Enhanced nasopharyngeal infection and shedding associated with an epidemic lineage of emm3 group A Streptococcus

Virulence. 2017 Oct 3;8(7):1390-1400. doi: 10.1080/21505594.2017.1325070. Epub 2017 May 1.

Abstract

Background: A group A Streptococcus (GAS) lineage of genotype emm3, sequence type 15 (ST15) was associated with a 6 month upsurge in invasive GAS disease in the UK. The epidemic lineage (Lineage C) had lost 2 typical emm3 prophages, Φ315.1 and Φ315.2 associated with the superantigen ssa, but gained a different prophage (ΦUK-M3.1) associated with a different superantigen, speC and a DNAse spd1.

Methods and results: The presence of speC and spd1 in Lineage C ST15 strains enhanced both in vitro mitogenic and DNase activities over non-Lineage C ST15 strains. Invasive disease models in Galleria mellonella and SPEC-sensitive transgenic mice, revealed no difference in overall invasiveness of Lineage C ST15 strains compared with non-Lineage C ST15 strains, consistent with clinical and epidemiological analysis. Lineage C strains did however markedly prolong murine nasal infection with enhanced nasal and airborne shedding compared with non-Lineage C strains. Deletion of speC or spd1 in 2 Lineage C strains identified a possible role for spd1 in airborne shedding from the murine nasopharynx.

Conclusions: Nasopharyngeal infection and shedding of Lineage C strains was enhanced compared with non-Lineage C strains and this was, in part, mediated by the gain of the DNase spd1 through prophage acquisition.

Keywords: DNases; Streptococcus pyogenes; epidemic upsurge; genotype emm3; group A Streptococcus; invasive group A streptococcal disease; nasopharyngeal infection; prophage; serotype M3; superantigens.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Bacterial / genetics*
  • Antigens, Bacterial / metabolism
  • Bacterial Outer Membrane Proteins / genetics*
  • Bacterial Outer Membrane Proteins / metabolism
  • Carrier Proteins / genetics*
  • Carrier Proteins / metabolism
  • Female
  • Genotype
  • Humans
  • Mice
  • Moths
  • Nasopharyngeal Diseases / epidemiology
  • Nasopharyngeal Diseases / microbiology*
  • Prophages / genetics
  • Prophages / physiology
  • Streptococcal Infections / epidemiology
  • Streptococcal Infections / microbiology*
  • Streptococcus pyogenes / genetics
  • Streptococcus pyogenes / pathogenicity
  • Streptococcus pyogenes / physiology*
  • Streptococcus pyogenes / virology
  • United Kingdom / epidemiology
  • Virulence

Substances

  • Antigens, Bacterial
  • Bacterial Outer Membrane Proteins
  • Carrier Proteins
  • streptococcal M protein