综合多种方法揭示了维斯提夫拉(Vestimentifera)适应深海的独特新陈代谢机制。

IF 13.8 1区 生物学 Q1 MICROBIOLOGY Microbiome Pub Date : 2024-11-16 DOI:10.1186/s40168-024-01960-4
Qinglei Sun, Zihao Yuan, Yuanyuan Sun, Li Sun
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引用次数: 0

摘要

背景:长尾管虫是一种深海定殖动物,人们首次在其体内观察到化自养共生现象。这些动物没有肠道,依靠内共生细菌合成有机化合物和提供营养。在分类学上,马尾藻属于鞘鳃纲和无针纲。与其他鞘形目动物相比,背心鱼类的特点是对热液喷口中普遍存在的硫化氢具有很强的耐受性,能在当地栖息地快速生长,身体结构由粗大的壳质管组成。导致这些特征的新陈代谢机制仍然难以捉摸:结果:比较基因组学发现,与其他无环类动物不同,背心鱼类具有三卤酮生成机制,而缺乏葡萄糖生成机制。转录组和代谢组分析检测到三卤糖-6-磷酸合成酶/磷酸酶(TPSP)的表达,TPSP是三卤酮生成的关键酶。除了三卤酮生成外,在马氏囊虫共生体中还发现了糖原生物合成,表现为糖原颗粒密集,但在其他Siboglinidae共生体中没有发现。对无脊椎动物 TPSP 的数据挖掘和分析表明,景天科以及蛇尾目、轮虫目、筇竹科和头索类的 TPSP 很可能起源于节肢动物门,可能是转座子介导的系统间基因转移的结果:本研究表明,细菌糖原生物合成在高效共生体-底栖动物合作中发挥着关键作用。这项研究为了解马氏囊虫的环境适应策略提供了一个新的视角,并为了解元古宙的代谢进化机制提供了新的视角。视频摘要。
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Integrated multi-approaches reveal unique metabolic mechanisms of Vestimentifera to adapt to deep sea.

Background: Vestimentiferan tubeworms are deep-sea colonizers, in which chemoautotrophic symbiosis was first observed. These animals are gutless and depend on endosymbiotic bacteria for organic compound synthesis and nutrition supply. Taxonomically, vestimentiferans belong to Siboglinidae and Annelida. Compared with other siboglinids, vestimentiferans are distinguished by high tolerance of the prevailing hydrogen sulfide in hydrothermal vents, rapid growth in local habitats, and a physical structure consisting of a thick chitinous tube. The metabolic mechanisms contributing to these features remain elusive.

Results: Comparative genomics revealed that unlike other annelids, vestimentiferans possessed trehaloneogenesis and lacked gluconeogenesis. Transcriptome and metabolome analyses detected the expression of trehalose-6-phosphate synthase/phosphatase (TPSP), the key enzyme of trehaloneogenesis, and trehalose production in vestimentiferan tissues. In addition to trehaloneogenesis, glycogen biosynthesis evidenced by packed glycogen granules was also found in vestimentiferan symbionts, but not in other Siboglinidae symbionts. Data mining and analyses of invertebrate TPSP revealed that the TPSP in Vestimentifera, as well as Cnidaria, Rotifera, Urochordata, and Cephalochordata, likely originated from Arthropoda, possibly as a result of transposon-mediated inter-phyla gene transfer.

Conclusion: This study indicates a critical role of bacterial glycogen biosynthesis in the highly efficient symbiont - vestimentiferan cooperation. This study provides a new perspective for understanding the environmental adaptation strategies of vestimentiferans and adds new insights into the mechanism of metabolic evolution in Metazoa. Video Abstract.

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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
期刊最新文献
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