Carbendazim-resistance associated β2 -tubulin substitutions increase deoxynivalenol biosynthesis by reducing the interaction between β2 -tubulin and IDH3 in Fusarium graminearum

Environ Microbiol. 2020 Feb;22(2):598-614. doi: 10.1111/1462-2920.14874. Epub 2019 Dec 4.

Abstract

Microtubule is a well-known structural protein participating in cell division, motility and vesicle traffic. In this study, we found that β2 -tubulin, one of the microtubule components, plays an important role in regulating secondary metabolite deoxynivalenol (DON) biosynthesis in Fusarium graminearum by interacting with isocitrate dehydrogenase subunit 3 (IDH3). We found IDH3 negatively regulate DON biosynthesis by reducing acetyl-CoA accumulation in F. graminearum and DON biosynthesis was stimulated by exogenous acetyl-CoA. In addition, the expression of IDH3 significantly decreased in the carbendazim-resistant mutant nt167 (Fgβ2 F167Y ). Furthermore, we found that carbendazim-resistance associated β2 -tubulin substitutions reducing the interaction intensity between β2 -tubulin and IDH3. Interestingly, we demonstrated that β2 -tubulin inhibitor carbendazim can disrupt the interaction between β2 -tubulin and IDH3. The decreased interaction intensity between β2 -tubulin and IDH3 resulted in the decreased expression of IDH3, which can cause the accumulation of acetyl-CoA, precursor of DON biosynthesis in F. graminearum. Thus, we revealed that carbendazim-resistance associated β2 -tubulin substitutions or carbendazim treatment increases DON biosynthesis by reducing the interaction between β2 -tubulin and IDH3 in F. graminearum. Taken together, the novel findings give the new perspectives of β2 -tubulin in regulating secondary metabolism in phytopathogenic fungi.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetyl Coenzyme A / metabolism
  • Amino Acid Substitution / genetics
  • Benzimidazoles / pharmacology*
  • Carbamates / pharmacology*
  • Drug Resistance, Fungal / genetics*
  • Fungicides, Industrial / pharmacology*
  • Fusarium / drug effects*
  • Fusarium / metabolism
  • Isocitrate Dehydrogenase / metabolism
  • Microtubules
  • Secondary Metabolism / physiology
  • Trichothecenes / metabolism*
  • Tubulin / genetics
  • Tubulin / metabolism

Substances

  • Benzimidazoles
  • Carbamates
  • Fungicides, Industrial
  • Trichothecenes
  • Tubulin
  • Acetyl Coenzyme A
  • Isocitrate Dehydrogenase
  • carbendazim
  • deoxynivalenol