Predicting antimicrobial resistance in Pseudomonas aeruginosa with machine learning-enabled molecular diagnostics.

Journal: EMBO molecular medicine
Published Date:

Abstract

Limited therapy options due to antibiotic resistance underscore the need for optimization of current diagnostics. In some bacterial species, antimicrobial resistance can be unambiguously predicted based on their genome sequence. In this study, we sequenced the genomes and transcriptomes of 414 drug-resistant clinical Pseudomonas aeruginosa isolates. By training machine learning classifiers on information about the presence or absence of genes, their sequence variation, and expression profiles, we generated predictive models and identified biomarkers of resistance to four commonly administered antimicrobial drugs. Using these data types alone or in combination resulted in high (0.8-0.9) or very high (> 0.9) sensitivity and predictive values. For all drugs except for ciprofloxacin, gene expression information improved diagnostic performance. Our results pave the way for the development of a molecular resistance profiling tool that reliably predicts antimicrobial susceptibility based on genomic and transcriptomic markers. The implementation of a molecular susceptibility test system in routine microbiology diagnostics holds promise to provide earlier and more detailed information on antibiotic resistance profiles of bacterial pathogens and thus could change how physicians treat bacterial infections.

Authors

  • Ariane Khaledi
    Department of Molecular Bacteriology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
  • Aaron Weimann
    Molecular Bacteriology Group, TWINCORE-Centre for Experimental and Clinical Infection Research, Hannover, Germany.
  • Monika Schniederjans
    Department of Molecular Bacteriology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
  • Ehsaneddin Asgari
    Molecular Cell Biomechanics Laboratory, Departments of Bioengineering and Mechanical Engineering, University of California, Berkeley, California 94720, United States of America.
  • Tzu-Hao Kuo
    Institute of Biomedical Informatics, National Yang-Ming University, Taipei 112, Taiwan. kzvito@gmail.com.
  • Antonio Oliver
    Servicio de Microbiología y Unidad de Investigación Hospital Universitario Son Espases, Instituto de Investigación Sanitaria Illes Balears (IdISPa), Palma de Mallorca, Spain.
  • Gabriel Cabot
    Servicio de Microbiología y Unidad de Investigación Hospital Universitario Son Espases, Instituto de Investigación Sanitaria Illes Balears (IdISPa), Palma de Mallorca, Spain.
  • Axel Kola
    Institute of Hygiene and Environmental Medicine, Charité - Universitätsmedizin Berlin, Berlin, Germany.
  • Petra Gastmeier
    Institute of Hygiene and Environmental Medicine, Charité - Universitätsmedizin Berlin, Berlin, Germany.
  • Michael Hogardt
    Institute of Medical Microbiology and Infection Control, University Hospital Frankfurt, Frankfurt/Main, Germany.
  • Daniel Jonas
    Faculty of Medicine, Institute for Infection Prevention and Hospital Epidemiology, Medical Center-University of Freiburg, Freiburg, Germany.
  • Mohammad Rk Mofrad
    Molecular Cell Biomechanics Laboratory, Departments of Bioengineering and Mechanical Engineering, University of California, Berkeley, CA, USA.
  • Andreas Bremges
    Computational Biology of Infection Research, Helmholtz Centre for Infection Research, Braunschweig, Germany.
  • Alice C McHardy
    Computational Biology of Infection Research, Helmholtz Centre for Infection Research, Braunschweig, Germany.
  • Susanne Häußler
    Institute of Animal Science, Physiology and Hygiene Unit, University of Bonn, Bonn 53115, Germany.