Comparison of the Vitek MS and Bruker Matrix-Assisted Laser Desorption Ionization-Time of Flight Mass Spectrometry Systems for Identification of Rhodococcus equi and Dietzia spp.

dc.contributor.authorde Alegría Puig, Carlos Ruiz
dc.contributor.authorPilares, Lilian
dc.contributor.authorMarco, Francesc
dc.contributor.authorVila, Jordi
dc.contributor.authorMartínez-Martínez, Luis
dc.contributor.authorNavas, Jesús
dc.date.accessioned2025-01-07T15:37:58Z
dc.date.available2025-01-07T15:37:58Z
dc.date.issued2017-05-10
dc.description.abstractRhodococcus equi causes pyogranulomatous pneumonia in domesticated animals and immunocompromised humans. Dietzia spp. are environmental bacteria that have rarely been associated with human infections. R. equi and Dietzia spp. are closely related actinomycetes. Phenotypic discrimination between R. equi and Dietzia on the basis of their Gram stain morphology and colony appearance is problematic. Matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS) is a fast, reliable, and cost-effective method for identification of a wide variety of microorganisms. We have evaluated the performance of Bruker Biotyper versus that of Vitek MS for identification of a collection of 154 isolates identified at the source as R. equi that includes isolates belonging to the genus Dietzia PCR amplification of the choE gene, encoding a cholesterol oxidase, and 16S rRNA sequencing were considered the reference methods for R. equi identification. Biotyper identified 131 (85.1%) of the 154 isolates at the species level, and this figure increased to 152 (98.7%) when the species cutoff was reduced from a score of ≥2.000 to ≥1.750. Vitek MS correctly identified at the species level 130 (84.4%) isolates as long as bacteria were extracted with ethanol but only 35 (22.7%) isolates when samples were prepared by direct extraction from colonies. The two systems allowed differentiation between R. equi and Dietzia spp., but identification of all Dietzia sp. isolates at the species level needed sequencing of the 16S rRNA gene.
dc.identifier.doi10.1128/JCM.00377-17
dc.identifier.essn1098-660X
dc.identifier.pmcPMC5483928
dc.identifier.pmid28490491
dc.identifier.pubmedURLhttps://pmc.ncbi.nlm.nih.gov/articles/PMC5483928/pdf
dc.identifier.unpaywallURLhttps://jcm.asm.org/content/jcm/55/7/2255.full.pdf
dc.identifier.urihttps://hdl.handle.net/10668/27285
dc.issue.number7
dc.journal.titleJournal of clinical microbiology
dc.journal.titleabbreviationJ Clin Microbiol
dc.language.isoen
dc.organizationSAS - Hospital Universitario Virgen del Rocío
dc.page.number2255-2260
dc.pubmedtypeComparative Study
dc.pubmedtypeEvaluation Study
dc.pubmedtypeJournal Article
dc.rights.accessRightsopen access
dc.subjectDietzia spp.
dc.subjectMALDI-TOF MS
dc.subjectRhodococcus equi
dc.subjectgenotypic identification
dc.subjectidentification
dc.subject.meshActinobacteria
dc.subject.meshBacteriological Techniques
dc.subject.meshDNA, Bacterial
dc.subject.meshDNA, Ribosomal
dc.subject.meshHumans
dc.subject.meshRNA, Ribosomal, 16S
dc.subject.meshSensitivity and Specificity
dc.subject.meshSequence Analysis, DNA
dc.subject.meshSpectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
dc.titleComparison of the Vitek MS and Bruker Matrix-Assisted Laser Desorption Ionization-Time of Flight Mass Spectrometry Systems for Identification of Rhodococcus equi and Dietzia spp.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number55

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