| CPC A61K 35/747 (2013.01) [A23L 5/00 (2016.08); A23L 33/135 (2016.08); A61K 9/0053 (2013.01); A61K 9/48 (2013.01); A61K 35/74 (2013.01); A61K 35/742 (2013.01); A61K 38/14 (2013.01); C12N 1/20 (2013.01); A23K 10/18 (2016.05); A23K 50/30 (2016.05); A61K 9/0031 (2013.01)] | 20 Claims |
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1. A pharmaceutical composition comprising a purified bacterial mixture, wherein the purified bacterial mixture consists of 7 to 10 bacterial strains, wherein the purified bacterial mixture comprises at least 7 of:
(i) a bacterial strain comprising a 16S rDNA sequence having at least 97% sequence identity to the nucleotide sequence of SEQ ID NO: 157;
(ii) a bacterial strain comprising a 16S rDNA sequence having at least 97% sequence identity to the nucleotide sequence of SEQ ID NO: 129;
(iii) a bacterial strain comprising a 16S rDNA sequence having at least 97% sequence identity to the nucleotide sequence of SEQ ID NO: 132;
(iv) a bacterial strain comprising a 16S rDNA sequence having at least 97% sequence identity to the nucleotide sequence of SEQ ID NO: 137;
(v) a bacterial strain comprising a 16S rDNA sequence having at least 97% sequence identity to the nucleotide sequence of SEQ ID NO: 124;
(vi) a bacterial strain comprising a 16S rDNA sequence having at least 97% sequence identity to the nucleotide sequence of SEQ ID NO: 141;
(vii) a bacterial strain comprising a 16S rDNA sequence having at least 97% sequence identity to the nucleotide sequence of SEQ ID NO: 146; and
(viii) a bacterial strain comprising a 16S rDNA sequence having at least 97% sequence identity to the nucleotide sequence of SEQ ID NO: 152,
wherein the bacterial strains are lyophilized.
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