Typing of vancomycin-resistant enterococci with MALDI-TOF mass spectrometry in a nosocomial outbreak setting

0301 basic medicine Enterococcus faecium Vancomycin-Resistant Enterococci/classification Disease Outbreaks Vancomycin-Resistant Enterococci 03 medical and health sciences Bacterial Typing Techniques/methods Matrix-Assisted Laser Desorption-Ionization/methods MALDI-TOF MS Humans Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization/methods Gram-Positive Bacterial Infections/microbiology Gram-Positive Bacterial Infections Enterococcus faecium/classification Cross Infection Spectrometry Reproducibility of Results Mass Bacterial Typing Techniques Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization VREfm Cross Infection/microbiology Vancomycin resistance
DOI: 10.1016/j.cmi.2018.03.020 Publication Date: 2018-03-23T22:57:43Z
ABSTRACT
To investigate the usefulness of matrix-assisted laser desorption ionization-time-of-flight mass spectrometry (MALDI-TOF MS) typing as a first-line epidemiological tool in a nosocomial outbreak of vancomycin-resistant Enterococcus faecium (VREfm).Fifty-five VREfm isolates, previously characterized by whole-genome sequencing (WGS), were included and analysed by MALDI-TOF MS. To take peak reproducibility into account, ethanol/formic acid extraction and other steps of the protocol were conducted in triplicate. Twenty-seven spectra were generated per isolate, and spectra were visually inspected to determine discriminatory peaks. The presence or absence of these was recorded in a peak scheme.Nine discriminatory peaks were identified. A characteristic pattern of these could distinguish between the three major WGS groups: WGS I, WGS II and WGS III. Only one of 38 isolates belonging to WGS I, WGS II or WGS III was misclassified. However, ten of the 17 isolates not belonging to WGS I, II or III displayed peak patterns indistinguishable from those of the outbreak strain.Using visual inspection of spectra, MALDI-TOF MS typing proved to be useful in differentiating three VREfm outbreak clones from each other. However, as non-outbreak isolates could not be reliably differentiated from outbreak clones, the practical value of this typing method for VREfm outbreak management was limited in our setting.
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