Evidence map›Paper›PMID 40662835›Full record

ArticleBioinformatics (Oxford, England)2025

Leveraging large language models to predict antibiotic resistance in Mycobacterium tuberculosis.

Conrad Testagrose, Sakshi Pandey, Mohammadali Serajian, Simone Marini, Mattia Prosperi, Christina Boucher

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Conrad TestagroseDepartment of Computer and Information Science and Engineering, University of Florida, Gainesville, FL 32611, United States.
Sakshi PandeyDepartment of Computer and Information Science and Engineering, University of Florida, Gainesville, FL 32611, United States.
Mohammadali SerajianDepartment of Computer and Information Science and Engineering, University of Florida, Gainesville, FL 32611, United States.
Simone MariniDepartment of Epidemiology, University of Florida, Gainesville, FL 32601, United States.ORCID 0000-0002-5704-3533
Mattia ProsperiDepartment of Epidemiology, University of Florida, Gainesville, FL 32601, United States.ORCID 0000-0002-9021-5595
Christina BoucherDepartment of Computer and Information Science and Engineering, University of Florida, Gainesville, FL 32611, United States.

Funding

Developing Computational Methods for Surveillance of Antimicrobial Resistant AgentsR01AI141810 · NIAID · UNIVERSITY OF FLORIDA · PI BOUCHER, CHRISTINA, PROSPERI, MATTIA · 2019 to 2023
$2.1M
Artificial Intelligence and Complex Computational ResearchNIAID NIH HHS R01AI14180NIAID NIH HHS R01 AI141810NIHNSFSCH INT-2013998
6 · The paper itself

Abstract

motivationAntibiotic resistance in Mycobacterium tuberculosis (MTB) poses a significant challenge to global public health. Rapid and accurate prediction of antibiotic resistance can inform treatment strategies and mitigate the spread of resistant strains. In this study, we present a novel approach leveraging large language models (LLMs) to predict antibiotic resistance in MTB (LLMTB). Our model is trained and evaluated on genomic data from 12 185 CRyPTIC isolates and their associated resistance profiles, utilizing natural language processing techniques to capture patterns and mutations linked to resistance. The model's architecture integrates state-of-the-art transformer-based LLMs, enabling the analysis of complex genomic sequences and the extraction of critical features relevant to antibiotic resistance.

resultsWe evaluate our model's performance using a comprehensive dataset of MTB strains, demonstrating its ability to achieve high performance in predicting resistance to various antibiotics. Unlike traditional machine learning methods, fine-tuning or few-shot learning opens avenues for LLMs to adapt to new or emerging drugs, thereby reducing reliance on extensive data curation. Beyond predictive accuracy, LLMTB uncovers deeper biological insights, identifying critical genes, intergenic regions, and novel resistance mechanisms. This method marks a transformative shift in resistance prediction and offers significant potential for enhancing diagnostic capabilities and guiding personalized treatment plans, ultimately contributing to the global effort to combat tuberculosis and antibiotic resistance. AVAILABILITY AND IMPLEMENTATION: All source code is publicly available at https://github.com/ctestagrose/LLMTB.

Indexed as

Drug Resistance, BacterialMycobacterium tuberculosisNatural Language ProcessingComputational BiologyGenome, BacterialHumansLarge Language ModelsMachine LearningMutation

Identifiers

PMID40662835
PMCPMC12261485

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.