Identification and characterization of parasitism genes from the pinewood nematode Bursaphelenchus xylophilus reveals a multilayered detoxification strategy

Mol Plant Pathol. 2016 Feb;17(2):286-95. doi: 10.1111/mpp.12280. Epub 2015 Jun 16.

Abstract

The migratory endoparasitic nematode Bursaphelenchus xylophilus, which is the causal agent of pine wilt disease, has phytophagous and mycetophagous phases during its life cycle. This highly unusual feature distinguishes it from other plant-parasitic nematodes and requires profound changes in biology between modes. During the phytophagous stage, the nematode migrates within pine trees, feeding on the contents of parenchymal cells. Like other plant pathogens, B. xylophilus secretes effectors from pharyngeal gland cells into the host during infection. We provide the first description of changes in the morphology of these gland cells between juvenile and adult life stages. Using a comparative transcriptomics approach and an effector identification pipeline, we identify numerous novel parasitism genes which may be important for the mediation of interactions of B. xylophilus with its host. In-depth characterization of all parasitism genes using in situ hybridization reveals two major categories of detoxification proteins, those specifically expressed in either the pharyngeal gland cells or the digestive system. These data suggest that B. xylophilus incorporates effectors in a multilayer detoxification strategy in order to protect itself from host defence responses during phytophagy.

Keywords: Bursaphelenchus xylophilus; effectors; gland cells; transcriptome; xenobiotic metabolism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Computational Biology
  • Gene Expression Regulation
  • Genes, Helminth*
  • Genetic Association Studies
  • Helminth Proteins / metabolism
  • Inactivation, Metabolic / genetics*
  • Parasites / genetics*
  • Pharynx / cytology
  • Pinus / parasitology*
  • Reproducibility of Results
  • Tylenchida / genetics*

Substances

  • Helminth Proteins