Role of the Streptococcus suis serotype 2 capsular polysaccharide in the interactions with dendritic cells is strain-dependent but remains critical for virulence

PLoS One. 2018 Jul 12;13(7):e0200453. doi: 10.1371/journal.pone.0200453. eCollection 2018.

Abstract

Streptococcus suis serotype 2 is an important porcine bacterial pathogen and zoonotic agent responsible for sudden death, septic shock, and meningitis. However, serotype 2 strains are heterogeneous, composed of a multitude of sequence types (STs) whose distribution greatly varies worldwide. Of the virulence factors presently described for S. suis, the capsular polysaccharide (CPS) is a critical factor implicated in a multitude of functions, including in impairment of phagocytosis and innate immune cell activation by masking underlying bacterial components. However, these roles have been described using Eurasian ST1 and ST7 strains, which greatly differ from North American ST25 strains. Consequently, the capacity of the CPS to mask surface antigens and putative virulence factors in non-Eurasian strains remains unknown. Herein, the role of the S. suis serotype 2 CPS of a prototype intermediate virulent North American ST25 strain, in comparison with that of a virulent European ST1 strain, with regards to interactions with dendritic cells, as well as virulence during the systemic phase of infection, was evaluated. Results demonstrated that the CPS remains critical for virulence and development of clinical disease regardless of strain background, due to its requirement for survival in blood. However, its role in the interactions with dendritic cells is strain-dependent. Consequently, certain key characteristics associated with the CPS are not necessarily applicable to all S. suis serotype 2 strains. This indicates that though certain factors may be important for S. suis serotype 2 virulence, strain background could be as determining, reiterating the need in using strains from varying backgrounds in order to better characterize the S. suis pathogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacterial Capsules / genetics
  • Bacterial Capsules / metabolism*
  • Cytokines / metabolism
  • Dendritic Cells / metabolism
  • Dendritic Cells / microbiology*
  • Escherichia coli
  • Female
  • Hydrophobic and Hydrophilic Interactions
  • Mice
  • Phagocytosis
  • Polysaccharides, Bacterial / metabolism*
  • Species Specificity
  • Streptococcal Infections / immunology
  • Streptococcal Infections / microbiology*
  • Streptococcal Infections / veterinary
  • Streptococcus suis / classification
  • Streptococcus suis / genetics
  • Streptococcus suis / metabolism*
  • Streptococcus suis / pathogenicity*
  • Virulence

Substances

  • Cytokines
  • Polysaccharides, Bacterial

Grants and funding

This work was supported by Natural Sciences and Engineering Research Council of Canada (http://www.nserc-crsng.gc.ca/index_eng.asp) - Grant #154280 to MG. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.