Qiao Liu, Xi Lu, Qiaofen Wu, Zhibiao Lu, Renjun Qin, Kui Huang, Xun Zou, Ke Xia, Yanni Yang, Shuo Qiu
{"title":"转录组学与生理分析相结合,为白芨对白孢子菌的抗性机制提供了新的思路。","authors":"Qiao Liu, Xi Lu, Qiaofen Wu, Zhibiao Lu, Renjun Qin, Kui Huang, Xun Zou, Ke Xia, Yanni Yang, Shuo Qiu","doi":"10.3389/fpls.2025.1604512","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong><i>Bletilla striata</i> (Orchidaceae) is a valuable traditional Chinese medicinal plant prized for its dried rhizomes. However, its cultivation faces significant challenges from leaf rust disease caused by <i>Coleosporium bletiae</i>, which causes substantial yield losses.</p><p><strong>Methods: </strong>To investigate host resistance mechanisms, we compared rust-resistant and susceptible <i>B. striata</i> accessions through integrated transcriptomic and physiological analyses.</p><p><strong>Results and discussion: </strong>Phenotypic observations revealed that while both resistant and susceptible plants developed rust spores by 2 days post-inoculation (dpi), the resistant accession exhibited a significantly slower progression of spore stack formation and lesion expansion on abaxial leaf surfaces over time. Integrated transcriptomic and physiological analyses revealed that the rust-resistant material of <i>B. striata</i> accessions exhibited faster and stronger defense responses to pathogen infection compared to susceptible plants. These responses were characterized by significant upregulation of DEGs associated with antioxidant defense systems, secondary metabolite biosynthesis, JA, SA, and BR signaling pathways, concurrent downregulation of DEGs involved in cell wall remodeling, and calcium-mediated signaling. Furthermore, rust pathogen inoculation triggered rapid physiological responses in resistant plants, including enhanced activity of defense-related enzymes (CAT, PAL, β-1,3-glucanase, and chitinase) and early accumulation of osmolytes (soluble sugars, soluble proteins, and proline). These coordinated molecular and biochemical responses effectively restricted pathogen colonization and spread. These findings delineate the molecular basis of rust resistance in <i>B. striata</i>, identifying key regulatory nodes in defense pathways that could be targeted through precision breeding or genetic engineering to develop durable resistance against <i>C. bletilla</i>.</p>","PeriodicalId":12632,"journal":{"name":"Frontiers in Plant Science","volume":"16 ","pages":"1604512"},"PeriodicalIF":4.1000,"publicationDate":"2025-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12301390/pdf/","citationCount":"0","resultStr":"{\"title\":\"Transcriptomics combined with physiological analysis provides insights into the mechanism of resistance to <i>Coleosporium bletiae</i> in <i>Bletilla striata</i>.\",\"authors\":\"Qiao Liu, Xi Lu, Qiaofen Wu, Zhibiao Lu, Renjun Qin, Kui Huang, Xun Zou, Ke Xia, Yanni Yang, Shuo Qiu\",\"doi\":\"10.3389/fpls.2025.1604512\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong><i>Bletilla striata</i> (Orchidaceae) is a valuable traditional Chinese medicinal plant prized for its dried rhizomes. However, its cultivation faces significant challenges from leaf rust disease caused by <i>Coleosporium bletiae</i>, which causes substantial yield losses.</p><p><strong>Methods: </strong>To investigate host resistance mechanisms, we compared rust-resistant and susceptible <i>B. striata</i> accessions through integrated transcriptomic and physiological analyses.</p><p><strong>Results and discussion: </strong>Phenotypic observations revealed that while both resistant and susceptible plants developed rust spores by 2 days post-inoculation (dpi), the resistant accession exhibited a significantly slower progression of spore stack formation and lesion expansion on abaxial leaf surfaces over time. Integrated transcriptomic and physiological analyses revealed that the rust-resistant material of <i>B. striata</i> accessions exhibited faster and stronger defense responses to pathogen infection compared to susceptible plants. These responses were characterized by significant upregulation of DEGs associated with antioxidant defense systems, secondary metabolite biosynthesis, JA, SA, and BR signaling pathways, concurrent downregulation of DEGs involved in cell wall remodeling, and calcium-mediated signaling. Furthermore, rust pathogen inoculation triggered rapid physiological responses in resistant plants, including enhanced activity of defense-related enzymes (CAT, PAL, β-1,3-glucanase, and chitinase) and early accumulation of osmolytes (soluble sugars, soluble proteins, and proline). These coordinated molecular and biochemical responses effectively restricted pathogen colonization and spread. These findings delineate the molecular basis of rust resistance in <i>B. striata</i>, identifying key regulatory nodes in defense pathways that could be targeted through precision breeding or genetic engineering to develop durable resistance against <i>C. bletilla</i>.