Evidence map›Paper›PMID 38007451›Full record

ArticleMicrobiome2023

Clec7a drives gut fungus-mediated host lipid deposition.

Jie Ma, Miao Zhou, Zehe Song, Yuankun Deng, Siting Xia, Yunxia Li, Xingguo Huang, Dingfu Xiao, Yulong Yin, Jie Yin

Open access · goldAbstract readVideo-Audio Media
In one paragraph

Article in Microbiome, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.8field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 18 citations in OpenAlex.

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  11. DietaryAnimals : an open access journal from MDPI · 2024
    Article
  12. Animals : an open access journal from MDPI · 2024
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  13. DietaryAnimals : an open access journal from MDPI · 2024
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Jie Ma *College of Animal Science and Technology, Hunan Agriculture University, Changsha, 410128, China.
Miao Zhou *College of Animal Science and Technology, Hunan Agriculture University, Changsha, 410128, China.
Zehe Song *College of Animal Science and Technology, Hunan Agriculture University, Changsha, 410128, China.
Yuankun DengCollege of Animal Science and Technology, Hunan Agriculture University, Changsha, 410128, China.
Siting XiaCollege of Animal Science and Technology, Hunan Agriculture University, Changsha, 410128, China.
Yunxia LiCollege of Animal Science and Technology, Hunan Agriculture University, Changsha, 410128, China.
Xingguo HuangCollege of Animal Science and Technology, Hunan Agriculture University, Changsha, 410128, China.
Dingfu XiaoCollege of Animal Science and Technology, Hunan Agriculture University, Changsha, 410128, China. xiaodingfu2001@163.com.
Yulong YinCollege of Animal Science and Technology, Hunan Agriculture University, Changsha, 410128, China.
Jie YinCollege of Animal Science and Technology, Hunan Agriculture University, Changsha, 410128, China. yinjie@hunau.edu.cn.
Hunan Agricultural University · CN

Funding

Earmarked Fund for China Agriculture Research System CARS-37National Key Research and Development Program of China 2022YFD1301500National Natural Science Foundation of China 32172761
6 · The paper itself

Abstract

backgroundCompared to that of bacteria, the role of gut fungi in obesity development remains unknown.

resultsHere, 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.

conclusionsTaken 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. Video Abstract.

Indexed as

Antifungal AgentsObesityAnimalsDectin-1Diet, High-FatFungiHumansLipidsMiceMice, Inbred C57BLSwineAntifungal AgentsClec7a protein, mouseDectin-1LipidsClec7aGut fungiLipid metabolism

Identifiers

PMID38007451
PMCPMC10675981
OpenAlexW4388999412

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.