Fusarium verticillioides (F. verticillioides) is a globally
recognized and
highly impactful fungal pathogen of maize, causing yield losses and
producing harmful mycotoxins that pose a threat to human and animal
health. However, the genetic tools available for studying this crucial
fungus are currently limited in comparison to other important fungal
pathogens. To address this, an efficient CRISPR/Cas9 genome editing
system based on an autonomously replicating plasmid with an AMA1 sequence
was established in this study. First, gene disruption of pyrG and pyrE via nonhomologous end-joining (NHEJ) pathway
was successfully achieved, with efficiency ranging from 66 to 100%.
Second, precise gene deletions were achieved with remarkable efficiency
using a dual sgRNA expression strategy. Third, the developed genome
editing system can be applied to generate designer chromosomes in F. verticillioides, as evidenced by the deletion
of a crucial 38 kb fragment required for fumonisin biosynthesis. Fourth,
the pyrG recycling system has been established and
successfully applied in F. verticillioides. Lastly, the developed ΔFUM1 and ΔFUM mutants can serve as biocontrol agents to reduce the
fumonisin B1 (FB1) contamination produced by
the toxigenic strain. Taken together, these significant advancements
in genetic manipulation and biocontrol strategies provide valuable
tools for studying and mitigating the impact of F.
verticillioides on maize crops.