Visceral adiposity in postmenopausal women is associated with a pro-inflammatory gut microbiome and immunogenic metabolic endotoxemia.

IF 13.8 1区 生物学 Q1 MICROBIOLOGY
Mohamed Gaber, Adam S Wilson, Amy E Millen, Kathleen M Hovey, Michael J LaMonte, Jean Wactawski-Wende, Heather M Ochs-Balcom, Katherine L Cook
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引用次数: 0

Abstract

Background: Obesity, and in particular abdominal obesity, is associated with an increased risk of developing a variety of chronic diseases. Obesity, aging, and menopause are each associated with differential shifts in the gut microbiome. Obesity causes chronic low-grade inflammation due to increased lipopolysaccharide (LPS) levels which is termed "metabolic endotoxemia." We examined the association of visceral adiposity tissue (VAT) area, circulating endotoxemia markers, and the gut bacterial microbiome in a cohort of aged postmenopausal women.

Methods: Fifty postmenopausal women (mean age 78.8 ± 5.3 years) who had existing adipose measurements via dual x-ray absorptiometry (DXA) were selected from the extremes of VAT: n = 25 with low VAT area (45.6 ± 12.5 cm2) and n = 25 with high VAT area (177.5 ± 31.3 cm2). Dietary intake used to estimate the Healthy Eating Index (HEI) score was assessed with a food frequency questionnaire. Plasma LPS, LPS-binding protein (LBP), anti-LPS antibodies, anti-flagellin antibodies, and anti-lipoteichoic acid (LTA) antibodies were measured by ELISA. Metagenomic sequencing was performed on fecal DNA. Female C57BL/6 mice consuming a high-fat or low-fat diet were treated with 0.4 mg/kg diet-derived fecal isolated LPS modeling metabolic endotoxemia, and metabolic outcomes were measured after 6 weeks.

Results: Women in the high VAT group showed increased Proteobacteria abundance and a lower Firmicutes/Bacteroidetes ratio. Plasma LBP concentration was positively associated with VAT area. Plasma anti-LPS, anti-LTA, and anti-flagellin IgA antibodies were significantly correlated with adiposity measurements. Women with high VAT showed significantly elevated LPS-expressing bacteria compared to low VAT women. Gut bacterial species that showed significant associations with both adiposity and inflammation (anti-LPS IgA and LBP) were Proteobacteria (Escherichia coli, Shigella spp., and Klebsiella spp.) and Veillonella atypica. Healthy eating index (HEI) scores negatively correlated with % body fat and anti-LPS IgA antibodies levels. Preclinical murine model showed that high-fat diet-fed mice administered a low-fat diet fecal-derived LPS displayed reduced body weight, decreased % body fat, and improved glucose tolerance test parameters when compared with saline-injected or high-fat diet fecal-derived LPS-treated groups consuming a high-fat diet.

Conclusions: Increased VAT in postmenopausal women is associated with elevated gut Proteobacteria abundance and immunogenic metabolic endotoxemia markers. Low-fat diet-derived fecal-isolated LPS improved metabolic parameters in high-fat diet-fed mice giving mechanistic insights into potential pro-health signaling mediated by under-acylated LPS isoforms. Video Abstract.

绝经后妇女的内脏脂肪与促炎性肠道微生物群和免疫性代谢内毒素血症有关。
背景:肥胖,尤其是腹部肥胖,与罹患各种慢性疾病的风险增加有关。肥胖、衰老和更年期都与肠道微生物组的不同变化有关。肥胖会导致脂多糖(LPS)水平升高,引起慢性低度炎症,这被称为 "代谢性内毒素血症"。我们研究了一组绝经后老年妇女的内脏脂肪组织(VAT)面积、循环内毒素血症标志物和肠道细菌微生物组之间的关系:通过双 X 射线吸收测量法(DXA)对 50 名绝经后妇女(平均年龄为 78.8 ± 5.3 岁)的脂肪组织进行了测量,并从中挑选出 VAT 的两个极端:低 VAT 面积(45.6 ± 12.5 cm2)n = 25 人,高 VAT 面积(177.5 ± 31.3 cm2)n = 25 人。用于估算健康饮食指数(HEI)得分的饮食摄入量是通过食物频率问卷进行评估的。血浆 LPS、LPS 结合蛋白 (LBP)、抗 LPS 抗体、抗鞭毛虫素抗体和抗脂变性胆酸 (LTA) 抗体均通过 ELISA 法检测。对粪便 DNA 进行了元基因组测序。对摄入高脂或低脂饮食的雌性 C57BL/6 小鼠进行 0.4 毫克/千克源自饮食的粪便分离 LPS 模拟代谢性内毒素血症处理,并在 6 周后测定代谢结果:结果:高 VAT 组妇女的蛋白质细菌丰度增加,而固醇菌/类杆菌比例降低。血浆 LBP 浓度与 VAT 面积呈正相关。血浆中的抗 LPS、抗 LTA 和抗鞭毛虫素 IgA 抗体与脂肪测量值显著相关。与脂肪含量低的妇女相比,脂肪含量高的妇女体内表达 LPS 的细菌明显增多。与脂肪率和炎症(抗 LPS IgA 和枸杞多糖)均有显著关联的肠道细菌种类是变形杆菌(大肠埃希氏菌、志贺氏菌属和克雷伯氏菌属)和非典型维氏菌。健康饮食指数(HEI)得分与体脂率和抗 LPS IgA 抗体水平呈负相关。临床前小鼠模型显示,与注射生理盐水或高脂饮食粪源性 LPS 处理组相比,摄入低脂饮食粪源性 LPS 的高脂饮食小鼠体重下降,体脂率降低,葡萄糖耐量试验参数改善:结论:绝经后妇女的增值脂肪增加与肠道变形杆菌丰度和免疫代谢内毒素血症指标升高有关。低脂饮食来源的粪便分离LPS改善了高脂饮食喂养小鼠的代谢参数,从机理上揭示了低酰化LPS异构体介导的潜在健康信号。视频摘要。
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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
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