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dc.contributor.authorYang, Jason H
dc.contributor.authorWright, Sarah N
dc.contributor.authorHamblin, Meagan
dc.contributor.authorMcCloskey, Douglas
dc.contributor.authorAlcantar, Miguel A
dc.contributor.authorSchrübbers, Lars
dc.contributor.authorLopatkin, Allison J
dc.contributor.authorSatish, Sangeeta
dc.contributor.authorNili, Amir
dc.contributor.authorPalsson, Bernhard O
dc.contributor.authorWalker, Graham C
dc.contributor.authorCollins, James J
dc.date.accessioned2021-10-27T20:11:08Z
dc.date.available2021-10-27T20:11:08Z
dc.date.issued2019
dc.identifier.urihttps://hdl.handle.net/1721.1/135182
dc.description.abstract© 2019 Elsevier Inc. Current machine learning techniques enable robust association of biological signals with measured phenotypes, but these approaches are incapable of identifying causal relationships. Here, we develop an integrated “white-box” biochemical screening, network modeling, and machine learning approach for revealing causal mechanisms and apply this approach to understanding antibiotic efficacy. We counter-screen diverse metabolites against bactericidal antibiotics in Escherichia coli and simulate their corresponding metabolic states using a genome-scale metabolic network model. Regression of the measured screening data on model simulations reveals that purine biosynthesis participates in antibiotic lethality, which we validate experimentally. We show that antibiotic-induced adenine limitation increases ATP demand, which elevates central carbon metabolism activity and oxygen consumption, enhancing the killing effects of antibiotics. This work demonstrates how prospective network modeling can couple with machine learning to identify complex causal mechanisms underlying drug efficacy. Causal metabolic pathways underlying antibiotic lethality in bacteria are illuminated by a network model-driven machine learning approach, overcoming limitations of existing “black-box” approaches that cannot reveal causal relationships from large biological datasets.
dc.language.isoen
dc.publisherElsevier BV
dc.relation.isversionof10.1016/J.CELL.2019.04.016
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs License
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourcePMC
dc.titleA White-Box Machine Learning Approach for Revealing Antibiotic Mechanisms of Action
dc.typeArticle
dc.contributor.departmentMassachusetts Institute of Technology. Institute for Medical Engineering & Science
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineering
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biology
dc.relation.journalCell
dc.eprint.versionAuthor's final manuscript
dc.type.urihttp://purl.org/eprint/type/JournalArticle
eprint.statushttp://purl.org/eprint/status/PeerReviewed
dc.date.updated2020-06-19T17:13:01Z
dspace.orderedauthorsYang, JH; Wright, SN; Hamblin, M; McCloskey, D; Alcantar, MA; Schrübbers, L; Lopatkin, AJ; Satish, S; Nili, A; Palsson, BO; Walker, GC; Collins, JJ
dspace.date.submission2020-06-19T17:13:03Z
mit.journal.volume177
mit.journal.issue6
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Needed


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