Method and system to modify an individual's gut-brain axis to provide neurocognitive protection
The present invention is directed to beneficially directing the bidirectional communication that exists between the brain and the gut so as to influence brain physiology, psychological responses and ultimately behavior in a positive manner by regulating an individual's mood, psychological symptoms, such as anxiety and depression and stress-related changes in brain function, by modifying the gut microbiome of an individual. An various embodiments, an individual's microbiome is modified in a manner to reduce the likelihood of stress, to reduce or treat symptoms affecting mental health and to promote the mental health of the individual. In certain embodiments, administration to an individual of at least three different bacteria species are combined to modify an individual's microbiome, selected from the group of Lacticaseibacillus paracasei, Coprococcus, Roseburia, Bifidobacterium, L. casei and Faecalibacterium prausnitzii , to reduce adverse psychological and/or physiological responses attendant to psychological stress. Other embodiments reduce certain bacterial populations, such as Veillonella and Megasphaer , while in other embodiments, bacteria that produce hydrogen sulfide, methane and acetate are reduced to beneficially affect an individual's mental health.
1. A method for modifying an individual's gut-brain axis to provide neurocognitive protection, comprising,
providing an individual human being with a population of beneficial bacteria selected from the group consisting of at least two bacteria selected from the group consisting of Blautia, Coprococcus, Faecalibacterium prausnitzii; Nitrosomonas eutropha, Roseburia intestinalis, Lactobacillus paracasei , and Lactobacillus plantarum;
administering fiber to the individual to maintain a therapeutically effective amount of the beneficial bacteria in the gut of the individual; and
reducing a number of bacteria in the gut of the individual selected from the group consisting of Pediococcus, Streptococcus, Enterococcus , and Leuconostoc bacteria.
2. The method of claim 1 , wherein said beneficial bacteria further comprises Akkermansia.
3. The method as set forth in claim 1 , wherein the beneficial bacteria are selected from the group consisting of bacterial species able to produce small chain fatty acids.
4. The method as set forth in claim 1 , wherein the beneficial bacteria produce butyrate.
5. The method as set forth in claim 1 , further comprising increasing the number of beneficial bacteria.
6. The method as set forth in claim 1 , wherein said beneficial bacteria generate tryptophan metabolites that act as aryl hydrocarbon receptor (AHR) agonists.
7. The method as set forth in claim 1 , wherein said beneficial bacteria produce tryptophan metabolites selected from the group consisting of indole-3-aldehyde, indole-3-ethanol, indole-3-pyruvate, and indole-3-acetic acid.
8. The method as set forth in claim 1 , wherein said beneficial bacteria further comprise Lactobacillus crispatus.
9. The method as set forth in claim 1 , wherein at least some bacteria in the bacterial formulation have been modified by using a using a clustered regularly interspaced short palindromic repeats (CRISPR) CRISPR associated protein (Cas) system or a CRISPR from Prevotella and Francisella 1 (Cpf1) system to enhance the generation of a tryptophan metabolites.
10. A method for modifying an individual's gut-brain axis to provide neurocognitive protection, comprising,
providing an individual human being with a population of beneficial bacteria selected from the group consisting of at least two bacteria selected from the group consisting of Blautia, Coprococcus, Faecalibacterium prausnitzii; Nitrosomonas eutropha, Roseburia intestinalis, Lactobacillus paracasei , and Lactobacillus plantarum;
administering fiber to the individual to maintain a therapeutically effective amount of the beneficial bacteria in the gut of the individual; and
wherein the bacterial formulation generates an amount of tryptophan metabolites sufficient to act as aryl hydrocarbon receptor (AHR) agonists and thereby reduce inflammation in the individual's gut.
11. The method as set forth in claim 10 , wherein at least some bacteria in the bacterial formulation have been modified by using a using a clustered regularly interspaced short palindromic repeats (CRISPR) CRISPR associated protein (Cas) system or a CRISPR from Prevotella and Francisella 1 (Cpf1) system to enhance the generation of a tryptophan metabolite.
12. The method as set forth in claim 10 , wherein the beneficial bacteria are encapsulated in a frangible enclosure.
13. The method as set forth in claim 10 , further comprising increasing the levels of Roseburia in the individual's gut microbiome.
14. The method as set forth in claim 10 , further comprising increasing the populations of at least two of the following in the individual's gut microbiome: Akkermansia muciniphila, Faecalibacterium prausnitzii, Bifidobacterium longum, Roseburia intestinalis, Coprococcus spp. and Veillonella.
15. The method as set forth in claim 10 , further comprising inhibiting monoacylglycerolacyltransferase-3 (MGAT3) synthesis in the individual to lower triacylglycerol (TAG) production.
16. The method as set forth in claim 10 , further comprising reducing bacteria in the gut of the individual selected from the group consisting of Pediococcus, Streptococcus, Enterococcus , and Leuconostoc bacteria.
17. The method as set forth in claim 10 , wherein a secretion of glucagon-like peptide-1 (GLP-1) is stimulated in the individual due to the production of butyrate by the beneficial bacteria.
18. The method as set forth in claim 10 , further comprising administering Bifidobacterium breve and B. longum in an amount sufficient to achieve at least one of the following: decrease the severity of diarrhea; and reduce the symptoms of celiac disease.
19. A method for modifying an individual's gut-brain axis to provide neurocognitive protection, comprising,
providing an individual human being with a population of beneficial bacteria selected from the group consisting of at least two bacteria selected from the group consisting of Coprococcus, Faecalibacterium prausnitzii; Roseburia intestinalis, Lactobacillus paracasei , and Lactobacillus plantarum;
administering fiber to the individual to maintain a therapeutically effective amount of the beneficial bacteria in the gut of the individual; and
wherein the bacterial formulation generates an amount of tryptophan metabolites sufficient to act as aryl hydrocarbon receptor (AHR) agonists and thereby reduce inflammation in the individual's gut.
20. The method as set forth in claim 19 , wherein the beneficial bacteria are encapsulated in a frangible enclosure.