Department of Microbiology and Cell Biology, Montana State Universitygrid.41891.35, Bozeman, Montana, USA.
Department of Chemical and Biological Engineering, Montana State Universitygrid.41891.35, Bozeman, Montana, USA.
Appl Environ Microbiol. 2021 Nov 10;87(23):e0159821. doi: 10.1128/AEM.01598-21. Epub 2021 Sep 29.
Little is known of how the confluence of subsurface and surface processes influences the assembly and habitability of hydrothermal ecosystems. To address this knowledge gap, the geochemical and microbial composition of a high-temperature, circumneutral hot spring in Yellowstone National Park was examined to identify the sources of solutes and their effect on the ecology of microbial inhabitants. Metagenomic analysis showed that populations comprising planktonic and sediment communities are archaeal dominated, are dependent on chemical energy (chemosynthetic), share little overlap in their taxonomic composition, and are differentiated by their inferred use of/tolerance to oxygen and mode of carbon metabolism. The planktonic community is dominated by putative aerobic/aerotolerant autotrophs, while the taxonomic composition of the sediment community is more evenly distributed and comprised of anaerobic heterotrophs. These observations are interpreted to reflect sourcing of the spring by anoxic, organic carbon-limited subsurface hydrothermal fluids and ingassing of atmospheric oxygen that selects for aerobic/aerotolerant organisms that have autotrophic capabilities in the water column. Autotrophy and consumption of oxygen by the planktonic community may influence the assembly of the anaerobic and heterotrophic sediment community. Support for this inference comes from higher estimated rates of genome replication in planktonic populations than sediment populations, indicating faster growth in planktonic populations. Collectively, these observations provide new insight into how mixing of subsurface waters and atmospheric oxygen create dichotomy in the ecology of hot spring communities and suggest that planktonic and sediment communities may have been less differentiated taxonomically and functionally prior to the rise of oxygen at ∼2.4 billion years ago (Gya). Understanding the source and availability of energy capable of supporting life in hydrothermal environments is central to predicting the ecology of microbial life on early Earth when volcanic activity was more widespread. Little is known of the substrates supporting microbial life in circumneutral to alkaline springs, despite their relevance to early Earth habitats. Using metagenomic and informatics approaches, water column and sediment habitats in a representative circumneutral hot spring in Yellowstone were shown to be dichotomous, with the former largely hosting aerobic/aerotolerant autotrophs and the latter primarily hosting anaerobic heterotrophs. This dichotomy is attributed to influx of atmospheric oxygen into anoxic deep hydrothermal spring waters. These results indicate that the ecology of microorganisms in circumneutral alkaline springs sourced by deep hydrothermal fluids was different prior to the rise of atmospheric oxygen ∼2.4 Gya, with planktonic and sediment communities likely to be less differentiated than contemporary circumneutral hot springs.
人们对地下和地表过程的汇合如何影响热液生态系统的组装和宜居性知之甚少。为了填补这一知识空白,本研究对黄石国家公园一处高温、近中性温泉的地球化学和微生物组成进行了考察,以确定溶质的来源及其对微生物栖息者生态的影响。宏基因组分析表明,由浮游生物和沉积物群落组成的种群主要由古菌组成,依赖于化学能量(化能合成),在分类组成上重叠很少,并且通过它们对氧气的推测使用/耐受性和碳代谢模式来区分。浮游生物群落主要由有氧/耐氧自养生物组成,而沉积物群落的分类组成则更为均匀,由厌氧异养生物组成。这些观察结果表明,温泉的水源是缺氧、有机碳有限的地下热液流体,并且大气氧气的内渗使有氧/耐氧生物得到选择,这些生物在水柱中具有自养能力。浮游生物群落的自养作用和对氧气的消耗可能会影响厌氧和异养沉积物群落的组装。这种推断得到了以下支持:与沉积物种群相比,浮游生物种群的基因组复制率估计更高,这表明浮游生物种群的生长速度更快。总的来说,这些观察结果提供了新的见解,即地下水和大气氧气的混合如何在温泉群落的生态学中产生二分法,并表明在约 24 亿年前(Gya)氧气出现之前,浮游生物和沉积物群落在分类和功能上可能没有那么分化。了解能够支持热液环境中生命的能量来源和可用性对于预测早期地球上微生物生命的生态学至关重要,因为那时火山活动更为普遍。尽管近中性至碱性泉对早期地球栖息地很重要,但人们对支持微生物生命的基质知之甚少。本研究使用宏基因组学和信息学方法,对黄石代表性近中性温泉的水柱和沉积物生境进行了研究,结果表明两者具有二分性,前者主要容纳有氧/耐氧自养生物,而后者主要容纳厌氧异养生物。这种二分性归因于大气氧气涌入缺氧深部热液泉水中。这些结果表明,在约 24 亿年前大气氧气上升之前,由深部热液流体供应的近中性碱性泉中的微生物生态学就有所不同,与当代近中性温泉相比,浮游生物和沉积物群落可能分化程度较低。