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Clec7a drives gut fungus-mediated host lipid deposition
BACKGROUND: Compared to that of bacteria, the role of gut fungi in obesity development remains unknown. RESULTS: Here, alterations in gut fungal biodiversity and composition were confirmed in obese pig models and high-fat diet (HFD)-fed mice. Antifungal drugs improved diet-induced obesity, while fun...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10675981/ https://www.ncbi.nlm.nih.gov/pubmed/38007451 http://dx.doi.org/10.1186/s40168-023-01698-5 |
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author | Ma, Jie Zhou, Miao Song, Zehe Deng, Yuankun Xia, Siting Li, Yunxia Huang, Xingguo Xiao, Dingfu Yin, Yulong Yin, Jie |
author_facet | Ma, Jie Zhou, Miao Song, Zehe Deng, Yuankun Xia, Siting Li, Yunxia Huang, Xingguo Xiao, Dingfu Yin, Yulong Yin, Jie |
author_sort | Ma, Jie |
collection | PubMed |
description | BACKGROUND: Compared to that of bacteria, the role of gut fungi in obesity development remains unknown. RESULTS: Here, alterations in gut fungal biodiversity and composition were confirmed in obese pig models and high-fat diet (HFD)-fed mice. Antifungal drugs improved diet-induced obesity, while fungal reconstruction by cohousing or fecal microbiota transplantation maintained the obese phenotype in HFD-fed mice. Fungal profiling identified 5 fungal species associated with obesity. Specifically, Ascomycota_sp. and Microascaceae_sp. were reduced in obese mice and negatively correlated with fat content. Oral supplementation with fungi was sufficient to prevent and treat diet-induced obesity. Clec7a, which is involved in fungal recognition, was highly expressed in HFD-fed mice. The Clec7a agonist accelerated diet-induced obesity, while Clec7a deficieny in mice resulted in resistance to diet-induced obesity and blocked the anti-obese effect of antifungal drugs and fungi. CONCLUSIONS: Taken together, these results indicate that gut fungi/Clec7a signaling is involved in diet-induced obesity and may have therapeutic implications as a biomarker for metabolic dysregulation in humans. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01698-5. |
format | Online Article Text |
id | pubmed-10675981 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-106759812023-11-25 Clec7a drives gut fungus-mediated host lipid deposition Ma, Jie Zhou, Miao Song, Zehe Deng, Yuankun Xia, Siting Li, Yunxia Huang, Xingguo Xiao, Dingfu Yin, Yulong Yin, Jie Microbiome Research BACKGROUND: Compared to that of bacteria, the role of gut fungi in obesity development remains unknown. RESULTS: Here, alterations in gut fungal biodiversity and composition were confirmed in obese pig models and high-fat diet (HFD)-fed mice. Antifungal drugs improved diet-induced obesity, while fungal reconstruction by cohousing or fecal microbiota transplantation maintained the obese phenotype in HFD-fed mice. Fungal profiling identified 5 fungal species associated with obesity. Specifically, Ascomycota_sp. and Microascaceae_sp. were reduced in obese mice and negatively correlated with fat content. Oral supplementation with fungi was sufficient to prevent and treat diet-induced obesity. Clec7a, which is involved in fungal recognition, was highly expressed in HFD-fed mice. The Clec7a agonist accelerated diet-induced obesity, while Clec7a deficieny in mice resulted in resistance to diet-induced obesity and blocked the anti-obese effect of antifungal drugs and fungi. CONCLUSIONS: Taken together, these results indicate that gut fungi/Clec7a signaling is involved in diet-induced obesity and may have therapeutic implications as a biomarker for metabolic dysregulation in humans. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01698-5. BioMed Central 2023-11-25 /pmc/articles/PMC10675981/ /pubmed/38007451 http://dx.doi.org/10.1186/s40168-023-01698-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Ma, Jie Zhou, Miao Song, Zehe Deng, Yuankun Xia, Siting Li, Yunxia Huang, Xingguo Xiao, Dingfu Yin, Yulong Yin, Jie Clec7a drives gut fungus-mediated host lipid deposition |
title | Clec7a drives gut fungus-mediated host lipid deposition |
title_full | Clec7a drives gut fungus-mediated host lipid deposition |
title_fullStr | Clec7a drives gut fungus-mediated host lipid deposition |
title_full_unstemmed | Clec7a drives gut fungus-mediated host lipid deposition |
title_short | Clec7a drives gut fungus-mediated host lipid deposition |
title_sort | clec7a drives gut fungus-mediated host lipid deposition |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10675981/ https://www.ncbi.nlm.nih.gov/pubmed/38007451 http://dx.doi.org/10.1186/s40168-023-01698-5 |
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