Lactiplantibacillus plantarum dfa1 Outperforms Enterococcus faecium dfa1 on Anti-Obesity in High Fat-Induced Obesity Mice Possibly through the Differences in Gut Dysbiosis Attenuation, despite the Similar Anti-Inflammatory Properties

Nutrients. 2021 Dec 25;14(1):80. doi: 10.3390/nu14010080.

Abstract

Fat reduction and anti-inflammation are commonly claimed properties of probiotics. Lactiplantibacillus plantarum and Enterococcus faecium were tested in high fat-induced obesity mice and in vitro experiments. After 16 weeks of probiotics, L. plantarum dfa1 outperforms E. faecium dfa1 on the anti-obesity property as indicated by body weight, regional fat accumulation, serum cholesterol, inflammatory cytokines (in blood and colon tissue), and gut barrier defect (FITC-dextran assay). With fecal microbiome analysis, L. plantarum dfa1 but not E. faecium dfa1 reduced fecal abundance of pathogenic Proteobacteria without an alteration in total Gram-negative bacteria when compared with non-probiotics obese mice. With palmitic acid induction, the condition media from both probiotics similarly attenuated supernatant IL-8, improved enterocyte integrity and down-regulated cholesterol absorption-associated genes in Caco-2 cell (an enterocyte cell line) and reduced supernatant cytokines (TNF-α and IL-6) with normalization of cell energy status (extracellular flux analysis) in bone-marrow-derived macrophages. Due to the anti-inflammatory effect of the condition media of both probiotics on palmitic acid-activated enterocytes was neutralized by amylase, the active anti-inflammatory molecules might, partly, be exopolysaccharides. As L. plantarum dfa1 out-performed E. faecium dfa1 in anti-obesity property, possibly through the reduced fecal Proteobacteria, with a similar anti-inflammatory exopolysaccharide; L. plantarum is a potentially better option for anti-obesity than E. faecium.

Keywords: Enterococcus faecium; Lactiplantibacillus plantarum; Lactobacillus plantarum; dysbiosis; high fat diet; obesity; probiotics.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents
  • Cholesterol / metabolism
  • Diet, High-Fat / adverse effects
  • Dysbiosis
  • Enterococcus faecium / physiology*
  • Enterocytes / drug effects
  • Enterocytes / metabolism
  • Feces / microbiology
  • Gastrointestinal Microbiome / drug effects*
  • Gene Expression Regulation / drug effects
  • Inflammation
  • Lactobacillaceae / physiology*
  • Male
  • Mice
  • Obesity / prevention & control*
  • Probiotics / pharmacology*

Substances

  • Anti-Inflammatory Agents
  • Cholesterol