Direct identification of pathogens from positive blood cultures using matrix‐assisted laser desorption‐ionization time‐of‐flight mass spectrometry. (24th December 2013)

• Record Type: Journal Article
• Authors: Rodríguez‐Sánchez, B.; Sánchez‐Carrillo, C.; Ruiz, A.; Marín, M.; Cercenado, E.; Rodríguez‐Créixems, M.; Bouza, E.; Greub, G.
• Is Part Of: Clinical microbiology and infection. Volume 20:Number 7(2014:Jul.)
• Page Start: O421
• Page End: O427
• Publication Date: 2013-12-24
• Subjects: Medical microbiology -- Periodicals; Diagnostic microbiology -- Periodicals; Communicable diseases -- Periodicals; Infection -- Periodicals; 616.01
• DOI: 10.1111/1469-0691.12455
• Languages: English
• ISSNs: 1198-743X

Abstract

<abstract abstract-type="main" id="clm12455-abs-0001"> <title>Abstract</title> <p>In recent years, matrix‐assisted laser desorption‐ionization time‐of‐flight (MALDI‐TOF) mass spectrometry (MS) has proved a rapid and reliable method for the identification of bacteria and yeasts that have already been isolated. The objective of this study was to evaluate this technology as a routine method for the identification of microorganisms directly from blood culture bottles (BCBs), before isolation, in a large collection of samples. For this purpose, 1000 positive BCBs containing 1085 microorganisms have been analysed by conventional phenotypic methods and by MALDI‐TOF MS. Discrepancies have been resolved using molecular methods: the amplification and sequencing of the 16S rRNA gene or the Superoxide Dismutase gene (sodA) for streptococcal isolates. MALDI‐TOF predicted a species‐ or genus‐level identification of 81.4% of the analysed microorganisms. The analysis by episode yielded a complete identification of 814 out of 1000 analysed episodes (81.4%). MALDI‐TOF identification is available for clinicians within hours of a working shift, as oppose to 18 h later when conventional identification methods are performed. Moreover, although further improvement of sample preparation for polymicrobial BCBs is required, the identification of more than one pathogen in the same BCB provides a valuable indication of unexpected pathogens when their presence may remain undetected in Gram staining. Implementation of MALDI‐TOF identification directly from the BCB provides a rapid and reliable identification of the causal pathogen within hours.</p> </abstract>