Faculty Opinions recommendation of A deep learning approach to antibiotic discovery.

Serge Mostowy, Ana T. López-Jiménez

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature 2020 peer-review

importance 8/10 partially solved Computational Drug Discovery Methods antibiotic drug discovery stage: research

Rapidly emerging antibiotic-resistant bacteria create an urgent need for new antibiotics with novel structures.

Antibiotic resistance threatens treatment of tuberculosis and drug-resistant pathogens like carbapenem-resistant Enterobacteriaceae.

A trained deep neural network predicted antibacterial activity across chemical libraries, discovering halicin plus eight other antibacterial compounds structurally unlike known antibiotics.

From 23 empirically tested predictions out of >107 million ZINC15 molecules, 8 antibacterial compounds identified; halicin active against M. tuberculosis and carbapenem-resistant Enterobacteriaceae and treated C. difficile and pan-resistant A. baumannii in murine models.

Deep learning yielded structurally novel antibiotic leads validated in vitro and in mouse models.

Venue Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
Published 2020
Work type peer-review
Authors Serge Mostowy, Ana T. López-Jiménez
Citations 0 (OpenAlex, at import time)
Model or method deep neural network
Organization not stated in source
Primary source https://doi.org/10.3410/f.737402248.793574353
Open access closed
Keywords halicin, antibiotic resistance, deep learning, drug discovery, ZINC15
8 / 10

major — millions of lives, an industry or a field

Abstract frames antibiotic resistance as rapidly emerging with growing need for new antibiotics; compounds active against M. tuberculosis, carbapenem-resistant Enterobacteriaceae, pan-resistant A. baumannii; no scale numbers.

Basis: inferred. Judged from the source text, which gives no explicit scale. Stated scale: not stated in source. Method and limits.

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