The Transcription Factor FgAtrR Regulates Asexual and Sexual Development, Virulence, and DON Production and Contributes to Intrinsic Resistance to Azole Fungicides in Fusarium graminearum

• Published in: Biology (Basel, Switzerland) Vol. 11; no. 2; p. 326
• Main Authors: Zhao, Yanxiang, Sun, Huilin, Li, Jingwen, Ju, Chao, Huang, Jinguang
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 18.02.2022; MDPI
• Subjects: ABC transporters; antifungal agents; Asexuality; Biosynthesis; Conidia; corn; Cultivars; Deletion mutant; Deoxynivalenol; Drug resistance; Fungi; fungicide resistance; Fungicides; Fusarium graminearum; Fusarium head blight; Gene regulation; Genes; Metabolic pathways; Mutants; mycotoxin; Pathogenicity; Perithecia; Pesticides; Pigmentation; plant pathogen; Prochloraz; Propiconazole; sequence analysis; sexual development; Sterols; Therapeutic targets; transcription (genetics); Transcription factors; transcriptional regulation; Virulence; wheat; Yeast; fungicide resistance; mycotoxin; plant pathogen; transcriptional regulation; Fusarium head blight
• ISSN: 2079-7737; 2079-7737
• DOI: 10.3390/biology11020326

Fusarium graminearum is the predominant causal agent of cereal Fusarium head blight disease (FHB) worldwide. The application of chemical fungicides such as azole antifungals is still the primary method for FHB control. However, to date, our knowledge of transcriptional regulation in the azole resistance of F. graminearum is quite limited. In this study, we identified and functionally characterized a Zn(II)2-Cys6 transcription factor FgAtrR in F. graminearum. We constructed a FgAtrR deletion mutant and found that deletion of FgAtrR resulted in faster radial growth with serious pigmentation defects, significantly reduced conidial production, and an inability to form perithecia. The pathogenicity of the ΔFgAtrR mutant on wheat spikes and corn silks was severely impaired with reduced deoxynivalenol production, while the tolerance to prochloraz and propiconazole of the deletion mutant was also significantly decreased. RNA-seq indicated that many metabolic pathways were affected by the deletion of FgAtrR. Importantly, FgAtrR could regulate the expression of the FgCYP51A and ABC transporters, which are the main contributors to azole resistance. These results demonstrated that FgAtrR played essential roles in asexual and sexual development, DON production, and pathogenicity, and contributed to intrinsic resistance to azole fungicides in F. graminearum. This study will help us improve the understanding of the azole resistance mechanism in F. graminearum.