高原盐碱湿地环境选择微生物功能而非分类物种。

IF 3.7 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Applied and Environmental Microbiology Pub Date : 2025-07-23 Epub Date: 2025-07-03 DOI:10.1128/aem.02206-24
Hongjie Zhang, Dayong Zhao, Qinglong L Wu, Jin Zeng
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引用次数: 0

摘要

高原盐碱湿地是一个研究不足的脆弱生态系统,了解高原盐碱湿地的微生物群落对预测全球气候变化背景下的生态系统功能至关重要。尽管其中一些湿地正在迅速萎缩和可能干涸,但我们对这个生态系统中微生物群落的了解仍然是支离破碎的。利用宏基因组测序技术,研究了青藏高原典型盐碱湿地错错龙湿地沉积物、表层根际土壤(Rsurface)、下表层根际土壤(Rsubsurface)、表层块状土壤(Bsurface)和下表层块状土壤(Bsubsurface)中甲烷、氮和硫循环基因/途径的分布及其微生物群落的形成机制。结果表明,沉积物的产甲烷功能电位较高,而甲烷氧化功能电位较低。5种生境的反硝化和异化硫酸盐还原电位随盐度的降低而增加,表现为沉积物表层< Rsubsurface < Bsubsurface。微生物群落的分类组成变化较大,但功能基因分布相对均匀,存在功能冗余。功能组成具有较大的确定性,而分类组成具有较大的随机性。在个别生境中也观察到类似的模式,确定性过程的相对重要性随着五个生境中盐度水平的增加而增加。此外,重建了188个非冗余的中等和高质量宏基因组组装基因组(MAGs),其中18个MAGs含有nod基因,这是一氧化氮歧化的标记基因。该研究通过强调极端环境对微生物功能的确定性选择,为研究微生物群落的形成机制提供了新的视角。重要性:了解微生物群落的形成机制是生态学的中心目标。然而,尽管高原盐碱湿地具有高海拔、低干扰、高盐度、对全球气候变化敏感、部分地区局部萎缩等独特的脆弱生态系统特征,但我们对其微生物群落的认识仍然是碎片化的。此外,以往对群落形成机制的研究主要集中在微生物的分类结构上,而忽略了它们的功能组成。本研究在全面了解高原盐碱湿地甲烷、氮和硫循环微生物群落分布格局的基础上,通过强调极端环境对微生物功能的确定性选择,为微生物群落形成机制提供了新的视角。这项研究还扩大了我们对含有nod基因的微生物多样性的理解,这可能在很大程度上有助于全球甲烷和氮的预算。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Environment selected microbial function rather than taxonomic species in a plateau saline-alkaline wetland.

Comprehending the microbial community in plateau saline-alkaline wetlands, an understudied and vulnerable ecosystem, is vital for predicting ecosystem functions within the context of global climate change. Despite the rapid shrinkage and potential drying up of some of these wetlands, our knowledge of the microbial community in this ecosystem remains fragmented. Here, we utilized metagenomic sequencing to investigate the distribution of methane, nitrogen, and sulfur cycling genes/pathways and formation mechanism of microbial communities across sediment, surface rhizosphere soils (Rsurface), subsurface rhizosphere soils (Rsubsurface), surface bulk soils (Bsurface), and subsurface bulk soils (Bsubsurface) in Cuochuolong Wetland, a typical saline-alkaline wetland located in the Tibetan Plateau. The results showed that sediment exhibited relatively higher functional potentials for methanogenesis but lower potentials for methane oxidation. Denitrification and dissimilatory sulfate reduction potentials increased with decreasing salinity across the five habitats, following the trend: sediment surface < Rsubsurface surface < Bsubsurface. The taxonomic compositions of microbial communities varied more dramatically, yet functional genes distributed relatively evenly, indicating functional redundancy. Greater determinacy was observed in functional compositions, whereas taxonomic compositions exhibited more stochasticity. Similar patterns were observed within individual habitats, with the relative importance of deterministic processes increasing as salinity levels increased across the five habitats. Additionally, 188 non-redundant medium- and high-quality metagenome-assembled genomes (MAGs) were reconstructed, with 18 MAGs containing the nod gene, a marker gene of disproportionation of nitric oxide. This study provided a novel perspective on the formation mechanism of microbial community by emphasizing the deterministic selection of extreme environments on microbial function.

Importance: Understanding the formation mechanism of microbial communities is a central goal in ecology. However, our understanding of microbial community remains fragmented in plateau saline-alkaline wetlands, despite their unique status as a vulnerable ecosystem characterized by high altitude, low disturbance, high salinity, sensitivity to global climate change, and localized shrinkage in some areas. Furthermore, previous studies on community formation mechanism have predominantly focused on microbial taxonomic structure, neglecting their functional compositions. Beyond providing a comprehensive understanding of the distribution patterns of methane, nitrogen, and sulfur cycling microbial communities within plateau saline-alkaline wetland, this study offers a novel perspective on formation mechanism of microbial community by emphasizing the deterministic selection of extreme environment on microbial function. This study also expands our comprehension of the diversity of microbes containing the nod gene, which may substantially contribute to global methane and nitrogen budgets.

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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
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