Key Technologies for Progressing Discovery of Microbiome-Based Medicines

被引:11
|
作者
Young, Remy B. [1 ,2 ,3 ]
Marcelino, Vanessa R. [1 ,4 ]
Chonwerawong, Michelle [1 ,4 ]
Gulliver, Emily L. [1 ,2 ,3 ,4 ]
Forster, Samuel C. [1 ,2 ,3 ,4 ]
机构
[1] Hudson Inst Med Res, Ctr Innate Immun & Infect Dis, Clayton, Vic, Australia
[2] Monash Univ, Monash Biomed Discovery Inst, Infect & Immun Program, Clayton, Vic, Australia
[3] Monash Univ, Dept Microbiol, Clayton, Vic, Australia
[4] Monash Univ, Dept Mol & Translat Sci, Clayton, Vic, Australia
来源
FRONTIERS IN MICROBIOLOGY | 2021年 / 12卷
基金
英国医学研究理事会;
关键词
microbiome; faecal transplant; gastrointestinal disorder; 16S rRNA sequencing; metagenomic sequencing; microbial genomics; bacteriotherapy; live biotherapeutics; HUMAN GUT MICROBIOME; LACTOBACILLUS-RHAMNOSUS; INTESTINAL MICROBIOTA; CLOSTRIDIUM-DIFFICILE; PROBIOTIC BACTERIA; GENE-EXPRESSION; MULTI-OMICS; IN-VITRO; T-CELLS; COLONIZATION;
D O I
10.3389/fmicb.2021.685935
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A growing number of experimental and computational approaches are illuminating the "microbial dark matter" and uncovering the integral role of commensal microbes in human health. Through this work, it is now clear that the human microbiome presents great potential as a therapeutic target for a plethora of diseases, including inflammatory bowel disease, diabetes and obesity. The development of more efficacious and targeted treatments relies on identification of causal links between the microbiome and disease; with future progress dependent on effective links between state-of-the-art sequencing approaches, computational analyses and experimental assays. We argue determining causation is essential, which can be attained by generating hypotheses using multi-omic functional analyses and validating these hypotheses in complex, biologically relevant experimental models. In this review we discuss existing analysis and validation methods, and propose best-practice approaches required to enable the next phase of microbiome research.
引用
收藏
页数:13
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