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Fast and Accurate Bacterial Species Identification in Urine Specimens Using LC-MS/MS Mass Spectrometry and Machine Learning.
Roux-Dalvai, Florence; Gotti, Clarisse; Leclercq, Mickaël; Hélie, Marie-Claude; Boissinot, Maurice; Arrey, Tabiwang N; Dauly, Claire; Fournier, Frédéric; Kelly, Isabelle; Marcoux, Judith; Bestman-Smith, Julie; Bergeron, Michel G; Droit, Arnaud.
Afiliación
  • Roux-Dalvai F; Proteomics platform, CHU de Québec - Université Laval Research Center, Québec City, Québec, Canada.
  • Gotti C; Proteomics platform, CHU de Québec - Université Laval Research Center, Québec City, Québec, Canada.
  • Leclercq M; Computational Biology Laboratory, CHU de Québec - Université Laval Research Center, Québec City, Québec, Canada.
  • Hélie MC; Centre de Recherche en Infectiologie de l'Université Laval, Axe Maladies Infectieuses et Immunitaires, Centre de Recherche du CHU de Québec-Université Laval, Québec City, Canada.
  • Boissinot M; Centre de Recherche en Infectiologie de l'Université Laval, Axe Maladies Infectieuses et Immunitaires, Centre de Recherche du CHU de Québec-Université Laval, Québec City, Canada.
  • Arrey TN; Thermo Fisher Scientific, Bremen, Germany.
  • Dauly C; Thermo Fisher Scientific, Bremen, Germany.
  • Fournier F; Proteomics platform, CHU de Québec - Université Laval Research Center, Québec City, Québec, Canada.
  • Kelly I; Proteomics platform, CHU de Québec - Université Laval Research Center, Québec City, Québec, Canada.
  • Marcoux J; Proteomics platform, CHU de Québec - Université Laval Research Center, Québec City, Québec, Canada.
  • Bestman-Smith J; Laboratoire de microbiologie-infectiologie, CHU de Québec-Université Laval, pavillon Hôpital de l'Enfant-Jésus, Québec City, Québec, Canada.
  • Bergeron MG; Centre de Recherche en Infectiologie de l'Université Laval, Axe Maladies Infectieuses et Immunitaires, Centre de Recherche du CHU de Québec-Université Laval, Québec City, Canada; Département de microbiologie-infectiologie et d'immunologie, Faculté de médecine, Université Laval, Québec City, Québec,
  • Droit A; Proteomics platform, CHU de Québec - Université Laval Research Center, Québec City, Québec, Canada; Computational Biology Laboratory, CHU de Québec - Université Laval Research Center, Québec City, Québec, Canada; Département de Médecine Moléculaire, Faculté de médecine, Université Laval, Québec City
Mol Cell Proteomics ; 18(12): 2492-2505, 2019 12.
Article en En | MEDLINE | ID: mdl-31585987
ABSTRACT
Fast identification of microbial species in clinical samples is essential to provide an appropriate antibiotherapy to the patient and reduce the prescription of broad-spectrum antimicrobials leading to antibioresistances. MALDI-TOF-MS technology has become a tool of choice for microbial identification but has several drawbacks it requires a long step of bacterial culture before analysis (≥24 h), has a low specificity and is not quantitative. We developed a new strategy for identifying bacterial species in urine using specific LC-MS/MS peptidic signatures. In the first training step, libraries of peptides are obtained on pure bacterial colonies in DDA mode, their detection in urine is then verified in DIA mode, followed by the use of machine learning classifiers (NaiveBayes, BayesNet and Hoeffding tree) to define a peptidic signature to distinguish each bacterial species from the others. Then, in the second step, this signature is monitored in unknown urine samples using targeted proteomics. This method, allowing bacterial identification in less than 4 h, has been applied to fifteen species representing 84% of all Urinary Tract Infections. More than 31,000 peptides in 190 samples were quantified by DIA and classified by machine learning to determine an 82 peptides signature and build a prediction model. This signature was validated for its use in routine using Parallel Reaction Monitoring on two different instruments. Linearity and reproducibility of the method were demonstrated as well as its accuracy on donor specimens. Within 4h and without bacterial culture, our method was able to predict the predominant bacteria infecting a sample in 97% of cases and 100% above the standard threshold. This work demonstrates the efficiency of our method for the rapid and specific identification of the bacterial species causing UTI and could be extended in the future to other biological specimens and to bacteria having specific virulence or resistance factors.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Bacterias / Proteínas Bacterianas / Bacteriuria / Cromatografía Liquida / Espectrometría de Masas en Tándem / Aprendizaje Automático Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Mol Cell Proteomics Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA Año: 2019 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Bacterias / Proteínas Bacterianas / Bacteriuria / Cromatografía Liquida / Espectrometría de Masas en Tándem / Aprendizaje Automático Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Mol Cell Proteomics Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA Año: 2019 Tipo del documento: Article País de afiliación: Canadá