Functionally distinct core microbes of Tricholoma matsutake revealed by cross-study analysis.

IF 12.7 1区 生物学 Q1 MICROBIOLOGY
Shinnam Yoo, Chang Wan Seo, Young Woon Lim
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引用次数: 0

Abstract

Background: Tricholoma matsutake (TM), a prized wild mushroom in Eurasia, hosts distinct microbiomes in its mycorrhizal zone (shiro), with some microbes known to benefit TM. However, no study has systematically compared shiro-inhabiting microbiomes across multiple studies from either taxonomic or functional perspectives.

Results: We first compiled bacterial and fungal amplicon sequences from public and newly generated datasets, then applied phylogenetic tree-based clustering to integrate technically heterogeneous sequences. This enabled the identification of core microbial phylotypes conserved in shiro from geographically diverse regions. We also revealed niche-specific phylotypes within the shiro, distinguishing those associated with soil, TM-colonized root, and fruitbody, thereby demonstrating clear niche differentiation. Functional predictions and experimental validation highlighted key roles of the microbes in degradation of aromatic compounds, utilization of plant-derived compounds, and fruitbody development.

Conclusions: Our cross-study integration of shiro microbial sequences identified core and niche-specific phylotypes with distinct ecological roles. This study lays a foundation for advancing ecological research and cultivation strategies for TM.

交叉研究揭示了松茸口蘑的功能核心微生物。
背景:松茸口蘑(Tricholoma matsutake, TM)是欧亚大陆一种珍贵的野生蘑菇,在其菌根区(shiro)拥有独特的微生物群,其中一些微生物已知对松茸口蘑有益。然而,没有一项研究从分类学或功能角度系统地比较了多个研究中居住的微生物组。结果:我们首先从公开的和新生成的数据集中编译细菌和真菌扩增子序列,然后应用基于系统发育树的聚类技术对异构序列进行整合。这使得从地理上不同的地区鉴定出在shiro中保守的核心微生物种型。我们还揭示了shiro内的生态位特异性种型,区分了与土壤、tm定殖根和子实体相关的种型,从而证明了明确的生态位分化。功能预测和实验验证强调了微生物在芳香化合物降解、植物源性化合物利用和子实体发育中的关键作用。结论:我们的交叉研究整合了shiro微生物序列,确定了具有不同生态作用的核心和生态位特异性种型。本研究为推进TM的生态研究和培育策略奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
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