Microbes and metabolites of a plant-parasite interaction: Deciphering the ecology of Tetrastigma host choice in the world’s largest parasitic flower, Rafflesia

IF 5.4 Q1 PLANT SCIENCES Current Plant Biology Pub Date : 2025-02-04 DOI:10.1016/j.cpb.2025.100456
Jeanmaire Molina , Roche C. de Guzman , Rinat Abzalimov , Wenkai Huang , Anusha Guruprasad , Ronniel Pedales , Adhityo Wicaksono , Destiny Davis , John Rey Callado , Hans Bänziger , Piyakaset Suksathan , William Eaton , Pride Yin , Marco Bürger , Mick Erickson , Stephen Jones , James Adams , Susan Pell
{"title":"Microbes and metabolites of a plant-parasite interaction: Deciphering the ecology of Tetrastigma host choice in the world’s largest parasitic flower, Rafflesia","authors":"Jeanmaire Molina ,&nbsp;Roche C. de Guzman ,&nbsp;Rinat Abzalimov ,&nbsp;Wenkai Huang ,&nbsp;Anusha Guruprasad ,&nbsp;Ronniel Pedales ,&nbsp;Adhityo Wicaksono ,&nbsp;Destiny Davis ,&nbsp;John Rey Callado ,&nbsp;Hans Bänziger ,&nbsp;Piyakaset Suksathan ,&nbsp;William Eaton ,&nbsp;Pride Yin ,&nbsp;Marco Bürger ,&nbsp;Mick Erickson ,&nbsp;Stephen Jones ,&nbsp;James Adams ,&nbsp;Susan Pell","doi":"10.1016/j.cpb.2025.100456","DOIUrl":null,"url":null,"abstract":"<div><div><em>Rafflesia,</em> known for producing the world’s largest flowers, is a holoparasite found only in Southeast Asia's rapidly diminishing tropical forests. Completely dependent on its <em>Tetrastigma</em> host plants, <em>Rafflesia</em> grows covertly within its host until flowering, but the ecological factors driving host susceptibility are unknown. With most <em>Rafflesia</em> species on the brink of extinction due to habitat loss, understanding the complex ecological interactions between <em>Rafflesia</em> and its host is crucial for conservation. In this study, we integrated metagenomic data with metabolomic profiles to identify potential functional relationships between microbial communities and specific metabolites, shedding light on their ecological roles in <em>Rafflesia's</em> life cycle. Key findings reveal that microbial taxa such as Microbacteriaceae and Nocardioidaceae correlate with elevated levels of polyphenols, particularly gallic acid derivatives, which may shape the chemical environment conducive to <em>Rafflesia</em> development. Complex-carbon-degrading bacteria thrive in the chemically distinct environment of <em>Rafflesia</em> buds, while an unknown group of Saccharimonadales was enriched in <em>Tetrastigma</em> host species. Docosenamide production in <em>Rafflesia</em> buds and their hosts may facilitate parasitic infection, while coumarin compounds in non-host <em>Tetrastigma</em> species may exert allelopathic effects. The enrichment of gallic acid derivatives, the phytohormone adenine, and gall-associated bacteria suggests that <em>Rafflesia</em> buds may function similarly to plant galls, manipulating host tissues to support their reproductive development. This study highlights the dynamic microbial shifts during <em>Rafflesia’</em>s development, emphasizing its symbiotic relationship with microbial communities and hosts. In identifying essential microbial and chemical conditions that could improve propagation techniques, this research has practical applications in ex situ conservation efforts, aiding in the rescue of the world’s largest flowers from the brink of extinction.</div></div>","PeriodicalId":38090,"journal":{"name":"Current Plant Biology","volume":"42 ","pages":"Article 100456"},"PeriodicalIF":5.4000,"publicationDate":"2025-02-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Plant Biology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2214662825000246","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Rafflesia, known for producing the world’s largest flowers, is a holoparasite found only in Southeast Asia's rapidly diminishing tropical forests. Completely dependent on its Tetrastigma host plants, Rafflesia grows covertly within its host until flowering, but the ecological factors driving host susceptibility are unknown. With most Rafflesia species on the brink of extinction due to habitat loss, understanding the complex ecological interactions between Rafflesia and its host is crucial for conservation. In this study, we integrated metagenomic data with metabolomic profiles to identify potential functional relationships between microbial communities and specific metabolites, shedding light on their ecological roles in Rafflesia's life cycle. Key findings reveal that microbial taxa such as Microbacteriaceae and Nocardioidaceae correlate with elevated levels of polyphenols, particularly gallic acid derivatives, which may shape the chemical environment conducive to Rafflesia development. Complex-carbon-degrading bacteria thrive in the chemically distinct environment of Rafflesia buds, while an unknown group of Saccharimonadales was enriched in Tetrastigma host species. Docosenamide production in Rafflesia buds and their hosts may facilitate parasitic infection, while coumarin compounds in non-host Tetrastigma species may exert allelopathic effects. The enrichment of gallic acid derivatives, the phytohormone adenine, and gall-associated bacteria suggests that Rafflesia buds may function similarly to plant galls, manipulating host tissues to support their reproductive development. This study highlights the dynamic microbial shifts during Rafflesia’s development, emphasizing its symbiotic relationship with microbial communities and hosts. In identifying essential microbial and chemical conditions that could improve propagation techniques, this research has practical applications in ex situ conservation efforts, aiding in the rescue of the world’s largest flowers from the brink of extinction.
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
求助全文
约1分钟内获得全文 去求助
来源期刊
Current Plant Biology
Current Plant Biology Agricultural and Biological Sciences-Plant Science
CiteScore
10.90
自引率
1.90%
发文量
32
审稿时长
50 days
期刊介绍: Current Plant Biology aims to acknowledge and encourage interdisciplinary research in fundamental plant sciences with scope to address crop improvement, biodiversity, nutrition and human health. It publishes review articles, original research papers, method papers and short articles in plant research fields, such as systems biology, cell biology, genetics, epigenetics, mathematical modeling, signal transduction, plant-microbe interactions, synthetic biology, developmental biology, biochemistry, molecular biology, physiology, biotechnologies, bioinformatics and plant genomic resources.
期刊最新文献
RTR_Lite_MobileNetV2: A lightweight and efficient model for plant disease detection and classification ABA-regulated JAZ1 suppresses phytoalexin biosynthesis by binding GmNAC42-1 in soybean Chitosan induces salicylic acid and methyl salicylate in banana plants and reduces colonisation by Fusarium oxysporum f. sp. cubense TR4 Integrating microplastic research in sustainable agriculture: Challenges and future directions for food production AI-enhanced 3D-QSAR screening of fragment-based novel designed molecules targeting Phalaris minor ACCase
×
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