Laser dissection-assisted phloem transcriptomics highlights the metabolic and physiological changes accompanying clubroot disease progression in oilseed rape.

IF 6.2 1区 生物学 Q1 PLANT SCIENCES The Plant Journal Pub Date : 2024-11-22 DOI:10.1111/tpj.17156
Sara Blicharz, Karolina Stefanowicz, William Truman, Aneta Basińska-Barczak, Deeksha Singh, Anna Kasprzewska, Nuria de Diego, Ondřej Vrobel, Sanja Ćavar Zeljković, Petr Tarkowski, Robert Malinowski
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Abstract

Plasmodiophora brassicae, a soil-borne biotroph, establishes galls as strong physiological sinks on Brassicaceae plants including Brassica napus and Arabidopsis thaliana. We compare transcriptional profiles of phloem dissected from leaf petioles and hypocotyls of healthy and infected B. napus plants. Our results highlight how pathogenesis accompanies phloem-mediated defence responses whilst exerting a strong influence on carbon-nitrogen (C-N) economy. We observe transcriptional changes indicating decreased aliphatic glucosinolate biosynthesis, fluctuating jasmonic acid responses, altered amino acid (AA) and nitrate transport, carbohydrate metabolism and modified cytokinin responses. Changes observed in phloem-dissected from upper versus lower plant organs point to phloem as a conduit in mediating C-N repartitioning, nutrition-related signalling and cytokinin dynamics over long distances during clubroot disease. To assess changes in physiology, we measured AAs, sugars and cytokinins, in phloem exudates from B. napus plants. Despite the decrease in most AA and sucrose levels, isopentyl-type cytokinins increased within infected plants. Furthermore, we employed Arabidopsis for visualising promoter activities of B. napus AA and N transporter orthologues and tested the impact of disrupted cytokinin transport during P. brassicae-induced gall formation using Atabcg14 mutants. Our physiological and microscopy studies show that the host developmental reaction to P. brassicae relies on cytokinin and is accompanied by intense nitrogen and carbon repartitioning. Overall, our work highlights the systemic aspects of host responses that should be taken into account when studying clubroot disease.

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激光解剖辅助韧皮部转录组学突出显示了伴随油菜棒状病害发展的代谢和生理变化。
Plasmodiophora brassicae 是一种土生生物营养体,它在十字花科植物(包括油菜和拟南芥)上形成的虫瘿是一种强大的生理汇。我们比较了从健康和受感染的油菜植物叶柄和下胚轴中提取的韧皮部转录谱。我们的研究结果突显了致病机理是如何伴随着韧皮部介导的防御反应,同时对碳氮(C-N)经济产生强烈影响的。我们观察到转录变化表明脂肪族葡糖苷酸生物合成减少、茉莉酸反应波动、氨基酸(AA)和硝酸盐转运改变、碳水化合物代谢和细胞分裂素反应改变。从植物上部器官和下部器官分离的韧皮部观察到的变化表明,韧皮部是球根病发生期间长距离介导碳-氮重新分配、营养相关信号和细胞分裂素动态的通道。为了评估生理变化,我们测量了油菜植株韧皮部渗出物中的 AAs、糖和细胞分裂素。尽管大多数 AA 和蔗糖含量都有所下降,但受感染植株体内的异戊基细胞分裂素含量却有所增加。此外,我们还利用拟南芥来观察油菜 AA 和 N 转运体直向同源物的启动子活动,并利用 Atabcg14 突变体测试了在黄铜穗芥诱导的虫瘿形成过程中细胞分裂素运输中断的影响。我们的生理学和显微镜研究表明,宿主对铜绿菌的发育反应依赖于细胞分裂素,并伴随着强烈的氮和碳重新分配。总之,我们的工作强调了宿主反应的系统性,在研究球根病时应将其考虑在内。
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来源期刊
The Plant Journal
The Plant Journal 生物-植物科学
CiteScore
13.10
自引率
4.20%
发文量
415
审稿时长
2.3 months
期刊介绍: Publishing the best original research papers in all key areas of modern plant biology from the world"s leading laboratories, The Plant Journal provides a dynamic forum for this ever growing international research community. Plant science research is now at the forefront of research in the biological sciences, with breakthroughs in our understanding of fundamental processes in plants matching those in other organisms. The impact of molecular genetics and the availability of model and crop species can be seen in all aspects of plant biology. For publication in The Plant Journal the research must provide a highly significant new contribution to our understanding of plants and be of general interest to the plant science community.
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