Integrative Biology Journals

JOURNAL OF FORESTRY RESEARCH ›› 2025, Vol. 36 ›› Issue (1): 1-.DOI: 10.1007/s11676-025-01854-7

• Original Paper •    

Transcriptomic and metabolomic analysis of fludioxonil‑induced stress response and resistance in the poplar leaf blight fungus (Alternaria alternata)

Mansoor Hayat1,2, Zhanbin Wang1,2, Xiaojing Liu1,2, Zarmina Gul3, Qian Bai1,2, Sajid Ali4   

  1. 1Key Laboratory of Forest Pathology, School of Forestry, Northeast Forestry University, Harbin 150040, People’s Republic of China 

    2Northeast Asia Biodiversity Center, Northeast Forestry University, Harbin 150040, People’s Republic of China 

    3Key Laboratory of Forest Plant Ecology, College of Chemistry, Chemical Engineering and Resource Utilization, Northeast Forestry University, Harbin 150040, People’s Republic of China 

    4State Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University, Harbin 150040, People’s Republic of China

  • Received:2024-12-31 Accepted:2025-02-19 Online:2025-05-04 Published:2025-01-01
  • Supported by:
    This study was supported by the Northeast Asia Biodiversity Research Center (grant number 411147021003).

Abstract: The predominant causal agent of poplar leaf blight is the pathogenic fungus Alternaria alternata (Fr.) Keissl., which exhibits host specificity toward Populus species. To elucidate the molecular response mechanisms of A. alternata under fludioxonil fungicide stress, the fungus was cultured at the half-maximal effective concentration (EC₅₀) of fludioxonil. Transcriptomic and metabolomic profiles were analyzed using mycelia harvested under these conditions. Comparative analysis revealed 1,001 differentially expressed genes (DEGs) in the resistant strain (RS) relative to the wild-type strain (WT), comprising 628 upregulated and 373 downregulated genes. Concurrently, 524 differentially accumulated metabolites (DAMs) were identified, with 336 upregulated and 188 downregulated metabolites. KEGG pathway enrichment demonstrated pronounced upregulation in glycerophospholipid metabolism, α-linolenic acid metabolism, nucleic acid biosynthesis, and glycosylation processes. Conversely, arachidonic acid and galactose metabolism pathways were suppressed. Significant downregulation was observed in phosphatidylinositol signaling, aflatoxin biosynthesis, and cutin/suberin/wax biosynthesis pathways. Transcriptomic profiling further indicated that upregulated DEGs were predominantly associated with amino sugar/nucleotide sugar metabolism, ABC transporters, aflatoxin biosynthesis, and purine metabolism, while downregulated DEGs were enriched in N-glycan biosynthesis, endoplasmic reticulum protein processing, steroid biosynthesis, and riboflavin metabolism. Fludioxonil exerted substantial inhibitory effects on fungal growth, pathogenicity, and metabolic activity. Mechanistically, A. alternata counteracted fungicide-induced stress through modulation of its antioxidant defense system. This integrative multi-omics study delineates the dynamic gene expression and metabolic reprogramming in A. alternata under fludioxonil exposure, providing novel insights into potential molecular targets and informing the development of next-generation fungicidal strategies for phytopathogen control.

Key words: Alternaria alternate, Fludioxonil, Resistance mechanism, Fungicide resistance, Transcriptomics and metabolomics analysis