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. 2014 May;52(5):1453–1458. doi: 10.1128/JCM.03355-13

TABLE 3.

Performance of the UCSC yeast database for Candida and non-Candida clinical isolates prospectively tested by MALDI-TOF MS analysisa

Organism No. of isolates tested No. of isolates with score of:
>2.0b ≥1.7 but <2.0c <1.7d
Species included in the database
    C. albicans 2,924 2,882 42 0
    C. glabrata 642 639 3 0
    C. parapsilosis 210 163 47 0
    C. tropicalis 203 176 27 0
    S. cerevisiae 178 157 21 0
    C. krusei 18 8 10 0
    C. norvegensis 12 2 10 0
    C. dubliniensis 5 5 0 0
    C. kefyr 5 2 2 1
    C. neoformans 5 4 1 0
    C. guilliermondii 3 2 0 1
    C. nivariensis 3 2 0 1
    T. inkin 3 1 1 1
    C. lusitaniae 2 0 1 1
    C. lambica 1 0 0 1
    C. pararugosa 1 0 0 1
    C. utilis 1 0 0 1
    G. candidum 1 0 0 1
    L. elongisporus 1 0 0 1
    P. caribbica 1 0 0 1
    P. membranifaciens 1 0 0 1
    T. asteroides 1 0 1 0
    Total 4,221 4,043 166 12
Species not included in the database
    Arxiozyma telluris 1 0 0 1
    Candida aaseri 1 0 0 1
    Candida blankii 1 0 0 1
    Candida famata 1 0 0 1
    Candida lipolytica 1 0 0 1
    Candida sloffiae 1 0 0 1
    Malassezia pachydermatis 1 0 0 1
    Pichia fabianii 1 0 0 1
    Rhodotorula glutinis 1 0 0 1
    Rhodotorula sloffiae 1 0 0 1
    Williopsis sp. 1 0 0 1
    Total 11 0 0 11
Overall species 4,232 4,043 166 23
ID (%) at the first run 95.5 4.0 0.5
ID (%) at the second run 99.5 0 0.5
a

Isolates were treated with the fast extraction protocol prior to MALDI-TOF MS analysis for identification.

b

A total of 1,676 (39.6%) isolates with scores of ≥2.3 (high-probable species identification by Bruker Daltonics) were from C. albicans (1,046 isolates), C. glabrata (491 isolates), C. parapsilosis (35 isolates), C. tropicalis (46 isolates), S. cerevisiae (32 isolates), C. krusei (8 isolates), C. norvegensis (2 isolates), C. dubliniensis (5 isolates), C. kefyr (2 isolates), C. neoformans (4 isolates), C. guilliermondii (2 isolates), and C. nivariensis (2 isolates).

c

Isolates were all identified to the species level after the second run of MALDI-TOF MS analysis.

d

Isolates were all identified by the rDNA sequence-based method.