Human-origin probiotic cocktail increases short-chain fatty acid production via modulation of mice and human gut microbiome

• Published in: Scientific reports 2018-08, Vol.8 (1), p.12649-15, Article 12649
• Main Authors: Nagpal, Ravinder, Wang, Shaohua, Ahmadi, Shokouh, Hayes, Joshua, Gagliano, Jason, Subashchandrabose, Sargurunathan, Kitzman, Dalane W., Becton, Thomas, Read, Russel, Yadav, Hariom
• Format: Article
• Language: English
• Subjects: 38; 38/77; 59; 631/326; 631/326/2565/2134; 64; 64/60; 692/4020; 692/4020/1503/2745; 82; 96; Acetic acid; Acid production; Antibiotics; Autoimmune diseases; Cell surface; Diabetes mellitus; Digestive system; Dysbacteriosis; Epithelial cells; Fatty acids; Gastrointestinal tract; Humanities and Social Sciences; Hydrophobicity; Immunological tolerance; Inoculation; Intestinal microflora; Intestine; Metabolites; Microbiomes; Microbiota; multidisciplinary; Probiotics; Propionic acid; Science; Science (multidisciplinary); Strains (organisms); Virulence
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-018-30114-4

The gut bacteria producing metabolites like short-chain fatty acids (SCFAs; e.g., acetate, propionate and butyrate), are frequently reduced in Patients with diabetes, obesity, autoimmune disorders, and cancers. Hence, microbiome modulators such as probiotics may be helpful in maintaining or even restoring normal gut microbiome composition to benefit host health. Herein, we developed a human-origin probiotic cocktail with the ability to modulate gut microbiota to increase native SCFA production. Following a robust protocol of isolation, characterization and safety validation of infant gut-origin Lactobacillus and Enterococcus strains with probiotic attributes (tolerance to simulated gastric and intestinal conditions, adherence to intestinal epithelial cells, absence of potential virulence genes, cell-surface hydrophobicity, and susceptibility to common antibiotics), we select 10 strains (5 from each genera) out of total 321 isolates. A single dose (oral gavage) as well as 5 consecutive doses of this 10-strain probiotic cocktail in mice modulates gut microbiome and increases SCFA production (particularly propionate and butyrate). Inoculation of these probiotics in human feces also increases SCFA production along with microbiome modulation. Results indicate that human-origin probiotic lactobacilli and enterococci could ameliorate gut microbiome dysbiosis and hence may prove to be a potential therapy for diseases involving reduced SCFAs production in the gut.