{"title":"Stomatal-based immunity differentiation across vascular plant lineages","authors":"Yuan-Yuan Zeng, Xu-Dong Liu, Guang-Qian Yao, Min-Hui Bi, Xiangling Fang, Kailiang Yu, Jinsheng He, Jianquan Liu, Timothy J. Brodribb, Xiang-Wen Fang","doi":"10.1111/nph.70077","DOIUrl":null,"url":null,"abstract":"<p>\n</p><ul>\n<li>Some plants are known to actively close their stomata in the presence of foliar pathogens, inhibiting pathogen entry into leaves, leading to ‘stoma-based immunity’ as the first line of defense. However, the variation in stoma-based innate immunity across the diversity of vascular plants remains unclear.</li>\n<li>Here, we investigated the stomatal response and guard cell signaling pathway in various seed plant, fern, and lycophyte species when exposed to the bacterial pathogens or pathogen-associated molecular patterns (PAMPs).</li>\n<li>We observed active stomatal closure in 10 seed plants when exposed to bacteria or PAMPs, whereas none of the nine fern and one lycophyte species exhibited this response. The PAMP flg22-induced reactive oxygen species burst was observed in all species, but the downstream signaling events, including cytosolic Ca<sup>2+</sup> accumulation, nitric oxide production, ion fluxes, vacuolar acidification, cytoplasmic pH elevation, vacuolar compartmentation, and disaggregation of the actin cytoskeleton in guard cells, were only observed in seed plants. No such changes were observed in the representatives of ferns and lycophytes.</li>\n<li>Our findings suggest a major difference in the regulation of stomatal immunity between seed plants and ferns and lycophytes under this study's conditions, unveiling physiological and biophysical mechanisms that may have underpinned the evolutionary adaptation of stomatal responses to pathogen attacks in seed plants.</li>\n</ul><p></p>","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"23 1","pages":""},"PeriodicalIF":8.3000,"publicationDate":"2025-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Phytologist","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/nph.70077","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Some plants are known to actively close their stomata in the presence of foliar pathogens, inhibiting pathogen entry into leaves, leading to ‘stoma-based immunity’ as the first line of defense. However, the variation in stoma-based innate immunity across the diversity of vascular plants remains unclear.
Here, we investigated the stomatal response and guard cell signaling pathway in various seed plant, fern, and lycophyte species when exposed to the bacterial pathogens or pathogen-associated molecular patterns (PAMPs).
We observed active stomatal closure in 10 seed plants when exposed to bacteria or PAMPs, whereas none of the nine fern and one lycophyte species exhibited this response. The PAMP flg22-induced reactive oxygen species burst was observed in all species, but the downstream signaling events, including cytosolic Ca2+ accumulation, nitric oxide production, ion fluxes, vacuolar acidification, cytoplasmic pH elevation, vacuolar compartmentation, and disaggregation of the actin cytoskeleton in guard cells, were only observed in seed plants. No such changes were observed in the representatives of ferns and lycophytes.
Our findings suggest a major difference in the regulation of stomatal immunity between seed plants and ferns and lycophytes under this study's conditions, unveiling physiological and biophysical mechanisms that may have underpinned the evolutionary adaptation of stomatal responses to pathogen attacks in seed plants.
期刊介绍:
New Phytologist is an international electronic journal published 24 times a year. It is owned by the New Phytologist Foundation, a non-profit-making charitable organization dedicated to promoting plant science. The journal publishes excellent, novel, rigorous, and timely research and scholarship in plant science and its applications. The articles cover topics in five sections: Physiology & Development, Environment, Interaction, Evolution, and Transformative Plant Biotechnology. These sections encompass intracellular processes, global environmental change, and encourage cross-disciplinary approaches. The journal recognizes the use of techniques from molecular and cell biology, functional genomics, modeling, and system-based approaches in plant science. Abstracting and Indexing Information for New Phytologist includes Academic Search, AgBiotech News & Information, Agroforestry Abstracts, Biochemistry & Biophysics Citation Index, Botanical Pesticides, CAB Abstracts®, Environment Index, Global Health, and Plant Breeding Abstracts, and others.