Rapid discrimination of Salmonella enterica serovar typhi from other serovars by MALDI-TOF mass spectrometry

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Abstract

Systemic infections caused by Salmonella enterica are an ongoing public health problem especially in Sub-Saharan Africa. Essentially typhoid fever is associated with high mortality particularly because of the increasing prevalence of multidrug-resistant strains. Thus, a rapid blood-culture based bacterial species diagnosis including an immediate sub-differentiation of the various serovars is mandatory. At present, MALDI-TOF based intact cell mass spectrometry (ICMS) advances to a widely used routine identification tool for bacteria and fungi. In this study, we investigated the appropriateness of ICMS to identify pathogenic bacteria derived from Sub-Saharan Africa and tested the potential of this technology to discriminate S. enterica subsp. enterica serovar Typhi (S. Typhi) from other serovars. Among blood culture isolates obtained from a study population suffering from febrile illness in Ghana, no major misidentifications were observed for the species identification process, but serovars of Salmonella enterica could not be distinguished using the commercially available Biotyper database. However, a detailed analysis of the mass spectra revealed several serovar-specific biomarker ions, allowing the discrimination of S. Typhi from others. In conclusion, ICMS is able to identify isolates from a sub-Saharan context and may facilitate the rapid discrimination of the clinically and epidemiologically important serovar S. Typhi and other non-S. Typhi serovars in future implementations. © 2012 Kuhns et al.

Figures

  • Table 1. Concordance of species identification by conventional and ICMS methods.
  • Figure 1. Value of BioTyper hit scores for S. Typhi identification. Negative values indicated higher false hit scores, positive values indicated higher correct hit scores. A value near zero indicated a similar score distribution between correct and false hits. doi:10.1371/journal.pone.0040004.g001
  • Figure 2. Relatedness of Salmonella enterica ICMS spectra reflects serotype. (A) Global cluster analysis of S. enterica isolates. (B) Enlargement of major clusters from (A). Serovars: S. Typhi (red), S. Typhimurium (green), S. Enteritidis (yellow), others (blue). Isolate sources: G:Göttingen; R:Salmonella Reference Center; E:Eikwe; N:Nkawkaw; f:Fosso. Isolation time points in Ghana (E, N, and f only): not bold = 2006; bold = 2009 (C) Overlay of ICMS spectra contained in the four major clusters identifies at least one major peak (peak 2; m/z = 5713.9) specific to S. Typhi (red) and two major peaks (peaks 1 and 3; m/z = 5616.7 and m/z = 6009.7 respectively) specific for non-S. Typhi isolates (green, yellow and blue). Several other small peaks specific for S. Typhi were also seen (three example peaks indicated in cluster IIb by arrows, m/z = 2856.4, m/z = 3258.0, and m/z = 4716.3, respectively). doi:10.1371/journal.pone.0040004.g002

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CITATION STYLE

APA

Kuhns, M., Zautner, A. E., Rabsch, W., Zimmermann, O., Weig, M., Bader, O., & Groß, U. (2012). Rapid discrimination of Salmonella enterica serovar typhi from other serovars by MALDI-TOF mass spectrometry. PLoS ONE, 7(6). https://doi.org/10.1371/journal.pone.0040004

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