糖藻表面微生物组与代谢组相关性的多组学分析。

IF 3.5 3区 生物学 Q2 MICROBIOLOGY
Emilie Adouane, Cédric Hubas, Catherine Leblanc, Raphaël Lami, Soizic Prado
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引用次数: 0

摘要

欧洲一种重要的褐藻Saccharina latissima的微生物群对其健康、适应性和对病原体的抵抗力有显著影响。然而,对与该物种相关的微生物群落(细菌、真核生物和真菌)的多样性和功能的综合研究尚缺乏。利用元条形码技术,研究了拉底葡萄球菌的外生菌群,并将微生物多样性与代谢组学模式(LC-MS/MS)进行了关联。特定的表细菌和真核生物群落与核心微生物群一起栖息在S. latisima表面,而真菌群落则表现出更低且更异质性的多样性。代谢组学分析揭示了大量多样性的质量特征,包括推定注释的脂肪酸、氨基衍生物、氨基酸和萘呋喃。多因素分析将微生物多样性与主要由真菌和细菌驱动的表面代谢组变化联系起来。鉴定了两个分类群:一个与细菌联合体有关,另一个与真菌联合体有关,每个都与特定的代谢物相关。这项研究证明了核心细菌和真核微生物群与核心代谢组相关,并强调了个体间的差异。使用天然产物数据库对表面代谢组进行注释表明,许多代谢物可能参与物种间的化学相互作用。我们的研究结果建立了微生物群落结构和功能之间的联系,确定了两种微生物群落可能参与了拉底草的化学防御。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multi-omics analysis of the correlation between surface microbiome and metabolome in Saccharina latissima (Laminariales, Phaeophyceae).

The microbiome of Saccharina latissima, an important brown macroalgal species in Europe, significantly influences its health, fitness, and pathogen resistance. Yet, comprehensive studies on the diversity and function of microbial communities (bacteria, eukaryotes, and fungi) associated with this species are lacking. Using metabarcoding, we investigated the epimicrobiota of S. latissima and correlated microbial diversity with metabolomic patterns (liquid chromatography coupled to tandem mass spectrometry). Specific epibacterial and eukaryotic communities inhabit the S. latissima surface, alongside a core microbiota, while fungal communities show lower and more heterogeneous diversity. Metabolomic analysis revealed a large diversity of mass features, including putatively annotated fatty acids, amino derivatives, amino acids, and naphthofurans. Multiple-factor analysis linked microbial diversity with surface metabolome variations, driven mainly by fungi and bacteria. Two taxa groups were identified: one associated with bacterial consortia and the other with fungal consortia, each correlated with specific metabolites. This study demonstrated a core bacterial and eukaryotic microbiota associated with a core metabolome and highlighted interindividual variations. Annotating the surface metabolome using Natural Products databases suggested numerous metabolites potentially involved in interspecies chemical interactions. Our findings establish a link between microbial community structure and function, identifying two microbial consortia potentially involved in the chemical defense of S. latissima.

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来源期刊
FEMS microbiology ecology
FEMS microbiology ecology 生物-微生物学
CiteScore
7.50
自引率
2.40%
发文量
132
审稿时长
3 months
期刊介绍: FEMS Microbiology Ecology aims to ensure efficient publication of high-quality papers that are original and provide a significant contribution to the understanding of microbial ecology. The journal contains Research Articles and MiniReviews on fundamental aspects of the ecology of microorganisms in natural soil, aquatic and atmospheric habitats, including extreme environments, and in artificial or managed environments. Research papers on pure cultures and in the areas of plant pathology and medical, food or veterinary microbiology will be published where they provide valuable generic information on microbial ecology. Papers can deal with culturable and non-culturable forms of any type of microorganism: bacteria, archaea, filamentous fungi, yeasts, protozoa, cyanobacteria, algae or viruses. In addition, the journal will publish Perspectives, Current Opinion and Controversy Articles, Commentaries and Letters to the Editor on topical issues in microbial ecology. - Application of ecological theory to microbial ecology - Interactions and signalling between microorganisms and with plants and animals - Interactions between microorganisms and their physicochemical enviornment - Microbial aspects of biogeochemical cycles and processes - Microbial community ecology - Phylogenetic and functional diversity of microbial communities - Evolutionary biology of microorganisms
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