FgMsn2 negatively regulates general stress responses and autophagy in Fusarium graminearum

Effective adaptation to diverse stressors is essential for fungal survival and pathogenicity. The mechanisms underlying general stress responses in Fusarium graminearum , the pathogen responsible for Fusarium head blight (FHB) in cereal crops, remain unclear. In this study, we identify FgMsn2 as a n...

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Published inPhytopathology Research Vol. 7; no. 1; pp. 1 - 10
Main Authors Gu, Rongcheng, Jian, Yunqing, Liu, Zunyong
Format Journal Article
LanguageEnglish
Published London BioMed Central 19.06.2025
BMC
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ISSN2524-4167
2096-5362
2524-4167
DOI10.1186/s42483-025-00341-5

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Abstract Effective adaptation to diverse stressors is essential for fungal survival and pathogenicity. The mechanisms underlying general stress responses in Fusarium graminearum , the pathogen responsible for Fusarium head blight (FHB) in cereal crops, remain unclear. In this study, we identify FgMsn2 as a negative regulator of general stress responses in F. graminearum . Deletion of FgMsn2 leads to resistance of F. graminearum to oxidative, osmotic, and cell wall stresses. Mechanically, FgMsn2 represses autophagy by inhibiting the expression of autophagy-related genes, including FgATG8 , and stress conditions trigger the cytoplasmic localization of FgMsn2. Additionally, the Δ FgMsn2 mutants show significantly reduced virulence on wheat, indicating the critical role of FgMsn2 in pathogenicity. These findings uncover a unique regulatory function of FgMsn2, which contrasts with its positive role in stress responses reported in other fungi, and provide valuable insights for developing novel strategies to manage FHB.
AbstractList Effective adaptation to diverse stressors is essential for fungal survival and pathogenicity. The mechanisms underlying general stress responses in Fusarium graminearum , the pathogen responsible for Fusarium head blight (FHB) in cereal crops, remain unclear. In this study, we identify FgMsn2 as a negative regulator of general stress responses in F. graminearum . Deletion of FgMsn2 leads to resistance of F. graminearum to oxidative, osmotic, and cell wall stresses. Mechanically, FgMsn2 represses autophagy by inhibiting the expression of autophagy-related genes, including FgATG8 , and stress conditions trigger the cytoplasmic localization of FgMsn2. Additionally, the Δ FgMsn2 mutants show significantly reduced virulence on wheat, indicating the critical role of FgMsn2 in pathogenicity. These findings uncover a unique regulatory function of FgMsn2, which contrasts with its positive role in stress responses reported in other fungi, and provide valuable insights for developing novel strategies to manage FHB.
Abstract Effective adaptation to diverse stressors is essential for fungal survival and pathogenicity. The mechanisms underlying general stress responses in Fusarium graminearum, the pathogen responsible for Fusarium head blight (FHB) in cereal crops, remain unclear. In this study, we identify FgMsn2 as a negative regulator of general stress responses in F. graminearum. Deletion of FgMsn2 leads to resistance of F. graminearum to oxidative, osmotic, and cell wall stresses. Mechanically, FgMsn2 represses autophagy by inhibiting the expression of autophagy-related genes, including FgATG8, and stress conditions trigger the cytoplasmic localization of FgMsn2. Additionally, the ΔFgMsn2 mutants show significantly reduced virulence on wheat, indicating the critical role of FgMsn2 in pathogenicity. These findings uncover a unique regulatory function of FgMsn2, which contrasts with its positive role in stress responses reported in other fungi, and provide valuable insights for developing novel strategies to manage FHB.
Effective adaptation to diverse stressors is essential for fungal survival and pathogenicity. The mechanisms underlying general stress responses in Fusarium graminearum , the pathogen responsible for Fusarium head blight (FHB) in cereal crops, remain unclear. In this study, we identify FgMsn2 as a negative regulator of general stress responses in F. graminearum . Deletion of FgMsn2 leads to resistance of F. graminearum to oxidative, osmotic, and cell wall stresses. Mechanically, FgMsn2 represses autophagy by inhibiting the expression of autophagy-related genes, including FgATG8 , and stress conditions trigger the cytoplasmic localization of FgMsn2. Additionally, the Δ FgMsn2 mutants show significantly reduced virulence on wheat, indicating the critical role of FgMsn2 in pathogenicity. These findings uncover a unique regulatory function of FgMsn2, which contrasts with its positive role in stress responses reported in other fungi, and provide valuable insights for developing novel strategies to manage FHB.
ArticleNumber 53
Author Liu, Zunyong
Jian, Yunqing
Gu, Rongcheng
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Issue 1
Keywords Pathogenicity
FgMsn2
Stress response
Autophagy
Fusarium head blight
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Snippet Effective adaptation to diverse stressors is essential for fungal survival and pathogenicity. The mechanisms underlying general stress responses in Fusarium...
Effective adaptation to diverse stressors is essential for fungal survival and pathogenicity. The mechanisms underlying general stress responses in Fusarium...
Abstract Effective adaptation to diverse stressors is essential for fungal survival and pathogenicity. The mechanisms underlying general stress responses in...
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StartPage 1
SubjectTerms Autophagy
Biomedical and Life Sciences
FgMsn2
Fusarium graminearum
Fusarium head blight
Life Sciences
Pathogenicity
Plant Pathology
Plant Sciences
Stress response
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Title FgMsn2 negatively regulates general stress responses and autophagy in Fusarium graminearum
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