秀丽隐杆线虫与共生真菌微生物组成员加利福尼亚巴奈特菌的相互作用

IF 2.7 4区 生物学 Q2 ENVIRONMENTAL SCIENCES
Carola Petersen, Hanne Griem-Krey, Christina Martínez Christophersen, Hinrich Schulenburg, Michael Habig
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引用次数: 0

摘要

已知秀丽隐杆线虫以其环境中的细菌为食并与细菌相互作用,已成为微生物组研究的模式生物。然而,秀丽隐杆线虫是否以及如何与共生真菌相互作用在很大程度上仍然未知,尽管在其自然栖息地存在许多真菌物种。在这里,我们从秀丽隐杆线虫的中胚层实验中分离出酵母加州巴内特菌,并表征了其基因组和与线虫的相互作用。我们发现,像细菌微生物群一样,加州双胞杆菌可以在秀丽隐杆线虫的肠道中定植,并且可以作为成年线虫的唯一食物来源,尽管这种食物来源很差。然而,当与大肠杆菌OP50一起出现时,真菌可以导致更高的种群增长和改变觅食行为,这表明了一种依赖环境的益处。这种效应在不同的自然秀丽隐杆线虫菌株之间有所不同,这表明线虫与加州双胞杆菌的相互作用具有基因组基础。在真菌方面,尽管我们获得了完整组装和注释的加州双胞杆菌菌株基因组,但我们无法鉴定出与秀丽隐杆线虫和/或大肠杆菌OP50相互作用的任何明显候选基因。总的来说,我们的研究结果提供了一个有趣的例子,说明自然相互作用的真菌、细菌和动物之间的复杂性和多层次关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Interaction Between the Nematode Caenorhabditis elegans and Its Coexisting Fungal Microbiome Member Barnettozyma californica

The Interaction Between the Nematode Caenorhabditis elegans and Its Coexisting Fungal Microbiome Member Barnettozyma californica

The nematode Caenorhabditis elegans is known to feed on and interact with bacteria in its environment and has become a model organism for microbiome studies. However, whether and how C. elegans interacts with co-occurring fungi remains largely unknown, despite the presence of many fungal species in its natural habitat. Here, we isolate the yeast Barnettozyma californica from a mesocosm experiment with C. elegans and characterise its genome and interaction with the nematode. We find that, like bacterial microbiota, B. californica can colonise the intestine of C. elegans and can serve as a sole, albeit poor, food source for adult nematodes. Yet, when present together with Escherichia coli OP50, the fungus can lead to higher population growth and altered foraging behaviour, suggesting a context-dependent benefit. This effect varied between different natural C. elegans strains, suggesting a genomic basis for the nematode's interaction with B. californica. On the fungal side, we could not identify any obvious candidate genes for its interaction with C. elegans and/or E. coli OP50, despite obtaining a fully assembled and annotated genome of the isolated B. californica strain. Overall, our results provide an intriguing example of the complexity and multi-level relationship between naturally interacting fungi, bacteria and animals.

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来源期刊
Environmental Microbiology Reports
Environmental Microbiology Reports ENVIRONMENTAL SCIENCES-MICROBIOLOGY
CiteScore
6.00
自引率
3.00%
发文量
91
审稿时长
3.0 months
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.
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