Development of a clinically comprehensive database and a simple procedure for identification of molds from solid media by matrix-assisted laser desorption ionization …

AF Lau, SK Drake, LB Calhoun… - Journal of clinical …, 2013 - Am Soc Microbiol
AF Lau, SK Drake, LB Calhoun, CM Henderson, AM Zelazny
Journal of clinical microbiology, 2013Am Soc Microbiol
Matrix-assisted laser desorption ionization–time of flight mass spectrometry (MALDI-TOF
MS) is a powerful tool for the rapid and highly accurate identification of clinical pathogens
but has not been utilized extensively in clinical mycology due to challenges in developing an
effective protein extraction method and the limited databases available. Here, we developed
an alternate extraction procedure and constructed a highly stringent database comprising
294 individual isolates representing 76 genera and 152 species. To our knowledge, this is …
Abstract
Matrix-assisted laser desorption ionization–time of flight mass spectrometry (MALDI-TOF MS) is a powerful tool for the rapid and highly accurate identification of clinical pathogens but has not been utilized extensively in clinical mycology due to challenges in developing an effective protein extraction method and the limited databases available. Here, we developed an alternate extraction procedure and constructed a highly stringent database comprising 294 individual isolates representing 76 genera and 152 species. To our knowledge, this is the most comprehensive clinically relevant mold database developed to date. When challenged with 421 blinded clinical isolates from our institution, by use of the BioTyper software, accurate species-level (score of ≥2.0) and genus-level (score of ≥1.7) identifications were obtained for 370 (88.9%) and 18 (4.3%) isolates, respectively. No isolates were misidentified. Of the 33 isolates (7.8%) for which there was no identification (score of <1.7), 25 were basidiomycetes not associated with clinical disease and 8 were Penicillium species that were not represented in the database. Our library clearly outperformed the manufacturer's database that was obtained with the instrument, which identified only 3 (0.7%) and 26 (6.2%) isolates at species and genus levels, respectively. Identification was not affected by different culture conditions. Implementation into our routine workflow has revolutionized our mycology laboratory efficiency, with improved accuracy and decreased time for mold identification, eliminating reliance on traditional phenotypic features.
American Society for Microbiology