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. 2021 Jul 7;27(25):3837–3850. doi: 10.3748/wjg.v27.i25.3837

Table 2.

Mechanism of obesity induced by gut microbiota

Effect
Microbiota characteristics
Mechanism
Ref.
Increased energy absorption Expansion of Desulfovibrio and loss of Clostridia Elevated the expression of genes that control lipid absorption such as CD36 Petersen et al[44]
Extra energy for the host The inverse association between fecal SCFAs and gut microbiota diversity; Faecalibacterium prausnitzii, Roseburia faecis, and other Clostridiales increased; Akkermansia muciniphila, Alistipes finegoldii, Bacteroides, Christensenellaceae, Methanobrevibacter, and Oscillospira decreased Excessive SCFAs de la Cuesta-Zuluaga et al[49]
Increased appetite A community dominated by members of the Clostridial clusters XIVa and IV The levels of peptide YY and GLP-1 in obese patients decrease significantly Wu et al[54], Salehi et al[55], Federico et al[56]
Decreased Fat storage Germ free mice colonized with Lactobacillus paracasei Increase the expression of ANGPTL4, and inhibit LPL, leading to decreased fat storage Aronsson et al[59], Tazi et al[60]
Increased fat storage Transplanting gut microbes from conventionally raised mice into germ-free mice Increasing the expression of ChREBP and SREBP-1, Fiaf is inhibited, activate LPL, help triglycerides enter the circulatory system from the liver Bäckhed et al[19]
Decreased chronic inflammation Increase levels in the butyrate-producing bacteria such as Ruminococcaceae and Lachnospiraceae Inhibit pathways leading to the production of pro-inflammatory cytokines; Stimulate adipoliolysis and mitochondrial oxidative phosphorylation, thereby achieving greater energy consumption; Reduce LPS, thereby reducing chronic low-grade inflammation Kang et al[66], Lührs et al[67], Jia et al[68]
Interruption of circadian rhythm Bile salts biotransformation bacteria such as Lachnospiraceae, Clostridiaceae, Ruminococcaceae, Lactobacillus, Bacteroides, and Bifidobacterium Regulate transcription of key genes involved in circadian rhythm (Dbp, Per1/2) and lipid metabolism (Pparγ, Angptl4) Joyce et al[77], Parkar et al[78]

SCFAs: Short-chain fatty acids; LPL: Lipoprotein lipase; LPS: Lipopolysaccharide.