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Transfer learning predicts species-specific drug interactions in emerging pathogens.
Chung, Carolina H; Chang, David C; Rhoads, Nicole M; Shay, Madeline R; Srinivasan, Karthik; Okezue, Mercy A; Brunaugh, Ashlee D; Chandrasekaran, Sriram.
Afiliação
  • Chung CH; Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI, 48109, USA.
  • Chang DC; Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI, 48109, USA.
  • Rhoads NM; Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI, 48109, USA.
  • Shay MR; Department of Pharmacology, University of Michigan, Ann Arbor, MI, 48109, USA.
  • Srinivasan K; Cellular and Molecular Biology Program, University of Michigan Medical School, Ann Arbor, MI, 48109, USA.
  • Okezue MA; Department of Ophthalmology and Visual Sciences, University of Michigan Medical School, Ann Arbor, MI, 48109, USA.
  • Brunaugh AD; Department of Pharmaceutical Sciences, University of Michigan College of Pharmacy, Ann Arbor, MI, 48109, USA.
  • Chandrasekaran S; Department of Pharmaceutical Sciences, University of Michigan College of Pharmacy, Ann Arbor, MI, 48109, USA.
bioRxiv ; 2024 Jun 06.
Article em En | MEDLINE | ID: mdl-38895385
ABSTRACT
Machine learning (ML) algorithms are necessary to efficiently identify potent drug combinations within a large candidate space to combat drug resistance. However, existing ML approaches cannot be applied to emerging and under-studied pathogens with limited training data. To address this, we developed a transfer learning and crowdsourcing framework (TACTIC) to train ML models on data from multiple bacteria. TACTIC was built using 2,965 drug interactions from 12 bacterial strains and outperformed traditional ML models in predicting drug interaction outcomes for species that lack training data. Top TACTIC model features revealed genetic and metabolic factors that influence cross-species and species-specific drug interaction outcomes. Upon analyzing ~600,000 predicted drug interactions across 9 metabolic environments and 18 bacterial strains, we identified a small set of drug interactions that are selectively synergistic against Gram-negative (e.g., A. baumannii) and non-tuberculous mycobacteria (NTM) pathogens. We experimentally validated synergistic drug combinations containing clarithromycin, ampicillin, and mecillinam against M. abscessus, an emerging pathogen with growing levels of antibiotic resistance. Lastly, we leveraged TACTIC to propose selectively synergistic drug combinations to treat bacterial eye infections (endophthalmitis).

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article