Rumen protozoa are a hub for diverse hydrogenotrophic functions

IF 3.6 4区 生物学 Q2 ENVIRONMENTAL SCIENCES Environmental Microbiology Reports Pub Date : 2024-07-03 DOI:10.1111/1758-2229.13298
Ido Toyber, Raghawendra Kumar, Elie Jami
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Abstract

Ciliate protozoa are an integral part of the rumen microbial community involved in a variety of metabolic processes. These processes are thought to be in part the outcome of interactions with their associated prokaryotic community. For example, methane production is enhanced through interspecies hydrogen transfer between protozoa and archaea. We hypothesize that ciliate protozoa are host to a stable prokaryotic community dictated by specific functions they carry. Here, we modify the microbial community by varying the forage-to-concentrate ratios and show that, despite major changes in the prokaryotic community, several taxa remain stably associated with ciliate protozoa. By quantifying genes belonging to various known reduction pathways in the rumen, we find that the bacterial community associated with protozoa is enriched in genes belonging to hydrogen utilization pathways and that these genes correspond to the same taxonomic affiliations seen enriched in protozoa. Our results show that ciliate protozoa in the rumen may serve as a hub for various hydrogenotrophic functions and a better understanding of the processes driven by different protozoa may unveil the potential role of ciliates in shaping rumen metabolism.

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瘤胃原生动物是多种养氢功能的枢纽。
纤毛虫原生动物是瘤胃微生物群落中不可或缺的一部分,参与各种代谢过程。据认为,这些过程部分是与相关原核生物群落相互作用的结果。例如,甲烷的产生是通过原生动物和古细菌之间的种间氢转移来提高的。我们假设,纤毛虫原生动物是稳定的原核生物群落的宿主,这取决于它们所承载的特定功能。在这里,我们通过改变饲料与浓缩物的比例来改变微生物群落,结果表明,尽管原核生物群落发生了重大变化,但仍有几个类群与纤毛虫原生动物保持着稳定的联系。通过量化瘤胃中属于各种已知还原途径的基因,我们发现与原生动物相关的细菌群落中富含属于氢利用途径的基因,而且这些基因与原生动物中富含的分类群相同。我们的研究结果表明,瘤胃中的纤毛虫原生动物可能是各种氢营养功能的枢纽,更好地了解不同原生动物驱动的过程可能会揭示纤毛虫在塑造瘤胃代谢过程中的潜在作用。
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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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