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Drugging the microbiome: targeting small microbiome molecules
被引:2
|作者:
Sharma, Sachin
[1
]
Hegde, Pooja
[1
]
Panda, Subhankar
[1
]
Orimoloye, Moyosore
[1
]
Aldrich, Courtney C.
[1
]
机构:
[1] Univ Minnesota, Dept Med Chem, Minneapolis, MN 55455 USA
基金:
美国国家卫生研究院;
关键词:
FRAGILIS CAPSULAR POLYSACCHARIDE;
BETA-GLUCURONIDASE ACTIVITY;
HUMAN GUT MICROBIOME;
KLEBSIELLA-OXYTOCA;
FECAL MICROBIOTA;
METABOLISM;
INHIBITION;
CANCER;
TMAO;
DYSBIOSIS;
D O I:
10.1016/j.mib.2022.102234
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
The human microbiome represents a large and diverse collection of microbes that plays an integral role in human physiology and pathophysiology through interactions with the host and within the microbial community. While early work exploring links between microbiome signatures and diseases states has been associative, emerging evidence demonstrates the metabolic products of the human microbiome have more proximal causal effects on disease phenotypes. The therapeutic implications of this shift are profound as manipulation of the microbiome by the administration of live biotherapeutics, ongoing, can now be pursued alongside research efforts toward describing inhibitors of key microbiome enzymes involved in the biosynthesis of metabolites implicated in various disease states and processing of host-derived metabolites. With growing interest in 'drugging the microbiome', we review few notable microbial metabolites for which traditional drug -development campaigns have yielded compounds with therapeutic promise.
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