Metabolic Profile of Gut Microbiota and Levels of Trefoil Factors in Adults with Different Metabolic Phenotypes of Obesity
Obesity is associated with changes in the gut microbiota, as well as with increased permeability of the intestinal wall. In 130 non-obese volunteers, 57 patients with metabolically healthy obesity (MHO), and 76 patients with metabolically unhealthy obesity (MUHO), bacterial DNA was isolated from sto...
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Veröffentlicht in: | Molecular biology (New York) 2024-08, Vol.58 (4), p.728-744 |
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creator | Kolesnikova, I. M. Ganenko, L. A. Vasilyev, I. Yu Grigoryeva, T. V. Volkova, N. I. Roumiantsev, S. A. Shestopalov, A. V. |
description | Obesity is associated with changes in the gut microbiota, as well as with increased permeability of the intestinal wall. In 130 non-obese volunteers, 57 patients with metabolically healthy obesity (MHO), and 76 patients with metabolically unhealthy obesity (MUHO), bacterial DNA was isolated from stool samples, and the 16S rRNA gene was sequenced. The metabolic profile of the microbiota predicted by PICRUSt2 (
https://huttenhower.sph.harvard.edu/picrust/
) was more altered in patients with MUHO than MHO. Obesity, especially MUHO, was accompanied by an increase in the ability of the gut microbiota to degrade energy substrates, produce energy through oxidative phosphorylation, synthesize water-soluble vitamins (B1, B6, B7), nucleotides, heme, aromatic amino acids, and protective structural components of cells. Such changes may be a consequence of the microbiota adaptation to the MUHO-specific conditions. Thus, a vicious circle is formed, when MUHO promotes the depletion of the gut microbiome, and further degeneration of the latter contributes to the pathogenesis of metabolic disorders. The concentration of the trefoil factor family (TFF) in the serum of the participants was also determined. In MHO and MUHO patients, the TFF2 and TFF3 levels were increased, but we did not find significant associations of these changes with the metabolic profile of the gut microbiota. |
doi_str_mv | 10.1134/S0026893324700316 |
format | Article |
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https://huttenhower.sph.harvard.edu/picrust/
) was more altered in patients with MUHO than MHO. Obesity, especially MUHO, was accompanied by an increase in the ability of the gut microbiota to degrade energy substrates, produce energy through oxidative phosphorylation, synthesize water-soluble vitamins (B1, B6, B7), nucleotides, heme, aromatic amino acids, and protective structural components of cells. Such changes may be a consequence of the microbiota adaptation to the MUHO-specific conditions. Thus, a vicious circle is formed, when MUHO promotes the depletion of the gut microbiome, and further degeneration of the latter contributes to the pathogenesis of metabolic disorders. The concentration of the trefoil factor family (TFF) in the serum of the participants was also determined. In MHO and MUHO patients, the TFF2 and TFF3 levels were increased, but we did not find significant associations of these changes with the metabolic profile of the gut microbiota.</description><identifier>ISSN: 0026-8933</identifier><identifier>EISSN: 1608-3245</identifier><identifier>DOI: 10.1134/S0026893324700316</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>Biochemistry ; Biomedical and Life Sciences ; Cell Molecular Biology ; Digestive system ; Energy resources ; Gastrointestinal tract ; Human Genetics ; Intestinal microflora ; Life Sciences ; Metabolic disorders ; Metabolism ; Microbiomes ; Microbiota ; Nucleotide sequence ; Nucleotides ; Obesity ; Oxidative phosphorylation ; Phenotypes ; Phosphorylation ; rRNA 16S ; Trefoil factor ; Vitamin B6</subject><ispartof>Molecular biology (New York), 2024-08, Vol.58 (4), p.728-744</ispartof><rights>Pleiades Publishing, Ltd. 2024. ISSN 0026-8933, Molecular Biology, 2024, Vol. 58, No. 4, pp. 728–744. © Pleiades Publishing, Ltd., 2024.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c198t-b4e62283d470d6022956336afa9b2109c4492be3dbdd1191ba487bfcb9b49b843</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1134/S0026893324700316$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1134/S0026893324700316$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>315,782,786,27933,27934,41497,42566,51328</link.rule.ids></links><search><creatorcontrib>Kolesnikova, I. M.</creatorcontrib><creatorcontrib>Ganenko, L. A.</creatorcontrib><creatorcontrib>Vasilyev, I. Yu</creatorcontrib><creatorcontrib>Grigoryeva, T. V.</creatorcontrib><creatorcontrib>Volkova, N. I.</creatorcontrib><creatorcontrib>Roumiantsev, S. A.</creatorcontrib><creatorcontrib>Shestopalov, A. V.</creatorcontrib><title>Metabolic Profile of Gut Microbiota and Levels of Trefoil Factors in Adults with Different Metabolic Phenotypes of Obesity</title><title>Molecular biology (New York)</title><addtitle>Mol Biol</addtitle><description>Obesity is associated with changes in the gut microbiota, as well as with increased permeability of the intestinal wall. In 130 non-obese volunteers, 57 patients with metabolically healthy obesity (MHO), and 76 patients with metabolically unhealthy obesity (MUHO), bacterial DNA was isolated from stool samples, and the 16S rRNA gene was sequenced. The metabolic profile of the microbiota predicted by PICRUSt2 (
