PREVENTION OR TREATMENT OF HEPATIC STEATOSIS
This disclosure is concerned with Anaerobutyricum soehngenii or relative thereof for use in preventing and/or treating hepatic steatosis, particularly nonalcoholic fatty liver disease (NAFLD) and/or nonalcoholic steatohepatitis (NASH), wherein the use is for increasing bile acid plasma level for reducing liver inflammation and/or for reducing hepatic necroinflammatory activity score. The Anaerobutyricum soehngenii or relative thereof may be combined with at least one Bifidobacterium species, preferably Bifidobacterium animalis subspecies lactis or relative thereof and/or Bifidobacterium breve or relative thereof. In addition or alternatively, the Anaerobutyricum soehngenii or relative thereof may be combined with at least one Akkermansia species, preferably Akkermansia muciniphila or relative thereof. In addition or alternatively, the Anaerobutyricum soehngenii or relative thereof may be combined with at least one Lactobacillus species, preferably Lactobacillus acidophilus or relative thereof, Lactobacillus casei or relative thereof and/or Lactobacillus reuteri or relative thereof.
1 - 16 . (canceled)
17 . A method of preventing and/or treating hepatic steatosis in a subject, the method comprising:
administering to the subject Anaerobutyricum soehngenii or a relative thereof having a 16S rRNA gene sequence with at least 97% sequence identity with SEQ ID NO:1 or SEQ ID NO:2 so as to prevent and/or treat hepatic steatosis in the subject, wherein the A. soehngenii or relative thereof is combined with at least one Bifidobacterium species.
18 . The method according to claim 17 , wherein the at least one Bifidobacterium species is chosen from:
Bifidobacterium animalis subspecies lactis or a relative thereof having a 16S rRNA gene sequence with at least 97% sequence identity with SEQ ID NO:3; and/or
Bifidobacterium breve or a relative thereof having a 16S rRNA gene sequence with at least 97% sequence identity with SEQ ID NO:6.
19 . The method according to claim 17 , which reduces a hepatic necroinflammatory activity score for the subject.
20 . The method according to claim 17 , wherein the hepatic steatosis is nonalcoholic fatty liver disease (NAFLD) and/or nonalcoholic steatohepatitis (NASH).
21 . The method according to claim 17 , wherein the A. soehngenii or relative thereof is combined with at least one Bifidobacterium species and with at least one Akkermansia species.
22 . The method according to claim 21 , wherein the at least one Akkermansia species has been subjected to pasteurization.
23 . The method according to claim 21 , wherein the at least one Akkermansia species is Akkermansia muciniphila or a relative thereof having a 16S rRNA sequence with at least 97% sequence identity with SEQ ID NO:12.
24 . The method according to claim 17 , wherein the A. soehngenii or relative thereof is combined with at least one Bifidobacterium species and with at least one Lactobacillus species.
25 . The method according to claim 24 , wherein the at least one Lactobacillus species is chosen from:
Lactobacillus acidophilus or a relative thereof having a 16S rRNA sequence with at least 97% sequence identity with SEQ ID NO:14;
Lactobacillus casei or a relative thereof having a 16S rRNA sequence with at least 97% sequence identity with SEQ ID NO:15;
Lactobacillus reuteri or a relative thereof having a 16S rRNA sequence with at least 97% sequence identity with SEQ ID NO: 16; and/or
Lactobacillus rhamnosus or a relative thereof having a 16S IRNA sequence with at least 97% sequence identity with SEQ ID NO:17.
26 . The method according to claim 17 , which is comprised in fecal matter.
27 . The method according to claim 26 , wherein the fecal matter is obtained from a donor following a vegan diet.
28 . The method according to claim 26 , wherein at least 10 8 cells of the A. soehngenii or relative thereof are comprised in the fecal matter.
29 . The method according to claim 17 , wherein the A. soehngenii or relative thereof is administered in a micro-encapsulated or lyophilized form.
30 . The method according to claim 17 , wherein the A. soehngenii or relative thereof is administered in a composition comprising a physiologically acceptable carrier.
31 . The method according to claim 30 , wherein the A. soehngenii or relative thereof is present in the composition in an amount ranging from 10 4 to 10 15 colony forming units (CFU).
32 . The method according to claim 30 , wherein the composition is a pharmaceutical composition and/or food composition.