Sarah P. Esser, Victoria Turzynski, Julia Plewka, Julia Nuy, Carrie J. Moore, Indra Banas, André R. Soares, Janey Lee, Tanja Woyke, Alexander J. Probst
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引用次数: 0
摘要
Candidatus Altiarchaea广泛分布于水生地下生态系统中,具有高度保守的核心基因组,但该核心基因组对不同生物和非生物因素的基因表达适应性尚不清楚。在这里,我们研究了两个Ca. Altiarchaeum种群的亚转录组,它们在两个完全不同的地下生态系统中茁壮成长。在美国的高二氧化碳地下水系统Crystal Geyser中,Ca. Altiarchaeum crystalense与共生体Ca. Huberiarchaeum crystalense共生,而在德国的Muehlbacher硫化物泉中,高硫化物浓度的自流泉中,Ca. a. hamiconexum被病毒严重感染。我们在此针对它们的基因组绘制了元转录组读数,以分析它们核心基因组的原位表达谱。在537个共享基因簇中,331个被功能注释,130个在两个位点之间的表达显著不同。主要差异与参与细胞防御的基因有关,如CRISPR-Cas、病毒防御、复制、转录以及能量和碳代谢。我们的研究结果表明,地下的高古菌种群可能适应了他们的环境,但受到其他生物实体的影响,这些生物实体篡改了他们的核心代谢。因此,我们假设病毒和共生相互作用可能是深层生物圈中生物体的主要能量汇。
Differential Expression of Core Metabolic Functions in Candidatus Altiarchaeum Inhabiting Distinct Subsurface Ecosystems
Candidatus Altiarchaea are widespread across aquatic subsurface ecosystems and possess a highly conserved core genome, yet adaptations of this core genome to different biotic and abiotic factors based on gene expression remain unknown. Here, we investigated the metatranscriptome of two Ca. Altiarchaeum populations that thrive in two substantially different subsurface ecosystems. In Crystal Geyser, a high-CO2 groundwater system in the USA, Ca. Altiarchaeum crystalense co-occurs with the symbiont Ca. Huberiarchaeum crystalense, while in the Muehlbacher sulfidic spring in Germany, an artesian spring high in sulfide concentration, Ca. A. hamiconexum is heavily infected with viruses. We here mapped metatranscriptome reads against their genomes to analyse the in situ expression profile of their core genomes. Out of 537 shared gene clusters, 331 were functionally annotated and 130 differed significantly in expression between the two sites. Main differences were related to genes involved in cell defence like CRISPR-Cas, virus defence, replication, transcription and energy and carbon metabolism. Our results demonstrate that altiarchaeal populations in the subsurface are likely adapted to their environment while influenced by other biological entities that tamper with their core metabolism. We consequently posit that viruses and symbiotic interactions can be major energy sinks for organisms in the deep biosphere.
期刊介绍:
The journal is identical in scope to Environmental Microbiology, shares the same editorial team and submission site, and will apply the same high level acceptance criteria. The two journals will be mutually supportive and evolve side-by-side.
Environmental Microbiology Reports provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following:
the structure, activities and communal behaviour of microbial communities
microbial community genetics and evolutionary processes
microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors
microbes in the tree of life, microbial diversification and evolution
population biology and clonal structure
microbial metabolic and structural diversity
microbial physiology, growth and survival
microbes and surfaces, adhesion and biofouling
responses to environmental signals and stress factors
modelling and theory development
pollution microbiology
extremophiles and life in extreme and unusual little-explored habitats
element cycles and biogeochemical processes, primary and secondary production
microbes in a changing world, microbially-influenced global changes
evolution and diversity of archaeal and bacterial viruses
new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens.