Lower Density and Shorter Duration of Nasopharyngeal Carriage by Pneumococcal Serotype 1 (ST217) May Explain Its

Laura Bricio-Moreno1, Chrispin Chaguza1,2, Reham Yahya1

  • 1Institute of Infection and Global Health, Department of Clinical Infection, Microbiology, and Immunology, University of Liverpool, Liverpool, United Kingdom.

Mbio
|December 9, 2020
PubMed

Insights

Streptococcus pneumoniae serotype 1 can cause invasive pneumococcal disease (IPD) and establish nasopharyngeal carriage. This serotype may also increase IPD risk from other serotypes through complex interactions.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Immunology

Background:

  • Streptococcus pneumoniae is a leading cause of life-threatening infections like pneumonia, meningitis, and sepsis globally.
  • Invasive pneumococcal disease (IPD) disproportionately affects developing countries, with Serotype 1 being a significant contributor in sub-Saharan Africa.
  • Serotype 1 is paradoxically rarely found in nasopharyngeal carriage, a state usually preceding IPD, creating a dichotomy that requires investigation.

Purpose of the Study:

  • To investigate the pathogenic mechanisms of African Serotype 1 Streptococcus pneumoniae strains (sequence type 217).
  • To understand the ability of Serotype 1 to establish nasopharyngeal carriage, challenging existing assumptions.
  • To explore the interactions between Serotype 1 and other pneumococcal serotypes during co-colonization and their impact on disease.

Main Methods:

  • Utilized murine models to study nasopharyngeal carriage and invasive pneumococcal disease (IPD).
  • Characterized the pathogenesis of African Serotype 1 (ST217) strains.
  • Employed RNA sequencing to analyze the expression of virulence genes in Serotype 1.

Main Results:

  • ST217 Serotype 1 strains demonstrated high virulence in a mouse model of invasive pneumonia.
  • Contrary to expectations, Serotype 1 successfully established nasopharyngeal carriage in the murine model.
  • Serotype 1 presence promoted the proliferation of co-colonizing serotypes, suggesting an increased risk of IPD from other serotypes.
  • RNA sequencing revealed upregulation of key virulence genes related to inflammation and tissue invasiveness in Serotype 1.

Conclusions:

  • Serotype 1 exhibits a complex pathogenesis, capable of both causing invasive disease and establishing carriage.
  • Interactions with co-colonizing serotypes are crucial, potentially increasing the risk of IPD by other serotypes.
  • Findings offer new insights into pneumococcal transmission, disease progression, and have implications for vaccine efficacy and intervention strategies.