https://huttenhower.sph.harvard.edu/picrust/
) was more altered in patients with MUHO than MHO. Obesity, especially MUHO, was accompanied by an increase in the ability of the gut microbiota to degrade energy substrates, produce energy through oxidative phosphorylation, synthesize water-soluble vitamins (B1, B6, B7), nucleotides, heme, aromatic amino acids, and protective structural components of cells. Such changes may be a consequence of the microbiota adaptation to the MUHO-specific conditions. Thus, a vicious circle is formed, when MUHO promotes the depletion of the gut microbiome, and further degeneration of the latter contributes to the pathogenesis of metabolic disorders. The concentration of the trefoil factor family (TFF) in the serum of the participants was also determined. In MHO and MUHO patients, the TFF2 and TFF3 levels were increased, but we did not find significant associations of these changes with the metabolic profile of the gut microbiota.</description><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Cell Molecular Biology</subject><subject>Digestive system</subject><subject>Energy resources</subject><subject>Gastrointestinal tract</subject><subject>Human Genetics</subject><subject>Intestinal microflora</subject><subject>Life Sciences</subject><subject>Metabolic disorders</subject><subject>Metabolism</subject><subject>Microbiomes</subject><subject>Microbiota</subject><subject>Nucleotide sequence</subject><subject>Nucleotides</subject><subject>Obesity</subject><subject>Oxidative phosphorylation</subject><subject>Phenotypes</subject><subject>Phosphorylation</subject><subject>rRNA 16S</subject><subject>Trefoil factor</subject><subject>Vitamin B6</subject><issn>0026-8933</issn><issn>1608-3245</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp1kF9LwzAUxYMoOKcfwLeAz9X8a9Y8jummsDHB-VySNnEZtZlJ6pif3tQJexDhQuCec37hXACuMbrFmLK7F4QILwSlhI0QopifgAHmqMjSIj8Fg17Oev0cXISwQQinIQPwtdBRKtfYCj57Z2yjoTNw1kW4sJV3yroooWxrONefugm9uPLaONvAqayi8wHaFo7rrokB7mxcw3trjPa6TYQjeq1bF_db_QNYKh1s3F-CMyOboK9-3yF4nT6sJo_ZfDl7moznWYVFETPFNCekoHUqVnNEiMg5pVwaKRTBSFSMCaI0rVVdYyywkqwYKVMpoZhQBaNDcHPgbr376HSI5cZ1vk1flhQJxDHJaZ5c-OBKrUNIFcutt-_S70uMyv7E5Z8Tpww5ZELytm_aH8n_h74Bnj19mw</recordid><startdate>20240801</startdate><enddate>20240801</enddate><creator>Kolesnikova, I. 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https://huttenhower.sph.harvard.edu/picrust/
) was more altered in patients with MUHO than MHO. Obesity, especially MUHO, was accompanied by an increase in the ability of the gut microbiota to degrade energy substrates, produce energy through oxidative phosphorylation, synthesize water-soluble vitamins (B1, B6, B7), nucleotides, heme, aromatic amino acids, and protective structural components of cells. Such changes may be a consequence of the microbiota adaptation to the MUHO-specific conditions. Thus, a vicious circle is formed, when MUHO promotes the depletion of the gut microbiome, and further degeneration of the latter contributes to the pathogenesis of metabolic disorders. The concentration of the trefoil factor family (TFF) in the serum of the participants was also determined. In MHO and MUHO patients, the TFF2 and TFF3 levels were increased, but we did not find significant associations of these changes with the metabolic profile of the gut microbiota.</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><doi>10.1134/S0026893324700316</doi><tpages>17</tpages></addata></record> |
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subjects | Biochemistry Biomedical and Life Sciences Cell Molecular Biology Digestive system Energy resources Gastrointestinal tract Human Genetics Intestinal microflora Life Sciences Metabolic disorders Metabolism Microbiomes Microbiota Nucleotide sequence Nucleotides Obesity Oxidative phosphorylation Phenotypes Phosphorylation rRNA 16S Trefoil factor Vitamin B6 |
title | Metabolic Profile of Gut Microbiota and Levels of Trefoil Factors in Adults with Different Metabolic Phenotypes of Obesity |
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