May 2004
Volume 45, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2004
Use of the antimicrobial potentiator (TricideTM) to improve efficacy of medications against fungal keratitis pathogens.
Author Affiliations & Notes
  • W.L. Weinstein
    Small Animal Medicine and Surgery,
    University of Georgia, College of Veterinary Medicine, Athens, GA
  • P.A. Moore
    Small Animal Medicine and Surgery,
    University of Georgia, College of Veterinary Medicine, Athens, GA
  • U.M. Dietrich
    Small Animal Medicine and Surgery,
    University of Georgia, College of Veterinary Medicine, Athens, GA
  • R.E. Wooley
    Department of Medical Microbiology,
    University of Georgia, College of Veterinary Medicine, Athens, GA
  • B.W. Ritchie
    Department of Small Animal Medicine, Department of Medical Microbiology,
    University of Georgia, College of Veterinary Medicine, Athens, GA
  • S. Sanchez
    Department of Medical Microbiology, Athens Veterinary Diagnostic Laboratory,
    University of Georgia, College of Veterinary Medicine, Athens, GA
  • Footnotes
    Commercial Relationships  W.L. Weinstein, None; P.A. Moore, None; U.M. Dietrich, None; R.E. Wooley, University of Georgia Research Foundation to Molecular Therapeutics C, P; B.W. Ritchie, University of Georgia Research Foundation to Molecular Therapeutics F, I, E, P; S. Sanchez, None.
  • