School of Biotechnology, Institute of Agricultural Technology, Suranaree University of Technology.
School of Crop Production Technology, Institute of Agricultural Technology, Suranaree University of Technology.
Microbes Environ. 2023;38(1). doi: 10.1264/jsme2.ME22079.
Cercospora leaf spot (CLS) is caused by Cercospora canescens and is one of the most important diseases of mungbean (Vigna radiata). Cercospora leaf spot may result in economic loss in production areas. The present study investigated the potential of Bacillus velezensis S141 as a biocontrol agent for C. canescens PAK1 growth on culture plates. Cell-free secretions from a dual culture of S141+PAK1 inhibited fungal growth more than those from a single culture of S141. The biocontrol efficiency of S141 against Cercospora leaf spot on mungbean was then evaluated by spraying. The disease severity of Cercospora leaf spot was significantly reduced in plants treated with S141, with a control efficiency of 83% after 2 days of infection. Comparative transcriptomics and qRT-PCR ana-lyses of S141 during C. canescens inhibition were performed to elucidate the antifungal mechanisms underlying its antifungal activity against Cercospora leaf spot. According to the differentially expressed genes, most up-regulated genes involved in the biosynthetic genes encoding enzymatic hydrolases, including protease, β-glucanase, and N-acyl glucosaminase, were detected in strain S141 following its interaction. Moreover, genes related to secondary metabolites (surfactin, bacilysin, and bacillomycin D) were up-regulated. Collectively, these results suggest that S141 exhibited strong antifungal activity against C. canescens due to multiple enzymatic hydrolases and secondary metabolites. Therefore, the present study provides insights into the biological network responsible for the antifungal activity of B. velezensis S141 against C. canescens.
叶斑病(CLS)是由叶点霉引起的,是绿豆(Vigna radiata)最重要的病害之一。叶斑病可能导致生产区的经济损失。本研究调查了芽孢杆菌 S141 作为生防菌对 culture plates 上 C. canescens PAK1 生长的潜力。S141+PAK1 双培养物的无细胞分泌物对真菌生长的抑制作用强于 S141 单培养物的无细胞分泌物。然后通过喷洒评估 S141 对绿豆叶斑病的生防效率。用 S141 处理的植物的叶斑病严重程度显著降低,感染后 2 天的防治效率为 83%。对 S141 在抑制 C. canescens 过程中的比较转录组学和 qRT-PCR 分析,以阐明其对叶斑病的抗真菌机制。根据差异表达基因,在 S141 相互作用后,检测到大多数上调的基因参与编码酶水解酶的生物合成基因,包括蛋白酶、β-葡聚糖酶和 N-酰基葡糖胺酶。此外,与次级代谢产物(表面活性素、杆菌肽和杆菌霉素 D)相关的基因上调。综上所述,这些结果表明,S141 由于多种酶水解酶和次级代谢产物对 C. canescens 表现出强烈的抗真菌活性。因此,本研究为芽孢杆菌 S141 对 C. canescens 的抗真菌活性的生物网络提供了深入了解。