Gut microbiome and metabolome profiling in Framingham heart study reveals cholesterol-metabolizing bacteria

被引:36
|
作者
Li, Chenhao [1 ,2 ,3 ]
Strazar, Martin [1 ]
Mohamed, Ahmed M. T. [1 ,2 ,3 ]
Pacheco, Julian A. [1 ]
Walker, Rebecca L. [1 ]
Lebar, Tina [4 ]
Zhao, Shijie [1 ]
Lockart, Julia [1 ]
Dame, Andrea [1 ]
Thurimella, Kumar [1 ]
Jeanfavre, Sarah [1 ]
Brown, Eric M. [1 ]
Ang, Qi Yan [1 ]
Berdy, Brittany [1 ]
Sergio, Dallis [1 ]
Invernizzi, Rachele [1 ,2 ,3 ]
Tinoco, Antonio [5 ]
Pishchany, Gleb [1 ]
Vasan, Ramachandran S. [6 ,7 ,8 ,9 ,10 ,11 ]
Balskus, Emily [5 ,12 ]
Huttenhower, Curtis [1 ,13 ]
Vlamakis, Hera [1 ]
Clish, Clary [1 ]
Shaw, Stanley Y. [1 ,14 ]
Plichta, Damian R. [1 ]
Xavier, Ramnik J. [1 ,2 ,3 ]
机构
[1] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
[2] Harvard Med Sch, Massachusetts Gen Hosp, Ctr Computat & Integrat Biol, Boston, MA 02115 USA
[3] Harvard Med Sch, Massachusetts Gen Hosp, Dept Mol Biol, Boston, MA 02115 USA
[4] Harvard Univ, Wyss Inst Biolog Inspired Engn, Boston, MA 02115 USA
[5] Harvard Univ, Dept Chem & Chem Biol, Cambridge, MA USA
[6] Boston Univ, Framingham, MA USA
[7] NHLBIs Framingham Heart Study, Framingham, MA USA
[8] Boston Univ, Sch Med, Dept Med, Sect Prevent Med, Boston, MA USA
[9] Boston Univ, Sch Med, Dept Med, Sect Epidemiol, Boston, MA USA
[10] Boston Univ, Sch Med, Dept Med, Sect Cardiol, Boston, MA USA
[11] Univ Texas San Antonio, Sch Publ Hlth, San Antonio, TX USA
[12] Harvard Univ, Howard Hughes Med Inst, Cambridge, MA USA
[13] Harvard TH Chan Sch Publ Hlth, Boston, MA USA
[14] Harvard Med Sch, Brigham & Womens Hosp, Div Cardiovasc Med, Boston, MA USA
关键词
PROTEIN-COUPLED RECEPTOR; METHANOBREVIBACTER-SMITHII; PHOSPHATIDYLCHOLINE; CONVERSION; CARNITINE; ALIGNMENT; CATALOG; FAILURE; SEARCH; GENOME;
D O I
10.1016/j.cell.2024.03.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Accumulating evidence suggests that cardiovascular disease (CVD) is associated with an altered gut microbiome. Our understanding of the underlying mechanisms has been hindered by lack of matched multi-omic data with diagnostic biomarkers. To comprehensively profile gut microbiome contributions to CVD, we generated stool metagenomics and metabolomics from 1,429 Framingham Heart Study participants. We identified blood lipids and cardiovascular health measurements associated with microbiome and metabolome composition. Integrated analysis revealed microbial pathways implicated in CVD, including flavonoid, g-butyrobetaine, and cholesterol metabolism. Species from the Oscillibacter genus were associated with decreased fecal and plasma cholesterol levels. Using functional prediction and in vitro characterization of multiple representative human gut Oscillibacter isolates, we uncovered conserved cholesterol -metabolizing capabilities, including glycosylation and dehydrogenation. These findings suggest that cholesterol metabolism is a broad property of phylogenetically diverse Oscillibacter spp., with potential benefits for lipid homeostasis and cardiovascular health.
引用
收藏
页码:1834 / 1852.e19
页数:39
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