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人肠道共生菌DSM18205中多糖利用位点的转录描绘以及与典型物种在膳食植物聚糖上的共培养

Transcriptional delineation of polysaccharide utilization loci in the human gut commensal DSM18205 and co-culture with exemplar species on dietary plant glycans.

作者信息

Panwar Deepesh, Briggs Jonathon, Fraser Alexander S C, Stewart William A, Brumer Harry

机构信息

Michael Smith Laboratories, The University of British Columbia, Vancouver, British Columbia, Canada.

Department of Biochemistry and Molecular Biology, The University of British Columbia, Vancouver, British Columbia, Canada.

出版信息

Appl Environ Microbiol. 2025 Jan 31;91(1):e0175924. doi: 10.1128/aem.01759-24. Epub 2024 Dec 5.

Abstract

UNLABELLED

There is growing interest in members of the genus (family ) as members of a well-balanced human gut microbiota (HGM). are particularly associated with the consumption of a diet rich in plant polysaccharides comprising dietary fiber. However, understanding of the molecular basis of complex carbohydrate utilization in species is currently incomplete. Here, we used RNA sequencing (RNA-seq) of the type strain DSM 18205 (previously CB7) to define precisely individual polysaccharide utilization loci (PULs) and associated carbohydrate-active enzymes (CAZymes) that are implicated in the catabolism of common fruit, vegetable, and grain polysaccharides (. mixed-linkage β-glucans, xyloglucans, xylans, pectins, and inulin). Although many commonalities were observed, several of these systems exhibited significant compositional and organizational differences homologs in the better-studied (sister family ), which predominate in post-industrial HGM. Growth on β-mannans, β(1, 3)-galactans, and microbial β(1, 3)-glucans was not observed, due to an apparent lack of cognate PULs. Most notably, is unable to grow on starch, due to an incomplete starch utilization system (Sus). Subsequent transcriptional profiling of bellwether Ton-B-dependent transporter-encoding genes revealed that PUL upregulation is rapid and general upon transfer from glucose to plant polysaccharides, reflective of de-repression enabling substrate sensing. Distinct from previous observations of species, we were unable to observe clearly delineated substrate prioritization on a polysaccharide mixture designed to mimic diverse plant cell wall digesta. Finally, co-culture experiments generally indicated stable co-existence and lack of exclusive competition between and representative HGM species ( and ) on individual polysaccharides, except in cases where corresponding PULs were obviously lacking.

IMPORTANCE

There is currently a great level of interest in improving the composition and function of the human gut microbiota (HGM) to improve health. The bacterium is prevalent in people who eat plant-rich diets and is therefore associated with a healthy lifestyle. On one hand, our study reveals the specific molecular systems that enable to proliferate on individual plant polysaccharides. On the other, a growing body of data suggests that the inability of to grow on starch and animal glycans, which dominate in post-industrial diets, as well as host mucin, contributes strongly to its displacement from the HGM by species, in the absence of direct antagonism.

摘要

未标记

作为均衡人类肠道微生物群(HGM)的成员,[菌属名称]([科名])的细菌越来越受到关注。它们特别与富含包含膳食纤维的植物多糖的饮食摄入有关。然而,目前对[菌属名称]物种中复杂碳水化合物利用的分子基础的理解并不完整。在这里,我们使用模式菌株[菌株名称] DSM 18205(以前称为[菌株名称] CB7)的RNA测序(RNA-seq)来精确确定参与常见水果、蔬菜和谷物多糖(如混合连接的β-葡聚糖、木葡聚糖、木聚糖、果胶和菊粉)分解代谢的各个多糖利用位点(PULs)和相关的碳水化合物活性酶(CAZymes)。尽管观察到许多共性,但这些系统中的几个在研究更充分的[菌属名称](姐妹科)的同源物中表现出显著的组成和组织差异,[菌属名称]在工业化后的HGM中占主导地位。未观察到[菌株名称]在β-甘露聚糖、β(1, 3)-半乳聚糖和微生物β(1, 3)-葡聚糖上生长,这显然是由于缺乏相关的PULs。最值得注意的是,由于淀粉利用系统(Sus)不完整,[菌株名称]无法在淀粉上生长。随后对关键的依赖Ton-B转运蛋白编码基因的转录谱分析表明,从葡萄糖转移到植物多糖后,PUL的上调迅速且普遍,这反映了去阻遏从而实现底物感知。与之前对[菌属名称]物种的观察不同,在设计用于模拟[菌属名称]多样植物细胞壁消化物的多糖混合物上,我们无法清楚地观察到明确的底物优先选择。最后,共培养实验总体表明,在单个多糖上,[菌株名称]与代表性的HGM物种([物种名称1]和[物种名称2])之间通常稳定共存且不存在排他性竞争,除非明显缺乏相应的PULs。

重要性

目前人们对改善人类肠道微生物群(HGM)的组成和功能以增进健康有着极大的兴趣。[菌属名称]细菌在食用富含植物性食物的人群中普遍存在,因此与健康的生活方式相关。一方面,我们的研究揭示了使[菌株名称]能够在单个植物多糖上增殖的特定分子系统。另一方面,越来越多的数据表明,在没有直接拮抗作用的情况下,[菌株名称]无法在工业化后饮食中占主导地位的淀粉和动物聚糖以及宿主粘蛋白上生长,这极大地导致了它被[菌属名称]物种从HGM中取代。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c23a/11784079/631131e2601d/aem.01759-24.f001.jpg

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