Fusarium verticillioides is the primary pathogen causing ear rot and stalk rot in corn ( Zea mays ). It not only affects yields but also produces mycotoxins endangering both human and animal health. Aldehyde dehydrogenase (ALDH) is essential for the oxidation of aldehydes in living organisms, making it a potential target for human drug design. However, there are limited reports on its function in plant pathogenic fungus. In this study, we analyzed the expression levels and gene knockout mutants, revealing that ALDH genes FvALDH-43 and FvALDH-96 in F. verticillioides played significant roles in pathogenicity and resistance to low-temperature stress by affecting antioxidant capacity. Virtual screening for natural product inhibitors and molecular docking were performed targeting FvALDH-43 and FvALDH-96. Following the biological activity analysis, three natural flavonoid compounds featuring a 2-hydroxyphenol chromene were identified. Among these, Taxifolin exhibited the highest biological activity and low toxicity. Both in vitro and in vivo biological evaluations confirmed that Taxifolin targeted ALDH and inhibited its activity. These findings indicate that aldehyde dehydrogenase may serve as a promising target for the design of novel fungicides.
Keyphrases
- molecular docking
- endothelial cells
- induced pluripotent stem cells
- genome wide
- public health
- cancer therapy
- poor prognosis
- small molecule
- human health
- pluripotent stem cells
- molecular dynamics simulations
- oxidative stress
- dna methylation
- risk assessment
- genome wide identification
- climate change
- drug delivery
- adverse drug
- biofilm formation
- gene expression
- gram negative
- binding protein
- staphylococcus aureus
- genome wide analysis
- wild type
- electronic health record