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Acquisition of the arginine deiminase system benefits epiparasitic Saccharibacteria and their host bacteria in a mammalian niche environment.在哺乳动物生境中,精氨酸脱亚氨酶系统的获得使外寄生的 Saccharibacteria 及其宿主细菌受益。
Proc Natl Acad Sci U S A. 2022 Jan 11;119(2). doi: 10.1073/pnas.2114909119.
2
Episymbiotic Saccharibacteria suppresses gingival inflammation and bone loss in mice through host bacterial modulation.共生菌萨卡里巴菌通过宿主细菌调节抑制小鼠牙龈炎症和骨丢失。
Cell Host Microbe. 2021 Nov 10;29(11):1649-1662.e7. doi: 10.1016/j.chom.2021.09.009. Epub 2021 Oct 11.
3
Patterns of Gene Content and Co-occurrence Constrain the Evolutionary Path toward Animal Association in Candidate Phyla Radiation Bacteria.基因含量和共现模式限制了候选门辐射细菌向动物共生进化的路径。
mBio. 2021 Aug 31;12(4):e0052121. doi: 10.1128/mBio.00521-21. Epub 2021 Jul 13.
4
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Isolation and cultivation of candidate phyla radiation (TM7) bacteria in coculture with bacterial hosts.与细菌宿主共培养条件下候选门辐射类(TM7)细菌的分离与培养。
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The saccharibacterium TM7x elicits differential responses across its host range.该 saccharibacterium TM7x 在其宿主范围内引发不同的反应。
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8
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9
Acquisition and Adaptation of Ultra-small Parasitic Reduced Genome Bacteria to Mammalian Hosts.获取和适应超小型寄生减基因组细菌与哺乳动物宿主。
Cell Rep. 2020 Jul 21;32(3):107939. doi: 10.1016/j.celrep.2020.107939.
10
Insights Obtained by Culturing Saccharibacteria With Their Bacterial Hosts.从培养菌及其细菌宿主中获得的新认识
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共生关系建立过程中附生菌 Saccharibacteria 菌株 TM7x 的转录组。

Transcriptome of Epibiont Saccharibacteria Strain TM7x During the Establishment of Symbiosis.

机构信息

Department of Periodontics, University of Washingtongrid.34477.33, Seattle, Washington, USA.

Department of Microbiology, The Forsyth Institute, Cambridge, Massachusetts, USA.

出版信息

J Bacteriol. 2022 Sep 20;204(9):e0011222. doi: 10.1128/jb.00112-22. Epub 2022 Aug 17.

DOI:10.1128/jb.00112-22
PMID:35975994
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9487520/
Abstract

Saccharibacteria strain TM7x is a member of the broadly distributed candidate phylum radiation. These bacteria have ultrasmall cell sizes, have reduced genomes, and live as epibionts on the surfaces of other bacteria. The mechanisms by which they establish and maintain this relationship are not yet fully understood. The transcriptomes of the epibiont TM7x and its host bacteria strain XH001 were captured across the establishment of symbiosis during both the initial interaction and stable symbiosis. The results showed a dynamic interaction with large shifts in gene expression for both species between the initial encounter and stable symbiosis, notably in transporter genes. During stable symbiosis, the host XH001 showed higher gene expression for peptidoglycan biosynthesis, mannosylation, cell cycle and stress-related genes, whereas it showed lower expression of chromosomal partitioning genes. This was consistent with the elongated cell shape seen in XH001 infected with TM7x and our discovery that infection resulted in thickened cell walls. Within TM7x, increased pili, type IV effector genes, and arginine catabolism/biosynthesis gene expression during stable symbiosis implied a key role for these functions in the interaction. Consistent with its survival and persistence in the human microbiome as an obligate epibiont with reduced biosynthetic capacities, TM7x also showed higher levels of energy production and peptidoglycan biosynthesis, but lower expression of stress-related genes, during stable symbiosis. These results imply that TM7x and its host bacteria keep a delicate balance in order to sustain an episymbiotic lifestyle. type strain TM7x is the first cultivated member of the Saccharibacteria and the candidate phyla radiation (CPR). It was discovered to be ultrasmall in cell size with a highly reduced genome that establishes an obligate epibiotic relationship with its host bacterium. The CPR is a large, monophyletic radiation of bacteria with reduced genomes that includes Saccharibacteria. The vast majority of the CPR have yet to be cultivated, and our insights into these unique organisms to date have been derived from only a few Saccharibacteria species. Being obligate parasites, it is unknown how these ultrasmall Saccharibacteria, which are missing many biosynthetic pathways, are maintained at a high prevalence within the human microbiome as well as in the environment.

摘要

Saccharibacteria 菌株 TM7x 是广泛分布的候选门辐射的成员。这些细菌具有极小的细胞尺寸,基因组减少,并作为其他细菌表面的共生体生活。它们建立和维持这种关系的机制尚未完全了解。共生体建立过程中,共生体 TM7x 和其宿主细菌菌株 XH001 的转录组被捕获。结果表明,在初始相互作用和稳定共生期间,两种物种的基因表达都发生了巨大变化,尤其是转运蛋白基因。在稳定共生期间,宿主 XH001 表现出更高的肽聚糖生物合成、甘露糖基化、细胞周期和应激相关基因的表达,而染色体分配基因的表达则较低。这与感染 TM7x 的 XH001 中观察到的伸长细胞形状一致,我们发现感染导致细胞壁增厚。在 TM7x 中,稳定共生期间菌毛、IV 型效应基因和精氨酸分解/合成基因表达增加,这表明这些功能在相互作用中起着关键作用。与作为具有减少生物合成能力的必需共生体在人类微生物组中存活和持续存在一致,TM7x 在稳定共生期间也表现出更高的能量产生和肽聚糖生物合成水平,但应激相关基因的表达较低。这些结果表明,TM7x 和其宿主细菌为了维持共生生活方式保持着微妙的平衡。TM7x 是第一个被培养的 Saccharibacteria 和候选门辐射(CPR)成员。它的细胞大小极小,基因组高度减少,与宿主细菌建立了必需的共生关系。CPR 是一个具有减少基因组的大型单系细菌辐射,包括 Saccharibacteria。迄今为止,CPR 的绝大多数尚未被培养,我们对这些独特生物体的了解迄今为止仅来自少数几个 Saccharibacteria 物种。由于是专性寄生虫,目前还不清楚这些缺少许多生物合成途径的超小型 Saccharibacteria 是如何在人类微生物组和环境中保持高流行率的。