Akkermansia muciniphila inversely correlates with the onset of inflammation, altered adipose tissue metabolism and metabolic disorders during obesity in mice

Marc Schneeberger, Amandine Everard, Alícia G. Gómez-Valadés, Sébastien Matamoros, Sara Ramírez, Nathalie M. Delzenne, Ramón Gomis, Marc Claret, Patrice D. Cani

Scientific Reports · 2015 · 794 citations · 41 references

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TL;DR

Gut microbiota is increasingly recognized as a key factor in obesity, with diet‑induced obesity linked to gut microbial shifts and adiposity‑associated low‑grade inflammation, yet the precise microbial–inflammatory connection remains unclear. This study examined how a high‑fat diet affects metabolic parameters and gut microbiota composition over time in mice. Using multifactorial analysis, the authors correlated changes in Akkermansia muciniphila abundance with adipose tissue lipid‑metabolism and inflammation markers and circulating glucose, insulin, triglycerides, and leptin levels. They found that age and high‑fat diet strongly reduced Akkermansia muciniphila, while Bilophila wadsworthia increased, and that lower Akkermansia abundance was linked to disrupted adipose tissue homeostasis at obesity onset, underscoring its beneficial metabolic role.

Abstract

Recent evidence indicates that the gut microbiota plays a key role in the pathophysiology of obesity. Indeed, diet-induced obesity (DIO) has been associated to substantial changes in gut microbiota composition in rodent models. In the context of obesity, enhanced adiposity is accompanied by low-grade inflammation of this tissue but the exact link with gut microbial community remains unknown. In this report, we studied the consequences of high-fat diet (HFD) administration on metabolic parameters and gut microbiota composition over different periods of time. We found that Akkermansia muciniphila abundance was strongly and negatively affected by age and HFD feeding and to a lower extend Bilophila wadsworthia was the only taxa following an opposite trend. Different approaches, including multifactorial analysis, showed that these changes in Akkermansia muciniphila were robustly correlated with the expression of lipid metabolism and inflammation markers in adipose tissue, as well as several circulating parameters (i.e., glucose, insulin, triglycerides, leptin) from DIO mice. Thus, our data shows the existence of a link between gut Akkermansia muciniphila abundance and adipose tissue homeostasis on the onset of obesity, thus reinforcing the beneficial role of this bacterium on metabolism.

References

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