MALDI-TOF Mass Spectrometry as a Useful Tool for Identification of Enterococcus spp. from Wild Birds and Differentiation of Closely Related Species

J Microbiol Biotechnol. 2017 Jun 28;27(6):1128-1137. doi: 10.4014/jmb.1612.12036.

Abstract

The aim of this study was to explore the accuracy and feasibility of matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) in identifying bacteria from environmental sources, as compared with rpoA gene sequencing, and to evaluate the occurrence of bacteria of the genus Enterococcus in wild birds. In addition, a phyloproteomic analysis of certain Enterococcus species with spectral relationships was performed. The enterococci were isolated from 25 species of wild birds in central Europe (Poland). Proteomic (MALDI-TOF MS) and genomic (rpoA gene sequencing) methods were used to identify all the isolates. Using MALDI-TOF MS, all 54 (100%) isolates were identified as Enterococcus spp. Among these, 51 (94.4%) isolates were identified to the species level (log(score) > or =2.0), and three isolates (5.6%) were identified at a level of probable genus identification (log(score) 1.88-1.927). Phylogenetic analysis based on rpoA sequences confirmed that all enterococci had been correctly identified. Enterococcus faecalis was the most prevalent enterococcal species (50%) and Enterococcus faecium (33.3%) the second most frequent species, followed by Enterococcus hirae (9.3%), Enterococcus durans (3.7%), and Enterococcus casseliflavus (3.7%). The phyloproteomic analysis of the spectral profiles of the isolates showed that MALDI-TOF MS is able to differentiate among similar species of the genus Enterococcus.

Keywords: Enterococcus; MALDI-TOF MS; Wild birds; rpoA sequencing.

MeSH terms

  • Animals
  • Animals, Wild / microbiology
  • Birds / microbiology*
  • Enterococcus / classification
  • Enterococcus / isolation & purification*
  • Enterococcus faecalis / genetics
  • Enterococcus faecium / genetics
  • Humans
  • Phylogeny
  • Poland
  • Polymerase Chain Reaction / methods
  • Proteomics
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization / methods*