Incorporation of therapeutically modified bacteria into gut microbiota inhibits obesity

J Clin Invest. 2014 Aug;124(8):3391-406. doi: 10.1172/JCI72517. Epub 2014 Jun 24.

Abstract

Metabolic disorders, including obesity, diabetes, and cardiovascular disease, are widespread in Westernized nations. Gut microbiota composition is a contributing factor to the susceptibility of an individual to the development of these disorders; therefore, altering a person's microbiota may ameliorate disease. One potential microbiome-altering strategy is the incorporation of modified bacteria that express therapeutic factors into the gut microbiota. For example, N-acylphosphatidylethanolamines (NAPEs) are precursors to the N-acylethanolamide (NAE) family of lipids, which are synthesized in the small intestine in response to feeding and reduce food intake and obesity. Here, we demonstrated that administration of engineered NAPE-expressing E. coli Nissle 1917 bacteria in drinking water for 8 weeks reduced the levels of obesity in mice fed a high-fat diet. Mice that received modified bacteria had dramatically lower food intake, adiposity, insulin resistance, and hepatosteatosis compared with mice receiving standard water or control bacteria. The protective effects conferred by NAPE-expressing bacteria persisted for at least 4 weeks after their removal from the drinking water. Moreover, administration of NAPE-expressing bacteria to TallyHo mice, a polygenic mouse model of obesity, inhibited weight gain. Our results demonstrate that incorporation of appropriately modified bacteria into the gut microbiota has potential as an effective strategy to inhibit the development of metabolic disorders.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Acyltransferases / genetics
  • Acyltransferases / metabolism
  • Animals
  • Arabidopsis Proteins / genetics
  • Arabidopsis Proteins / metabolism
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Diet, High-Fat / adverse effects
  • Digestive System / microbiology*
  • Disease Models, Animal
  • Eating
  • Escherichia coli / genetics
  • Escherichia coli / metabolism
  • Female
  • Humans
  • Liver / metabolism
  • Liver / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Microbiota*
  • Obesity / microbiology*
  • Obesity / pathology
  • Obesity / therapy*
  • Phosphatidylethanolamines / metabolism
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Weight Gain

Substances

  • Arabidopsis Proteins
  • DNA-Binding Proteins
  • MHF2 protein, Arabidopsis
  • Phosphatidylethanolamines
  • Recombinant Proteins
  • Acyltransferases
  • phosphatidylethanolamine N-acyltransferase