• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

胆汁酸修饰酶的缺失影响细菌的适应性和全球代谢转录组。

Loss of bile acid-altering enzymes impacts bacterial fitness and the global metabolic transcriptome.

机构信息

Department of Biological Sciences, Genetics Program, College of Science, North Carolina State University , Raleigh, North Carolina, USA.

Department of Population Health and Pathobiology, College of Veterinary Medicine, North Carolina State University , Raleigh, North Carolina, USA.

出版信息

Microbiol Spectr. 2024 Jan 11;12(1):e0357623. doi: 10.1128/spectrum.03576-23. Epub 2023 Nov 29.

DOI:10.1128/spectrum.03576-23
PMID:38018975
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10783122/
Abstract

Recent work on bile salt hydrolases (BSHs) in Gram-negative bacteria, such as Bacteroides, has primarily focused on how they can impact host physiology. However, the benefits bile acid metabolism confers to the bacterium that performs it are not well understood. In this study, we set out to define if and how () uses its BSHs and hydroxysteroid dehydrogenase to modify bile acids to provide a fitness advantage for itself and . Genes encoding bile acid-altering enzymes were able to impact how responds to nutrient limitation in the presence of bile acids, specifically carbohydrate metabolism, affecting many polysaccharide utilization loci. This suggests that may be able to shift its metabolism, specifically its ability to target different complex glycans including host mucin, when it comes into contact with specific bile acids in the gut.

摘要

最近对革兰氏阴性菌(如拟杆菌属)中胆盐水解酶(BSHs)的研究主要集中在它们如何影响宿主生理学上。然而,执行胆汁酸代谢对细菌本身带来的益处尚不清楚。在这项研究中,我们旨在确定()是否以及如何利用其 BSH 和羟甾醇脱氢酶来修饰胆汁酸,为自身和提供适应优势。编码改变胆汁酸的酶的基因能够影响在存在胆汁酸的情况下对营养限制的反应,特别是碳水化合物代谢,影响许多多糖利用基因座。这表明,当与肠道中特定的胆汁酸接触时,可能能够改变其代谢,特别是靶向不同复杂聚糖(包括宿主粘蛋白)的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2bb/10783122/8f76811d2f09/spectrum.03576-23.f006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2bb/10783122/90c3707185bc/spectrum.03576-23.f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2bb/10783122/8e448217da53/spectrum.03576-23.f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2bb/10783122/b57b444c0c73/spectrum.03576-23.f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2bb/10783122/1efd56b96858/spectrum.03576-23.f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2bb/10783122/61a6f88d3ea4/spectrum.03576-23.f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2bb/10783122/8f76811d2f09/spectrum.03576-23.f006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2bb/10783122/90c3707185bc/spectrum.03576-23.f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2bb/10783122/8e448217da53/spectrum.03576-23.f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2bb/10783122/b57b444c0c73/spectrum.03576-23.f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2bb/10783122/1efd56b96858/spectrum.03576-23.f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2bb/10783122/61a6f88d3ea4/spectrum.03576-23.f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2bb/10783122/8f76811d2f09/spectrum.03576-23.f006.jpg

