Disease
Microbiota ☳
Metabolome
Factor
Eubacterium ⇒ Eubacterium rectale {10000528}
Record Keys
Parent:
Definition: Eubacterium rectale
Details
Initialisation date: 2021-04-12
Meta Information
Rank:
Domain:
Zone: [ ]
Enzyme: [ ]
Function: [ ]
Notes: Shared Reference Notes
[1.1 ]
- Eubacterium rectale subspecies harboring flagellin-encoding genes were associated with a predominantly #Meat-based diet
[1.2 ]
[1.3 ] Eubacterium rectale , one of the most prevalent human gut bacteria, can produce #Lauroyl tryptamine .
- Auroyl tryptamine is able to bind a human receptor that plays a key role in regulating the immune system and controlling inflammation.
[1.4 ] [#Behcet’s Disease ] Eubacterium rectale (a kind of #Butyrate -producing bacteria) in BD mice, which can upregulate NK1.1+ cells and reduce serum IL-17 levels and disease severity scores, sharing the partial mechanism of #Colchicine , which is used to treat BD patients.
[1.5 ] [#Alzheimer’s disease ] [#Bacteroides fragilis ] [#Amyloid-beta ] #Amyloid deposits was associated with greater abundance of proinflammatory taxa (#Escherichia /#Shigella ), which were in turn correlated with proinflammatory cytokines, and with reduced abundance of Eubacterium rectale and B. fragilis, 2 taxa with anti-inflammatory activity
[1.6 ] [#Covid-19 ] #Bifidobacteria species and Eubacterium rectale , with lower severity, and pro-inflammatory bacteria such as #Prevotella copri with higher severity.
[1.7 ] [#Alzheimer’s disease ] Eubacterium rectale (anti-inflammatory taxon).
- a decrease in #Firmicutes and #Bifidobacterium and increased levels of #Proteobacteria , #Actinobacteria
- a disputed frequency of #Bacteroidetes in various studies..
[1.8 ] [#Bacteroides massiliensis ] #Prostate cancer > a higher relative abundance of Bacteriodes massiliensis as well as decreased relative abundances of #Faecalibacterium prausnitzii and Eubacterium rectale in the stool from men with PCa compared to the controls.
[1.9 ] [#Chronic fatigue syndrome ] #Faecalibacterium prausnitzii and Eubacterium rectale , which are both recognized as abundant, health-promoting #Butyrate producers in the human gut, were reduced in ME/CFS.
- deficient microbial capacity for #Butyrate synthesis.
- The abundance of #Faecalibacterium prausnitzii was inversely associated with fatigue severity.
[#Actinomyces massiliensis ] - #Athletes from 16 different sports > dominated by a single or a combination of five species, namely Eubacterium rectale , Polynucleobacter necessarius, #Faecalibacterium prausnitzii , #Bacteroides vulgatus , and #Gordonibacter massiliensis.
- Species such as #Bifidobacterium animalis , #Lactobacillus acidophilus , #Prevotella intermedia , and F. prausnitzii were associated with #Athletes participating in high dynamic component sports.
[1.11 ] [#Diabetes Type 1 ] #Villanella , #Clostridium , and #Bacteroides and a decreased quantity of #Lactobacillus , Eubacterium rectale , #Blautia coccoides , and #Bifidobacterium in #Children with type 1 diabetes.
[1.12 ] [#Resistant starch ] #Ruminococcus bromii , and #Bifidobacterium adolescentis , and also to a lesser extent by Eubacterium rectale and #Bacteroides thetaiotaomicron .
