Coral‐associated Symbiodiniaceae exhibit host specificity but lack phylosymbiosis, with Cladocopium and Durusdinium showing different cophylogenetic patterns

IF 8.3 1区 生物学 Q1 PLANT SCIENCES
New Phytologist Pub Date : 2025-05-03 DOI:10.1111/nph.70184
Jiaxin Li, Zhuang Shao, Keke Cheng, Qingsong Yang, Huimin Ju, Xiaoyu Tang, Si Zhang, Jie Li
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引用次数: 0

Abstract

Summary Altering the composition of the Symbiodiniaceae community to adapt to anomalous sea water warming represents a potential survival mechanism for scleractinian corals. However, the processes of Symbiodiniaceae assembly and long‐standing evolution of coral–Symbiodiniaceae interactions remain unclear. Here, we utilized ITS2 (internal transcribed spacer 2) amplicon sequencing and the SymPortal framework to investigate the diversity and specificity of Symbiodiniaceae across 39 scleractinian coral species. Furthermore, we tested phylosymbiosis and cophylogeny between coral hosts and their Symbiodiniaceae. In our study, environmental samples exhibited the highest Symbiodiniaceae diversity. Cladocopium and Durusdinium dominated the Symbiodiniaceae communities, with significant β‐diversity differences among coral species. Additionally, host specificity was widespread in Symbiodiniaceae, especially Durusdinium spp., yet lacked a phylosymbiotic pattern. Moreover, Cladocopium spp. showed cophylogenetic congruence with their hosts, while there was no evidence for Durusdinium spp. Furthermore, host switching was the predominant evolutionary event, implying its contribution to Cladocopium diversification. These findings suggest that Symbiodiniaceae assembly does not recapitulate host phylogeny, and host specificity alone does not drive phylosymbiosis or cophylogeny. As environmental reservoirs, free‐living Symbiodiniaceae may influence symbiotic communities. Additionally, Durusdinium–coral associations lack cophylogenetic signals, indicating more flexible partnerships than Cladocopium. Overall, our results enhance understanding of Symbiodiniaceae assembly and coral–Symbiodiniaceae evolutionary interactions.
与珊瑚相关的共生科表现出宿主特异性,但缺乏系统共生,Cladocopium和Durusdinium表现出不同的共同发育模式
改变共生科群落组成以适应异常海水变暖是硬核珊瑚的一种潜在生存机制。然而,共生体科的组装过程和珊瑚-共生体科相互作用的长期进化尚不清楚。本研究利用ITS2 (internal transcripiting spacer 2)扩增子测序和SymPortal框架研究了39种核状珊瑚中共生二科的多样性和特异性。此外,我们还测试了珊瑚宿主与其共生科之间的系统共生和共生体发育。在我们的研究中,环境样品表现出最高的共生菌科多样性。Cladocopium和Durusdinium在共生珊瑚科群落中占主导地位,各珊瑚种间β‐多样性差异显著。此外,寄主特异性在共生科中广泛存在,尤其是Durusdinium spp.,但缺乏系统共生模式。此外,Cladocopium spp.与寄主的亲缘进化是一致的,而Durusdinium spp.与寄主的亲缘进化是不一致的。这些发现表明,共生科的组合并不概括宿主系统发育,宿主特异性本身并不驱动系统共生或共同发育。作为环境水库,自由生活的共生菌科可能影响共生群落。此外,durusdini - coral组合缺乏共同发育信号,表明比Cladocopium更灵活的伙伴关系。总的来说,我们的研究结果增强了对共生体科植物组装和珊瑚-共生体科植物进化相互作用的理解。
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来源期刊
New Phytologist
New Phytologist 生物-植物科学
自引率
5.30%
发文量
728
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.
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