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两个内共生单胞菌进化枝与其珊瑚宿主洛氏鹿角珊瑚之间共生相互作用的基因组预测。

Genomic prediction of symbiotic interactions between two Endozoicomonas clades and their coral host, Acropora loripes.

作者信息

Gotze Cecilie R, Tandon Kshitij, Philip Gayle K, Dungan Ashley M, Maire Justin, Høj Lone, Blackall Linda L, Oppen Madeleine J H van

机构信息

School of BioSciences, The University of Melbourne, Parkville, VIC, 3010, Australia.

Australian Institute of Marine Science, Townsville, QLD, 4810, Australia.

出版信息

Anim Microbiome. 2025 Sep 25;7(1):94. doi: 10.1186/s42523-025-00455-3.

DOI:10.1186/s42523-025-00455-3
PMID:40999549
Abstract

BACKGROUND

The bacterial genus Endozoicomonas is a predominant member of the coral microbiome, widely recognised for its ubiquity and ability to form high-density aggregates within coral tissues. Hence, investigating its metabolic interplay with coral hosts offers critical insights into its ecological roles and contributions to coral health and resilience.

RESULTS

Using long- and short-read whole-genome sequencing of 11 Endozoicomonas strains from Acropora loripes, genome sizes were found to range between 5.8 and 7.1 Mbp. Phylogenomic analysis identified two distinct clades within the family Endozoicomonadaceae. Metabolic reconstruction uncovered clade-specific pathways, including the degradation of holobiont-derived carbon and lipids (e.g., galactose, starch, triacylglycerol, D-glucuronate), the latter of which suggests involvement of Endozoicomonas in host 'sex-type' steroid hormone metabolism. A clade-specific type 6 Secretion System (T6SS) and predicted effector molecules were identified, potentially facilitating coral-bacterium symbiosis. Additionally, genomic analyses revealed diverse phosphorus acquisition strategies, implicating Endozoicomonas in holobiont phosphorus cycling and stress responses.

CONCLUSIONS

This study reveals clade-specific genomic signatures of Endozoicomonas supporting its mutualistic lifestyle within corals. Findings suggests possible roles in nutrient cycling, reproductive health, and stress resilience, offering novel insights into coral holobiont functioning.

摘要

背景

内共生单胞菌属是珊瑚微生物群的主要成员,因其广泛存在以及能够在珊瑚组织内形成高密度聚集体而广为人知。因此,研究其与珊瑚宿主的代谢相互作用,对于深入了解其生态作用以及对珊瑚健康和恢复力的贡献至关重要。

结果

通过对来自鹿角珊瑚的11株内共生单胞菌菌株进行长读长和短读长全基因组测序,发现基因组大小在5.8至7.1兆碱基对之间。系统发育基因组学分析在内共生单胞菌科中确定了两个不同的进化枝。代谢重建揭示了进化枝特异性途径,包括全生物衍生的碳和脂质(如半乳糖、淀粉、三酰甘油、D-葡萄糖醛酸)的降解,后者表明内共生单胞菌参与宿主“性别类型”类固醇激素代谢。鉴定出一种进化枝特异性的6型分泌系统(T6SS)和预测的效应分子,可能促进珊瑚与细菌的共生。此外,基因组分析揭示了多种磷获取策略,表明内共生单胞菌参与全生物的磷循环和应激反应。

结论

本研究揭示了内共生单胞菌的进化枝特异性基因组特征,支持其在珊瑚体内的共生生活方式。研究结果表明其在营养循环、生殖健康和应激恢复力方面可能发挥的作用,为珊瑚全生物功能提供了新的见解。

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本文引用的文献

1
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ISME J. 2025 Mar 28. doi: 10.1093/ismejo/wraf059.
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Bacterial capsules: Occurrence, mechanism, and function.细菌荚膜:发生、机制与功能。
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Tissue-associated and vertically transmitted bacterial symbiont in the coral Pocillopora acuta.石珊瑚 Pocillopora acuta 组织相关和垂直传播的细菌共生体。
ISME J. 2024 Jan 8;18(1). doi: 10.1093/ismejo/wrad027.
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Frenemies on the reef? Resolving the coral-Endozoicomonas association.珊瑚礁上的亦敌亦友?解析珊瑚-内共生菌的共生关系。
Trends Microbiol. 2024 May;32(5):422-434. doi: 10.1016/j.tim.2023.11.006. Epub 2024 Jan 11.
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DNA from non-viable bacteria biases diversity estimates in the corals Acropora loripes and Pocillopora acuta.来自无法存活细菌的DNA会使鹿角珊瑚和尖锐小枝鹿角珊瑚的多样性估计产生偏差。
Environ Microbiome. 2023 Dec 8;18(1):86. doi: 10.1186/s40793-023-00541-6.
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Phosphorus nutrition strategies in a Symbiodiniacean species: Implications in coral-alga symbiosis facing increasing phosphorus deficiency in future warmer oceans.在 Symbiodiniacean 物种中的磷营养策略:在未来更温暖的海洋中面临日益增加的磷缺乏的情况下,对珊瑚藻共生关系的影响。
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Gut microbial beta-glucuronidase: a vital regulator in female estrogen metabolism.肠道微生物β-葡萄糖醛酸酶:女性雌激素代谢中的重要调节因子。
Gut Microbes. 2023 Jan-Dec;15(1):2236749. doi: 10.1080/19490976.2023.2236749.
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Ecology of Endozoicomonadaceae in three coral genera across the Pacific Ocean.太平洋中三个珊瑚属内生滴虫科的生态学研究。
Nat Commun. 2023 Jun 1;14(1):3037. doi: 10.1038/s41467-023-38502-9.
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Colocalization and potential interactions of and chlamydiae in microbial aggregates of the coral .和衣原体在珊瑚微生物聚集体中的共定位和潜在相互作用。
Sci Adv. 2023 May 19;9(20):eadg0773. doi: 10.1126/sciadv.adg0773. Epub 2023 May 17.
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