- in the mixed bacterial and fecal incubations, RS degradation is impossible in the absence of R. bromii
Intervention in Disease
Author: MetaBiomIdentifier: 10000528URL: https://www.metabiom.org/microbiota/473/eubacterium-rectaleKeywords: Microbiome, Dysbiosis, Microbiota, Organism, Bacteria
Common References
[1.1 ] Diet and gut microbiome interactions of relevance for symptoms in irritable bowel syndrome 80001736 ]
[1.2 ] Sulfoquinovose is a select nutrient of prominent bacteria and a source of hydrogen sulfide in the human gut 80001764 ]
[1.3 ] Gut-inhabiting Clostridia build human GPCR ligands by conjugating neurotransmitters with diet- and human-derived fatty acids 80001868 ]
[1.4 ] Findings on the Relationship Between Intestinal Microbiome and Vasculitis 80002464 ]
[1.5 ] Role of the gut microbiota in the development of various neurological diseases 80002479 ]
[1.6 ] COVID-19 severity is associated with population-level gut microbiome variations 80002553 ]
[1.7 ] The gut microbiome in Alzheimer’s disease: what we know and what remains to be explored 80002733 ]
[1.8 ] Dysbiotic microbes and how to find them: a review of microbiome profiling in prostate cancer 80002745 ]
[1.9 ] Deficient butyrate-producing capacity in the gut microbiome is associated with bacterial network disturbances and fatigue symptoms in ME/CFS 80002751 ]
[1.10 ] Intertwined Relationship of Mitochondrial Metabolism, Gut Microbiome and Exercise Potential 80003004 ]
[1.11 ] Gut Microbiome–Brain Alliance: A Landscape View into Mental and Gastrointestinal Health and Disorders 80003039 ]
[1.12 ] Prebiotics: Definition, Types, Sources, Mechanisms, and Clinical Applications 80003325 ]
[1.13 ] Intestinal floras of populations that have a high risk of colon cancer 80001116 ]
[1.14 ] Association of brain amyloidosis with pro-inflammatory gut bacterial taxa and peripheral inflammation markers in cognitively impaired elderly. 80000280 ]
[1.15 ] Probiotics improve renal function, glucose, lipids, inflammation and oxidative stress in diabetic kidney disease: a systematic review and meta-analysis 80002470 ]
[1.16 ] Altered gut microbiota and short chain fatty acids in Chinese children with autism spectrum disorder 80000947 ]
[1.17 ] Altered gut microbiota and microbial biomarkers associated with chronic kidney disease 80000867 ]
[1.18 ] Alterations of the human gut microbiome in liver cirrhosis 80000668 ]
[1.19 ] Real-time polymerase chain reaction quantification of specific butyrate-producing bacteria, Desulfovibrio and Enterococcus faecalis in the feces of patients with colorectal cancer. 80000301 ]
[1.20 ] Dysbiosis signatures of gut microbiota in coronary artery disease 80000879 ]
[1.21 ] Alterations in gut microbiota of patients with COVID-19 during time of hospitalization 80001420 ]
[1.22 ] Dysbiosis of fecal microbiota in Crohn’s Disease patients as revealed by a custom phylogenetic microarray 80000285 ]
[1.23 ] Spatial organization and composition of the mucosal flora in patients with inflammatory bowel disease 80000610 ]
[1.24 ] Metagenomic evidence for taxonomic dysbiosis and functional imbalance in the gastrointestinal tracts of children with cystic fibrosis 80000395 ]
[1.25 ] Toward defining the autoimmune microbiome for type 1 diabetes 80000310 ]
[1.26 ] A metagenome-wide association study of gut microbiota in type 2 diabetes. 80000240 ]
[1.27 ] Aberrant gut microbiota alters host metabolome and impacts renal failure in humans and rodents 80001376 ]
[1.28 ] Intestinal microbiota is altered in patients with gastric cancer from Shanxi Province, China 80001028 ]
[1.29 ] Altered gut microbiota profile in patients with generalized anxiety disorder 80001066 ]
[1.30 ] Dysbiosis and compositional alterations with aging in the gut microbiota of patients with heart failure. 80000396 ]
[1.31 ] Imbalance of gut microbiome and intestinal epithelial barrier dysfunction in patients with high blood pressure 80000785 ]
[1.32 ] Fecal microbiota profiles in treatment-naïve pediatric inflammatory bowel disease - associations with disease phenotype, treatment, and outcome 80000963 ]
[1.33 ] Dysbiosis in the gut microbiota of patients with multiple sclerosis, with a striking depletion of species belonging to Clostridia XIVa and IV clusters. 80000233 ]
[1.34 ] The gut microbiome signatures discriminate healthy from pulmonary tuberculosis patients 80001136 ]
[1.35 ] Fecal microbiota in early rheumatoid arthritis 80001229 ]
[1.36 ] Gut microbiota dysbiosis in male patients with chronic traumatic complete spinal cord injury 80000938 ]
[1.37 ] Gut microbiota differs between children with inflammatory bowel disease and healthy siblings in taxonomic and functional composition: a metagenomic analysis 80000660 ]
[1.38 ] Rethinking healthy eating in light of the gut microbiome 80002441 ]
[1.39 ] Next Generation Microbiome Research: Identification of Keystone Species in the Metabolic Regulation of Host-Gut Microbiota Interplay 80002163 ]
