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      Gut Microbiota and Type 2 Diabetes Mellitus: Association, Mechanism, and Translational Applications

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          Abstract

          Gut microbiota has attracted widespread attention due to its crucial role in disease pathophysiology, including type 2 diabetes mellitus (T2DM). Metabolites and bacterial components of gut microbiota affect the initiation and progression of T2DM by regulating inflammation, immunity, and metabolism. Short-chain fatty acids, secondary bile acid, imidazole propionate, branched-chain amino acids, and lipopolysaccharide are the main molecules related to T2DM. Many studies have investigated the role of gut microbiota in T2DM, particularly those butyrate-producing bacteria. Increasing evidence has demonstrated that fecal microbiota transplantation and probiotic capsules are useful strategies in preventing diabetes. In this review, we aim to elucidate the complex association between gut microbiota and T2DM inflammation, metabolism, and immune disorders, the underlying mechanisms, and translational applications of gut microbiota. This review will provide novel insight into developing individualized therapy for T2DM patients based on gut microbiota immunometabolism.

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          Most cited references115

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          WITHDRAWN: Global and regional diabetes prevalence estimates for 2019 and projections for 2030 and 2045: results from the International Diabetes Federation Diabetes Atlas, 9th edition

          To provide global estimates of diabetes prevalence for 2019 and projections for 2030 and 2045.
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            An obesity-associated gut microbiome with increased capacity for energy harvest.

            The worldwide obesity epidemic is stimulating efforts to identify host and environmental factors that affect energy balance. Comparisons of the distal gut microbiota of genetically obese mice and their lean littermates, as well as those of obese and lean human volunteers have revealed that obesity is associated with changes in the relative abundance of the two dominant bacterial divisions, the Bacteroidetes and the Firmicutes. Here we demonstrate through metagenomic and biochemical analyses that these changes affect the metabolic potential of the mouse gut microbiota. Our results indicate that the obese microbiome has an increased capacity to harvest energy from the diet. Furthermore, this trait is transmissible: colonization of germ-free mice with an 'obese microbiota' results in a significantly greater increase in total body fat than colonization with a 'lean microbiota'. These results identify the gut microbiota as an additional contributing factor to the pathophysiology of obesity.
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              From Dietary Fiber to Host Physiology: Short-Chain Fatty Acids as Key Bacterial Metabolites.

              A compelling set of links between the composition of the gut microbiota, the host diet, and host physiology has emerged. Do these links reflect cause-and-effect relationships, and what might be their mechanistic basis? A growing body of work implicates microbially produced metabolites as crucial executors of diet-based microbial influence on the host. Here, we will review data supporting the diverse functional roles carried out by a major class of bacterial metabolites, the short-chain fatty acids (SCFAs). SCFAs can directly activate G-coupled-receptors, inhibit histone deacetylases, and serve as energy substrates. They thus affect various physiological processes and may contribute to health and disease.
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                Author and article information

                Contributors
                Journal
                Mediators Inflamm
                Mediators Inflamm
                mi
                Mediators of Inflammation
                Hindawi
                0962-9351
                1466-1861
                2021
                17 August 2021
                : 2021
                : 5110276
                Affiliations
                1Central Laboratory, Weifang People's Hospital, Weifang 261000, China
                2Department of Scientific Research Management, Weifang People's Hospital, Weifang 261000, China
                3Central Laboratory of the First Affiliated Hospital, Weifang Medical University, Weifang 261000, China
                4Department of Nuclear Medicine, Weifang People's Hospital, Weifang 261000, China
                5Clinical Laboratory, Weifang People's Hospital, Weifang 261000, China
                Author notes

                Academic Editor: Bingjie Gu

                Author information
                https://orcid.org/0000-0003-3264-0881
                https://orcid.org/0000-0002-1170-6805
                Article
                10.1155/2021/5110276
                8384524
                34447287
                a865122f-a042-404f-9867-e0b353404462
                Copyright © 2021 Lili Zhang et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 14 April 2021
                : 26 July 2021
                Funding
                Funded by: Science and Technology Development Program of Weifang
                Award ID: 2020TX084
                Funded by: Shandong Science and Technology Development Program
                Award ID: 2016WS0657
                Funded by: Natural Science Foundation of Shandong Province
                Award ID: ZR2020KC001
                Categories
                Review Article

                Immunology
                Immunology

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