Fluoroquinolone therapy in a rabbit model of post-LASIK methicillin-resistant Staphylococcus aureus keratitis
- PMID: 18242457
- DOI: 10.1016/j.jcrs.2007.10.022
Fluoroquinolone therapy in a rabbit model of post-LASIK methicillin-resistant Staphylococcus aureus keratitis
Abstract
Purpose: To develop a rabbit model of post-laser in situ keratomileusis (LASIK) methicillin-resistant Staphylococcus aureus (MRSA) keratitis for studying fluoroquinolone prophylaxis and treatment.
Setting: Department of Microbiology, University of Mississippi Medical Center, Jackson, Mississippi, USA.
Methods: An MRSA keratitis isolate (5 microL, 500 colony forming units [CFU]) was inoculated underneath a corneal flap. Bacterial growth and pathology were determined by quantitative cultures (CFU) and slitlamp examination, respectively. The effectiveness of commercial moxifloxacin and gatifloxacin formulations was compared in 3 regimens: prophylaxis (4 drops before inoculation), early therapy (single drop hourly from 4 to 9 hours postinfection), and late therapy (single drop hourly from 10 to 15 hours postinfection). Zones of bacterial inhibition to known in vivo antibiotic concentrations were determined.
Results: Bacteria grew to a maximum of approximately 10(6) CFU/cornea within 10 hours postinfection. The slitlamp examination scores showed pathologic changes beginning 10 hours postinfection and progressed throughout the infection. For prophylaxis, eyes treated with moxifloxacin had significantly fewer CFU than gatifloxacin-treated eyes or untreated controls (both P < or = .0001). During early treatment, the antibiotics were equally effective in reducing CFU relative to untreated controls (P < or = .0001). In late treatment, gatifloxacin and moxifloxacin caused significant reductions in CFU relative to untreated controls (P < or = .0007 and P < or = .0001, respectively). Moxifloxacin produced zones of bacterial inhibition significantly larger than those produced by gatifloxacin.
Conclusions: Methicillin-resistant S aureus inoculation beneath a rabbit corneal flap produced an infection that was useful for quantitative microbiological studies. A significant advantage in using moxifloxacin relative to gatifloxacin was observed in prophylaxis of keratitis (P = .0001).
Similar articles
-
Penetration and effectiveness of prophylactic fluoroquinolones in experimental methicillin-sensitive or methicillin-resistant Staphylococcus aureus anterior chamber infections.J Cataract Refract Surg. 2010 Dec;36(12):2160-7. doi: 10.1016/j.jcrs.2010.06.070. J Cataract Refract Surg. 2010. PMID: 21111321
-
Efficacy of besifloxacin in a rabbit model of methicillin-resistant Staphylococcus aureus keratitis.Cornea. 2009 Oct;28(9):1055-60. doi: 10.1097/ICO.0b013e31819e34cb. Cornea. 2009. PMID: 19724203
-
Efficacy of besifloxacin in an early treatment model of methicillin-resistant Staphylococcus aureus keratitis.J Ocul Pharmacol Ther. 2010 Apr;26(2):193-8. doi: 10.1089/jop.2009.0121. J Ocul Pharmacol Ther. 2010. PMID: 20334537
-
Antibiotic Resistance in the Treatment of Staphylococcus aureus Keratitis: a 20-Year Review.Cornea. 2015 Jun;34(6):698-703. doi: 10.1097/ICO.0000000000000431. Cornea. 2015. PMID: 25811722 Free PMC article. Review.
-
In vitro and in vivo potency of moxifloxacin and moxifloxacin ophthalmic solution 0.5%, a new topical fluoroquinolone.Surv Ophthalmol. 2005 Nov;50 Suppl 1:S16-31. doi: 10.1016/j.survophthal.2005.06.002. Surv Ophthalmol. 2005. PMID: 16257308 Review.
Cited by
-
Animal models of bacterial keratitis.J Biomed Biotechnol. 2011;2011:680642. doi: 10.1155/2011/680642. Epub 2011 Jan 4. J Biomed Biotechnol. 2011. PMID: 21274270 Free PMC article. Review.
-
Secretory Leukoprotease Inhibitor: A Native Antimicrobial Protein in the Innate Immune Response in a Rat Model of S. aureus Keratitis.J Ophthalmol. 2009;2009:259393. doi: 10.1155/2009/259393. Epub 2009 Oct 15. J Ophthalmol. 2009. PMID: 20309414 Free PMC article.
-
Research progress on animal models of corneal epithelial-stromal injury.Int J Ophthalmol. 2023 Nov 18;16(11):1890-1898. doi: 10.18240/ijo.2023.11.23. eCollection 2023. Int J Ophthalmol. 2023. PMID: 38028511 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical