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Potential therapeutic implications of histidine catabolism by the gut microbiota in NAFLD patients with morbid obesity
The gut microbiota contributes to the pathophysiology of non-alcoholic fatty liver disease (NAFLD). Histidine is a key energy source for the microbiota, scavenging it from the host. Its role in NAFLD is poorly known. Plasma metabolomics, liver transcriptomics, and fecal metagenomics were performed i...
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Published in: | Cell reports. Medicine 2023-12, Vol.4 (12), p.101341-101341, Article 101341 |
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creator | Quesada-Vázquez, Sergio Castells-Nobau, Anna Latorre, Jèssica Oliveras-Cañellas, Núria Puig-Parnau, Irene Tejera, Noemi Tobajas, Yaiza Baudin, Julio Hildebrand, Falk Beraza, Naiara Burcelin, Rémy Martinez-Gili, Laura Chilloux, Julien Dumas, Marc-Emmanuel Federici, Massimo Hoyles, Lesley Caimari, Antoni Del Bas, Josep M Escoté, Xavier Fernández-Real, José-Manuel Mayneris-Perxachs, Jordi |
description | The gut microbiota contributes to the pathophysiology of non-alcoholic fatty liver disease (NAFLD). Histidine is a key energy source for the microbiota, scavenging it from the host. Its role in NAFLD is poorly known. Plasma metabolomics, liver transcriptomics, and fecal metagenomics were performed in three human cohorts coupled with hepatocyte, rodent, and Drosophila models. Machine learning analyses identified plasma histidine as being strongly inversely associated with steatosis and linked to a hepatic transcriptomic signature involved in insulin signaling, inflammation, and trace amine-associated receptor 1. Circulating histidine was inversely associated with Proteobacteria and positively with bacteria lacking the histidine utilization (Hut) system. Histidine supplementation improved NAFLD in different animal models (diet-induced NAFLD in mouse and flies, ob/ob mouse, and ovariectomized rats) and reduced de novo lipogenesis. Fecal microbiota transplantation (FMT) from low-histidine donors and mono-colonization of germ-free flies with Enterobacter cloacae increased triglyceride accumulation and reduced histidine content. The interplay among microbiota, histidine catabolism, and NAFLD opens therapeutic opportunities. |
doi_str_mv | 10.1016/j.xcrm.2023.101341 |
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Histidine is a key energy source for the microbiota, scavenging it from the host. Its role in NAFLD is poorly known. Plasma metabolomics, liver transcriptomics, and fecal metagenomics were performed in three human cohorts coupled with hepatocyte, rodent, and Drosophila models. Machine learning analyses identified plasma histidine as being strongly inversely associated with steatosis and linked to a hepatic transcriptomic signature involved in insulin signaling, inflammation, and trace amine-associated receptor 1. Circulating histidine was inversely associated with Proteobacteria and positively with bacteria lacking the histidine utilization (Hut) system. Histidine supplementation improved NAFLD in different animal models (diet-induced NAFLD in mouse and flies, ob/ob mouse, and ovariectomized rats) and reduced de novo lipogenesis. Fecal microbiota transplantation (FMT) from low-histidine donors and mono-colonization of germ-free flies with Enterobacter cloacae increased triglyceride accumulation and reduced histidine content. The interplay among microbiota, histidine catabolism, and NAFLD opens therapeutic opportunities.