DHXT1, a Virulence Factor of Dactylellina haptotyla, Regulates Pathogenicity by Participating in Trap Formation and Metabolite Synthesis

Int J Mol Sci. 2024 Jul 5;25(13):7384. doi: 10.3390/ijms25137384.

Abstract

The capsule-associated protein 10 gene (CAP10) is indispensable due to its involvement in pod formation and virulence maintenance in Cryptococcus neoformans. The function of the CAP10 gene in nematode-predatory fungi remains unreported. As a typical nematode-trapping fungus, Dactylellina haptotyla efficiently captures nematodes using adhesive knobs, which has potential applications in the biological control of plant-parasitic nematodes. In this study, we investigated the function of DHXT1 (a CAP10 homologous protein) in D. haptotyla-nematode interactions based on the disruption and overexpression of DHXT1, phenotypic analysis and metabolomic analysis. As a result, it was shown that the disruption of the DHXT1 gene causes a marked decrease in the number of adhesive knobs, and on the contrary, the overexpression of the DHXT1 gene causes a substantial increase in the number of adhesive knobs. Interestingly, the variety of metabolites increased with the disruption of the DHXT1 and decreased with the overexpression of the DHXT1 gene. The results suggest that DHXT1 effects pathogenicity through its involvement in adhesive knobs' formation and metabolite synthesis and serves as a key virulence factor in D. haptotyla.

Keywords: CAP10; Dactylellina haptotyla; adhesive knob formation; metabolites; virulence factor.

MeSH terms

  • Animals
  • Fungal Proteins* / genetics
  • Fungal Proteins* / metabolism
  • Plant Diseases / microbiology
  • Plant Diseases / parasitology
  • Virulence
  • Virulence Factors* / genetics
  • Virulence Factors* / metabolism

Substances

  • Virulence Factors
  • Fungal Proteins

Grants and funding

This work was supported in part by the National Key R&D Program of China (2023 YFD1400400), the National Natural Science Foundation of China (32270132), the Science and Technology Major Project from Yunnan Province (202201BC070004) and the Special fund of the Yunnan University “double first-class” construction. We are grateful to the Microbial Library of the Germplasm Bank of Wild Species from Southwest China for preserving and providing experimental strains.