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本文引用的文献

1
Functional Microbial Responses to Alcohol Abstinence in Patients With Alcohol Use Disorder.酒精使用障碍患者戒酒时的功能性微生物反应
Front Physiol. 2020 Apr 24;11:370. doi: 10.3389/fphys.2020.00370. eCollection 2020.
2
Fecal Microbiome Distinguishes Alcohol Consumption From Alcoholic Hepatitis But Does Not Discriminate Disease Severity.粪便微生物组可区分酒精摄入与酒精性肝炎,但无法区分疾病严重程度。
Hepatology. 2020 Jul;72(1):271-286. doi: 10.1002/hep.31178.
3
Whole-Virome Analysis Sheds Light on Viral Dark Matter in Inflammatory Bowel Disease.全病毒组分析揭示炎症性肠病中的病毒暗物质。
Cell Host Microbe. 2019 Dec 11;26(6):764-778.e5. doi: 10.1016/j.chom.2019.10.009. Epub 2019 Nov 19.
4
Bacteriophage targeting of gut bacterium attenuates alcoholic liver disease.噬菌体靶向肠道细菌可减轻酒精性肝病。
Nature. 2019 Nov;575(7783):505-511. doi: 10.1038/s41586-019-1742-x. Epub 2019 Nov 13.
5
The Candida albicans exotoxin candidalysin promotes alcohol-associated liver disease.白色念珠菌外毒素白念珠菌溶素促进酒精相关性肝病。
J Hepatol. 2020 Mar;72(3):391-400. doi: 10.1016/j.jhep.2019.09.029. Epub 2019 Oct 10.
6
The Human Gut Virome Is Highly Diverse, Stable, and Individual Specific.人类肠道病毒组高度多样化、稳定且具有个体特异性。
Cell Host Microbe. 2019 Oct 9;26(4):527-541.e5. doi: 10.1016/j.chom.2019.09.009.
7
Intestinal Fungal Dysbiosis and Systemic Immune Response to Fungi in Patients With Alcoholic Hepatitis.酒精性肝炎患者肠道真菌失调与真菌的全身免疫反应。
Hepatology. 2020 Feb;71(2):522-538. doi: 10.1002/hep.30832. Epub 2019 Aug 20.
8
Epstein-Barr virus infection is associated with a higher Child-Pugh score and may predict poor prognoses for patients with liver cirrhosis.爱泼斯坦-巴尔病毒感染与较高的Child-Pugh 评分相关,并且可能预示着肝硬化患者的预后不良。
BMC Gastroenterol. 2019 Jun 18;19(1):94. doi: 10.1186/s12876-019-1021-1.
9
Serum and Fecal Oxylipins in Patients with Alcohol-Related Liver Disease.血清和粪便氧化脂质在酒精性肝病患者中的变化。
Dig Dis Sci. 2019 Jul;64(7):1878-1892. doi: 10.1007/s10620-019-05638-y. Epub 2019 May 10.
10
Gut mucosal virome alterations in ulcerative colitis.溃疡性结肠炎患者的肠道黏膜病毒组改变。
Gut. 2019 Jul;68(7):1169-1179. doi: 10.1136/gutjnl-2018-318131. Epub 2019 Mar 6.

酒精性肝炎患者的肠道病毒组。

Intestinal Virome in Patients With Alcoholic Hepatitis.

机构信息

Department of Medicine, University of California San Diego, La Jolla, CA.

Department of Medicine, VA San Diego Healthcare System, San Diego, CA.

出版信息

Hepatology. 2020 Dec;72(6):2182-2196. doi: 10.1002/hep.31459. Epub 2020 Oct 10.

DOI:10.1002/hep.31459
PMID:32654263
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8159727/
Abstract

BACKGROUND AND AIMS

Alcoholic hepatitis (AH) is a severe manifestation of alcohol-associated liver disease (ALD) with high mortality. Although gut bacteria and fungi modulate disease severity, little is known about the effects of the viral microbiome (virome) in patients with ALD.

APPROACH AND RESULTS

We extracted virus-like particles from 89 patients with AH who were enrolled in a multicenter observational study, 36 with alcohol use disorder (AUD), and 17 persons without AUD (controls). Virus-like particles from fecal samples were fractionated using differential filtration techniques, and metagenomic sequencing was performed to characterize intestinal viromes. We observed an increased viral diversity in fecal samples from patients with ALD, with the most significant changes in samples from patients with AH. Escherichia-, Enterobacteria-, and Enterococcus phages were over-represented in fecal samples from patients with AH, along with significant increases in mammalian viruses such as Parvoviridae and Herpesviridae. Antibiotic treatment was associated with higher viral diversity. Specific viral taxa, such as Staphylococcus phages and Herpesviridae, were associated with increased disease severity, indicated by a higher median Model for End-Stage Liver Disease score, and associated with increased 90-day mortality.

CONCLUSIONS

In conclusion, intestinal viral taxa are altered in fecal samples from patients with AH and associated with disease severity and mortality. Our study describes an intestinal virome signature associated with AH.

摘要

背景与目的

酒精性肝炎(AH)是一种严重的酒精相关肝病(ALD)表现,死亡率较高。尽管肠道细菌和真菌会影响疾病的严重程度,但对于 ALD 患者病毒微生物组(病毒组)的影响知之甚少。

方法和结果

我们从参加多中心观察性研究的 89 名 AH 患者中提取病毒样颗粒,其中 36 名患有酒精使用障碍(AUD),17 名无 AUD(对照组)。使用差速过滤技术对粪便样本中的病毒样颗粒进行分离,并进行宏基因组测序以描述肠道病毒组。我们观察到 ALD 患者粪便样本中的病毒多样性增加,AH 患者的样本变化最为显著。肠道中埃希氏菌、肠杆菌和肠球菌噬菌体过度表达,同时哺乳动物病毒如细小病毒科和疱疹病毒科的数量也显著增加。抗生素治疗与病毒多样性增加相关。特定的病毒分类群,如葡萄球菌噬菌体和疱疹病毒科,与疾病严重程度相关,表现为更高的终末期肝病模型评分中位数,并且与 90 天死亡率增加相关。

结论

总之,AH 患者粪便样本中的肠道病毒分类群发生改变,与疾病严重程度和死亡率相关。我们的研究描述了与 AH 相关的肠道病毒组特征。