• 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

人类肠道微生物群:简化且稳定的无菌大鼠模型的特征。

Human intestinal microbiota: characterization of a simplified and stable gnotobiotic rat model.

机构信息

German Institute of Human Nutrition Potsdam Rehbruecke, Department of Gastrointestinal Microbiology, Nuthetal, Germany.

出版信息

Gut Microbes. 2011 Jan-Feb;2(1):25-33. doi: 10.4161/gmic.2.1.14651.

DOI:10.4161/gmic.2.1.14651
PMID:21637015
Abstract

The study of host microbe interactions is hampered by the complexity and inter-individual variability of the human gut microbiota. Therefore, a simplified human intestinal microbiota (SIHUMI) consisting of seven bacterial species was introduced into germfree rats. Species selection was based on numerical importance and fermentative abilities in the human gut. Association of the rats with the SIHUMI (Anaerostipes caccae, Bacteroides thetaiotaomicron, Bifidobacterium longum, Blautia producta, Clostridium ramosum, Escherichia coli and Lactobacillus plantarum) resulted in increased faecal concentrations of short chain fatty acids compared to germfree animals. Since the faecal butyrate concentration was low (0.9 ± 0.5 µmol/g dry matter) the SIHUMI was complemented with Clostridium butyricum. This extended bacterial community (SIHUMIx) led to an increased faecal butyrate concentration of 1.5 ± 0.7 µmol/g dry matter. Besides forming SCFA, the SIHUMIx was capable of degrading mucins, β-aspartylglycine and bilirubin. These features are characteristic of conventional animals but not observed in germfree animals. Dietary interventions with modifications in fibre and fat content led to changes in the proportion of community members. The relative increase of one member of this community in response to a high-fat diet reflects the situation reported for obese mice and human subjects. The strength of the model communities is their remarkable stability over time and their easy transfer to the offspring.

摘要

宿主微生物相互作用的研究受到人类肠道微生物菌群复杂性和个体间变异性的阻碍。因此,引入了由 7 种细菌组成的简化人类肠道微生物群(SIHUMI)到无菌大鼠中。物种选择基于在人类肠道中的数量重要性和发酵能力。与 SIHUMI(厌氧梭菌、拟杆菌、双歧杆菌、布劳特氏菌、脆弱拟杆菌、大肠杆菌和植物乳杆菌)相关联的大鼠导致粪便中短链脂肪酸浓度增加,与无菌动物相比。由于粪便丁酸浓度较低(0.9±0.5µmol/g 干物质),因此用丁酸梭菌补充 SIHUMI。这种扩展的细菌群落(SIHUMIx)导致粪便丁酸浓度增加到 1.5±0.7µmol/g 干物质。除了形成 SCFA 外,SIHUMIx 还能够降解粘蛋白、β-天冬氨酸甘氨酸和胆红素。这些特征是常规动物的特征,但在无菌动物中观察不到。饮食干预中纤维和脂肪含量的改变导致群落成员比例的变化。该群落中一个成员的相对增加对高脂肪饮食的反应反映了肥胖小鼠和人类受试者的情况。模型群落的优势在于它们具有显著的时间稳定性,并且易于传递给后代。

