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Exploratory Study on Application of MALDI-TOF-MS to Detect SARS-CoV-2 Infection in Human Saliva
Monique Melo Costa1,2,3, Hugo Martin1,2,3, Bertrand Estellon4
1Unité Parasitologie et Entomologie, Département Microbiologie et Maladies Infectieuses, Institut de Recherche Biomédicale des Armées, 91220 Marseille, France.
A new PCR-free method using mass spectrometry and machine learning on saliva samples shows promise for diagnosing COVID-19. This approach offers a potential alternative to RT-qPCR, especially for initial diagnosis and later stages of infection.
Area of Science:
- Biotechnology
- Infectious Disease Diagnostics
- Computational Biology
Background:
- The COVID-19 pandemic necessitated rapid and accurate diagnostic methods.
- Current gold standard, RT-qPCR, has limitations including invasiveness, cost, and supply chain issues.
- Development of alternative, non-invasive diagnostic tools is crucial for managing outbreaks.
Purpose of the Study:
- To develop and evaluate a PCR-free diagnostic method for SARS-CoV-2 using MALDI-TOF MS and ML on saliva.
- To compare the performance of this novel method against RT-qPCR for COVID-19 diagnosis.
- To assess the diagnostic utility of MALDI-TOF MS and ML profiling of saliva across different time points post-infection.
Main Methods:
- Saliva samples were collected from COVID-19 positive patients and healthy controls at D0, D10, and D30.
- Matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) was used to generate spectral profiles.
- Machine learning models, including Support Vector Machine with Linear Kernel (SVM-LK), were trained and tested for classification.
Main Results:
- Nine spectral peaks significantly differentiated SARS-CoV-2 positive patients from controls at D0.
- The SVM-LK model achieved high accuracy (85.2%) on the training set and 88.9% on D0 independent samples.
- Performance decreased at later time points, with 80.8% accuracy at D30 and 64.3% at D10.
Conclusions:
- MALDI-TOF MS combined with ML offers a promising PCR-free supplementary tool for COVID-19 diagnosis.
- The method demonstrates strong performance for initial diagnosis and later stages (D30).
- Diagnostic accuracy is reduced for convalescent samples (D10), indicating potential limitations for this specific time window.
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