SsNEP2 Plays a Role in the Interaction Between Sclerotinia sclerotiorum and Coniothyrium minitans

<i>Sclerotinia sclerotiorum</i>, a fungal pathogen that is spread worldwide and causes serious diseases on crops, can be parasitized specifically by the mycoparasite <i>Coniothyrium minitans</i>. <i>SsNEP2,</i> encoding a necrosis-inducing protein in <i>S. sclerotiorum,</i> was previously inferred to play a role in the virulence to host plants. In this study, silencing of <i>SsNEP2</i> in <i>S. sclerotiorum</i> had no significant (<i>p</i> < 0.01) influence on mycelial morphology, while overexpression led to lower mycelial growth and more branches. When amended with the fermentation broth of the <i>SsNEP2</i> silencing mutants, conidial germination of <i>C. minitans</i> was promoted, while conidial production decreased. When parasitized by <i>C. minitans</i>, enhanced resistance of the <i>SsNEP2</i> silencing mutants and weaker resistance of the overexpressed transformants were observed compared to the wild-type <i>S. sclerotiorum</i> strain 1980. In addition, the expression of <i>SsNEP2</i> in <i>C. minitans</i> enhanced mycelial parasitism on <i>S. sclerotiorum</i> and restored the effect of silencing <i>SsNEP2</i> in <i>S. sclerotiorum</i> on mycoparasitism. Thus, we highlight the role of <i>SsNEP2</i> as a PAMP-like protein in the mycoparasitism between <i>C. minitans</i> and its host fungus <i>S. sclerotiorum. SsNEP2</i> can be used to promote the biological potential of <i>C. minitans</i>.

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Publication Details

Journal
Journal of Fungi
Published
2025-02-16
DOI
https://doi.org/10.3390/jof11020151
Citations
1
Primary Topic
Plant pathogens and resistance mechanisms
Type
article
Field-Weighted Citation Impact
1.75

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article

SsNEP2 Plays a Role in the Interaction Between Sclerotinia sclerotiorum and Coniothyrium minitans

Huizhang Zhao, Yànpíng Fù, Jiāsēn Chéng, Zihang Zhu et al.
1 citations
Journal of Fungi
Plant pathogens and resistance mechanisms
1.75
article

SsNEP2 Plays a Role in the Interaction Between Sclerotinia sclerotiorum and Coniothyrium minitans

Huizhang Zhao, Yànpíng Fù, Jiāsēn Chéng, Zihang Zhu, Dàohóng Jiāng, Jiǎtāo Xiè, Haixuan Wang, Yueli Xu
article en
1 citations

Abstract

<i>Sclerotinia sclerotiorum</i>, a fungal pathogen that is spread worldwide and causes serious diseases on crops, can be parasitized specifically by the mycoparasite <i>Coniothyrium minitans</i>. <i>SsNEP2,</i> encoding a necrosis-inducing protein in <i>S. sclerotiorum,</i> was previously inferred to play a role in the virulence to host plants. In this study, silencing of <i>SsNEP2</i> in <i>S. sclerotiorum</i> had no significant (<i>p</i> < 0.01) influence on mycelial morphology, while overexpression led to lower mycelial growth and more branches. When amended with the fermentation broth of the <i>SsNEP2</i> silencing mutants, conidial germination of <i>C. minitans</i> was promoted, while conidial production decreased. When parasitized by <i>C. minitans</i>, enhanced resistance of the <i>SsNEP2</i> silencing mutants and weaker resistance of the overexpressed transformants were observed compared to the wild-type <i>S. sclerotiorum</i> strain 1980. In addition, the expression of <i>SsNEP2</i> in <i>C. minitans</i> enhanced mycelial parasitism on <i>S. sclerotiorum</i> and restored the effect of silencing <i>SsNEP2</i> in <i>S. sclerotiorum</i> on mycoparasitism. Thus, we highlight the role of <i>SsNEP2</i> as a PAMP-like protein in the mycoparasitism between <i>C. minitans</i> and its host fungus <i>S. sclerotiorum. SsNEP2</i> can be used to promote the biological potential of <i>C. minitans</i>.

Journal of FungiVol. 11(2)
Huazhong Agricultural University (CN), Hubei Academy of Agricultural Sciences (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 17%
Plant pathogens and resistance mechanisms
1.75
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