A Novel Lineage of Endosymbiotic Actinomycetales: Genome Reduction and Acquisition of New Functions in Bifidobacteriaceae Associated With Termite Gut Flagellates

IF 4.3 2区 生物学 Q2 MICROBIOLOGY Environmental microbiology Pub Date : 2025-01-08 DOI:10.1111/1462-2920.70010
Joana Kästle Silva, Vincent Hervé, Undine S. Mies, Katja Platt, Andreas Brune
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Abstract

Cellulolytic flagellates are essential for the symbiotic digestion of lignocellulose in the gut of lower termites. Most species are associated with host-specific consortia of bacterial symbionts from various phyla. 16S rRNA-based diversity studies and taxon-specific fluorescence in situ hybridization revealed a termite-specific clade of Actinomycetales that colonise the cytoplasm of Trichonympha spp. and other gut flagellates, representing the only known case of intracellular Actinomycetota in protists. Comparative analysis of eleven metagenome-assembled genomes from lower termites allowed us to describe them as new genera of Bifidobacteriaceae. Like the previously investigated Candidatus Ancillula trichonymphae, they ferment sugars via the bifidobacterium shunt but, unlike their free-living relatives, experienced significant genome erosion. Additionally, they acquired new functions by horizontal gene transfer from other gut bacteria, including the capacity to produce hydrogen. Members of the genus Ancillula (average genome size 1.56 ± 0.2 Mbp) retained most pathways for the synthesis of amino acids, including a threonine/serine exporter, providing concrete evidence for the basis of the mutualistic relationship with their host. By contrast, Opitulatrix species (1.23 ± 0.1 Mbp) lost most of their biosynthetic capacities, indicating that an originally mutualistic symbiosis is on the decline.

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一个新的内共生放线菌谱系:与白蚁肠道鞭毛虫相关的双歧杆菌科基因组还原和新功能的获得
分解纤维素的鞭毛虫是低等白蚁肠道中木质纤维素的共生消化所必需的。大多数种类与来自不同门的细菌共生体的宿主特异性联合体有关。基于16S rrna的多样性研究和分类群特异性荧光原位杂交发现了一个白蚁特异性的放线菌分支,该分支定植于毛菌属和其他肠道鞭毛虫的细胞质中,代表了原生生物中唯一已知的细胞内放线菌群。对低等白蚁的11个元基因组组装基因组进行比较分析,使我们能够将它们描述为双歧杆菌科新属。与之前研究的滴管候选菌一样,它们通过双歧杆菌分流器发酵糖,但与它们自由生活的亲戚不同,它们经历了显著的基因组侵蚀。此外,它们通过其他肠道细菌的水平基因转移获得了新的功能,包括产生氢的能力。蚁属成员(平均基因组大小为1.56±0.2 Mbp)保留了大部分氨基酸合成途径,包括苏氨酸/丝氨酸输出通路,为与其宿主的互惠关系提供了具体证据。相比之下,Opitulatrix物种(1.23±0.1 Mbp)失去了大部分生物合成能力,表明原本互利共生的共生关系正在下降。
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来源期刊
Environmental microbiology
Environmental microbiology 环境科学-微生物学
CiteScore
9.90
自引率
3.90%
发文量
427
审稿时长
2.3 months
期刊介绍: Environmental Microbiology 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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