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AoSho1 and AoOpy2 are involved in the regulation of mycelial growth, sporulation, osmoregulation, and pathogenicity in Arthrobotrys oligospora

ABSTRACT: Arthrobotrys oligospora, a widely distributed nematode-trapping fungus, utilises adhesive mycelial nets (traps) to capture nematodes. As key components of the MAPK cascade, Sho1 and Opy2 are critical in the fungal stress response. This study examined the roles of homologous Sho1 (AoSho1) and Opy2 (AoOpy2) through gene knockdown, phenotypic analysis, and multi-omics approaches. The results revealed that knockdown of Aosho1 and Aoopy2 led to reduced mycelial growth, a significant decrease in spore production, trap formation, and nematode predation capacity. Furthermore, deletion of Aosho1 and Aoopy2 increased autophagic activity and heightened sensitivity to osmotic stress. Transcriptome analysis indicated that AoOpy2 functions as a multifaceted regulator in fungal growth, development, and environmental adaptation. Metabolomics data also suggested that AoSho1 and AoOpy2 are involved in several metabolic pathways. In conclusion, AoSho1 and AoOpy2 are essential for mycelial growth, osmoregulation, and the pathogenicity of A. oligospora. This study lays the groundwork for understanding the roles and potential mechanisms of the MAPK signalling pathway in the development and pathogenicity of nematode-trapping fungi.

ORGANISM(S): Orbilia oligospora

PROVIDER: GSE306156 | GEO | 2025/08/27

REPOSITORIES: GEO

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Project description:As a dynamic structure with a barrier between the cell and the outside world, maintenance of cell wall integrity (CWI) is important for fungal growth, development and pathogenicity processes. Here we characterized a MADS-box transcription factor RlmA (AoRlmA) downstream of the CWI regulatory pathway in the nematode-trapping fungus Arthrobotrys oligospora. Deletion of AorlmA caused a reduction in mycelial growth and the number of nuclei, and significant downregulation of transcript levels of genes related to nucleus synthesis and DNA damage repair, such as rad3, spo11, and rad25. Meanwhile, the ΔAorlmA mutant strains showed a significant reduction in spore production compared with the wild-type (WT) strain, and the transcript levels of sporulation-related genes was downregulated in the ΔAorlmA mutant during the early and middle stages of condiation, such as flbA, medA, and vosA. Meanwhile, the mycelial cell wall of the ΔAorlmA mutant strain showed breakage. Also, the transcript levels of genes related to cell wall synthesis were significantly down-regulated in the mutant strain compared to the WT strain, and the mutant strain was more sensitive to stresses of cell wall synthesis disruptors, oxidative stress and osmotic stress than the WT strain. Compared with the WT strain, the ΔAorlmA mutant strain not only had a reduced number of traps and nematicidal ability, but also, the shape of the traps of the mutants has also changed. In addition, In addition, AoRlmA also regulates autophagy and endocytosis. Transcriptome analysis of ΔAorlmA mutant strains showed that AorlmA regulates redox, cell wall synthesis, DNA replication and damage repair, and pathogenic processes. Metabolomic analysis showed that AorlmA is involved in the biosynthesis of secondary metabolites of A. oligospora. To summarise, our data suggest that AorlmA is involved in growth, sporulation, spore germination, maintenance of cell wall integrity, DNA replication and damage repair, pathogenesis, autophagy and secondary metabolite biosynthesis processes.

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AoSho1 and AoOpy2 are involved in the regulation of mycelial growth, sporulation, osmoregulation, and pathogenicity in Arthrobotrys oligospora

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