Cerato-platanin induces resistance in Arabidopsis leaves through stomatal perception, overexpression of salicylic acid- and ethylene-signalling genes and camalexin biosynthesis

PLoS One. 2014 Jun 26;9(6):e100959. doi: 10.1371/journal.pone.0100959. eCollection 2014.

Abstract

Microbe-associated molecular patterns (MAMPs) lead to the activation of the first line of plant defence. Few fungal molecules are universally qualified as MAMPs, and proteins belonging to the cerato-platanin protein (CPP) family seem to possess these features. Cerato-platanin (CP) is the name-giving protein of the CPP family and is produced by Ceratocystis platani, the causal agent of the canker stain disease of plane trees (Platanus spp.). On plane tree leaves, the biological activity of CP has been widely studied. Once applied on the leaf surface, CP acts as an elicitor of defence responses. The molecular mechanism by which CP elicits leaves is still unknown, and the protective effect of CP against virulent pathogens has not been clearly demonstrated. In the present study, we tried to address these questions in the model plant Arabidopsis thaliana. Our results suggest that stomata rapidly sense CP since they responded to the treatment with ROS signalling and stomatal closure, and that CP triggers salicylic acid (SA)- and ethylene (ET)-signalling pathways, but not the jasmonic acid (JA)-signalling pathway, as revealed by the expression pattern of 20 marker genes. Among these, EDS1, PAD4, NPR1, GRX480, WRKY70, ACS6, ERF1a/b, COI1, MYC2, PDF1.2a and the pathogenesis-related (PR) genes 1-5. CP rapidly induced MAPK phosphorylation and induced the biosynthesis of camalexin within 12 hours following treatment. The induction of localised resistance was shown by a reduced susceptibility of the leaves to the infection with Botrytis cinerea and Pseudomonas syringae pv. tomato. These results contribute to elucidate the key steps of the signalling process underlying the resistance induction in plants by CP and point out the central role played by the stomata in this process.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arabidopsis / drug effects
  • Arabidopsis / genetics*
  • Arabidopsis / metabolism*
  • Arabidopsis Proteins / genetics*
  • Arabidopsis Proteins / metabolism*
  • Drug Resistance
  • Ethylenes / metabolism
  • Fungal Proteins / pharmacology
  • Gene Expression Regulation, Plant / drug effects
  • Hydrogen Peroxide / metabolism
  • Indoles / metabolism*
  • Mitogen-Activated Protein Kinases / metabolism
  • Phosphorylation
  • Plant Leaves / genetics*
  • Plant Leaves / metabolism*
  • Plant Stomata / drug effects
  • Plant Stomata / genetics
  • Plant Stomata / metabolism
  • Reactive Oxygen Species / metabolism
  • Salicylic Acid / metabolism
  • Signal Transduction
  • Thiazoles / metabolism*

Substances

  • Arabidopsis Proteins
  • Ethylenes
  • Fungal Proteins
  • Indoles
  • Reactive Oxygen Species
  • Thiazoles
  • camalexin
  • ethylene
  • Hydrogen Peroxide
  • Mitogen-Activated Protein Kinases
  • Salicylic Acid

Grants and funding

This work was supported by Ministero Italiano dell’Università e della Ricerca Scientifica, Progetti di Ricerca di Interesse Nazionale (PRIN) 2009 (http://prin.miur.it/). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.