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Prediction of antibiotic resistance mechanisms using a protein language model
Open accessPreprint — published as 10.1093/bioinformatics/btae550 · Paper page
Abstract
Motivation: Antibiotic resistance has emerged as a major global health threat, with an increasing number of bacterial infections becoming difficult to treat. Predicting the underlying resistance mechanisms of antibiotic resistance genes (ARGs) is crucial for understanding and combating this problem. However, existing methods struggle to accurately predict resistance mechanisms for ARGs with low similarity to known sequences and lack sufficient interpretability of the prediction models. Results: In this study, we present a novel approach for predicting ARG resistance mechanisms using Protein-BERT, a protein language model based on deep learning. Our method outperforms state-of-the-art techniques on diverse ARG datasets, including those with low homology to the training data, highlighting its potential for predicting the resistance mechanisms of unknown ARGs. Attention analysis of the model reveals that it considers biologically relevant features, such as conserved amino acid residues and antibiotic target binding sites, when making predictions. These findings provide valuable insights into the molecular basis of antibiotic resistance and demonstrate the interpretability of protein language models, offering a new perspective on their application in bioinformatics. Availability: The source code is available for free at https://github.com/hmdlab/ARG-BERT . The output results of the model are published at https://waseda.box.com/v/ARG-BERT-suppl . Contact: mhamada@waseda.jp
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Metadata
- Authors
- Yagimoto, K., Hosoda, S., Sato, M., & Hamada, M.
- Affiliations
- Waseda University (JP)
- Hitachi (Japan) (JP)
- Corresponding author
- Hamada, Michiaki
- Venue
- Bioinformatics
- Publisher
- openRxiv
- Published
- 2024-05-06
- Volume
- 40
- Issue
- 10
- ISSN
- 1367-4803 (ISSN-L)
- PMC
- PMC11464418
- OpenAlex
- W4402428761
- Cited by
- 25
- References
- 1
- Citations by year
- 2026: 18 · 2025: 6 · 2024: 1
- FWCI
- 3.12
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- Bioinformatics (publishedVersion, cc-by)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- Japan Agency for Medical Research and Development (JP22ama121055, JP21ae0121049, JP21gm0010008)
- Japan Society for the Promotion of Science (22H04925, 23H00509, 20H00624)
- Topics
- Health Sciences › Medicine › Microbiology (medical) › Antibiotic Resistance in Bacteria
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Machine Learning in Bioinformatics
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Drug Discovery › Computational Drug Discovery Methods
- Keywords
- antibiotic resistance mechanisms, antibiotic resistance genes, protein language models, interpretability, attention analysis, conserved residues, bacterial antibiotic resistance
- MeSH terms
- Deep Learning, Anti-Bacterial Agents, Drug Resistance, Microbial, Computational Biology, Drug Resistance, Bacterial
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