{"title":"食肉植物丛枝菌根共生的收敛损失","authors":"Héctor Montero, Matthias Freund, Kenji Fukushima","doi":"10.1111/nph.70544","DOIUrl":null,"url":null,"abstract":"Summary<jats:list list-type=\"bullet\"> <jats:list-item>Most land plants form the ancient arbuscular mycorrhizal (AM) symbiosis, while carnivory is a younger trait that evolved in several angiosperm orders. The two biotic interactions similarly help plants acquire mineral nutrients, raising the question of whether they can coexist. However, the mycorrhizal status of carnivorous plants has long remained speculative.</jats:list-item> <jats:list-item>We surveyed the occurrence of AM‐associated genes across carnivorous plant lineages, performed AM fungal inoculation assays, and microscopically evaluated the patterns of colonization.</jats:list-item> <jats:list-item>We found convergent losses of the AM trait either coincident with or predating the emergence of carnivory. Exceptionally, the carnivorous plant <jats:italic>Roridula gorgonias</jats:italic> retains symbiosis‐related genes and forms arbuscules. The youngest carnivorous lineage, <jats:italic>Brocchinia reducta</jats:italic>, showed signatures of the early stages of AM trait loss. An AM‐associated <jats:italic>CHITINASE</jats:italic> gene encodes a digestive enzyme in the carnivorous plant <jats:italic>Cephalotus</jats:italic>, suggesting gene co‐option.</jats:list-item> <jats:list-item>We uncovered a mutually exclusive trend of AM symbiosis and carnivory, with only rare instances of coexistence. These findings illuminate the largely unexplored processes by which plant nutritional strategies evolve and supplant one another over time.</jats:list-item> </jats:list>","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"207 1","pages":""},"PeriodicalIF":8.1000,"publicationDate":"2025-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Convergent losses of arbuscular mycorrhizal symbiosis in carnivorous plants\",\"authors\":\"Héctor Montero, Matthias Freund, Kenji Fukushima\",\"doi\":\"10.1111/nph.70544\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Summary<jats:list list-type=\\\"bullet\\\"> <jats:list-item>Most land plants form the ancient arbuscular mycorrhizal (AM) symbiosis, while carnivory is a younger trait that evolved in several angiosperm orders. The two biotic interactions similarly help plants acquire mineral nutrients, raising the question of whether they can coexist. However, the mycorrhizal status of carnivorous plants has long remained speculative.</jats:list-item> <jats:list-item>We surveyed the occurrence of AM‐associated genes across carnivorous plant lineages, performed AM fungal inoculation assays, and microscopically evaluated the patterns of colonization.</jats:list-item> <jats:list-item>We found convergent losses of the AM trait either coincident with or predating the emergence of carnivory. Exceptionally, the carnivorous plant <jats:italic>Roridula gorgonias</jats:italic> retains symbiosis‐related genes and forms arbuscules. The youngest carnivorous lineage, <jats:italic>Brocchinia reducta</jats:italic>, showed signatures of the early stages of AM trait loss. An AM‐associated <jats:italic>CHITINASE</jats:italic> gene encodes a digestive enzyme in the carnivorous plant <jats:italic>Cephalotus</jats:italic>, suggesting gene co‐option.</jats:list-item> <jats:list-item>We uncovered a mutually exclusive trend of AM symbiosis and carnivory, with only rare instances of coexistence. These findings illuminate the largely unexplored processes by which plant nutritional strategies evolve and supplant one another over time.</jats:list-item> </jats:list>\",\"PeriodicalId\":214,\"journal\":{\"name\":\"New Phytologist\",\"volume\":\"207 1\",\"pages\":\"\"},\"PeriodicalIF\":8.1000,\"publicationDate\":\"2025-09-26\",\"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.70544\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Phytologist","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/nph.70544","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
Convergent losses of arbuscular mycorrhizal symbiosis in carnivorous plants
SummaryMost land plants form the ancient arbuscular mycorrhizal (AM) symbiosis, while carnivory is a younger trait that evolved in several angiosperm orders. The two biotic interactions similarly help plants acquire mineral nutrients, raising the question of whether they can coexist. However, the mycorrhizal status of carnivorous plants has long remained speculative.We surveyed the occurrence of AM‐associated genes across carnivorous plant lineages, performed AM fungal inoculation assays, and microscopically evaluated the patterns of colonization.We found convergent losses of the AM trait either coincident with or predating the emergence of carnivory. Exceptionally, the carnivorous plant Roridula gorgonias retains symbiosis‐related genes and forms arbuscules. The youngest carnivorous lineage, Brocchinia reducta, showed signatures of the early stages of AM trait loss. An AM‐associated CHITINASE gene encodes a digestive enzyme in the carnivorous plant Cephalotus, suggesting gene co‐option.We uncovered a mutually exclusive trend of AM symbiosis and carnivory, with only rare instances of coexistence. These findings illuminate the largely unexplored processes by which plant nutritional strategies evolve and supplant one another over time.
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.