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本文引用的文献

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Colonic microbiota is associated with inflammation and host epigenomic alterations in inflammatory bowel disease.肠道微生物群与炎症性肠病中的炎症和宿主表观遗传改变有关。
Nat Commun. 2020 Mar 23;11(1):1512. doi: 10.1038/s41467-020-15342-5.
2
Long-term dietary intervention reveals resilience of the gut microbiota despite changes in diet and weight.长期饮食干预可使肠道微生物组保持稳定,尽管饮食和体重发生了变化。
Am J Clin Nutr. 2020 Jun 1;111(6):1127-1136. doi: 10.1093/ajcn/nqaa046.
3
Mediterranean diet intervention alters the gut microbiome in older people reducing frailty and improving health status: the NU-AGE 1-year dietary intervention across five European countries.地中海饮食干预改变老年人的肠道微生物组,减少虚弱并改善健康状况:跨越五个欧洲国家的 NU-AGE 为期一年的饮食干预。
Gut. 2020 Jul;69(7):1218-1228. doi: 10.1136/gutjnl-2019-319654. Epub 2020 Feb 17.
4
Age-Related Differences in the Gut Microbiome of Rhesus Macaques.恒河猴肠道微生物组的年龄相关差异。
J Gerontol A Biol Sci Med Sci. 2020 Jun 18;75(7):1293-1298. doi: 10.1093/gerona/glaa048.
5
Cellular senescence contributes to age-dependent changes in circulating extracellular vesicle cargo and function.细胞衰老导致循环细胞外囊泡货物和功能随年龄的变化。
Aging Cell. 2020 Mar;19(3):e13103. doi: 10.1111/acel.13103. Epub 2020 Jan 21.
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Microbial genomes from non-human primate gut metagenomes expand the primate-associated bacterial tree of life with over 1000 novel species.非人类灵长类动物肠道宏基因组中的微生物基因组扩展了灵长类动物相关细菌的生命之树,其中包含超过 1000 个新物种。
Genome Biol. 2019 Dec 28;20(1):299. doi: 10.1186/s13059-019-1923-9.
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Dietary butyrate suppresses inflammation through modulating gut microbiota in high-fat diet-fed mice.饮食丁酸通过调节高脂肪饮食喂养小鼠的肠道微生物群来抑制炎症。
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Intestinal Inflammation Modulates the Epithelial Response to Butyrate in Patients With Inflammatory Bowel Disease.肠道炎症调节炎症性肠病患者对丁酸盐的上皮反应。
Inflamm Bowel Dis. 2020 Jan 1;26(1):43-55. doi: 10.1093/ibd/izz119.
9
Nondigestible carbohydrates, butyrate, and butyrate-producing bacteria.不可消化的碳水化合物、丁酸盐和产生丁酸盐的细菌。
Crit Rev Food Sci Nutr. 2019;59(sup1):S130-S152. doi: 10.1080/10408398.2018.1542587. Epub 2018 Dec 22.
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Front Immunol. 2018 Aug 14;9:1832. doi: 10.3389/fimmu.2018.01832. eCollection 2018.

猴子的结肠黏膜微生物组群落随年龄变化的相关变化。

Age-Related Colonic Mucosal Microbiome Community Shifts in Monkeys.

机构信息

Department of Pathology, Wake Forest School of Medicine, Medical Center Boulevard, Winston-Salem, North Carolina.

School of Medicine, University of Tasmania, Australia.

出版信息

J Gerontol A Biol Sci Med Sci. 2021 Oct 13;76(11):1906-1914. doi: 10.1093/gerona/glaa256.

DOI:10.1093/gerona/glaa256
PMID:33021628
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8514065/
Abstract

Age-related changes in gut microbiome impact host health. The interactive relationship between the microbiome and physiological systems in an aged body system remains to be clearly defined, particularly in the context of inflammation. Therefore, we aimed to evaluate systemic inflammation, microbial translocation (MT), and differences between fecal and mucosal microbiomes. Ascending colon mucosal biopsies, fecal samples, and blood samples from healthy young and old female vervet monkeys were collected for 16S rRNA gene sequencing, MT, and cytokine analyses, respectively. To demonstrate microbial co-occurrence patterns, we used Kendall's tau correlation measure of interactions between microbes. We found elevated levels of plasma LBP-1, MCP-1, and CRP in old monkeys, indicative of higher MT and systemic inflammation. Microbiome analysis revealed significant differences specific to age. At the phylum level, abundances of pathobionts such as Proteobacteria were increased in the mucosa of old monkeys. At the family level, Helicobacteriaceae was highly abundant in mucosal samples (old); in contrast, Ruminococcaceae were higher in the fecal samples of old monkeys. We found significantly lower Firmicutes:Bacteroidetes ratio and lower abundance of butyrate-producing microbes in old monkeys, consistent with less healthy profiles. Microbial community co-occurrence analysis on mucosal samples revealed 13 nodes and 41 associations in the young monkeys, but only 12 nodes and 21 associations in the old monkeys. Our findings provide novel insights into systemic inflammation and gut microbial interactions, highlight the importance of the mucosal niche, and facilitate further understanding of the decline in the stability of the microbial community with aging.

摘要

肠道微生物组的年龄相关性变化影响宿主健康。微生物组与衰老机体系统生理系统之间的相互作用关系尚待明确界定,尤其是在炎症方面。因此,我们旨在评估系统性炎症、微生物易位(MT)以及粪便和黏膜微生物组之间的差异。我们分别从健康的年轻和老年雌性长尾猕猴收集升结肠黏膜活检、粪便样本和血液样本,用于 16S rRNA 基因测序、MT 和细胞因子分析。为了展示微生物的共同发生模式,我们使用 Kendall's tau 相互作用测量来衡量微生物之间的相互作用。我们发现老年猴血浆 LBP-1、MCP-1 和 CRP 水平升高,表明 MT 和系统性炎症增加。微生物组分析显示出特定于年龄的显著差异。在门水平上,黏膜中病原体如变形菌门的丰度在老年猴中增加。在科水平上,Helicobacteriaceae 在黏膜样本中高度丰富(老年);相反,在老年猴的粪便样本中,Ruminococcaceae 较高。我们发现,老年猴的厚壁菌门:拟杆菌门比例显著降低,丁酸产生菌丰度降低,这与不太健康的特征一致。对黏膜样本的微生物群落共发生分析显示,年轻猴中有 13 个节点和 41 个关联,而老年猴中只有 12 个节点和 21 个关联。我们的研究结果为系统性炎症和肠道微生物相互作用提供了新的见解,强调了黏膜生态位的重要性,并有助于进一步了解随着年龄增长微生物群落稳定性的下降。