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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...

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Autores principales: Ma, Jie, Zhou, Miao, Song, Zehe, Deng, Yuankun, Xia, Siting, Li, Yunxia, Huang, Xingguo, Xiao, Dingfu, Yin, Yulong, Yin, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
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.
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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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