Strategizing the human microbiome for small molecules: Approaches and perspectives

被引:2
|
作者
Hussain, Aehtesham [1 ]
Patwekar, Umera [1 ]
Mongad, Dattatray S. [1 ]
Shouche, Yogesh S. [1 ]
机构
[1] NCMR Natl Ctr Cell Sci NCCS, Pune 411007, Maharashtra, India
关键词
human microbes; microbial secondary metabolites; genome mining; metabolic engineering; biosynthetic gene clusters; chemical analytics; culture-omics; BIOSYNTHETIC GENE CLUSTERS; CHAIN FATTY-ACIDS; NATURAL-PRODUCTS; CLINICAL-TRIAL; DISCOVERY; METABOLITES; ANTIBIOTICS; ACTIVATION; DIVERSITY; MICROCINS;
D O I
10.1016/j.drudis.2022.103459
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Studies of the human microbiome are providing a deeper understanding of its significance to human health, and increasing evidence links the microbiota with several diseases. Nevertheless, the exact mechanisms involved in human-microbe interactions are mostly undefined. The genomic potential of the human microbiome to biosynthesize distinct molecules outmatches its known chemical space, and small-molecule discovery in this context remains in its infancy. The profiling of microbiome-derived small molecules and their contextualization through cause-effect mechanistic studies may provide a better understanding of host-microbe interactions, guide new therapeutic interventions, and modulate microbiome-based therapies. This review describes the advances, approaches, and allied challenges in mining new microbial scaffolds from the human microbiome using genomic, microbe cultivation, and chemical analytic platforms. In the future, the complete biological characterization of a single microbe-derived molecule that has a specific therapeutic application could resolve the current limitations of microbiota-modulating therapies.
引用
收藏
页码:1 / 9
页数:9
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