Compositions comprising bacterial strains
US-2017143773-A1 · May 25, 2017 · US
US11007233B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11007233-B2 |
| Application number | US-201916714092-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 13, 2019 |
| Priority date | Jun 14, 2017 |
| Publication date | May 18, 2021 |
| Grant date | May 18, 2021 |
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The invention provides compositions comprising bacterial strains for treating and preventing neurodegenerative disorders.
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The invention claimed is: 1. A pharmaceutical composition comprising a dried bacteria strain of the species Megasphaera massiliensis, wherein the bacteria strain comprises a 16S rRNA gene sequence that has at least 96% sequence identity to the polynucleotide sequence of SEQ ID NO: 2, as determined by a Smith-Waterman homology search algorithm using an affine gap search with a gap open penalty of 12, a gap extension penalty of 2, and a Blocks Substitution Matrix (BLOSUM) of 62, and a pharmaceutically acceptable excipient, diluent, or carrier. 2. The pharmaceutical composition of claim 1 , wherein the bacteria strain is present in the pharmaceutical composition in an amount that comprises from about 1×10 3 to about 1×10 11 colony forming units (CFU)/g of the bacteria strain with respect to the total weight of the pharmaceutical composition. 3. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition is formulated for oral, rectal, nasal, buccal, sublingual, or subcutaneous administration. 4. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition is formulated for delivery to an intestine of the subject. 5. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition is encapsulated. 6. The pharmaceutical composition of claim 1 , wherein pharmaceutical composition comprises an enteric coating. 7. The pharmaceutical composition of claim 1 , further comprising an additional therapeutic agent. 8. The pharmaceutical composition of claim 1 , wherein the bacteria strain comprises a 16S rRNA gene sequence that has at least 99% sequence identity to the polynucleotide sequence of SEQ ID NO:2, as determined by a Smith-Waterman homology search algorithm using an affine gap search with a gap open penalty of 12, a gap extension penalty of 2, and a Blocks Substitution Matrix (BLOSUM) of 62. 9. The pharmaceutical composition of claim 1 , wherein the bacteria strain comprises a 16S rRNA gene sequence that is the polynucleotide sequence of SEQ ID NO:2. 10. The pharmaceutical composition of claim 1 , wherein the bacteria strain is the bacteria strain deposited under accession number NCIMB 42787. 11. A method of treating a neurological condition associated with neuroinflammation, oxidative stress, or neurodegeneration in a subject in need thereof comprising: administering to the subject a pharmaceutical composition comprising a therapeutically effective amount of a bacteria strain of the species Megasphaera massiliensis , wherein the bacteria strain comprises a 16S rRNA gene sequence that has at least 96% sequence identity to the polynucleotide sequence of SEQ ID NO:2, as determined by a Smith-Waterman homology search algorithm using an affine gap search with a gap open penalty of 12, a gap extension penalty of 2, and a Blocks Substitution Matrix (BLOSUM) of 62, thereby treating the neurological condition associated with neuroinflammation, oxidative stress, or neurodegeneration in the subject. 12. The method of claim 11 , wherein the bacteria strain is the bacteria strain deposited under accession number NCIMB 42787. 13. The method of claim 11 , wherein administering comprises oral, rectal, nasal, buccal, sublingual, or subcutaneous administration. 14. The method of claim 11 , wherein the bacteria strain comprises a 16S rRNA gene sequence that has at least 99% sequence identity to the polynucleotide sequence of SEQ ID NO:2, as determined by a Smith-Waterman homology search algorithm using an affine gap search with a gap open penalty of 12, a gap extension penalty of 2, and a Blocks Substitution Matrix (BLOSUM) of 62. 15. The method of claim 11 , wherein the pharmaceutical composition is encapsulated. 16. The method of claim 11 , wherein the bacteria strain is dried. 17. The method of claim 11 , wherein the subject is human.
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