The Vta1 transcriptional regulator is required for microsclerotia melanization in Verticillium dahliae

Fungal Biol. 2020 May;124(5):490-500. doi: 10.1016/j.funbio.2020.01.007. Epub 2020 Jan 31.

Abstract

Many fungi are able to produce resting structures, which ensure survival and protect them against various stresses in their habitat such as exposure to UV light, temperature variations, drought as well as changing pH and nutrient conditions. Verticillium dahliae is a plant pathogenic fungus that forms melanized resting structures, called microsclerotia, for survival of time periods without a host. These highly stress resistant microsclerotia persist in the soil for many years and are therefore problematic for an effective treatment of the fungus. The Verticillium transcription activator of adhesion 1 (Vta1) was initially identified as one of several transcriptional regulators that rescue adhesion in non-adhesive Saccharomyces cerevisiae cells. Vta2 and Vta3 are required for early steps in plant infection and colonization and additionally control microsclerotia formation. Here, we show that Vta1 function is different, because it is dispensable for root colonization and infection. Vta1 is produced in the fungal cell during microsclerotia development. Analysis of the deletion mutant revealed that the absence of Vta1 allows microsclerotia production, but they are colorless and no more melanized. Vta1 is required for melanin production and activates transcription of melanin biosynthesis genes including the polyketide synthase encoding PKS1 and the laccase LAC1. The primary function of Vta1 in melanin production is important for survival of microsclerotia as resting structures of V. dahliae.

Keywords: Melanin production; Plant pathogen; Resting structure; Transcription factor; Verticillium spp.; Verticillium transcription activator of adhesion 1 (Vta1).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ascomycota* / genetics
  • Ascomycota* / metabolism
  • Fungal Proteins* / genetics
  • Gene Expression Regulation, Fungal
  • Melanins* / genetics
  • Plant Diseases / microbiology
  • Transcription Factors* / genetics

Substances

  • Fungal Proteins
  • Melanins
  • Transcription Factors

Supplementary concepts

  • Verticillium dahliae