对新型蝠鲼功能的深入研究揭示了它们在秘鲁亚马逊泥炭地中的多功能代谢作用。

IF 3.7 2区 生物学 Q2 MICROBIOLOGY
Michael J Pavia, Arkadiy I Garber, Sarah Avalle, Franco Macedo-Tafur, Rodil Tello-Espinoza, Hinsby Cadillo-Quiroz
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引用次数: 0

摘要

热带泥炭地土壤有机碳的分解受到微生物群落功能组成的影响。在本研究中,我们在之前工作的基础上,从亚马逊帕斯塔萨-马拉尼翁前陆盆地(PMFB)的热带泥炭地中恢复了共 28 个元基因组组装基因组(MAGs),这些基因组被归类为Bathyarchaeia。通过系统发生组分析,我们确定了 PMFB 中的九个属级支系,其中四个支系组成了泥炭地特有的推定新科("Candidatus Paludivitaceae")。我们重点研究了 Ca.Paludivitaceae MAGs,因为这组MAGs很新颖,而且人们对它们在热带泥炭地中的作用了解有限。对这些 MAGs 的功能分析显示,这个假定的家族包括兼性厌氧菌,具有氧气、硫化物或氮氧化的遗传潜力。这种新陈代谢的多功能性可以与乙炔、丙醇或脯氨酸的发酵结合起来。在 Ca.Paludivitaceae 以外的其他支系可能具有乙酰生成和新氨基酸生物合成的能力,并编码大量的 Fe3+ 转运体。最重要的是,Ca.Paludivitaceae 被认为是羧营养型生物,能够利用 CO 产生能量或生产生物质。通过这种新陈代谢,它们可以排出环境中的 CO(甲烷生成的副产品),或产生 CO2 和 H2 等甲烷生成底物。总之,我们的研究结果表明,热带泥炭地中的褐藻属(Bathyarchaeia)具有复杂的新陈代谢和不同的品系,因此有必要进一步评估它们在这些生态系统中的作用:本研究通过组装 28 个新的元基因组扩展了巴氏菌科(Candidatus Paludivitaceae)家族,为了解它们在泥炭地生态系统中的代谢多样性和生态意义提供了新的视角。通过全面的系统发生和功能分析,我们阐明了它们潜在的独特兼性厌氧能力和一氧化碳解毒潜力。这项研究强调了它们在碳循环和温室气体调节中的关键作用。这些发现对于解决影响泥炭土壤稳定性的微生物过程至关重要,为以前未充分探索和代表性不足的古生物种群的生态作用提供了新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Functional insights of novel Bathyarchaeia reveal metabolic versatility in their role in peatlands of the Peruvian Amazon.

The decomposition of soil organic carbon within tropical peatlands is influenced by the functional composition of the microbial community. In this study, building upon our previous work, we recovered a total of 28 metagenome-assembled genomes (MAGs) classified as Bathyarchaeia from the tropical peatlands of the Pastaza-Marañón Foreland Basin (PMFB) in the Amazon. Using phylogenomic analyses, we identified nine genus-level clades to have representatives from the PMFB, with four forming a putative novel family ("Candidatus Paludivitaceae") endemic to peatlands. We focus on the Ca. Paludivitaceae MAGs due to the novelty of this group and the limited understanding of their role within tropical peatlands. Functional analysis of these MAGs reveals that this putative family comprises facultative anaerobes, possessing the genetic potential for oxygen, sulfide, or nitrogen oxidation. This metabolic versatility can be coupled to the fermentation of acetoin, propanol, or proline. The other clades outside Ca. Paludivitaceae are putatively capable of acetogenesis and de novo amino acid biosynthesis and encode a high amount of Fe3+ transporters. Crucially, the Ca. Paludivitaceae are predicted to be carboxydotrophic, capable of utilizing CO for energy generation or biomass production. Through this metabolism, they could detoxify the environment from CO, a byproduct of methanogenesis, or produce methanogenic substrates like CO2 and H2. Overall, our results show the complex metabolism and various lineages of Bathyarchaeia within tropical peatlands pointing to the need to further evaluate their role in these ecosystems.

Importance: With the expansion of the Candidatus Paludivitaceae family by the assembly of 28 new metagenome assembled genomes, this study provides novel insights into their metabolic diversity and ecological significance in peatland ecosystems. From a comprehensive phylogenic and functional analysis, we have elucidated their putative unique facultative anaerobic capabilities and CO detoxification potential. This research highlights their crucial role in carbon cycling and greenhouse gas regulation. These findings are essential for resolving the microbial processes affecting peat soil stability, offering new perspectives on the ecological roles of previously underexplored and underrepresented archaeal populations.

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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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