Faecalibacterium prausnitzii as a potential Antiatherosclerotic microbe

普氏粪杆菌 肠道菌群 生物 代谢组学 基因组 冠状动脉疾病 体内 微生物群 疾病 免疫学 医学 内科学 生物信息学 生物化学 生物技术 基因
作者
Haitao Yang,Zhihui Jiang,Yi Yang,Tingting Wu,Ying‐Ying Zheng,Yitong Ma,Xiang Xie
出处
期刊:Cell Communication and Signaling [Springer Nature]
卷期号:22 (1) 被引量:9
标识
DOI:10.1186/s12964-023-01464-y
摘要

Abstract Background The gut microbiota plays a crucial role in coronary artery disease (CAD) development, but limited attention has been given to the role of the microbiota in preventing this disease. This study aimed to identify key biomarkers using metagenomics and untargeted metabolomics and verify their associations with atherosclerosis. Methods A total of 371 participants, including individuals with various CAD types and CAD-free controls, were enrolled. Subsequently, significant markers were identified in the stool samples through gut metagenomic sequencing and untargeted metabolomics. In vivo and in vitro experiments were performed to investigate the mechanisms underlying the association between these markers and atherosclerosis. Results Faecal omics sequencing revealed that individuals with a substantial presence of Faecalibacterium prausnitzii had the lowest incidence of CAD across diverse CAD groups and control subjects. A random forest model confirmed the significant relationship between F. prausnitzii and CAD incidence. Notably, F. prausnitzii emerged as a robust, independent CAD predictor. Furthermore, our findings indicated the potential of the gut microbiota and gut metabolites to predict CAD occurrence and progression, potentially impacting amino acid and vitamin metabolism. F. prausnitzii mitigated inflammation and exhibited an antiatherosclerotic effect on ApoE −/− mice after gavage. This effect was attributed to reduced intestinal LPS synthesis and reinforced mechanical and mucosal barriers, leading to decreased plasma LPS levels and an antiatherosclerotic outcome. Conclusions Sequencing of the samples revealed a previously unknown link between specific gut microbiota and atherosclerosis. Treatment with F. prausnitzii may help prevent CAD by inhibiting atherosclerosis.

科研通智能强力驱动
Strongly Powered by AbleSci AI

祝大家在新的一年里科研腾飞
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
俏皮的豌豆完成签到 ,获得积分20
5秒前
化学课die表完成签到 ,获得积分10
8秒前
8秒前
偷得浮生半日闲完成签到,获得积分10
10秒前
淡然冬灵完成签到,获得积分10
13秒前
JamesPei应助善良板栗采纳,获得10
14秒前
17秒前
三月完成签到,获得积分10
21秒前
YY完成签到 ,获得积分10
24秒前
charleslam发布了新的文献求助10
25秒前
嘎嘎嘎嘎完成签到,获得积分10
25秒前
想上985完成签到,获得积分10
34秒前
清脆冬日完成签到 ,获得积分10
39秒前
40秒前
无极微光应助gtgwm采纳,获得20
41秒前
桥豆麻袋完成签到,获得积分10
43秒前
我是老大应助meizu采纳,获得10
45秒前
孙同学发布了新的文献求助10
45秒前
苹果冬莲完成签到,获得积分10
47秒前
文艺完成签到 ,获得积分10
48秒前
火离猫完成签到,获得积分10
49秒前
龙腾岁月完成签到 ,获得积分10
49秒前
一个千年猪妖完成签到 ,获得积分10
51秒前
领导范儿应助孙同学采纳,获得10
53秒前
火星上的雨柏完成签到 ,获得积分10
54秒前
54秒前
Mito2009完成签到,获得积分10
55秒前
乐枫完成签到 ,获得积分10
55秒前
研友-wbg-LjbQIL完成签到 ,获得积分10
56秒前
忧虑的墨镜完成签到 ,获得积分10
58秒前
meizu发布了新的文献求助10
1分钟前
无辜的猎豹完成签到 ,获得积分10
1分钟前
可靠的南露完成签到,获得积分10
1分钟前
照亮世界的ay完成签到,获得积分10
1分钟前
meizu完成签到,获得积分10
1分钟前
优雅的WAN完成签到 ,获得积分10
1分钟前
假装新疆人烤大串儿完成签到 ,获得积分10
1分钟前
Tonald Yang发布了新的文献求助10
1分钟前
不安听露完成签到 ,获得积分10
1分钟前
山是山三十三完成签到 ,获得积分10
1分钟前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Les Mantodea de guyane 2500
Common Foundations of American and East Asian Modernisation: From Alexander Hamilton to Junichero Koizumi 600
Signals, Systems, and Signal Processing 510
Discrete-Time Signals and Systems 510
Campbell Walsh Wein Urology 3-Volume Set 12th Edition 200
Three-dimensional virtual model for robot-assisted partial nephrectomy in totally endophytic renal tumors: a propensity-score matching analysis with a control group 200
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 计算机科学 有机化学 物理 生物化学 纳米技术 复合材料 内科学 化学工程 人工智能 催化作用 遗传学 数学 基因 量子力学 物理化学
热门帖子
关注 科研通微信公众号,转发送积分 5866638
求助须知:如何正确求助?哪些是违规求助? 6425336
关于积分的说明 15654717
捐赠科研通 4981580
什么是DOI,文献DOI怎么找? 2686691
邀请新用户注册赠送积分活动 1629491
关于科研通互助平台的介绍 1587499