TY - JOUR
T1 - Drugging the microbiome
T2 - targeting small microbiome molecules
AU - Sharma, Sachin
AU - Hegde, Pooja V
AU - Panda, Subhankar
AU - Orimoloye, Moyosore O
AU - Aldrich, Courtney C.
N1 - Funding Information:
This work was supported by grants ( AI143784 and AI136445 ) from the National Institutes of Health .
Publisher Copyright:
© 2022 Elsevier Ltd
PY - 2023/2
Y1 - 2023/2
N2 - 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.
AB - 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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U2 - 10.1016/j.mib.2022.102234
DO - 10.1016/j.mib.2022.102234
M3 - Review article
C2 - 36399893
AN - SCOPUS:85141991447
SN - 1369-5274
VL - 71
JO - Current Opinion in Microbiology
JF - Current Opinion in Microbiology
M1 - 102234
ER -