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Enhanced diagnosis of multi-drug-resistant microbes using group association modeling and machine learning

Author

Listed:
  • Julian G. Saliba

    (Tulane University School of Medicine
    Tulane University School of Science and Engineering)

  • Wenshu Zheng

    (Tulane University School of Medicine
    Tulane University School of Medicine)

  • Qingbo Shu

    (Tulane University School of Medicine
    Tulane University School of Medicine)

  • Liqiang Li

    (Shenzhen Third People’s Hospital
    National Clinical Research Center for Infectious Diseases)

  • Chi Wu

    (Shenzhen Third People’s Hospital
    National Clinical Research Center for Infectious Diseases)

  • Yi Xie

    (Sichuan University)

  • Christopher J. Lyon

    (Tulane University School of Medicine
    Tulane University School of Medicine)

  • Jiuxin Qu

    (Shenzhen Third People’s Hospital
    National Clinical Research Center for Infectious Diseases)

  • Hairong Huang

    (Beijing Chest Hospital of Capital Medical University)

  • Binwu Ying

    (Sichuan University)

  • Tony Ye Hu

    (Tulane University School of Medicine
    Tulane University School of Medicine)

Abstract

New solutions are needed to detect genotype-phenotype associations involved in microbial drug resistance. Herein, we describe a Group Association Model (GAM) that accurately identifies genetic variants linked to drug resistance and mitigates false-positive cross-resistance artifacts without prior knowledge. GAM analysis of 7,179 Mycobacterium tuberculosis (Mtb) isolates identifies gene targets for all analyzed drugs, revealing comparable performance but fewer cross-resistance artifacts than World Health Organization (WHO) mutation catalogue approach, which requires expert rules and precedents. GAM also reveals generalizability, demonstrating high predictive accuracy with 3,942 S. aureus isolates. GAM refinement by machine learning (ML) improves predictive accuracy with small or incomplete datasets. These findings were validated using 427 Mtb isolates from three sites, where GAM inputs are also found to be more suitable in ML prediction models than WHO inputs. GAM + ML could thus address the limitations of current drug resistance prediction methods to improve treatment decisions for drug-resistant microbial infections.

Suggested Citation

  • Julian G. Saliba & Wenshu Zheng & Qingbo Shu & Liqiang Li & Chi Wu & Yi Xie & Christopher J. Lyon & Jiuxin Qu & Hairong Huang & Binwu Ying & Tony Ye Hu, 2025. "Enhanced diagnosis of multi-drug-resistant microbes using group association modeling and machine learning," Nature Communications, Nature, vol. 16(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-58214-6
    DOI: 10.1038/s41467-025-58214-6
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    References listed on IDEAS

    as
    1. Natalie J. E. Waller & Chen-Yi Cheung & Gregory M. Cook & Matthew B. McNeil, 2023. "The evolution of antibiotic resistance is associated with collateral drug phenotypes in Mycobacterium tuberculosis," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
    2. Danesh Moradigaravand & Martin Palm & Anne Farewell & Ville Mustonen & Jonas Warringer & Leopold Parts, 2018. "Prediction of antibiotic resistance in Escherichia coli from large-scale pan-genome data," PLOS Computational Biology, Public Library of Science, vol. 14(12), pages 1-17, December.
    3. Maha R. Farhat & Luca Freschi & Roger Calderon & Thomas Ioerger & Matthew Snyder & Conor J. Meehan & Bouke de Jong & Leen Rigouts & Alex Sloutsky & Devinder Kaur & Shamil Sunyaev & Dick van Soolingen , 2019. "GWAS for quantitative resistance phenotypes in Mycobacterium tuberculosis reveals resistance genes and regulatory regions," Nature Communications, Nature, vol. 10(1), pages 1-11, December.
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