4.7 Article

Factors Associated With MALDI-TOF Mass Spectral Quality of Species Identification in Clinical Routine Diagnostics

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fcimb.2021.646648

关键词

MALDI-TOF mass spectrometry; quality control; standardisation; species identification; microbial diagnostics

资金

  1. Personalized Health at ETHZ (D-BSSE)
  2. University of Basel [PMB-03-17]
  3. Swiss National Science Foundation [P1BSP3-184342]
  4. Swiss National Science Foundation (SNF) [P1BSP3_184342] Funding Source: Swiss National Science Foundation (SNF)

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Accurate and timely identification of bacterial species is crucial in clinical diagnostics, and MALDI-TOF MS is a widely used method for this purpose. However, challenges in species identification persist due to incomplete databases, closely related species, and vaguely defined spectral quality. This study identified quality measures for MALDI-TOF MS, optimized spectral quality, and found that factors such as using formic acid, measuring young bacterial colonies, and frequent calibration can improve mass spectral quality. Additionally, differences in spectral quality were observed between different bacterial taxa, with optimal measurement conditions varying for each taxon.
Background An accurate and timely identification of bacterial species is critical in clinical diagnostics. Species identification allows a potential first adaptation of empiric antibiotic treatments before the resistance profile is available. Matrix assisted Laser Desorption Ionization Time of Flight mass spectrometry (MALDI-TOF MS) is a widely used method for bacterial species identification. However, important challenges in species identification remain. These arise from (i) incomplete databases, (ii) close relatedness of species of interest, and (iii) spectral quality, which is currently vaguely defined. Methods We selected 47 clinically relevant bacterial isolates from 39 species, which can be challenging to identify by MALDI-TOF MS. We measured these isolates under various analytical conditions on two MALDI-TOF MS systems. First, we identified spectral features, which were associated with correct species identification in three different databases. Considering these features, we then systematically compared spectra produced with three different sample preparation protocols. In addition, we varied quantities of bacterial colony material applied and bacterial colony age. Results We identified (i) the number of ribosomal marker peaks detected, (ii) the median relative intensity of ribosomal marker peaks, (iii) the sum of the intensity of all detected peaks, (iv) a high measurement precision, and (v) reproducibility of peaks to act as good proxies of spectral quality. We found that using formic acid, measuring bacterial colonies at a young age, and frequently calibrating the MALDI-TOF MS device increase mass spectral quality. We further observed significant differences in spectral quality between different bacterial taxa and optimal measurement conditions vary per taxon. Conclusion We identified and applied quality measures for MALDI-TOF MS and optimized spectral quality in routine settings. Phylogenetic marker peaks can be reproducibly detected and provide an increased resolution and the ability to distinguish between challenging species such as those within the Enterobacter cloacae complex, Burkholderia cepacia complex, or viridans streptococci.

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