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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.
2
Composition of gut microbiota in patients with toxigenic Clostridioides (Clostridium) difficile: Comparison between subgroups according to clinical criteria and toxin gene load.产毒艰难梭菌(梭状芽孢杆菌)患者肠道微生物群的组成:根据临床标准和毒素基因载量的亚组比较。
PLoS One. 2019 Feb 20;14(2):e0212626. doi: 10.1371/journal.pone.0212626. eCollection 2019.
3
A defined commensal consortium elicits CD8 T cells and anti-cancer immunity.特定共生菌群可诱导 CD8+T 细胞及抗肿瘤免疫。
Nature. 2019 Jan;565(7741):600-605. doi: 10.1038/s41586-019-0878-z. Epub 2019 Jan 23.
4
A role for bacterial urease in gut dysbiosis and Crohn's disease.细菌脲酶在肠道菌群失调和克罗恩病中的作用。
Sci Transl Med. 2017 Nov 15;9(416). doi: 10.1126/scitranslmed.aah6888.
5
The Human Intestinal Microbiome in Health and Disease.健康与疾病中的人类肠道微生物群
N Engl J Med. 2016 Dec 15;375(24):2369-2379. doi: 10.1056/NEJMra1600266.
6
Microbiome data distinguish patients with Clostridium difficile infection and non-C. difficile-associated diarrhea from healthy controls.微生物组数据可将艰难梭菌感染患者、非艰难梭菌相关性腹泻患者与健康对照区分开来。
mBio. 2014 May 6;5(3):e01021-14. doi: 10.1128/mBio.01021-14.
7
An introduction to causal inference.因果推断导论。
Int J Biostat. 2010 Feb 26;6(2):Article 7. doi: 10.2202/1557-4679.1203.

促进微生物组研究转化进展的策略。

Strategies to Facilitate Translational Advances from Microbiome Surveys.

机构信息

Department of Biostatistics, University of Washington, Seattle, WA, USA.

Microbiome Research Initiative, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.

出版信息

Trends Microbiol. 2020 May;28(5):329-330. doi: 10.1016/j.tim.2020.02.002. Epub 2020 Mar 4.

DOI:10.1016/j.tim.2020.02.002
PMID:32298611
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8118166/
Abstract

Manipulating the microbiome has enormous potential to treat important human diseases. Microbiome surveys are often used to identify potential therapeutic targets by finding associations between microbial elements and disease status. We argue that many reported associations between the microbiome and disease are incompatible with translational research because they are insufficiently specific. We encourage the clear specification of manipulable microbial elements that can be tested in follow-up randomized experiments, and we provide multiple examples of specific and nonspecific microbial elements.

摘要

微生物组的操纵具有治疗重要人类疾病的巨大潜力。通过寻找微生物与疾病状态之间的关联,微生物组调查通常用于确定潜在的治疗靶点。我们认为,由于不够具体,许多报道的微生物组与疾病之间的关联与转化研究是不兼容的。我们鼓励明确规定可在后续随机实验中进行测试的可操作微生物元素,并提供了多个具体和非具体微生物元素的示例。