Genome-scale metabolic reconstruction of 7,302 human microorganisms for personalized medicine
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60460709%3A41340%2F23%3A94096" target="_blank" >RIV/60460709:41340/23:94096 - isvavai.cz</a>
Result on the web
<a href="https://www.nature.com/articles/s41587-022-01628-0" target="_blank" >https://www.nature.com/articles/s41587-022-01628-0</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1038/s41587-022-01628-0" target="_blank" >10.1038/s41587-022-01628-0</a>
Alternative languages
Result language
angličtina
Original language name
Genome-scale metabolic reconstruction of 7,302 human microorganisms for personalized medicine
Original language description
The human microbiome influences the efficacy and safety of a wide variety of commonly prescribed drugs. Designing precision medicine approaches that incorporate microbial metabolism would require strain and molecule-resolved, scalable computational modeling. Here, we extend our previous resource of genome-scale metabolic reconstructions of human gut microorganisms with a greatly expanded version. AGORA2 (assembly of gut organisms through reconstruction and analysis, version 2) accounts for 7,302 strains, includes strain-resolved drug degradation and biotransformation capabilities for 98 drugs, and was extensively curated based on comparative genomics and literature searches. The microbial reconstructions performed very well against three independently assembled experimental datasets with an accuracy of 0,72 to 0,84, surpassing other reconstruction resources and predicted known microbial drug transformations with an accuracy of 0,81. We demonstrate that AGORA2 enables personalized, strain-resolved modeling by predicting the drug conversion potential of the gut microbiomes from 616 patients with colorectal cancer and controls, which greatly varied between individuals and correlated with age, sex, body mass index and disease stages. AGORA2 serves as a knowledge base for the human microbiome and paves the way to personalized, predictive analysis of host microbiome metabolic interactions.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10602 - Biology (theoretical, mathematical, thermal, cryobiology, biological rhythm), Evolutionary biology
Result continuities
Project
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Continuities
S - Specificky vyzkum na vysokych skolach
Others
Publication year
2023
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
NATURE BIOTECHNOLOGY
ISSN
1087-0156
e-ISSN
1087-0156
Volume of the periodical
41
Issue of the periodical within the volume
1
Country of publishing house
CZ - CZECH REPUBLIC
Number of pages
22
Pages from-to
1320-1331
UT code for WoS article
000916149200003
EID of the result in the Scopus database
2-s2.0-85146589321