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dc.contributor.authorZvezdanova, Margarita Estreya
dc.contributor.authorEscribano, Pilar
dc.contributor.authorRuiz, Adrián
dc.contributor.authorMartínez-Jiménez, María del Carmen
dc.contributor.authorPelaez, Teresa
dc.contributor.authorCollazos, Ana
dc.contributor.authorGuinea, Jesús
dc.contributor.authorBouza, Emilio
dc.contributor.authorRodríguez-Sánchez, Belén
dc.date.accessioned2024-02-05T14:20:01Z
dc.date.available2024-02-05T14:20:01Z
dc.date.issued2019
dc.identifier.citationof Medical Microbiology, 304(8), 1192-1198. https://doi.org/10.1016/j.ijmm.2014.08.012 Zvezdanova, M. E., Escribano, P., Ruiz, A., Martínez-Jiménez, M. C., Peláez, T., Collazos, A., Guinea, J., Bouza, E., & Rodríguez-Sánchez, B. (2019). Increased species-assignment of filamentous fungi using MALDI-TOF MS coupled with a simplified sample processing and an in-house library. Medical Mycology, 57(1), 63-70. https://doi.org/10.1093/mmy/myx154es
dc.identifier.issn1369-3786
dc.identifier.otherhttps://academic.oup.com/mmyes
dc.identifier.urihttp://hdl.handle.net/20.500.12020/1190
dc.description.abstractIn this study we evaluated the capacity of MALDI-TOF MS (Bruker Daltonics, Bremen, Germany) to identify clinical mould isolates. We focused on two aspects of MALDI-TOF MS identification: the sample processing and the database. Direct smearing of the sample was compared with a simplified processing consisting of mechanical lysis of the moulds followed by a protein extraction step. Both methods were applied to all isolates and the Filamentous Fungi Library 1.0 (Bruker Daltonics) was used for their identification. This approach allowed the correct species-level identification of 25/34 Fusarium spp. and 10/10 Mucor circinelloides isolates using the simplified sample processing. In addition, 7/34 Fusarium spp. and 1/21 Pseudallescheria/Scedosporium spp. isolates were correctly identified at the genus level. The remaining isolates–60–could not be identified using the commercial database, mainly because of the low number of references for some species and the absence of others. Thus, an in-house library was built with 63 local isolates previously characterized using DNA sequence analysis. Its implementation allowed the accurate identification at the species level of 94 isolates (91.3%) and the remaining nine isolates (8.7%) were correctly identified at the genus level. No misidentifications at genus level were detected. In conclusion, with improvements of both the sample preparation and the feeding of the database, MALDI-TOF MS is a reliable, ready to usemethod to identify moulds of clinical origin in an accurate, rapid, and cost-effective manner.es
dc.language.isoenes
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleIncreased species-assignment of filamentous fungi using MALDI-TOF MS coupled with a simplified sample processing and an in-house libraryes
dc.typearticlees
dc.identifier.doihttps://doi.org/10.1093/mmy/myx154
dc.issue.number1es
dc.journal.titleMedical Mycologyes
dc.page.initial63es
dc.page.final70es
dc.relation.projectIDThis study has been supported by the Miguel Servet Program (Carlos III Health Institute and Ministry of Science and Innovation (ISCIII-MICINN) CP14/00220) from the Health Research Fund (FIS) of the Carlos III Health Institute (ISCIII), Madrid, Spain, partially financed by the by the European Regional Development Fund (FEDER) ‘A way of making Europe.’ BRS (CPI14/00220),es
dc.rights.accessRightsopenAccesses
dc.subject.areaCiencias Biomédicases
dc.subject.keywordFilamentous Fungies
dc.subject.keywordRoutine identificationes
dc.subject.keywordMALDI-TOF MSes
dc.subject.keywordGene sequencinges
dc.subject.unesco2414 Microbiologíaes
dc.volume.number57es


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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