Invasion of the stigma by oomycete pathogenic hyphae or pollen tubes: striking similarities and differences.

IF 5.6 2区 生物学 Q1 PLANT SCIENCES Journal of Experimental Botany Pub Date : 2024-10-30 DOI:10.1093/jxb/erae308
Lucie Riglet, Sophie Hok, Naïma Kebdani-Minet, Joëlle Le Berre, Mathieu Gourgues, Frédérique Rozier, Vincent Bayle, Lesli Bancel-Vallée, Valérie Allasia, Harald Keller, Martine Da Rocha, Agnés Attard, Isabelle Fobis-Loisy
{"title":"Invasion of the stigma by oomycete pathogenic hyphae or pollen tubes: striking similarities and differences.","authors":"Lucie Riglet, Sophie Hok, Naïma Kebdani-Minet, Joëlle Le Berre, Mathieu Gourgues, Frédérique Rozier, Vincent Bayle, Lesli Bancel-Vallée, Valérie Allasia, Harald Keller, Martine Da Rocha, Agnés Attard, Isabelle Fobis-Loisy","doi":"10.1093/jxb/erae308","DOIUrl":null,"url":null,"abstract":"<p><p>Both the pollen tube and hyphae of filamentous pathogens penetrate the outer layer of the host and then grow within host tissues. Early epidermal responses are decisive for the outcome of these two-cell interaction processes. We identified a single cell type, the papilla in the stigma of Arabidospis, as a tool to conduct a comprehensive comparative analysis on how an epidermal cell responds to the invasion of an unwanted pathogen or a welcome pollen tube. We showed that Phytophtora parasitica, a root oomycete, effectively breaches the stigmatic cell wall and develops as a biotroph within the papilla cytoplasm. These invasive features resemble the behaviour exhibited by the pathogen within its natural host cell, but diverge from the manner in which the pollen tube progresses, being engulfed within the papilla cell wall. Quantitative analysis revealed that both invaders trigger reorganization of the stigmatic endomembrane system and the actin cytoskeleton. While some remodelling processes are shared between the two interactions, others appear more specific towards the respective invader. These findings underscore the remarkable ability of an epidermal cell to differentiate between two types of invaders, thereby enabling it to trigger the most suitable response during the onset of invasion.</p>","PeriodicalId":15820,"journal":{"name":"Journal of Experimental Botany","volume":" ","pages":"6258-6274"},"PeriodicalIF":5.6000,"publicationDate":"2024-10-30","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/erae308","RegionNum":2,"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

Both the pollen tube and hyphae of filamentous pathogens penetrate the outer layer of the host and then grow within host tissues. Early epidermal responses are decisive for the outcome of these two-cell interaction processes. We identified a single cell type, the papilla in the stigma of Arabidospis, as a tool to conduct a comprehensive comparative analysis on how an epidermal cell responds to the invasion of an unwanted pathogen or a welcome pollen tube. We showed that Phytophtora parasitica, a root oomycete, effectively breaches the stigmatic cell wall and develops as a biotroph within the papilla cytoplasm. These invasive features resemble the behaviour exhibited by the pathogen within its natural host cell, but diverge from the manner in which the pollen tube progresses, being engulfed within the papilla cell wall. Quantitative analysis revealed that both invaders trigger reorganization of the stigmatic endomembrane system and the actin cytoskeleton. While some remodelling processes are shared between the two interactions, others appear more specific towards the respective invader. These findings underscore the remarkable ability of an epidermal cell to differentiate between two types of invaders, thereby enabling it to trigger the most suitable response during the onset of invasion.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
卵菌病原菌丝或花粉管侵入柱头:惊人的相似之处和不同之处。
丝状病原体的菌丝和花粉管都能穿透寄主外层,并在寄主组织内生长。表皮的早期反应对这些双细胞相互作用过程的结果起着决定性作用。我们确定了一种单一的细胞类型,即大连阿拉伯纺锤体(Arabidospis thaliana)柱头的乳头,并以此为工具,对表皮细胞如何应对不受欢迎的病原体或花粉管的入侵进行了全面的比较分析。我们的研究表明,根部卵菌 Phytophtora parasitica 能有效地突破柱头细胞壁,并在乳头细胞质内发育成生物营养体。这些入侵特征与病原体在其天然宿主细胞内的行为相似,但与花粉管在乳头细胞壁内被吞噬的方式不同。定量分析显示,两种入侵者都会引发柱头内膜系统和肌动蛋白细胞骨架的重组。虽然有些重塑过程在两种相互作用中是共享的,但其他过程似乎对各自的入侵者更具特异性。这些发现强调了表皮细胞区分两种入侵者的非凡能力,从而使其能够在入侵开始时触发最合适的反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Journal of Experimental Botany
Journal of Experimental Botany 生物-植物科学
CiteScore
12.30
自引率
4.30%
发文量
450
审稿时长
1.9 months
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.
期刊最新文献
Gibberellins: Extending the Green Revolution. Investigating biological nitrogen fixation via single-cell transcriptomics. TORquing chromatin: the regulatory role of TOR kinase on chromatin function. Innovative modeling on the effects of low-temperature stress on rice yields. Accounting for the impact of genotype and environment on variation in leaf respiration of wheat in Mexico and Australia.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1