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Symptomatic atherosclerosis is associated with an altered gut metagenome

机译:有症状的动脉粥样硬化与肠道基因组改变有关

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Recent findings have implicated the gut microbiota as a contributor of metabolic diseases through the modulation of host metabolism and inflammation. Atherosclerosis is associated with lipid accumulation and inflammation in the arterial wall, and bacteria have been suggested as a causative agent of this disease. Here we use shotgun sequencing of the gut metagenome to demonstrate that the genus Collinsella was enriched in patients with symptomatic atherosclerosis, defined as stenotic atherosclerotic plaques in the carotid artery leading to cerebrovascular events, whereas Roseburia and Eubacterium were enriched in healthy controls. Further characterization of the functional capacity of the metagenomes revealed that patient gut metagenomes were enriched in genes encoding peptidoglycan synthesis and depleted in phytoene dehydrogenase; patients also had reduced serum levels of beta-carotene. Our findings suggest that the gut metagenome is associated with the inflammatory status of the host and patientswith symptomatic atherosclerosis harbor characteristic changes in the gut metagenome.
机译:最近的发现暗示肠道微生物群通过调节宿主代谢和炎症而成为代谢疾病的贡献者。动脉粥样硬化与脂质蓄积和动脉壁炎症有关,并且细菌被认为是该疾病的病原体。在这里,我们使用肠道元基因组的shot弹枪测序来证明Collinsella属在患有症状性动脉粥样硬化的患者中富集,定义为导致脑血管事件的颈动脉狭窄性动脉粥样硬化斑块,而Roseburia和Eubacterium在健康对照中富集。对元基因组功能能力的进一步表征表明,患者的肠道元基因组富含编码肽聚糖合成的基因,并富含八氢番茄红素脱氢酶。患者的血清β-胡萝卜素水平也降低了。我们的发现表明,肠道元基因组与宿主的炎症状态相关,并且有症状的动脉粥样硬化患者在肠道元基因组中具有特征性变化。

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