相似文献

1
Loss of bile acid-altering enzymes impacts bacterial fitness and the global metabolic transcriptome.胆汁酸修饰酶的缺失影响细菌的适应性和全球代谢转录组。
Microbiol Spectr. 2024 Jan 11;12(1):e0357623. doi: 10.1128/spectrum.03576-23. Epub 2023 Nov 29.
2
Loss of bile acid altering enzymes impact bacterial fitness and the global metabolic transcriptome.胆汁酸改变酶的缺失会影响细菌适应性和整体代谢转录组。
bioRxiv. 2023 Jun 27:2023.06.27.546749. doi: 10.1101/2023.06.27.546749.
3
metabolic activity decreases with polysaccharide molecular weight.代谢活性随多糖分子量的降低而降低。
mBio. 2024 Mar 13;15(3):e0259923. doi: 10.1128/mbio.02599-23. Epub 2024 Feb 20.
4
Symbiotic Human Gut Bacteria with Variable Metabolic Priorities for Host Mucosal Glycans.对宿主黏膜聚糖具有可变代谢优先级的共生人类肠道细菌。
mBio. 2015 Nov 10;6(6):e01282-15. doi: 10.1128/mBio.01282-15.
5
Reciprocal Prioritization to Dietary Glycans by Gut Bacteria in a Competitive Environment Promotes Stable Coexistence.肠道细菌在竞争环境下对膳食糖的相互优先化促进稳定共存。
mBio. 2017 Oct 10;8(5):e01068-17. doi: 10.1128/mBio.01068-17.
6
A Novel Family of RNA-Binding Proteins Regulate Polysaccharide Metabolism in .一种新型 RNA 结合蛋白家族调控. 中的多糖代谢。
J Bacteriol. 2021 Oct 12;203(21):e0021721. doi: 10.1128/JB.00217-21. Epub 2021 Jul 12.
7
Functional genetics of human gut commensal Bacteroides thetaiotaomicron reveals metabolic requirements for growth across environments.人类肠道共生拟杆菌的功能遗传学研究揭示了其在不同环境中生长的代谢需求。
Cell Rep. 2021 Mar 2;34(9):108789. doi: 10.1016/j.celrep.2021.108789.
8
Regulated expression of polysaccharide utilization and capsular biosynthesis loci in biofilm and planktonic Bacteroides thetaiotaomicron during growth in chemostats.在恒化器中生长时,生物膜和浮游态拟杆菌中多糖利用和荚膜生物合成基因座的调控表达。
Biotechnol Bioeng. 2014 Jan;111(1):165-73. doi: 10.1002/bit.24994. Epub 2013 Jul 30.
9
Recognition and degradation of plant cell wall polysaccharides by two human gut symbionts.人体肠道共生菌对植物细胞壁多糖的识别与降解。
PLoS Biol. 2011 Dec;9(12):e1001221. doi: 10.1371/journal.pbio.1001221. Epub 2011 Dec 20.
10
Prioritization of polysaccharide utilization and control of regulator activation in Bacteroides thetaiotaomicron.多形拟杆菌中多糖利用的优先级及调节因子激活的控制
Mol Microbiol. 2017 Apr;104(1):32-45. doi: 10.1111/mmi.13609. Epub 2017 Feb 3.

引用本文的文献

1
A genotoxin associated with colorectal cancer linked to gut dysbiosis in children with cystic fibrosis.一种与囊性纤维化患儿肠道微生物群失调相关的、与结直肠癌有关的基因毒素。
bioRxiv. 2025 Sep 4:2025.09.04.674286. doi: 10.1101/2025.09.04.674286.
2
Lipidomics, Microbiota, and Intestinal Infection Outcome.脂质组学、微生物群与肠道感染结果
Int J Mol Sci. 2025 Aug 24;26(17):8214. doi: 10.3390/ijms26178214.
3
Zeta CrAss-like Phages, a Separate Phage Family Using a Variety of Adaptive Mechanisms to Persist in Their Hosts.类Zeta CrAss噬菌体,一个利用多种适应性机制在宿主中持续存在的独立噬菌体家族。

