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Predicting and generating antibiotics against future pathogens with ApexOracle

arXiv 2507.07862 ↗First posted 10 Jul 2025cs.LG q-bio.QMcited by 0

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Abstract (arXiv)

Antimicrobial resistance (AMR) is escalating and outpacing current antibiotic development. Thus, discovering antibiotics effective against emerging pathogens is becoming increasingly critical. However, existing approaches cannot rapidly identify effective molecules against novel pathogens or emerging drug-resistant strains. Here, we introduce ApexOracle, an artificial intelligence (AI) model that both predicts the antibacterial potency of existing compounds and designs de novo molecules active against strains it has never encountered. Departing from models that rely solely on molecular features, ApexOracle incorporates pathogen-specific context through the integration of molecular features captured via a foundational discrete diffusion language model and a dual-embedding framework that combines genomic- and literature-derived strain representations. Across diverse bacterial species and chemical modalities, ApexOracle consistently outperformed state-of-the-art approaches in activity prediction and demonstrated reliable transferability to novel pathogens with little or no antimicrobial data. Its unified representation-generation architecture further enables the in silico creation of "new-to-nature" molecules with high predicted efficacy against priority threats. By pairing rapid activity prediction with targeted molecular generation, ApexOracle offers a scalable strategy for countering AMR and preparing for future infectious-disease outbreaks.

Key facts. No citing papers in the map yet (data through 14 Oct 2026). Builds on 8 of its 52 references that are in the map. First posted on arXiv 10 Jul 2025.

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References · 8

  1. 2022Scalable Diffusion Models with Transformerscited by 6,054
  2. 2024Qwen2.5 Technical Reportcited by 4,942
  3. 2024Simple and Effective Masked Diffusion Language Modelscited by 848
  4. 2021Large-Scale Chemical Language Representations Capture Molecular Structure and Propertiescited by 206
  5. 2024Simple Guidance Mechanisms for Discrete Diffusion Modelscited by 155
  6. 2022ChemBERTa-2: Towards Chemical Foundation Modelscited by 127
  7. 2023A Group Symmetric Stochastic Differential Equation Model for Molecule Multi-modal Pretrainingcited by 32
  8. 2024UniGEM: A Unified Approach to Generation and Property Prediction for Moleculescited by 21

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  6. 2026Agentic Discovery of Non-Canonical Antimicrobial Peptides with AMPGAN v3
  7. 2026Bridging the Evidence-to-Execution Gap:A Reflective Agent for Multi-Objective Peptide Design
  8. 2026MAC-AMP: A Closed-Loop Multi-Agent Collaboration System for Multi-Objective Antimicrobial Peptide Design