The protein inventory of Clostridium difficile grown in complex and minimal medium

Proteomics Clin Appl. 2016 Oct;10(9-10):1068-1072. doi: 10.1002/prca.201600069. Epub 2016 Sep 12.

Abstract

The intestinal pathogen Clostridium difficile is causing an increasing number of infections often characterized by severity and high relapse rates. Profound knowledge of the physiology of the pathogen could help to develop new treatment strategies. Proteomics, a valuable tool to study bacterial physiology, was used in this work to establish a benchmark proteome of reference strain C. difficile 630Δerm with MS-based details on all identified proteins. Our elaborate annotation and visualization of C. difficile 630Δerm 3764 ORFs will serve as a valuable base for researchers having to evaluate global expression studies. To exemplify expression variability, protein expression of late exponentially growing cells in complex brain-heart infusion medium and C. difficile minimal medium was compared. Noteworthy results of this comparison are as follows: (i) the higher expression of enzymes for the biosynthesis of some vitamins and purine and (ii) downregulation of proteins involved in butanoate fermentation in C. difficile minimal medium. However, the abundance of proteins involved in DNA metabolism, protein synthesis, and the cell envelope showed no variation between the two growth media.

Keywords: Benchmark proteome; Clostridium difficile; Comprehensive peptide dataset; Label-free protein quantification; Voronoi treemaps.

MeSH terms

  • Bacterial Proteins / metabolism*
  • Butyric Acid / metabolism
  • Clostridioides difficile / drug effects
  • Clostridioides difficile / growth & development*
  • Clostridioides difficile / metabolism*
  • Culture Media / chemistry*
  • Fermentation / drug effects
  • Inosine Monophosphate / biosynthesis
  • Proteomics*

Substances

  • Bacterial Proteins
  • Culture Media
  • Butyric Acid
  • Inosine Monophosphate