Deep Learning of Dual Plasma Fingerprints for High‐Performance Infection Classification

Abstract Infection classification is the key for choosing the proper treatment plans. Early determination of the causative agents is critical for disease control. Host responses analysis can detect variform and sensitive host inflammatory responses to ascertain the presence and type of the infection. However, traditional host‐derived inflammatory indicators are insufficient for clinical infection classification. Fingerprints‐based omic analysis has attracted increasing attention globally for analyzing the complex host systemic immune response. A single type of fingerprints is not applicable for infection classification (area under curve (AUC) of 0.550–0.617). Herein, an infection classification platform based on deep learning of dual plasma fingerprints (DPFs‐DL) is developed. The DPFs with high reproducibility (coefficient of variation <15%) are obtained at low sample consumption (550 nL native plasma) using inorganic nanoparticle and organic matrix assisted laser desorption/ionization mass spectrometry. A classifier (DPFs‐DL) for viral versus bacterial infection discrimination (AUC of 0.775) and coronavirus disease 2019 (COVID‐2019) diagnosis (AUC of 0.917) is also built. Furthermore, a metabolic biomarker panel of two differentially regulated metabolites, which may serve as potential biomarkers for COVID‐19 management (AUC of 0.677–0.883), is constructed. This study will contribute to the development of precision clinical care for infectious diseases.