Host-to-Host Transmission of Streptococcus pneumoniae Is Driven by Its Inflammatory Toxin, Pneumolysin

Cell Host Microbe. 2017 Jan 11;21(1):73-83. doi: 10.1016/j.chom.2016.12.005.

Abstract

Host-to-host transmission is a critical step for infection. Here we studied transmission of the opportunistic pathogen Streptococcus pneumoniae in an infant mouse model. Transmission from nasally colonized pups required high levels of bacterial shedding in nasal secretions and was temporally correlated with, and dependent upon, the acute inflammatory response. Pneumolysin, a pore-forming cytotoxin and major virulence determinant, was both necessary and sufficient to promote inflammation, which increased shedding and allowed for intralitter transmission. Direct contact between pups was not required for transmission indicating the importance of an environmental reservoir. An additional in vivo effect of pneumolysin was to enhance bacterial survival outside of the host. Our findings provide experimental evidence of a microbial strategy for transit to new hosts and explain why an organism expresses a toxin that damages the host upon which it depends.

Keywords: bacteria; colonization; infection; pneumococcus; pneumolysin; shedding; toxin; transmission.

MeSH terms

  • Animals
  • Bacterial Load
  • Bacterial Proteins / metabolism
  • Disease Models, Animal
  • Inflammation / immunology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Pneumococcal Infections / microbiology
  • Pneumococcal Infections / transmission*
  • Respiratory System / immunology
  • Respiratory System / microbiology*
  • Respiratory System / pathology
  • Streptococcus pneumoniae / pathogenicity*
  • Streptolysins / metabolism*

Substances

  • Bacterial Proteins
  • Streptolysins
  • plY protein, Streptococcus pneumoniae