Wang Chun, Yang Kexin, Jibril Sauban Musa, Wang Ruoping, Li Chengyun, Wang Yi
State Key Laboratory for Conservation and Utilization of Bio-Resources in Yunnan, Yunnan Agricultural University, Kunming 650201, China.
Yunnan-CABI Joint Laboratory for Integrated Prevention and Control of Transboundary Pests, Yunnan Agricultural University, Kunming 650201, China.
J Fungi (Basel). 2025 Mar 17;11(3):227. doi: 10.3390/jof11030227.
Rice brown spot disease, caused by , is a significant fungal disease that poses a major threat to global rice production. Despite its widespread impact, genomic studies of remain limited, particularly those involving high-quality genomic data. In this study, we performed whole-genome sequencing of the strain RBD1, which was isolated from the demonstration field for upland rice cultivation in Haozhiba Village, Lancang County, Pu'er City, Yunnan Province, China, using a combination of second-generation Illumina sequencing and third-generation Single-Molecule Real-Time (SMRT) sequencing. The assembled genome was 37.5 Mb in size with a G + C content of 49.39%, containing 42 contigs with a contig N50 of 2.0 Mb. Genomic analysis identified genes related to carbon, nitrogen, and lipid metabolism, highlighting the strain's metabolic flexibility under diverse environmental conditions and host interactions. Additionally, we identified pathogenicity-related genes involved in MAPK signaling, G protein signaling, and oxidative stress responses. Under 1.2 M sorbitol-induced osmotic stress, we observed significant differences in growth responses between RBD1 and the rice blast fungus H7. Transcriptomic analysis using Illumina sequencing revealed that RBD1 responds to osmotic stress by enhancing carbohydrate metabolism, fatty acid degradation, and amino acid synthesis, while H7 primarily relies on protein synthesis to enhance growth tolerance. This study provides a valuable foundation for understanding the pathogenic mechanisms of rice brown spot and future disease control strategies.
由[病原体名称未给出]引起的水稻褐条斑病是一种对全球水稻生产构成重大威胁的重要真菌病害。尽管其影响广泛,但对[病原体名称未给出]的基因组研究仍然有限,特别是那些涉及高质量基因组数据的研究。在本研究中,我们使用第二代Illumina测序和第三代单分子实时(SMRT)测序相结合的方法,对从中国云南省普洱市澜沧县浩治坝村旱稻种植示范田分离的[病原体名称未给出]菌株RBD1进行了全基因组测序。组装后的基因组大小为37.5 Mb,G + C含量为49.39%,包含42个重叠群,重叠群N50为2.0 Mb。基因组分析确定了与碳、氮和脂质代谢相关的基因,突出了该菌株在不同环境条件和宿主相互作用下的代谢灵活性。此外,我们还鉴定了参与MAPK信号传导、G蛋白信号传导和氧化应激反应的致病性相关基因。在1.2 M山梨醇诱导的渗透胁迫下,我们观察到RBD1与稻瘟病菌H7在生长反应上存在显著差异。使用Illumina测序进行的转录组分析表明,RBD1通过增强碳水化合物代谢、脂肪酸降解和氨基酸合成来应对渗透胁迫,而H7主要依靠蛋白质合成来提高生长耐受性。本研究为理解水稻褐条斑病的致病机制和未来的病害控制策略提供了有价值的基础。