Surface layer proteins from virulent Clostridium difficile ribotypes exhibit signatures of positive selection with consequences for innate immune response

BMC Evol Biol. 2017 Mar 23;17(1):90. doi: 10.1186/s12862-017-0937-8.

Abstract

Background: Clostridium difficile is a nosocomial pathogen prevalent in hospitals worldwide and increasingly common in the community. Sequence differences have been shown to be present in the Surface Layer Proteins (SLPs) from different C. difficile ribotypes (RT) however whether these differences influence severity of infection is still not clear.

Results: We used a molecular evolutionary approach to analyse SLPs from twenty-six C. difficile RTs representing different slpA sequences. We demonstrate that SLPs from RT 027 and 078 exhibit evidence of positive selection (PS). We compared the effect of these SLPs to those purified from RT 001 and 014, which did not exhibit PS, and demonstrate that the presence of sites under positive selection correlates with ability to activate macrophages. SLPs from RTs 027 and 078 induced a more potent response in macrophages, with increased levels of IL-6, IL-12p40, IL-10, MIP-1α, MIP-2 production relative to RT 001 and 014. Furthermore, RTs 027 and 078 induced higher expression of CD40, CD80 and MHC II on macrophages with decreased ability to phagocytose relative to LPS.

Conclusions: These results tightly link sequence differences in C. difficile SLPs to disease susceptibility and severity, and suggest that positively selected sites in the SLPs may play a role in driving the emergence of hyper-virulent strains.

Keywords: Clostridium difficile; Positive selection; Protein evolution; Protein functional shift; Surface layer protein; Virulence.

MeSH terms

  • Bacterial Proteins / genetics
  • Bacterial Proteins / immunology*
  • Clostridioides difficile / classification
  • Clostridioides difficile / immunology
  • Clostridioides difficile / pathogenicity
  • Clostridium Infections / immunology*
  • Clostridium Infections / microbiology
  • Humans
  • Immunity, Innate
  • Macrophages / immunology
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / immunology*
  • Phagocytosis
  • Phylogeny
  • Ribotyping

Substances

  • Bacterial Proteins
  • Membrane Glycoproteins
  • S-layer proteins