Functionally redundant Rho GTPases Cdc42 and RacA regulate aflatoxin synthesis and pathogenicity in Aspergillus flavus by controlling morphogenesis, oxidative balance and energy metabolism

Rho GTPases Cdc42 and RacA share significant sequence homology and are conserved among eukaryotic species. These proteins act as molecular switches in various signal transduction pathways by cycling between GTP-bound (active) and GDP-bound (inactive) states. However, their specific functions in A. flavus remain understudied.

The research team developed a CRISPR/Cas9 system utilizing 5S rRNA and tRNA-gRNA tandem arrays, achieving over 95% single gene editing efficiency and 75% dual gene editing efficiency. Phenotypic and transcriptome analyses revealed significant functional redundancy between cdc42 and racA. The researchers found that conidial germination was significantly accelerated in the mutants, with early germination driven by increased hydrolase activity and ATP levels. Loss of cdc42 or racA resulted in reduced pathogenicity, impaired cell wall integrity, reduced aflatoxin production, and disrupted oxidative systems. These proteins regulate the generation of reactive oxygen species (ROS) by interacting with NoxR, the regulatory subunit of NADPH oxidase (Nox). Cdc42 and RacA play opposing roles in fatty acid β-oxidation and pyruvate metabolism. Simultaneous loss of function of both genes is lethal, as evidenced by the inability of the ∆cdc42racAtetOn mutant to grow in medium lacking doxycycline.

This study reveals the critical roles of the closely related genes cdc42 and racA in the growth, development, and metabolism of A. flavus. These findings provide potential targets for mitigating the harmful effects of A. flavus and aflatoxins.

See the article: Functionally redundant Rho GTPases Cdc42 and RacA regulate aflatoxin synthesis and pathogenicity in Aspergillus flavus by controlling morphogenesis, oxidative balance and energy metabolism