Press release

Embargoed by Nature Metabolism until Monday, March 9 at 12pm (Eastern Time) 

Bacteria potentially involved in the development of type 2 diabetes


Newswise — Québec City/Hamilton, ON (March 9, 2020) – Bacteria may be involved in the development of type 2 diabetes, according to a study published today in Nature Metabolism by researchers from Université Laval, the Québec Heart and Lung Institute (IUCPQ), and McMaster University. 

The authors found that the blood, liver, and certain abdominal fat deposits in diabetics have a different bacterial signature than in non-diabetics. 

The researchers demonstrated this using blood and tissue samples from 40 patients suffering from severe obesity taken during bariatric surgery. Half of the participants suffered from type 2 diabetes, while the other subjects showed insulin resistance without being diabetic. 

The researchers identified the bacterial genetic material in each of the tissues sampled, which came from the liver and three abdominal fat deposits. Based on the type of bacteria present and their relative abundance, the researchers were able to determine the bacterial signature for each tissue. 

Their analysis revealed that the bacterial signature in diabetics was not the same as in non-diabetics. It also showed that the total number of bacteria varied from one tissue to another, and was highest in the liver and the greater omentum (a fatty tissue connecting the stomach and the transverse colon), two areas that play an important role in metabolic regulation.

“Our findings suggest that in people suffering from severe obesity, bacteria or fragments of bacteria are associated with the development of type 2 diabetes,” said the lead author, André Marette, professor at Université Laval’s Faculty of Medicine and researcher at the IUCPQ research centre.

According to the study, the bacterial genetic material detected in the tissues most likely comes from the intestine. 

“We know that the intestinal barrier is more permeable in obese patients,” said Professor Marette. “Our hypothesis is that living bacteria and bacterial fragments cross this barrier and set off an inflammatory process that ultimately prevents insulin from doing its job, which is to regulate blood glucose levels by acting on metabolic tissues.” 

Fernando Forato Anhê, an author on the paper and a postdoctoral research fellow at McMaster, added: “Location, location location...Beyond knowing the names of bacteria, their location is key to understanding how gut microbes influence host metabolism." 

Professor Marette and his collaborators will be able to pursue their research further thanks to a $2 million grant they were recently awarded by the Canadian Institutes of Health Research. 

“Our next objective is to determine if the bacteria found in the liver and fat deposits of people suffering from severe obesity are also present in those who are overweight or moderately obese,” said André Marette. 

“We also want to see if certain pathogenic bacteria found in the tissues can trigger type 2 diabetes in an animal model. And lastly, we want to find out if certain beneficial bacteria found in these tissues can be used to prevent the development of the disease. If so, they might lead us to a new family of probiotic bacteria or a source of bacteria-based treatments to help fight diabetes,” he said.

The authors of the study published in Nature Metabolism are Fernando Forato Anhê (Université Laval and McMaster University); Benjamin Jensen, Thibault Varin, Simon Marceau, Laurent Biertho, André Tchernof, and André Marette (Université Laval and IUCPQ); Michael Surette and Jonathan Schertzer (McMaster University); and Florence Servant, Sebastian Van Blerk, and Benjamin Lelouvier (Vaiomer). The study was funded by a Bariatric Care Team Grant from CIHR and the REMISSION Project.




Note to Editors : Photo attached of Fernando Forato Anhê, an author on the paper and a postdoctoral research fellow at McMaster. Credit McMaster University.



Jean-François Huppé

Media Relations

Université Laval

418 656-7785

[email protected]


Veronica McGuire

Media Relations

McMaster University

905 525-9140, ext. 22169 [email protected]