Machine Learning Assisted MALDI Mass Spectrometry for Rapid Antimicrobial Resistance Prediction in Clinicals.

Journal: Analytical chemistry
PMID:

Abstract

Antimicrobial susceptibility testing (AST) plays a critical role in assessing the resistance of individual microbial isolates and determining appropriate antimicrobial therapeutics in a timely manner. However, conventional AST normally takes up to 72 h for obtaining the results. In healthcare facilities, the global distribution of vancomycin-resistant (VRE) infections underscores the importance of rapidly determining VRE isolates. Here, we developed an integrated antimicrobial resistance (AMR) screening strategy by combining matrix-assisted laser desorption ionization mass spectrometry (MALDI-MS) with machine learning to rapidly predict VRE from clinical samples. Over 400 VRE and vancomycin-susceptible (VSE) isolates were analyzed using MALDI-MS at different culture times, and a comprehensive dataset comprising 2388 mass spectra was generated. Algorithms including the support vector machine (SVM), SVM with L1-norm, logistic regression, and multilayer perceptron (MLP) were utilized to train the classification model. Validation on a panel of clinical samples (external patients) resulted in a prediction accuracy of 78.07%, 80.26%, 78.95%, and 80.54% for each algorithm, respectively, all with an AUROC above 0.80. Furthermore, a total of 33 mass regions were recognized as influential features and elucidated, contributing to the differences between VRE and VSE through the Shapley value and accuracy, while tandem mass spectrometry was employed to identify the specific peaks among them. Certain ribosomal proteins, such as A0A133N352 and R2Q455, were tentatively identified. Overall, the integration of machine learning with MALDI-MS has enabled the rapid determination of bacterial antibiotic resistance, greatly expediting the usage of appropriate antibiotics.

Authors

  • Weibo Gao
    Department of Radiology, Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710004, Shannxi, China.
  • Hang Li
    Beijing Academy of Quantum Information Sciences, Beijing 100193, China.
  • Jingxian Yang
    Department of Clinical Laboratory, Aerospace Center Hospital, Beijing 100039, China.
  • Jinming Zhang
    Key Laboratory for Biomechanics and Mechanobiology of Chinese Education Ministry, Beijing Advanced Innovation Centre for Biomedical Engineering, School of Biological Science and Medical Engineering, Beihang University, Beijing 100083, People's Republic of China.
  • Rongxin Fu
    Department of Biomedical Engineering, School of Medicine, Tsinghua University, Beijing, China.
  • Jiaxi Peng
    Department of Chemistry, University of Toronto, Toronto ON M5S 3H6, Canada.
  • Yechen Hu
    Department of Chemistry, University of Toronto, Toronto ON M5S 3H6, Canada.
  • Yitong Liu
    Science of Information and Communication Engineering, Beijing University of Posts and Telecommunications, Beijing 100876, China.
  • Yingshi Wang
    Department of Clinical Laboratory, Aerospace Center Hospital, Beijing 100039, China.
  • Shuang Li
    Clinical and Research Center for Infectious Diseases, Beijing Youan Hospital, Capital Medical University, Beijing, China.
  • Shuailong Zhang
    Donnelly Centre for Cellular and Biomolecular Research, University of Toronto, Toronto, ON M5S 3E1, Canada.