通过交叉饲养相互作用从蜂巢中分离的放线菌新属Melissospora conviva gen. nov., sp. nov.。

IF 2 3区 生物学 Q4 MICROBIOLOGY
Déborah Tellatin, Luc Cornet, Valdes Snauwaert, Philippe Compère, Marc Ongena, Loïc Quinton, Nudzejma Stulanovic, Silvia Ribeiro Monteiro, Augustin Rigolet, Pierre Burguet, Petra Van Damme, Lorena Carro, Sébastien Rigali
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引用次数: 0

摘要

大多数微生物在标准实验室条件下仍然无法培养,限制了我们对微生物多样性和生态相互作用的理解。这种不可培养性的一个主要原因是当细菌从其自然群落中移除时,失去了获得必需交叉喂养代谢物的途径。在一项针对蜜蜂蜂巢放线菌的生物勘探活动中,我们发现了5株需要共同培养才能恢复生长的菌株(DT32、DT45T、DT55、DT59和DT194),这表明它们依赖于原生栖息地的微生物相互作用。全基因组测序和系统发育分析将这些分离物定位在小单孢菌科的一个独特谱系中,与小单孢菌属的五个官方认可的分支分开。显微、化学分类和生理特征的结合进一步支持了它们的独特性。值得注意的是,它们表现出高度的营养不良,无法使用所有测试的碳源,可能是由于与其他小单孢科相比,基因组减少(4.6 Mbp)。与它们最近的小单孢子菌亲戚进行的全基因组比较显示,在关键的代谢途径中,包括乙醛酸绕道和enterner - doudoroff途径,基因丢失,这可能解释了它们的代谢依赖。这些发现揭示了一个高度专门化的、生态适应的谱系,具有深刻的进化分歧,并进一步支持微生物相互依存分离策略来探索微生物暗物质。本文提出了放线菌门的新属和新种Melissospora conviva,以分离物DT45T为典型的模式种和模式菌株,已在公共馆藏中保存,登记号为DSM 117791和LMG 33580。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Melissospora conviva gen. nov., sp. nov., a novel actinobacterial genus isolated from beehive through cross-feeding interactions.

Most micro-organisms remain unculturable under standard laboratory conditions, limiting our understanding of microbial diversity and ecological interactions. One major cause of this uncultivability is the loss of access to essential cross-fed metabolites when bacteria are removed from their natural communities. During a bioprospecting campaign targeting actinomycetes of an Apis mellifera beehive, we identified five isolates (DT32, DT45T, DT55, DT59 and DT194) that required co-cultivation for growth recovery, suggesting a dependence on microbial interactions in their native habitat. Whole-genome sequencing and phylogenetic analysis positioned these isolates within a distinct lineage of Micromonosporaceae, separate from the five officially recognized clades of the Micromonospora genus. A combination of microscopic, chemotaxonomic and physiological characterizations further supported their uniqueness. Notably, they exhibited high auxotrophy, being unable to use all carbon sources tested, likely due to genome reduction (4.6 Mbp) compared to other Micromonosporaceae. Pangenomic comparisons with their closest Micromonospora relatives revealed gene losses in key metabolic pathways, including the glyoxylate bypass and the Entner-Doudoroff pathway, which may explain their metabolic reliance. These findings reveal a highly specialized, ecologically adapted lineage with deep evolutionary divergence and further support microbial interdependence isolation strategies to explore the microbial dark matter. We propose Melissospora conviva as a novel genus and species within the Actinomycetota phylum, with isolate DT45T as the representative type species and type strain, which has been deposited in public collections under the accession numbers DSM 117791 and LMG 33580.

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来源期刊
CiteScore
5.20
自引率
21.40%
发文量
426
审稿时长
1 months
期刊介绍: Published by the Microbiology Society and owned by the International Committee on Systematics of Prokaryotes (ICSP), a committee of the Bacteriology and Applied Microbiology Division of the International Union of Microbiological Societies, International Journal of Systematic and Evolutionary Microbiology is the leading forum for the publication of novel microbial taxa and the ICSP’s official journal of record for prokaryotic names. The journal welcomes high-quality research on all aspects of microbial evolution, phylogenetics and systematics, encouraging submissions on all prokaryotes, yeasts, microfungi, protozoa and microalgae across the full breadth of systematics including: Identification, characterisation and culture preservation Microbial evolution and biodiversity Molecular environmental work with strong taxonomic or evolutionary content Nomenclature Taxonomy and phylogenetics.
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