Staphylococcus aureus infection of the rabbit cornea following topical administration

Aihua Tang1, Charles L Balzli, Armando R Caballero

  • 1Department of Microbiology, University of Mississippi Medical Center, Jackson, MS 39216, USA.

Current Eye Research
|August 25, 2012
PubMed
Abstract

Insights

A unique Staphylococcus aureus strain (UMCR1) can topically infect the rabbit cornea, causing significant inflammation and damage. This finding is crucial for understanding ocular infections caused by virulent S. aureus strains.

Area of Science:

  • Ophthalmology
  • Microbiology
  • Infectious Diseases

Background:

  • Staphylococcus aureus is a common cause of bacterial keratitis.
  • The mechanisms by which S. aureus infects the cornea, particularly virulent strains, are not fully understood.

Purpose of the Study:

  • To evaluate the ability of different S. aureus strains to infect the rabbit cornea after topical application.
  • To investigate a particularly virulent S. aureus strain (UMCR1) for its corneal infectivity.

Main Methods:

  • Scarified rabbit corneas were inoculated topically or intrastromally with S. aureus strains.
  • Corneal infection was assessed by slit lamp examination (SLE), bacterial culture (log CFU), and histopathology.
  • Inflammation was quantified by polymorphonuclear leukocyte (PMN) assays.
  • Hemolysin titers and interactions with tears/corneal cells were analyzed.

Main Results:

  • Intrastromal injection of all strains led to severe keratitis.
  • Topical inoculation with four strains resulted in no infection.
  • Strain UMCR1 successfully infected the cornea topically, causing high SLE scores, extensive PMN infiltration, epithelial destruction, and edema.
  • UMCR1 efficiently invaded human corneal epithelial cells but lacked high hemolysin titers or tear resistance.

Conclusions:

  • A specific S. aureus strain (UMCR1) can cause topical infectious keratitis in rabbits.
  • This strain's ability to infect the cornea, anterior chamber, and conjunctiva suggests a common mechanism for overcoming host defenses at these ocular sites.