Manan Shah, Till L. V. Bornemann, Julia K. Nuy, Martin W. Hahn, Alexander J. Probst, Daniela Beisser, Jens Boenigk
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引用次数: 0
摘要
了解环境中错综复杂的微生物相互作用至关重要。养分与细菌之间的关系尤其如此,因为磷、氮和有机碳的可用性会影响细菌的种群动态。有人认为,低营养条件会促使基因组精简的进化过程。这一过程有助于保存稀缺的营养物质,并使细菌得以增殖。基因组精简与基因组特性有关,如 %GC 含量、编码σ因子的基因、编码区百分比、基因冗余以及细胞运动和 ATP 结合盒转运体等过程中的功能转变。目前的研究旨在揭示营养对浮游淡水细菌基因组大小、%GC 含量和功能特性的影响。我们对许多元基因组特征群落进行了更精细的分类。我们的研究证实了营养水平与基因组特性之间的相互作用。它还强调了不同营养类型(尤其是磷和氮)对这些特性的不同影响。我们观察到功能特征与基因组大小的协变关系。较大的基因组在运动、环境相互作用和调控基因方面表现出丰富的途径。ABC 转运体基因反映了环境中营养物质的可用性,小基因组可能更依赖于来自其他生物的代谢物。我们还讨论了不同门类为适应寡营养环境而采取的不同策略。这些发现有助于我们了解复杂微生物群落的基因组适应性。
Genome-resolved metagenomics reveals the effect of nutrient availability on bacterial genomic properties across 44 European freshwater lakes
Understanding intricate microbial interactions in the environment is crucial. This is especially true for the relationships between nutrients and bacteria, as phosphorus, nitrogen and organic carbon availability are known to influence bacterial population dynamics. It has been suggested that low nutrient conditions prompt the evolutionary process of genome streamlining. This process helps conserve scarce nutrients and allows for proliferation. Genome streamlining is associated with genomic properties such as %GC content, genes encoding sigma factors, percent coding regions, gene redundancy, and functional shifts in processes like cell motility and ATP binding cassette transporters, among others. The current study aims to unveil the impact of nutrition on the genome size, %GC content, and functional properties of pelagic freshwater bacteria. We do this at finer taxonomic resolutions for many metagenomically characterized communities. Our study confirms the interplay of trophic level and genomic properties. It also highlights that different nutrient types, particularly phosphorus and nitrogen, impact these properties differently. We observed a covariation of functional traits with genome size. Larger genomes exhibit enriched pathways for motility, environmental interaction, and regulatory genes. ABC transporter genes reflect the availability of nutrients in the environment, with small genomes presumably relying more on metabolites from other organisms. We also discuss the distinct strategies different phyla adopt to adapt to oligotrophic environments. The findings contribute to our understanding of genomic adaptations within complex microbial communities.
期刊介绍:
Environmental Microbiology 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