopsis Proteins / metabolism
  • Arabidopsis* / genetics
  • Arabidopsis* / immunology
  • Arabidopsis* / parasitology
  • Electron Transport Complex III* / metabolism
  • Gene Expression Regulation, Plant
  • Helminth Proteins / genetics
  • Helminth Proteins / metabolism
  • Iron-Sulfur Proteins / genetics
  • Iron-Sulfur Proteins / metabolism
  • Mutation / genetics
  • Plant Diseases / immunology
  • Plant Diseases / parasitology
  • Plant Immunity*
  • Plastids* / metabolism
  • Protein Binding
  • Reactive Oxygen Species* / metabolism
  • Tylenchoidea* / pathogenicity
  • Tylenchoidea* / physiology

Substances

  • Reactive Oxygen Species
  • Rieske iron-sulfur protein
  • Electron Transport Complex III
  • Helminth Proteins
  • Arabidopsis Proteins
  • Iron-Sulfur Proteins

Associated data

  • RefSeq/AF531162