Abstract

Type 2 diabetes is a leading cause of morbidity and a common risk of several disorders. Identifying the microbial ecology changes is essential for disease prediction, therapy, and prevention. Thus, our study is aimed at investigating the intestinal microbiota among healthy and type 2 diabetes individuals and exploring the effect of antidiabetic agents on gut bacterial flora. 24 type 2 diabetes (metformin, glimepiride, and nontherapeutic subgroups; N = 8) and 24 healthy control subjects were enrolled in this study, and intestinal bacterial microbiota was investigated by analyzing V3-V4 regions of 16S rRNA gene sequence. Numerous alterations were observed in the gut microbial community of diabetic individuals. These changes were characterized by a significant lowered abundance of Faecalibacterium, Fusobacterium, Dialister, and Elusimicrobium in the nontherapeutic subgroup compared to the healthy control group. Likewise, correlation analysis showed a substantial decline in gut microbiota richness and diversity with the duration of illness. Furthermore, antidiabetic agents restored to some extent the richness and diversity of gut microbiota and improved the abundance of many beneficial bacteria with a significant increase of Methanobrevibacter in the metformin subcategory compared to the nontherapeutic subgroup. In return, they decreased the abundance of some opportunistic pathogens. The findings of this study have added a novel understanding about the pathogenesis of the disease and the mechanisms underlying antidiabetic therapy, which are of potential interest for therapeutic lines and further studies.

Highlights

  • Gut microbiota are miscellaneous groups of microorganisms that inhabit the gastrointestinal tract (GIT) of both humans and animals

  • Type 2 diabetes mellitus (T2DM) belongs to a cluster of broadly distributed chronic disorders that result from the disruption of sugar metabolism and homeostasis

  • Between healthy control (HC) and either T2DM individuals or NT subgroup, there was no significant variations in the distribution of the study participants among gender, marital status, residence, education level, and occupation as well as body mass index (BMI)

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Summary

Introduction

Gut microbiota are miscellaneous groups of microorganisms that inhabit the gastrointestinal tract (GIT) of both humans and animals. It has coexisted with the body in a symbiotic relationship, with significant metabolic and regulatory functions. Type 2 diabetes mellitus (T2DM) belongs to a cluster of broadly distributed chronic disorders that result from the disruption of sugar metabolism and homeostasis. It has complicated mechanisms and multiple factors implicated [3, 4]. Increasing evidence suggests that the intestinal flora has a significant effect in the development of metabolic disorders, which is attributed to dysbiosis of microbial communities and metabolites. Insulin resistance does not exclusively result from overweight and involves a complex interplay of multiple factors such as the gut ecosystem and immune response

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