Ethylene-Cytokinin Interaction Determines Early Defense Response of Wheat against Stagonospora nodorum Berk

Biomolecules. 2021 Jan 28;11(2):174. doi: 10.3390/biom11020174.

Abstract

Ethylene, salicylic acid (SA), and jasmonic acid are the key phytohormones involved in plant immunity, and other plant hormones have been demonstrated to interact with them. The classic phytohormone cytokinins are important participants of plant defense signaling. Crosstalk between ethylene and cytokinins has not been sufficiently studied as an aspect of plant immunity and is addressed in the present research. We compared expression of the genes responsible for hormonal metabolism and signaling in wheat cultivars differing in resistance to Stagonospora nodorum in response to their infection with fungal isolates, whose virulence depends on the presence of the necrotrophic effector SnTox3. Furthermore, we studied the action of the exogenous cytokinins, ethephon (2-chloroethylphosphonic acid, ethylene-releasing agent) and 1-methylcyclopropene (1-MCP, inhibitor of ethylene action) on infected plants. Wheat susceptibility was shown to develop due to suppression of reactive oxygen species production and decreased content of active cytokinins brought about by SnTox3-mediated activation of the ethylene signaling pathway. SnTox3 decreased cytokinin content most quickly by its activated glucosylation in an ethylene-dependent manner and, furthermore, by oxidative degradation and inhibition of biosynthesis in ethylene-dependent and ethylene-independent manners. Exogenous zeatin application enhanced wheat resistance against S. nodorum through inhibition of the ethylene signaling pathway and upregulation of SA-dependent genes. Thus, ethylene inhibited triggering of SA-dependent resistance mechanism, at least in part, by suppression of the cytokinin signaling pathway.

Keywords: NADPH oxidases; SnTox3; Stagonospora nodorum; crosstalk; cytokinins; ethylene; necrotrophic effectors; plant–microbe interaction; reactive oxygen species.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ascomycota / metabolism*
  • Cytokinins / chemistry*
  • Cytokinins / metabolism
  • Ethylenes / chemistry*
  • Gene Expression Regulation, Plant
  • Hormones / metabolism
  • Hydrogen Peroxide
  • NADPH Oxidases / metabolism
  • Plant Diseases / microbiology
  • Plant Immunity
  • Plant Proteins / metabolism
  • Reactive Oxygen Species
  • Respiratory Burst
  • Seeds / metabolism
  • Signal Transduction
  • Superoxides
  • Triticum / metabolism*

Substances

  • Cytokinins
  • Ethylenes
  • Hormones
  • Plant Proteins
  • Reactive Oxygen Species
  • Superoxides
  • ethylene
  • Hydrogen Peroxide
  • NADPH Oxidases

Supplementary concepts

  • Parastagonospora nodorum