</p>\",\"PeriodicalId\":12632,\"journal\":{\"name\":\"Frontiers in Plant Science\",\"volume\":\"16 \",\"pages\":\"1604512\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2025-07-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12301390/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Frontiers in Plant Science\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.3389/fpls.2025.1604512\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q1\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Plant Science","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3389/fpls.2025.1604512","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
Transcriptomics combined with physiological analysis provides insights into the mechanism of resistance to Coleosporium bletiae in Bletilla striata.
Introduction: Bletilla striata (Orchidaceae) is a valuable traditional Chinese medicinal plant prized for its dried rhizomes. However, its cultivation faces significant challenges from leaf rust disease caused by Coleosporium bletiae, which causes substantial yield losses.
Methods: To investigate host resistance mechanisms, we compared rust-resistant and susceptible B. striata accessions through integrated transcriptomic and physiological analyses.
Results and discussion: Phenotypic observations revealed that while both resistant and susceptible plants developed rust spores by 2 days post-inoculation (dpi), the resistant accession exhibited a significantly slower progression of spore stack formation and lesion expansion on abaxial leaf surfaces over time. Integrated transcriptomic and physiological analyses revealed that the rust-resistant material of B. striata accessions exhibited faster and stronger defense responses to pathogen infection compared to susceptible plants. These responses were characterized by significant upregulation of DEGs associated with antioxidant defense systems, secondary metabolite biosynthesis, JA, SA, and BR signaling pathways, concurrent downregulation of DEGs involved in cell wall remodeling, and calcium-mediated signaling. Furthermore, rust pathogen inoculation triggered rapid physiological responses in resistant plants, including enhanced activity of defense-related enzymes (CAT, PAL, β-1,3-glucanase, and chitinase) and early accumulation of osmolytes (soluble sugars, soluble proteins, and proline). These coordinated molecular and biochemical responses effectively restricted pathogen colonization and spread. These findings delineate the molecular basis of rust resistance in B. striata, identifying key regulatory nodes in defense pathways that could be targeted through precision breeding or genetic engineering to develop durable resistance against C. bletilla.
期刊介绍:
In an ever changing world, plant science is of the utmost importance for securing the future well-being of humankind. Plants provide oxygen, food, feed, fibers, and building materials. In addition, they are a diverse source of industrial and pharmaceutical chemicals. Plants are centrally important to the health of ecosystems, and their understanding is critical for learning how to manage and maintain a sustainable biosphere. Plant science is extremely interdisciplinary, reaching from agricultural science to paleobotany, and molecular physiology to ecology. It uses the latest developments in computer science, optics, molecular biology and genomics to address challenges in model systems, agricultural crops, and ecosystems. Plant science research inquires into the form, function, development, diversity, reproduction, evolution and uses of both higher and lower plants and their interactions with other organisms throughout the biosphere. Frontiers in Plant Science welcomes outstanding contributions in any field of plant science from basic to applied research, from organismal to molecular studies, from single plant analysis to studies of populations and whole ecosystems, and from molecular to biophysical to computational approaches.
Frontiers in Plant Science publishes articles on the most outstanding discoveries across a wide research spectrum of Plant Science. The mission of Frontiers in Plant Science is to bring all relevant Plant Science areas together on a single platform.