</description><identifier>ISSN: 2666-3791</identifier><identifier>EISSN: 2666-3791</identifier><identifier>DOI: 10.1016/j.xcrm.2023.101341</identifier><identifier>PMID: 38118419</identifier><language>eng</language><publisher>United States: Cell Press</publisher><subject>Animals ; Diet, High-Fat ; Gastrointestinal Microbiome - physiology ; Histidine - therapeutic use ; Humans ; Life Sciences ; Mice ; Non-alcoholic Fatty Liver Disease - drug therapy ; Obesity, Morbid ; Rats</subject><ispartof>Cell reports. Medicine, 2023-12, Vol.4 (12), p.101341-101341, Article 101341</ispartof><rights>Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>2023 The Authors 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c437t-54d6c32732cb862f784cc254695c2bccb2ae65af173d08268e2805dc79f791dc3</citedby><cites>FETCH-LOGICAL-c437t-54d6c32732cb862f784cc254695c2bccb2ae65af173d08268e2805dc79f791dc3</cites><orcidid>0000-0001-9523-7024</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10772641/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10772641/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38118419$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-04528666$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Quesada-Vázquez, Sergio</creatorcontrib><creatorcontrib>Castells-Nobau, Anna</creatorcontrib><creatorcontrib>Latorre, Jèssica</creatorcontrib><creatorcontrib>Oliveras-Cañellas, Núria</creatorcontrib><creatorcontrib>Puig-Parnau, Irene</creatorcontrib><creatorcontrib>Tejera, Noemi</creatorcontrib><creatorcontrib>Tobajas, Yaiza</creatorcontrib><creatorcontrib>Baudin, Julio</creatorcontrib><creatorcontrib>Hildebrand, Falk</creatorcontrib><creatorcontrib>Beraza, Naiara</creatorcontrib><creatorcontrib>Burcelin, Rémy</creatorcontrib><creatorcontrib>Martinez-Gili, Laura</creatorcontrib><creatorcontrib>Chilloux, Julien</creatorcontrib><creatorcontrib>Dumas, Marc-Emmanuel</creatorcontrib><creatorcontrib>Federici, Massimo</creatorcontrib><creatorcontrib>Hoyles, Lesley</creatorcontrib><creatorcontrib>Caimari, Antoni</creatorcontrib><creatorcontrib>Del Bas, Josep M</creatorcontrib><creatorcontrib>Escoté, Xavier</creatorcontrib><creatorcontrib>Fernández-Real, José-Manuel</creatorcontrib><creatorcontrib>Mayneris-Perxachs, Jordi</creatorcontrib><title>Potential therapeutic implications of histidine catabolism by the gut microbiota in NAFLD patients with morbid obesity</title><title>Cell reports. Medicine</title><addtitle>Cell Rep Med</addtitle><description>The gut microbiota contributes to the pathophysiology of non-alcoholic fatty liver disease (NAFLD). Histidine is a key energy source for the microbiota, scavenging it from the host. Its role in NAFLD is poorly known. Plasma metabolomics, liver transcriptomics, and fecal metagenomics were performed in three human cohorts coupled with hepatocyte, rodent, and Drosophila models. Machine learning analyses identified plasma histidine as being strongly inversely associated with steatosis and linked to a hepatic transcriptomic signature involved in insulin signaling, inflammation, and trace amine-associated receptor 1. Circulating histidine was inversely associated with Proteobacteria and positively with bacteria lacking the histidine utilization (Hut) system. Histidine supplementation improved NAFLD in different animal models (diet-induced NAFLD in mouse and flies, ob/ob mouse, and ovariectomized rats) and reduced de novo lipogenesis. Fecal microbiota transplantation (FMT) from low-histidine donors and mono-colonization of germ-free flies with Enterobacter cloacae increased triglyceride accumulation and reduced histidine content. The interplay among microbiota, histidine catabolism, and NAFLD opens therapeutic opportunities.</description><subject>Animals</subject><subject>Diet, High-Fat</subject><subject>Gastrointestinal Microbiome - physiology</subject><subject>Histidine - therapeutic use</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>Mice</subject><subject>Non-alcoholic Fatty Liver Disease - drug therapy</subject><subject>Obesity, Morbid</subject><subject>Rats</subject><issn>2666-3791</issn><issn>2666-3791</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNpdUU1v1DAQtSpQW5X-AQ7IRzjs4o_ETk5o1dIPaUV7gLNlO04zqyQOtrOw_x5HW6rCaUZv3nv2zEPoPSVrSqj4vFv_tmFYM8L4AvCCnqBzJoRYcVnTN6_6M3QZ444QwkpKK05O0RmvclfQ-hztH31yYwLd49S5oCc3J7AYhqkHqxP4MWLf4g5iggZGhzOoje8hDtgcFg1-mhMewAZvwCeNYcTfNjfbazxlebaO-BekDg8-GGiwNy5COrxDb1vdR3f5XC_Qj5uv36_uVtuH2_urzXZlCy7TqiwaYTmTnFlTCdbKqrCWlYWoS8uMtYZpJ0rdUskbUjFROVaRsrGybvPijeUX6MvRd5rN4Bqb_xN0r6YAgw4H5TWofycjdOrJ7xUlUjJR0Ozw6ejQ_ae722zVgpGiZFW-9X7hfnx-Lfifs4tJDRCt63s9Oj9HxepMlpTxhcqO1Hy3GINrX7wpUUvAaqeWgNUSsDoGnEUfXm_zIvkbJ_8DIx2kbQ</recordid><startdate>20231219</startdate><enddate>20