Heterologous Expression Screens in Nicotiana benthamiana Identify a Candidate Effector of the Wheat Yellow Rust Pathogen that Associates with Processing Bodies

PLoS One. 2016 Feb 10;11(2):e0149035. doi: 10.1371/journal.pone.0149035. eCollection 2016.

Abstract

Rust fungal pathogens of wheat (Triticum spp.) affect crop yields worldwide. The molecular mechanisms underlying the virulence of these pathogens remain elusive, due to the limited availability of suitable molecular genetic research tools. Notably, the inability to perform high-throughput analyses of candidate virulence proteins (also known as effectors) impairs progress. We previously established a pipeline for the fast-forward screens of rust fungal candidate effectors in the model plant Nicotiana benthamiana. This pipeline involves selecting candidate effectors in silico and performing cell biology and protein-protein interaction assays in planta to gain insight into the putative functions of candidate effectors. In this study, we used this pipeline to identify and characterize sixteen candidate effectors from the wheat yellow rust fungal pathogen Puccinia striiformis f sp tritici. Nine candidate effectors targeted a specific plant subcellular compartment or protein complex, providing valuable information on their putative functions in plant cells. One candidate effector, PST02549, accumulated in processing bodies (P-bodies), protein complexes involved in mRNA decapping, degradation, and storage. PST02549 also associates with the P-body-resident ENHANCER OF mRNA DECAPPING PROTEIN 4 (EDC4) from N. benthamiana and wheat. We propose that P-bodies are a novel plant cell compartment targeted by pathogen effectors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Basidiomycota / genetics
  • Basidiomycota / metabolism*
  • Basidiomycota / pathogenicity
  • Chromatography, Liquid
  • Computer Simulation
  • Fungal Proteins / metabolism*
  • Gene Expression Profiling
  • Gene Expression Regulation, Plant*
  • Green Fluorescent Proteins / metabolism
  • Microscopy, Confocal
  • Nicotiana / microbiology*
  • Open Reading Frames
  • Plant Diseases / microbiology
  • Plant Leaves / metabolism
  • Plant Leaves / microbiology
  • Protein Interaction Mapping
  • RNA, Messenger / metabolism
  • Tandem Mass Spectrometry
  • Triticum / microbiology
  • Virulence

Substances

  • Fungal Proteins
  • RNA, Messenger
  • Green Fluorescent Proteins

Grants and funding

BP, CL, and SD were supported by the French National Research Agency through the Labex ARBRE (ANR-12-LABXARBRE-01) and the Young Scientist Grant POPRUST (ANR-2010-JCJC-1709-01). BP and CL are supported by an INRA Contrat Jeune Scientifique. BP was supported by the European Union, in the framework of the Marie-Curie FP7 COFUND People Programme, through the award of an AgreenSkills’ fellowship (under grant agreement n° 267196). BP, JS, JW, KVK, DGOS, and SK are supported by the Biotechnology and Biological Sciences Research Council and the Gatsby Charitable Foundation. DGOS is supported by a Leverhulme early career fellowship and a fellowship in computational biology at TGAC, in partnership with the John Innes Centre. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.