The expression of the genes involved in redox metabolism and hydrogen peroxide balance is associated with the resistance of cowpea [Vigna unguiculata (L.) Walp.] to the hemibiotrophic fungus Colletotrichum gloeosporioides

J Plant Physiol. 2019 Feb:233:73-83. doi: 10.1016/j.jplph.2018.12.009. Epub 2019 Jan 2.

Abstract

Correlations between the transcriptional responses of genes that encode superoxide dismutase (SOD), catalase (CAT), ascorbate peroxidase (APX), and peroxiredoxin (Prx) enzymes and Colletotrichum gloeosporioides development in cowpea leaves were assessed. Each of these genes is involved in the redox metabolism and hydrogen peroxide balance. Although electron microscopy revealed that conidia adhered to and germinated on the leaf cuticle, the inoculated cowpea leaves did not show any characteristic anthracnose symptoms. The adhered and germinated conidia showed irregular surfaces and did not develop further. This was apparently due to increased leaf H2O2 levels in response to inoculation with C. gloeosporioides. During the early stages post inoculation, cowpea leaves elevated the H2O2 content and modulated the defense gene expression, as well as associated pathways. During the later stages, the increased expression of the CuZnSODI and CuZnSODII genes suggested an active superoxide dismutation to further elevate H2O2 levels, which indicated that higher H2O2 content may function as a toxic agent that kills the fungus. The second increase in H2O2 production above the threshold level was correlated with the expression of the APXI, CATI, CATII, PrxIIBCD, and PrxIIE genes, which resulted in a coordinated pattern to establish an appropriate balance between H2O2 generation and scavenging. Therefore, appropriate H2O2 content in cowpea leaves inhibited C. gloeosporioides development and maintained intracellular redox homeostasis to avoid uncontrolled programmed cell death and necrosis in cowpea leaves.

Keywords: C. gloeosporioides; Cowpea; Defense gene expression; H(2)O(2); Redox metabolism; Vigna unguiculata.

MeSH terms

  • Ascorbate Peroxidases / metabolism
  • Catalase / metabolism
  • Colletotrichum* / ultrastructure
  • Disease Resistance / physiology*
  • Gene Expression Profiling
  • Gene Expression Regulation, Plant / physiology
  • Genes, Plant / physiology
  • Hydrogen Peroxide / metabolism*
  • Lipid Peroxidation
  • Microscopy, Electron, Scanning
  • Oxidation-Reduction*
  • Peroxiredoxins / metabolism
  • Plant Diseases / microbiology
  • Plant Leaves / metabolism
  • Plant Leaves / microbiology
  • Real-Time Polymerase Chain Reaction
  • Superoxide Dismutase / metabolism
  • Vigna / genetics
  • Vigna / microbiology*
  • Vigna / physiology

Substances

  • Hydrogen Peroxide
  • Ascorbate Peroxidases
  • Peroxiredoxins
  • Catalase
  • Superoxide Dismutase