231219</enddate><creator>Quesada-Vázquez, Sergio</creator><creator>Castells-Nobau, Anna</creator><creator>Latorre, Jèssica</creator><creator>Oliveras-Cañellas, Núria</creator><creator>Puig-Parnau, Irene</creator><creator>Tejera, Noemi</creator><creator>Tobajas, Yaiza</creator><creator>Baudin, Julio</creator><creator>Hildebrand, Falk</creator><creator>Beraza, Naiara</creator><creator>Burcelin, Rémy</creator><creator>Martinez-Gili, Laura</creator><creator>Chilloux, Julien</creator><creator>Dumas, Marc-Emmanuel</creator><creator>Federici, Massimo</creator><creator>Hoyles, Lesley</creator><creator>Caimari, Antoni</creator><creator>Del Bas, Josep M</creator><creator>Escoté, Xavier</creator><creator>Fernández-Real, José-Manuel</creator><creator>Mayneris-Perxachs, Jordi</creator><general>Cell Press</general><general>Elsevier</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>1XC</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-9523-7024</orcidid></search><sort><creationdate>20231219</creationdate><title>Potential therapeutic implications of histidine catabolism by the gut microbiota in NAFLD patients with morbid obesity</title><author>Quesada-Vázquez, Sergio ; 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Medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Quesada-Vázquez, Sergio</au><au>Castells-Nobau, Anna</au><au>Latorre, Jèssica</au><au>Oliveras-Cañellas, Núria</au><au>Puig-Parnau, Irene</au><au>Tejera, Noemi</au><au>Tobajas, Yaiza</au><au>Baudin, Julio</au><au>Hildebrand, Falk</au><au>Beraza, Naiara</au><au>Burcelin, Rémy</au><au>Martinez-Gili, Laura</au><au>Chilloux, Julien</au><au>Dumas, Marc-Emmanuel</au><au>Federici, Massimo</au><au>Hoyles, Lesley</au><au>Caimari, Antoni</au><au>Del Bas, Josep M</au><au>Escoté, Xavier</au><au>Fernández-Real, José-Manuel</au><au>Mayneris-Perxachs, Jordi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Potential therapeutic implications of histidine catabolism by the gut microbiota in NAFLD patients with morbid obesity</atitle><jtitle>Cell reports. Medicine</jtitle><addtitle>Cell Rep Med</addtitle><date>2023-12-19</date><risdate>2023</risdate><volume>4</volume><issue>12</issue><spage>101341</spage><epage>101341</epage><pages>101341-101341</pages><artnum>101341</artnum><issn>2666-3791</issn><eissn>2666-3791</eissn><abstract>The gut microbiota contributes to the pathophysiology of non-alcoholic fatty liver disease (NAFLD). Histidine is a key energy source for the microbiota, scavenging it from the host. Its role in NAFLD is poorly known. Plasma metabolomics, liver transcriptomics, and fecal metagenomics were performed in three human cohorts coupled with hepatocyte, rodent, and Drosophila models. Machine learning analyses identified plasma histidine as being strongly inversely associated with steatosis and linked to a hepatic transcriptomic signature involved in insulin signaling, inflammation, and trace amine-associated receptor 1. Circulating histidine was inversely associated with Proteobacteria and positively with bacteria lacking the histidine utilization (Hut) system. Histidine supplementation improved NAFLD in different animal models (diet-induced NAFLD in mouse and flies, ob/ob mouse, and ovariectomized rats) and reduced de novo lipogenesis. Fecal microbiota transplantation (FMT) from low-histidine donors and mono-colonization of germ-free flies with Enterobacter cloacae increased triglyceride accumulation and reduced histidine content. The interplay among microbiota, histidine catabolism, and NAFLD opens therapeutic opportunities.</abstract><cop>United States</cop><pub>Cell Press</pub><pmid>38118419</pmid><doi>10.1016/j.xcrm.2023.101341</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-9523-7024</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Diet, High-Fat Gastrointestinal Microbiome - physiology Histidine - therapeutic use Humans Life Sciences Mice Non-alcoholic Fatty Liver Disease - drug therapy Obesity, Morbid Rats |
title | Potential therapeutic implications of histidine catabolism by the gut microbiota in NAFLD patients with morbid obesity |
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