Evolutionary history of tyrosine-supplementing endosymbionts in pollen-feeding beetles.

IF 10.8 1区 环境科学与生态学 Q1 ECOLOGY ISME Journal Pub Date : 2024-01-08 DOI:10.1093/ismejo/wrae080
Jürgen C Wierz, Matthew L Gimmel, Selina Huthmacher, Tobias Engl, Martin Kaltenpoth
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Abstract

Many insects feeding on nutritionally challenging diets like plant sap, leaves, or wood engage in ancient associations with bacterial symbionts that supplement limiting nutrients or produce digestive or detoxifying enzymes. However, the distribution, function, and evolutionary dynamics of microbial symbionts in insects exploiting other plant tissues or relying on a predacious diet remain poorly understood. Here, we investigated the evolutionary history and function of the intracellular gamma-proteobacterial symbiont "Candidatus Dasytiphilus stammeri" in soft-winged flower beetles (Coleoptera, Melyridae, Dasytinae) that transition from saprophagy or carnivory to palynivory (pollen-feeding) between larval and adult stage. Reconstructing the distribution of the symbiont within the Dasytinae phylogeny unraveled not only a long-term coevolution, originating from a single acquisition event with subsequent host-symbiont codiversification, but also several independent symbiont losses. The analysis of 20 different symbiont genomes revealed that their genomes are severely eroded. However, the universally retained shikimate pathway indicates that the core metabolic contribution to their hosts is the provisioning of tyrosine for cuticle sclerotization and melanization. Despite the high degree of similarity in gene content and order across symbiont strains, the capacity to synthesize additional essential amino acids and vitamins and to recycle urea is retained in some but not all symbionts, suggesting ecological differences among host lineages. This report of tyrosine-provisioning symbionts in insects with saprophagous or carnivorous larvae and pollen-feeding adults expands our understanding of tyrosine supplementation as an important symbiont-provided benefit across a broad range of insects with diverse feeding ecologies.

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食花粉甲虫体内补充酪氨酸的内共生体的进化史。
许多以植物汁液、叶片或木材等具有营养挑战性的食物为食的昆虫与细菌共生体建立了古老的联系,这些共生体可补充限制性营养物质或产生消化或解毒酶。然而,人们对利用其他植物组织或以捕食为生的昆虫体内微生物共生体的分布、功能和进化动态仍然知之甚少。在这里,我们研究了软翅花甲虫(Melyridae, Dasytinae)细胞内γ-蛋白细菌共生体 "Candidatus Dasytiphilus stammeri "的进化历史和功能。通过重建共生体在菊形目系统发育中的分布,揭示了一种长期的共同进化过程,这种进化源于一次宿主获得共生体的事件,随后宿主-共生体发生了融合,但也有几次独立的共生体消失。对 20 个不同共生体基因组的分析表明,这些共生体的基因组受到了严重侵蚀。不过,普遍保留的莽草酸途径表明,共生体对宿主的核心代谢贡献是为角质层硬化和黑色化提供酪氨酸。尽管不同共生菌株的基因含量和排列顺序高度相似,但一些共生菌株(而非所有共生菌株)保留了合成其他必需氨基酸和维生素以及回收尿素的能力,这表明宿主品系之间存在生态差异。这篇关于嗜食或肉食性幼虫和以花粉为食的成虫中酪氨酸供应共生体的报告,拓展了我们对酪氨酸补充作为一种重要的共生体提供的益处的认识,这种益处广泛存在于具有不同取食生态的昆虫中。
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来源期刊
ISME Journal
ISME Journal 环境科学-生态学
CiteScore
22.10
自引率
2.70%
发文量
171
审稿时长
2.6 months
期刊介绍: The ISME Journal covers the diverse and integrated areas of microbial ecology. We encourage contributions that represent major advances for the study of microbial ecosystems, communities, and interactions of microorganisms in the environment. Articles in The ISME Journal describe pioneering discoveries of wide appeal that enhance our understanding of functional and mechanistic relationships among microorganisms, their communities, and their habitats.
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