Bledina Dede, Eoghan P Reeves, Maren Walter, Wolfgang Bach, Rudolf Amann, Anke Meyerdierks
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引用次数: 0
摘要
热液喷口系统释放的还原化合物是深海的重要能源。栖息在热液羽流中的化学自养微生物氧化这些化合物,特别是氢和还原硫,以获得固定二氧化碳所需的能量。在这里,我们分析了大西洋中脊沿岸四个热液系统的浮游生物群落:在此,我们结合长读 16S rRNA 基因分析、荧光原位杂交、元组学和热力学计算,分析了位于大西洋中脊的四个热液系统:伊里诺夫斯科、塞梅诺夫-2、洛加切夫-1 和阿沙泽-2 的浮游生物群落。这些热液羽流中的微生物群落主要是Sulfurimonas和SUP05。对Sulfurimonas和SUP05 MAGs及其在羽流中的基因转录的研究表明,氢和硫驱动了一种生态位分区。除了硫和氢氧化外,栖息在羽流中的一个新的 SAR202 支系(此处称为羧基球菌属)还具有通过反向 TCA 循环进行 CO 氧化和 CO2 固定的能力。这两种途径在其他富氢羽流(包括冯达姆喷口区)中也有大量转录。在伊里诺夫斯科非浮力羽流中,深层羧基球菌的相对丰度高达 4% (1.0 x 103 个细胞 ml-1),在非热液影响的深海元基因组中也很丰富(高达 5 RPKM)。因此,一氧化碳可能不是来自热液(1.9-4 μM),而是来自热液中的生物活动,它可能是热液羽流中的重要能量来源。总之,这项研究揭示了大西洋中脊羽流中细菌群落的化学自养潜力。
Bacterial chemolithoautotrophy in ultramafic plumes along the Mid-Atlantic Ridge.
Hydrothermal vent systems release reduced chemical compounds that act as an important energy source in the deep sea. Chemolithoautotrophic microbes inhabiting hydrothermal plumes oxidize these compounds, in particular, hydrogen and reduced sulfur, to obtain the energy required for CO2 fixation. Here, we analysed the planktonic communities of four hydrothermal systems located along the Mid-Atlantic Ridge: Irinovskoe, Semenov-2, Logatchev-1, and Ashadze-2, by combining long-read 16S rRNA gene analysis, fluorescence in situ hybridization, meta-omics, and thermodynamic calculations. Sulfurimonas and SUP05 dominated the microbial communities in these hydrothermal plumes. Investigation of Sulfurimonas and SUP05 MAGs, and their gene transcription in plumes indicated a niche partitioning driven by hydrogen and sulfur. In addition to sulfur and hydrogen oxidation, a novel SAR202 clade inhabiting the plume, here referred to as genus Carboxydicoccus, harbours the capability for CO oxidation and CO2 fixation via reverse TCA cycle. Both pathways were also highly transcribed in other hydrogen-rich plumes, including the Von Damm vent field. Carboxydicoccus profundi reached up to 4% relative abundance (1.0 x 103 cell ml- 1) in Irinovskoe non-buoyant plume and was also abundant in non-hydrothermally influenced deep-sea metagenomes (up to 5 RPKM). Therefore, CO, which is probably not sourced from the hydrothermal fluids (1.9-5.8 μM), but rather from biological activities within the rising fluid, may serve as a significant energy source in hydrothermal plumes. Taken together, this study sheds light on the chemolithoautotrophic potential of the bacterial community in Mid-Atlantic Ridge plumes.
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.