在珊瑚进化过程中,微生物介导的生长和防御之间权衡的证据。

IF 4.9 Q1 MICROBIOLOGY Animal microbiome Pub Date : 2025-01-03 DOI:10.1186/s42523-024-00370-z
Hannah E Epstein, Tanya Brown, Ayọmikun O Akinrinade, Ryan McMinds, F Joseph Pollock, Dylan Sonett, Styles Smith, David G Bourne, Carolina S Carpenter, Rob Knight, Bette L Willis, Mónica Medina, Joleah B Lamb, Rebecca Vega Thurber, Jesse R Zaneveld
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引用次数: 0

摘要

背景:生命史策略之间的进化权衡在动物进化中很重要。由于微生物可以影响宿主生理的多个方面,包括生长速度和对疾病或应激的易感性,动物-微生物共生的变化有可能调节生活史的权衡。硬核珊瑚提供了一个生物多样性,数据丰富,生态相关的宿主系统来探索这个想法。结果:采用比较方法,通过进行跨物种珊瑚微生物组调查(“全球珊瑚微生物组计划”)并将结果与长期全球疾病流行和珊瑚性状数据相结合,我们测试了珊瑚微生物组是否与4.25亿年珊瑚进化中的疾病易感性相关。在系统发育的背景下解释这些数据,我们表明微生物优势预测疾病易感性,并将这种优势与疾病的关联追溯到一个推定有益的共生属,内生单胞菌。珊瑚组织内植单胞菌的相对丰度解释了40个珊瑚属中30%的疾病易感性变异和60%的微生物组优势变异,同时也与高生长率密切相关。结论:珊瑚内生单胞菌共生的进化与疾病患病率和生长速率相关,并具有一定的中介作用。探索这些发现的机制基础对于我们理解微生物共生如何影响动物生活史权衡是很重要的。
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Evidence for microbially-mediated tradeoffs between growth and defense throughout coral evolution.

Background: Evolutionary tradeoffs between life-history strategies are important in animal evolution. Because microbes can influence multiple aspects of host physiology, including growth rate and susceptibility to disease or stress, changes in animal-microbial symbioses have the potential to mediate life-history tradeoffs. Scleractinian corals provide a biodiverse, data-rich, and ecologically-relevant host system to explore this idea.

Results: Using a comparative approach, we tested if coral microbiomes correlate with disease susceptibility across 425 million years of coral evolution by conducting a cross-species coral microbiome survey (the "Global Coral Microbiome Project") and combining the results with long-term global disease prevalence and coral trait data. Interpreting these data in their phylogenetic context, we show that microbial dominance predicts disease susceptibility, and traced this dominance-disease association to a single putatively beneficial symbiont genus, Endozoicomonas. Endozoicomonas relative abundance in coral tissue explained 30% of variation in disease susceptibility and 60% of variation in microbiome dominance across 40 coral genera, while also correlating strongly with high growth rates.

Conclusions: These results demonstrate that the evolution of Endozoicomonas symbiosis in corals correlates with both disease prevalence and growth rate, and suggest a mediating role. Exploration of the mechanistic basis for these findings will be important for our understanding of how microbial symbioses influence animal life-history tradeoffs.

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