Ocular virulence of capsule-deficient streptococcus pneumoniae in a rabbit keratitis model

Julian M Reed1, Richard J O'Callaghan, Dalia O Girgis

  • 1Department of Microbiology, Immunology, and Parasitology, LSU Health Sciences Center, New Orleans, LA 70112, USA.

Abstract

Insights

Streptococcus pneumoniae lacking a capsule showed significant virulence in rabbit keratitis models, mirroring encapsulated strains. However, this noncapsular strain proved avirulent in mouse models, highlighting capsule-dependent virulence.

Area of Science:

  • Microbiology
  • Ophthalmology
  • Infectious Diseases

Background:

  • Streptococcus pneumoniae is a leading cause of bacterial keratitis.
  • The role of the bacterial capsule in S. pneumoniae virulence is well-established.
  • Nonencapsulated strains are often considered less virulent, but their ocular pathogenicity requires further investigation.

Purpose of the Study:

  • To determine the ocular virulence of noncapsular Streptococcus pneumoniae.
  • To compare the virulence of encapsulated and noncapsular S. pneumoniae strains in a rabbit keratitis model.
  • To assess the role of the capsule in S. pneumoniae pathogenesis.

Main Methods:

  • Infection of mice with encapsulated (Avery's strain) and noncapsular (strain R6) S. pneumoniae to monitor mortality.
  • Intracorneal inoculation of rabbit eyes with both strains (10^5 CFUs).
  • Quantification of bacterial loads in corneas at 20 and 48 hours post-infection.
  • Slit-lamp examination (SLE) of rabbit eyes at 24, 36, and 48 hours to assess pathology.

Main Results:

  • The noncapsular strain demonstrated significant ocular virulence in rabbits, causing similar pathological effects to the encapsulated strain.
  • Bacterial loads were comparable between strains at 20 hours, but significantly higher for the encapsulated strain at 48 hours.
  • In contrast, the encapsulated strain caused 100% mortality in mice, while the noncapsular strain was avirulent.

Conclusions:

  • Noncapsular Streptococcus pneumoniae exhibits significant ocular virulence, comparable to its encapsulated counterpart in a rabbit keratitis model.
  • The bacterial capsule is critical for systemic virulence in mice but not for establishing ocular infection in rabbits.
  • These findings underscore the complex role of the S. pneumoniae capsule in host-specific pathogenesis.

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