本文引用的文献

1
Parabacteroides distasonis ameliorates hepatic fibrosis potentially via modulating intestinal bile acid metabolism and hepatocyte pyroptosis in male mice.拟杆菌属缓解肝纤维化的作用可能是通过调节雄性小鼠肠道胆汁酸代谢和肝细胞焦亡实现的。
Nat Commun. 2023 Apr 1;14(1):1829. doi: 10.1038/s41467-023-37459-z.
2
Gut-microbiome-expressed 3β-hydroxysteroid dehydrogenase degrades estradiol and is linked to depression in premenopausal females.肠道微生物表达的 3β-羟类固醇脱氢酶降解雌二醇,并与绝经前女性的抑郁有关。
Cell Metab. 2023 Apr 4;35(4):685-694.e5. doi: 10.1016/j.cmet.2023.02.017. Epub 2023 Mar 17.
3
Bile salt hydrolases shape the bile acid landscape and restrict Clostridioides difficile growth in the murine gut.
Int J Mol Sci. 2025 Aug 8;26(16):7694. doi: 10.3390/ijms26167694.
4
Effects of Celastrol-Enriched Peanuts on Metabolic Health and the Development of Atherosclerosis.富含雷公藤红素的花生对代谢健康及动脉粥样硬化发展的影响。
Nutrients. 2025 Apr 23;17(9):1418. doi: 10.3390/nu17091418.
5
New insights into microbial bile salt hydrolases: from physiological roles to potential applications.微生物胆汁盐水解酶的新见解:从生理作用到潜在应用
Front Microbiol. 2025 Feb 12;16:1513541. doi: 10.3389/fmicb.2025.1513541. eCollection 2025.
6
Investigation of Bile Salt Hydrolase Activity in Human Gut Bacteria Reveals Production of Conjugated Secondary Bile Acids.对人体肠道细菌中胆汁盐水解酶活性的研究揭示了共轭次级胆汁酸的产生。
bioRxiv. 2025 Jan 16:2025.01.16.633392. doi: 10.1101/2025.01.16.633392.
7
Enzymatic Regulation of the Gut Microbiota: Mechanisms and Implications for Host Health.肠道微生物群的酶促调节:机制及其对宿主健康的影响
Biomolecules. 2024 Dec 20;14(12):1638. doi: 10.3390/biom14121638.
8
Bile acids impact the microbiota, host, and dynamics providing insight into mechanisms of efficacy of FMTs and microbiota-focused therapeutics.胆汁酸影响微生物群、宿主和动态,为深入了解 FMT 和专注于微生物组的治疗方法的疗效机制提供了线索。
Gut Microbes. 2024 Jan-Dec;16(1):2393766. doi: 10.1080/19490976.2024.2393766. Epub 2024 Sep 3.
9
Barcoded overexpression screens in gut Bacteroidales identify genes with roles in carbon utilization and stress resistance.肠道拟杆菌门的条码过表达筛选鉴定出在碳利用和应激抗性中起作用的基因。
Nat Commun. 2024 Aug 5;15(1):6618. doi: 10.1038/s41467-024-50124-3.
10
Pathogenic strains can emerge from gut-resident commensals.致病菌株可能源自肠道内的共生菌。
bioRxiv. 2024 Jun 19:2024.06.19.599758. doi: 10.1101/2024.06.19.599758.
胆汁盐水解酶塑造了胆汁酸图谱,并限制了艰难梭菌在小鼠肠道中的生长。
Nat Microbiol. 2023 Apr;8(4):611-628. doi: 10.1038/s41564-023-01337-7. Epub 2023 Mar 13.
4
Deoxycholic acid exacerbates intestinal inflammation by modulating interleukin-1 expression and tuft cell proportion in dextran sulfate sodium-induced murine colitis.脱氧胆酸通过调节白细胞介素-1 的表达和微绒毛细胞比例加剧葡聚糖硫酸钠诱导的小鼠结肠炎的肠道炎症。
PeerJ. 2023 Feb 15;11:e14842. doi: 10.7717/peerj.14842. eCollection 2023.
5
Bile salt hydrolase in non-enterotoxigenic Bacteroides potentiates colorectal cancer.非肠产毒型拟杆菌中的胆汁盐水解酶促进结直肠癌。
Nat Commun. 2023 Feb 10;14(1):755. doi: 10.1038/s41467-023-36089-9.
6
Bacteroides vulgatus Ameliorates Lipid Metabolic Disorders and Modulates Gut Microbial Composition in Hyperlipidemic Rats.脆弱拟杆菌改善高脂血症大鼠的脂代谢紊乱并调节肠道微生物组成。
Microbiol Spectr. 2023 Feb 14;11(1):e0251722. doi: 10.1128/spectrum.02517-22. Epub 2023 Jan 10.
7
Enterococci enhance Clostridioides difficile pathogenesis.肠球菌增强艰难梭菌的发病机制。
Nature. 2022 Nov;611(7937):780-786. doi: 10.1038/s41586-022-05438-x. Epub 2022 Nov 16.
8
The Proteome of Extracellular Vesicles Produced by the Human Gut Bacteria Bacteroides thetaiotaomicron Is Influenced by Environmental and Host-Derived Factors.人肠道细菌拟杆菌 Bacteroides thetaiotaomicron 产生的细胞外囊泡的蛋白质组受环境和宿主来源因素的影响。
Appl Environ Microbiol. 2022 Aug 23;88(16):e0053322. doi: 10.1128/aem.00533-22. Epub 2022 Aug 2.
9
Oxidative ornithine metabolism supports non-inflammatory C. difficile colonization.氧化鸟氨酸代谢支持无炎症的艰难梭菌定植。
Nat Metab. 2022 Jan;4(1):19-28. doi: 10.1038/s42255-021-00506-4. Epub 2022 Jan 6.
10
A single sulfatase is required to access colonic mucin by a gut bacterium.一种肠道细菌需要单一的硫酸盐酶才能接触结肠黏液。
Nature. 2021 Oct;598(7880):332-337. doi: 10.1038/s41586-021-03967-5. Epub 2021 Oct 6.