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真菌病毒感染会下调……以削弱……病菌的致病性。(你提供的原文中部分内容不完整,导致翻译可能不太准确完整)

The infection of mycovirus down regulates to weaken the pathogenicity of the f. sp. .

作者信息

Zhang Jingyi, Li Chenjiao, You Shaopeng, Feng Yuyao, Liu Mingyi, Li Bo, Wang Shutong, Cao Keqiang, Wang Yanan

机构信息

College of Plant Protection, Hebei Agricultural University, Baoding, Hebei, China.

出版信息

Front Plant Sci. 2025 Jul 22;16:1598183. doi: 10.3389/fpls.2025.1598183. eCollection 2025.

Abstract

This study explored the association between differentially expressed miRNA Aa-milR13 in f. sp. strains with and without virus infection, and the regulation of fungal host pathogenicity by viruses. MiRNA sequencing was conducted on a hypovirulent strain (QY21) with compound infection of Alternaria alternata chrysovirus 1 (AaCV1) and Alternaria alternata magoulivirus 1 (AaMV1), a hypovirulent strain (QY21-C1) with single AaMV1 infection, and a virus-free strain (QY21-C2). Fourteen miRNAs with significant differential expression were identified. Aa-milR13 was significantly downregulated in virus-infected strains and validated by RT-qPCR. Structural analysis of the Aa-milR13 sequence identified that the mature Aa-milR13 is located at the 5' end of its precursor stem-loop structure. Knockout of Aa-milR13 in QY21-C2 resulted in slower hyphal growth, darker colony color, and reduced pathogenicity, resembling virus-infected strains. Conversely, overexpression of Aa-milR13 led to accelerated hyphal growth, lighter colony color, and significantly enhanced pathogenicity.Three target genes of Aa-milR13, subtilisin-like protein (AaSLP,cinr CC77DRAFT_1100266), DUF431-domain-containing protein (DUF431, CC77DRAFT_1022347), and high-affinity nitrate transporter NrtB (NrtB, CC77DRAFT_1056077), were predicted and confirmed by RT-qPCR to be negatively correlated with Aa-milR13 expression. Bioinformatics analysis indicated that Aa-milR13 targets the CDS regions of the potential target genes through cleavage, with Watson-Crick pairing of AU, CG, wobble pairing of GU, and various pairing patterns such as AA, AC, AG, GG, UU, UC, etc. This study suggests that fungal virus infection downregulates Aa-milR13, upregulating its targets, potentially contributing to reduced fungal pathogenicity. This is the first report of small RNAs acting as an intermediate bridge in the regulation of fungi virulence by fungal viruses. The research results lay the foundation for elucidating the mechanism of small RNA-involved regulation of fungi hypovirulence by fungal viruses and provide theoretical support for the use of fungal viruses in the control of crop fungal diseases.

摘要

本研究探讨了在感染病毒和未感染病毒的链格孢菌菌株中差异表达的微小RNA Aa - milR13与病毒对真菌宿主致病性的调控之间的关联。对一株同时感染链格孢盘多毛孢病毒1(AaCV1)和链格孢马古病毒1(AaMV1)的低毒力菌株(QY21)、一株仅感染AaMV1的低毒力菌株(QY21 - C1)以及一株无病毒菌株(QY21 - C2)进行了微小RNA测序。鉴定出14个具有显著差异表达的微小RNA。Aa - milR13在病毒感染菌株中显著下调,并通过RT - qPCR进行了验证。对Aa - milR13序列的结构分析表明,成熟的Aa - milR13位于其前体茎环结构的5'端。在QY21 - C2中敲除Aa - milR13导致菌丝生长变慢、菌落颜色变深以及致病性降低,类似于病毒感染菌株。相反,过表达Aa - milR13导致菌丝生长加速、菌落颜色变浅以及致病性显著增强。预测了Aa - milR13的三个靶基因,枯草杆菌蛋白酶样蛋白(AaSLP,cinr CC77DRAFT_1100266)、含DUF431结构域的蛋白(DUF431,CC77DRAFT_1022347)和高亲和力硝酸盐转运蛋白NrtB(NrtB,CC77DRAFT_1056077),并通过RT - qPCR证实它们与Aa - milR13的表达呈负相关。生物信息学分析表明,Aa - milR13通过切割作用靶向潜在靶基因的编码区,存在AU的沃森 - 克里克配对、CG配对、GU的摆动配对以及AA、AC、AG、GG、UU、UC等多种配对模式。本研究表明,真菌病毒感染下调Aa - milR13,上调其靶标,可能导致真菌致病性降低。这是关于小RNA在真菌病毒调控真菌毒力中作为中间桥梁作用的首次报道。研究结果为阐明真菌病毒通过小RNA调控真菌低毒力的机制奠定了基础,并为利用真菌病毒防治作物真菌病害提供了理论支持。

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