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在单次粪便微生物群移植后,儿童微生物群对性别匹配小鼠脂肪和肠道发育的影响会持续到成年期。

Effects of children's microbiota on adipose and intestinal development in sex-matched mice persist into adulthood following a single fecal microbiota transplantation.

作者信息

La Rosa Federica, Guzzardi Maria Angela, Pardo-Tendero Mercedes, Barone Monica, Ruocco Chiara, Conti Gabriele, Panetta Daniele, Riabitch Daria, Bernardi Silvia, Giorgetti Assuero, Campani Daniela, Monleon Daniel, Nisoli Enzo, Brigidi Patrizia, Iozzo Patricia

机构信息

Institute of Clinical Physiology, National Research Council, via Moruzzi 1, 56124 Pisa, Italy.

Department of Pathology, University of Valencia, Health Research Institute INCLIVA/CIBERFES for Frailty and Healthy Aging, Blasco Ibañez, 15, 46010, Valencia, Spain.

出版信息

Mol Metab. 2025 Jul;97:102157. doi: 10.1016/j.molmet.2025.102157. Epub 2025 Apr 25.

DOI:10.1016/j.molmet.2025.102157
PMID:40288637
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12139018/
Abstract

BACKGROUND

The global prevalence of obesity and type 2 diabetes, particularly among children, is rising, yet the long-term impacts of early-life fecal microbiota transplantation (FMT) on metabolic health remain poorly understood.

OBJECTIVES

To investigate how early-life FMT from children to young, sex-matched mice influences metabolic outcomes and adipose tissue function in later, adult life.

METHODS

Germ-free mice were colonized with fecal microbiota from either lean children or children with obesity. The impacts on brown adipose tissue (BAT), white adipose tissue (WAT), glucose metabolism, and gut health were analyzed in male and female mice. Microbial communities and metabolite profiles were characterized using sequencing and metabolomics.

RESULTS

Male mice receiving FMT from obese donors exhibited marked BAT whitening and impaired amino acid and glucose metabolism. In contrast, female recipients developed hyperglycemia, accompanied by gut barrier dysfunction and WAT impairment. Distinct microbial and metabolite profiles were associated with these phenotypes: Collinsella and trimethylamine in females; and Paraprevotella, Collinsella, Lachnospiraceae NK4A136, Bacteroides, Coprobacillus, and multiple metabolites in males. These phenotypic effects persisted despite changes in host environment and diet.

CONCLUSIONS

Early-life FMT induced long-lasting effects on the metabolic landscape, profoundly affecting adipose tissue function and systemic glucose homeostasis in adulthood. Donor dietary habits correlated with the fecal microbial profiles observed in recipient mice. These findings highlight the critical need for identifying and leveraging beneficial exposures during early development to combat obesity and diabetes.

摘要

背景

肥胖和2型糖尿病的全球患病率正在上升,尤其是在儿童中,但早期粪便微生物群移植(FMT)对代谢健康的长期影响仍知之甚少。

目的

研究儿童早期向性别匹配的年轻小鼠进行粪便微生物群移植如何影响成年后期的代谢结果和脂肪组织功能。

方法

将无菌小鼠用来自瘦儿童或肥胖儿童的粪便微生物群进行定殖。分析雄性和雌性小鼠对棕色脂肪组织(BAT)、白色脂肪组织(WAT)、葡萄糖代谢和肠道健康的影响。使用测序和代谢组学对微生物群落和代谢物谱进行表征。

结果

接受肥胖供体粪便微生物群移植的雄性小鼠表现出明显的棕色脂肪组织变白以及氨基酸和葡萄糖代谢受损。相比之下,雌性受体出现高血糖,伴有肠道屏障功能障碍和白色脂肪组织受损。不同的微生物和代谢物谱与这些表型相关:雌性中的柯林斯菌和三甲胺;雄性中的副普雷沃菌、柯林斯菌、毛螺菌科NK4A136、拟杆菌属、粪芽孢杆菌属以及多种代谢物。尽管宿主环境和饮食发生了变化,这些表型效应仍然存在。

结论

早期粪便微生物群移植对代谢格局产生了持久影响,深刻影响了成年期的脂肪组织功能和全身葡萄糖稳态。供体的饮食习惯与受体小鼠中观察到的粪便微生物谱相关。这些发现凸显了在早期发育过程中识别和利用有益暴露以对抗肥胖和糖尿病的迫切需求。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659b/12139018/708aca771358/figs4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659b/12139018/fd4a2e49f0f9/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659b/12139018/813ceb2f0ec5/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659b/12139018/21bdf1c8119b/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659b/12139018/1aeb9247c34c/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659b/12139018/e0514f444a24/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659b/12139018/06fb2698c699/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659b/12139018/3784719415c0/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659b/12139018/031d34adca76/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659b/12139018/ec551a834f30/figs1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659b/12139018/80b963da7e69/figs2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659b/12139018/91e627ea1c1e/figs3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659b/12139018/708aca771358/figs4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659b/12139018/fd4a2e49f0f9/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659b/12139018/813ceb2f0ec5/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659b/12139018/21bdf1c8119b/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659b/12139018/1aeb9247c34c/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659b/12139018/e0514f444a24/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659b/12139018/06fb2698c699/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659b/12139018/3784719415c0/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659b/12139018/031d34adca76/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659b/12139018/ec551a834f30/figs1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659b/12139018/80b963da7e69/figs2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659b/12139018/91e627ea1c1e/figs3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659b/12139018/708aca771358/figs4.jpg

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