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Published on: February 6, 2021
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.
Purpose:
Determine the ocular virulence of noncapsular Streptococcus pneumoniae in a rabbit keratitis model.
Methods:
Mice were infected intraperitoneally with 10(5) colony-forming units (CFUs) of Avery's strain (capsular type 2) or strain R6 (a noncapsular derivative of type 2), and mortality was monitored daily. In addition, 10(5) CFU of each strain was injected into rabbit corneas. Bacterial loads in rabbit corneas were determined at 20 or 48 hours after infection. Slit lamp examination (SLE) of rabbit eyes was performed at 24, 36, and 48 hours after infection. Controls included corneas inoculated with bacterial suspension medium and UV-killed bacteria.
Results:
One hundred percent mortality was observed in mice infected intraperitoneally with the encapsulated strain at 2 days after infection, whereas all mice infected with the nonencapsulated strain survived for 21 days. The nonencapsulated strain caused the same pathologic effects in the rabbit cornea as the encapsulated strain at 24, 36, and 48 hours after infection (P > or = 0.080). Control corneas showed no pathologic effects and had significantly lower SLE scores than corneas infected with live bacteria (P < or = 0.001). Mean bacteria log CFU +/- SEM recovered at 20 hours after infection were 7.069 +/- 0.094 for the encapsulated and 6.533 +/- 0.116 for the nonencapsulated strain (P = 0.001). Bacteria recovered from the corneas at 48 hours after infection were 6.712 +/- 0.349 and 1.807 +/- 0.462 for the encapsulated and nonencapsulated strains, respectively (P < 0.001).
Conclusions:
The S. pneumoniae noncapsular strain was as virulent in the rabbit cornea as was the encapsulated strain, but unlike the encapsulated strain, was avirulent in the mouse peritoneum.
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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