Are1-mediated nitrogen metabolism is associated with iron regulation in the mycoparasite Trichoderma atroviride

Microbiol Res. 2024 Dec:289:127907. doi: 10.1016/j.micres.2024.127907. Epub 2024 Sep 24.

Abstract

Trichoderma atroviride is a mycoparasitic fungus with antagonistic activity against fungal pathogens and is used as a pathogen control agent alternative to synthetic fungicides. Sensing nutrient availability in the environment and adjusting metabolism for optimal growth, development and reproduction is essential for adaptability and is relevant to its mycoparasitic activity. During mycoparasitism, secondary metabolites are produced to weaken the fungal prey and support the attack. Are1-like proteins act as major GATA-type transcription factors in the activation of genes subject to nitrogen catabolite repression. Since the quality and quantity of nitrogen has been proven particularly relevant in remodeling the biosynthesis of secondary metabolites in fungi, we decided to functionally characterize Are1, the ortholog of Aspergillus nidulans AreA, in T. atroviride. We show that the growth of the T. atroviride ∆are1 mutant is impaired in comparison to the wild type on several nitrogen sources. Deletion of are1 enhanced sensitivity to oxidative and cell-wall stressors and altered the mycoparasitic activity. We were able to identify for the first time a link between Are1 and iron homeostasis via a regulatory mechanism that does not appear to be strictly linked to the nitrogen source, but rather to an independent role of the transcription factor.

Keywords: Are1; Nitrogen catabolite regulation; Siderophore biosynthesis; Trichoderma atroviride.

MeSH terms

  • Aspergillus nidulans / genetics
  • Aspergillus nidulans / metabolism
  • Fungal Proteins* / genetics
  • Fungal Proteins* / metabolism
  • GATA Transcription Factors / genetics
  • GATA Transcription Factors / metabolism
  • Gene Deletion
  • Gene Expression Regulation, Fungal*
  • Homeostasis
  • Hypocreales* / genetics
  • Hypocreales* / growth & development
  • Hypocreales* / metabolism
  • Iron* / metabolism
  • Nitrogen* / metabolism
  • Oxidative Stress
  • Secondary Metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism

Substances

  • Nitrogen
  • Iron
  • Fungal Proteins
  • GATA Transcription Factors
  • Transcription Factors

Supplementary concepts

  • Trichoderma atroviride