Lactobacillus fermentum FTDC 8312 combats hypercholesterolemia via alteration of gut microbiota

• Published in: Journal of biotechnology Vol. 262; pp. 75 - 83
• Main Authors: Lye, Huey-Shi, Kato, Tamotsu, Low, Wai-Yee, Taylor, Todd D., Prakash, Tulika, Lew, Lee-Ching, Ohno, Hiroshi, Liong, Min-Tze
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 20.11.2017
• Subjects: Animals; Anticholesteremic Agents; Apolipoprotein A-I; Bacteria - classification; Bacteria - genetics; Bile Acids and Salts - analysis; Body Weight; Cholesterol; Cholesterol - blood; Cholesterol, Dietary - adverse effects; Diet; DNA, Bacterial - genetics; Feces - chemistry; Gastrointestinal Microbiome - genetics; Genes, Bacterial - genetics; Gut microbiota; Hypercholesterolemia - drug therapy; Lactobacillus; Lactobacillus fermentum - genetics; Lipid Metabolism - drug effects; Lipids - blood; Lipoproteins - blood; Lipoproteins, HDL - blood; Lipoproteins, LDL - blood; Male; Mice; Mice, Inbred BALB C; Phospholipids - blood; Probiotics - therapeutic use; RNA, Ribosomal, 16S - genetics; Sterols - analysis; Triglycerides - blood; Whole Genome Sequencing; Gut microbiota; Cholesterol; Lactobacillus
• ISSN: 0168-1656; 1873-4863
• DOI: 10.1016/j.jbiotec.2017.09.007

•Reduction of cholesterol in hypercholesterolemic mice by L. fermentum FTDC 8312.•This was accompanied by increased fecal bile excretion.•The importance of gut microbiota on hypercholesterolemia.•The unconventional benefit of a probiotic; a new potential for integrative medicine. In this study, hypercholesterolemic mice fed with Lactobacillus fermentum FTDC 8312 after a seven-week feeding trial showed a reduction in serum total cholesterol (TC) levels, accompanied by a decrease in serum low-density lipoprotein cholesterol (LDL-C) levels, an increase in serum high-density lipoprotein cholesterol (HDL-C) levels, and a decreased ratio of apoB100:apoA1 when compared to those fed with control or a type strain, L. fermentum JCM 1173. These have contributed to a decrease in atherogenic indices (TC/HDL-C) of mice on the FTDC 8312 diet. Serum triglyceride (TG) levels of mice fed with FTDC 8312 and JCM 1173 were comparable to those of the controls. A decreased ratio of cholesterol and phospholipids (C/P) was also observed for mice fed with FTDC 8312, leading to a decreased number of spur red blood cells (RBC) formation in mice. Additionally, there was an increase in fecal TC, TG, and total bile acid levels in mice on FTDC 8312 diet compared to those with JCM 1173 and controls. The administration of FTDC 8312 also altered the gut microbiota population such as an increase in the members of genera Akkermansia and Oscillospira, affecting lipid metabolism and fecal bile excretion in the mice. Overall, we demonstrated that FTDC 8312 exerted a cholesterol lowering effect that may be attributed to gut microbiota modulation.