相似文献

1
Human intestinal microbiota: characterization of a simplified and stable gnotobiotic rat model.人类肠道微生物群:简化且稳定的无菌大鼠模型的特征。
Gut Microbes. 2011 Jan-Feb;2(1):25-33. doi: 10.4161/gmic.2.1.14651.
2
Isolation of lactate-utilizing butyrate-producing bacteria from human feces and in vivo administration of Anaerostipes caccae strain L2 and galacto-oligosaccharides in a rat model.从人粪便中分离利用乳酸产生丁酸的细菌,并在大鼠模型中对粪厌氧棒状菌L2菌株和低聚半乳糖进行体内给药。
FEMS Microbiol Ecol. 2008 Dec;66(3):528-36. doi: 10.1111/j.1574-6941.2008.00528.x. Epub 2008 Jun 12.
3
Oligofructose and long-chain inulin: influence on the gut microbial ecology of rats associated with a human faecal flora.低聚果糖和长链菊粉:对与人类粪便菌群相关的大鼠肠道微生物生态的影响。
Br J Nutr. 2001 Aug;86(2):291-300. doi: 10.1079/bjn2001403.
4
Clostridium ramosum promotes high-fat diet-induced obesity in gnotobiotic mouse models.多枝梭菌在悉生小鼠模型中促进高脂饮食诱导的肥胖。
mBio. 2014 Sep 30;5(5):e01530-14. doi: 10.1128/mBio.01530-14.
5
The Intestinal Microbiota in Metabolic Disease.代谢性疾病中的肠道微生物群
Nutrients. 2016 Apr 6;8(4):202. doi: 10.3390/nu8040202.
6
Association of germ-free mice with a simplified human intestinal microbiota results in a shortened intestine.无菌小鼠与简化的人类肠道微生物群结合会导致肠道缩短。
Gut Microbes. 2014 Mar-Apr;5(2):176-82. doi: 10.4161/gmic.28203. Epub 2014 Feb 13.
7
Clostridium butyricum, a butyrate-producing probiotic, inhibits intestinal tumor development through modulating Wnt signaling and gut microbiota.丁酸梭菌是一种产生丁酸的益生菌,通过调节 Wnt 信号通路和肠道微生物群来抑制肠道肿瘤的发展。
Cancer Lett. 2020 Jan 28;469:456-467. doi: 10.1016/j.canlet.2019.11.019. Epub 2019 Nov 14.
8
Following the community development of SIHUMIx - a new intestinal model for bioreactor use.随着用于生物反应器的新型肠道模型SIHUMIx的群落发展。
Gut Microbes. 2020 Jul 3;11(4):1116-1129. doi: 10.1080/19490976.2019.1702431. Epub 2020 Jan 10.
9
Exopolysaccharides produced by Bifidobacterium longum IPLA E44 and Bifidobacterium animalis subsp. lactis IPLA R1 modify the composition and metabolic activity of human faecal microbiota in pH-controlled batch cultures.长双歧杆菌 IPLA E44 和动物双歧杆菌亚种。乳双歧杆菌 IPLA R1 产生的胞外多糖改变了 pH 控制批次培养中人体粪便微生物群的组成和代谢活性。
Int J Food Microbiol. 2009 Nov 15;135(3):260-7. doi: 10.1016/j.ijfoodmicro.2009.08.017. Epub 2009 Aug 19.
10
A Mesocosm of Lactobacillus johnsonii, Bifidobacterium longum, and Escherichia coli in the mouse gut.小鼠肠道中约氏乳杆菌、长双歧杆菌和大肠杆菌的微宇宙。
DNA Cell Biol. 2009 Aug;28(8):413-22. doi: 10.1089/dna.2009.0873.

引用本文的文献

1
StrainR2 accurately deconvolutes strain-level abundances in synthetic microbial communities.StrainR2能够准确地解析合成微生物群落中菌株水平的丰度。
Bioinformatics. 2025 Aug 2;41(8). doi: 10.1093/bioinformatics/btaf440.
2
Bacterial microcompartments and energy metabolism drive gut colonization by Bilophila wadsworthia.细菌微区室与能量代谢促进沃兹沃思嗜胆菌在肠道的定殖。
Nat Commun. 2025 May 30;16(1):5049. doi: 10.1038/s41467-025-60180-y.
3
Food colorant brilliant blue causes persistent functional and structural changes in an in vitro simplified microbiota model system.
食用色素亮蓝在体外简化微生物群模型系统中引起持续的功能和结构变化。
ISME Commun. 2025 Mar 22;5(1):ycaf050. doi: 10.1093/ismeco/ycaf050. eCollection 2025 Jan.
4
The host genotype actively shapes its microbiome across generations in laboratory mice.在实验室小鼠中,宿主基因型会在几代之间积极塑造其微生物群。
Microbiome. 2024 Dec 5;12(1):256. doi: 10.1186/s40168-024-01954-2.
5
Measuring and understanding information storage and transfer in a simulated human gut microbiome.测量和理解模拟人类肠道微生物组中的信息存储和传输。
PLoS Comput Biol. 2024 Sep 17;20(9):e1012359. doi: 10.1371/journal.pcbi.1012359. eCollection 2024 Sep.
6
An model system for testing chemical effects on microbiome-immune interactions - examples with BPX and PFAS mixtures.用于测试化学物质对微生物组-免疫相互作用影响的模型系统 - 以 BPX 和 PFAS 混合物为例。
Front Immunol. 2024 Jun 17;15:1298971. doi: 10.3389/fimmu.2024.1298971. eCollection 2024.
7
Surrogate modeling and control of medical digital twins.医学数字孪生的代理建模与控制
ArXiv. 2024 May 20:arXiv:2402.05750v2.
8
Designing function-specific minimal microbiomes from large microbial communities.从大型微生物群落中设计功能特定的最小微生物群。
NPJ Syst Biol Appl. 2024 May 3;10(1):46. doi: 10.1038/s41540-024-00373-1.
9
A Gnotobiotic Mouse Model with Divergent Equol-Producing Phenotypes: Potential for Determining Microbial-Driven Health Impacts of Soy Isoflavone Daidzein.具有不同产_EQUOL 表型的无菌小鼠模型:确定大豆异黄酮染料木黄酮的微生物驱动健康影响的潜力。
Nutrients. 2024 Apr 6;16(7):1079. doi: 10.3390/nu16071079.
10
High-throughput screening of the effects of 90 xenobiotics on the simplified human gut microbiota model (SIHUMIx): a metaproteomic and metabolomic study.90种外源性物质对简化人类肠道微生物群模型(SIHUMIx)影响的高通量筛选:一项元蛋白质组学和代谢组学研究
Front Microbiol. 2024 Feb 20;15:1349367. doi: 10.3389/fmicb.2024.1349367. eCollection 2024.