Component
Relative abundance of faecal Bacteroides
Relative abundance of faecal Bacteroides. Species, exposure and limitations are retained in each linked claim.
1 recorded relationships. Experimental role, claim status and evidence remain attached to each record.
How nutrients influence it
Every nutrient with a recorded effect on this component, credited to the nutrient that acted rather than the chapter that recorded it. Open a nutrient to see the findings and the conditions they were measured under.
Other things that act on it
Enzymes, hormones, genes, and other components with a recorded effect. These are not nutrients, so they do not count toward the arrows above. Each finding names the chapter that recorded it.
How nutrients reach it in more than one step
Chains of two or more recorded steps that end here, grouped by the nutrient they start from. Each step is a separate finding, so a chain is a route a mechanism could take, not proof that it does.
Tracing routes…
What it does
Every recorded relationship this component is part of, grouped by its role. Plain wording comes first; the technical statement follows.
Where it participates (unsigned role)
Co-culture was used to isolate KLE1738 which required the presence of Bacteroides fragilis to grow, bioassay-driven purification of the supernatant led to isolation of the growth factor which surprisingly is the major inhibitory neurotransmitter GABA, GABA was the only tested nutrient that supported the growth of KLE1738, a variety of GABA-producing bacteria were isolated and Bacteroides species produced large quantities of GABA, transcriptome analysis of human stool from healthy individuals showed that GABA-producing pathways are actively expressed by Bacteroides, Parabacteroides and Escherichia species, and relative abundance levels of faecal Bacteroides are negatively correlated with brain signatures associated with depression.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/gaba-research/30531975.abstract.txt", "locator": "Indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "c5ec17a6d5ab61a71d407f753583383c556fb07e10434eb3a3c7b42e4d0953f9", "start_char": 0, "end_char": 1773, "text_sha256": "c5ec17a6d5ab61a71d407f753583383c556fb07e10434eb3a3c7b42e4d0953f9"}
- experimental_model
- Co-culture isolation with bioassay-driven purification, genome-based metabolic modelling, stool transcriptomics and brain imaging
- exposure
- A gut isolate that grows only in the presence of another species, and the growth factor it requires
- limitations
- The correlation with depression imaging is observational and the causal direction is not established. The bacteriology is direct.
- nutrient_topic
- GABA research collection; topical membership is not evidence of a direct clinical effect, and the sign of a GABA response depends on the chloride gradient of the cell it was measured in. · Gamma-aminobutyric acid
- organism
- Human
- plain_language
- One gut bacterium cannot grow without this molecule and another makes it in quantity, and the human gut expresses both halves.
- primary_references
- [gb-p30531975] GABA-modulating bacteria of the human gut microbiota. (2019). https://pubmed.ncbi.nlm.nih.gov/30531975/ DOI: 10.1038/s41564-018-0307-3
- tissue_or_cell_type
- Gut microbiota and brain
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Co-culture isolation with bioassay-driven purification, genome-based metabolic modelling, stool transcriptomics and brain imaging · source_derived_draft · unverified_draft
### gb-gut-bacteria-make-and-consume-gaba Co-culture was used to isolate KLE1738 which required the presence of Bacteroides fragilis to grow, bioassay-driven purification of the supernatant led to isolation of the growth factor which surprisingly is the major inhibitory neurotransmitter GABA, GABA was the only tested nutrient that supported the growth of KLE1738, a variety of GABA-producing bacteria were isolated and Bacteroides species produced large quantities of GABA, transcriptome analysis of human stool from healthy individuals showed that GABA-producing pathways are actively expressed by Bacteroides, Parabacteroides and Escherichia species, and relative abundance levels of faecal Bacteroides are negatively correlated with brain signatures associated with depression. Condition category: normal nutrient_topic: GABA research collection; topical membership is not evidence of a direct clinical effect, and the sign of a GABA response depends on the chloride gradient of the cell it was measured in. plain_language: One gut bacterium cannot grow without this molecule and another makes it in quantity, and the human gut expresses both halves. organism: Human tissue_or_cell_type: Gut microbiota and brain experimental_model: Co-culture isolation with bioassay-driven purification, genome-based metabolic modelling, stool transcriptomics and brain imaging limitations: The correlation with depression imaging is observational and the causal direction is not established. The bacteriology is direct. exposure: A gut isolate that grows only in the presence of another species, and the growth factor it requires evidence_span: {"source_cache": "artifacts/gaba-research/30531975.abstract.txt", "locator": "Indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "c5ec17a6d5ab61a71d407f753583383c556fb07e10434eb3a3c7b42e4d0953f9", "start_char": 0, "end_char": 1773, "text_sha256": "c5ec17a6d5ab61a71d407f753583383c556fb07e10434eb3a3c7b42e4d0953f9"} [gb-p30531975] GABA-modulating bacteria of the human gut microbiota. (2019). https://pubmed.ncbi.nlm.nih.gov/30531975/ DOI: 10.1038/s41564-018-0307-3
Complete structured claim and evidence
The events it takes part in
A mechanism often involves more than two components. These are the full events, with every participant and its role.
Situations it appears in
Low-supply and faulty-machinery situations recorded in the chapters where this component plays a part.
In the sources
Preserved passages that mention this component, quoted exactly. Open one to read it in context.
Open hypotheses
Proposed ideas that involve this component. They are labeled as hypotheses and do not change any recorded statement.
This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.