{"title":"转录组学和功能分析揭示了葡萄孢菌在玫瑰中定植的复杂景观。","authors":"Rui Li, Juanni Yao, Jiaying Xiao, Yue Ming, Daofeng Liu, Yueqing Cao, Zhensheng Kang, Zhengguo Li, Yulin Cheng","doi":"10.1093/jxb/eraf219","DOIUrl":null,"url":null,"abstract":"<p><p>Botrytis cinerea (Bc) is a notorious necrotrophic fungal pathogen that colonizes different plant tissues. Gray mold caused by Bc is a great threat to rose (Rosa sp.), one of the most important ornamental plants worldwide, but colonization strategies of Bc in rose tissues remain unexplored. Here, we report a comprehensive investigation of the mechanisms underlying Bc colonization in rose leaf and petal by integrated transcriptomic and functional analyses. Multiple genes involved in the biogenesis of ribosome, an organelle for protein synthesis, were commonly upregulated during Bc colonization in leaf and petal. Application of inhibitors targeting fungal ribosome biogenesis, coupled with gene disruption assays, demonstrated the contribution of ribosome biogenesis to Bc colonization in leaf and petal. Notably, genes associated with nitrogen transport, carbohydrate metabolism, and protein glycosylation contributed to Bc colonization, and some of them were tissue-specific virulence factors. Through in silico secretome analysis and functional verification, we identified seven novel plant cell death-inducing effectors and one of them contributed to Bc colonization in leaf and petal. This study reveals a complex unexplored landscape of Bc colonization in rose and also advances the understanding of plant-pathogen interactions.</p>","PeriodicalId":15820,"journal":{"name":"Journal of Experimental Botany","volume":" ","pages":""},"PeriodicalIF":5.6000,"publicationDate":"2025-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Transcriptomic and functional analyses reveal a complex unexplored landscape of Botrytis cinerea colonization in rose.\",\"authors\":\"Rui Li, Juanni Yao, Jiaying Xiao, Yue Ming, Daofeng Liu, Yueqing Cao, Zhensheng Kang, Zhengguo Li, Yulin Cheng\",\"doi\":\"10.1093/jxb/eraf219\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Botrytis cinerea (Bc) is a notorious necrotrophic fungal pathogen that colonizes different plant tissues. Gray mold caused by Bc is a great threat to rose (Rosa sp.), one of the most important ornamental plants worldwide, but colonization strategies of Bc in rose tissues remain unexplored. Here, we report a comprehensive investigation of the mechanisms underlying Bc colonization in rose leaf and petal by integrated transcriptomic and functional analyses. Multiple genes involved in the biogenesis of ribosome, an organelle for protein synthesis, were commonly upregulated during Bc colonization in leaf and petal. Application of inhibitors targeting fungal ribosome biogenesis, coupled with gene disruption assays, demonstrated the contribution of ribosome biogenesis to Bc colonization in leaf and petal. Notably, genes associated with nitrogen transport, carbohydrate metabolism, and protein glycosylation contributed to Bc colonization, and some of them were tissue-specific virulence factors. Through in silico secretome analysis and functional verification, we identified seven novel plant cell death-inducing effectors and one of them contributed to Bc colonization in leaf and petal. This study reveals a complex unexplored landscape of Bc colonization in rose and also advances the understanding of plant-pathogen interactions.</p>\",\"PeriodicalId\":15820,\"journal\":{\"name\":\"Journal of Experimental Botany\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":5.6000,\"publicationDate\":\"2025-05-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Experimental Botany\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1093/jxb/eraf219\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Experimental Botany","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/jxb/eraf219","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
Transcriptomic and functional analyses reveal a complex unexplored landscape of Botrytis cinerea colonization in rose.
Botrytis cinerea (Bc) is a notorious necrotrophic fungal pathogen that colonizes different plant tissues. Gray mold caused by Bc is a great threat to rose (Rosa sp.), one of the most important ornamental plants worldwide, but colonization strategies of Bc in rose tissues remain unexplored. Here, we report a comprehensive investigation of the mechanisms underlying Bc colonization in rose leaf and petal by integrated transcriptomic and functional analyses. Multiple genes involved in the biogenesis of ribosome, an organelle for protein synthesis, were commonly upregulated during Bc colonization in leaf and petal. Application of inhibitors targeting fungal ribosome biogenesis, coupled with gene disruption assays, demonstrated the contribution of ribosome biogenesis to Bc colonization in leaf and petal. Notably, genes associated with nitrogen transport, carbohydrate metabolism, and protein glycosylation contributed to Bc colonization, and some of them were tissue-specific virulence factors. Through in silico secretome analysis and functional verification, we identified seven novel plant cell death-inducing effectors and one of them contributed to Bc colonization in leaf and petal. This study reveals a complex unexplored landscape of Bc colonization in rose and also advances the understanding of plant-pathogen interactions.
期刊介绍:
The Journal of Experimental Botany publishes high-quality primary research and review papers in the plant sciences. These papers cover a range of disciplines from molecular and cellular physiology and biochemistry through whole plant physiology to community physiology.
Full-length primary papers should contribute to our understanding of how plants develop and function, and should provide new insights into biological processes. The journal will not publish purely descriptive papers or papers that report a well-known process in a species in which the process has not been identified previously. Articles should be concise and generally limited to 10 printed pages.