Affiliation:
1. Laboratoire de Bactériologie-Hygiène, Institut Fédératif de Biologie, Centre Hospitalo-Universitaire, Toulouse, France
2. Université Paul Sabatier-Toulouse III, Toulouse, France
Abstract
ABSTRACT
Discrimination between
Streptococcus pneumoniae
and its close relatives of the viridans group is a common difficulty in matrix-assisted laser desorption ionization–time of flight (MALDI-TOF) mass spectrometry-based identification. In the present study, the performances of the Vitek MS MALDI-TOF mass spectrometry system were assessed using 334 pneumococci, 166 other
S. mitis
group streptococci, 184 non-
S. mitis
group streptococci, and 19 related alpha- and nonhemolytic aerobic Gram-positive catalase-negative coccal isolates. Pneumococci had been identified by means of optochin susceptibility and bile solubility or serotyping, and other isolates mainly by use of RapidID32 Strep strips. In case of discordant or low-discrimination results, genotypic methods were used. The sensitivity of the Vitek MS for the identification of
S. pneumoniae
was 99.1%, since only three bile-insoluble isolates were misidentified as
Streptococcus mitis
/
Streptococcus oralis
. Conversely, two optochin-resistant pneumococci were correctly identified (specificity, 100%). Three
Streptococcus pseudopneumoniae
isolates were also correctly identified. Among nonpneumococcal isolates, 90.8% (
n
= 335) were correctly identified to the species or subspecies level and 2.4% (
n
= 9) at the group level. For the remaining 25 isolates, the Vitek MS proposed a bacterial species included in the list of possible species suggested by genotypic methods, except for 4 isolates which were not identified due to the absence of the species in the database. According to our study, the Vitek MS displays performance similar to that of the optochin susceptibility test for routine identification of pneumococcal isolates. Moreover, the Vitek MS is efficient for the identification of other viridans group streptococci and related isolates, provided that the species are included in the database.
Publisher
American Society for Microbiology
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