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 in | Phytopathology Research Vol. 7; no. 1; pp. 1 - 10 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
London
BioMed Central
19.06.2025
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ISSN | 2524-4167 2096-5362 2524-4167 |
DOI | 10.1186/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. |
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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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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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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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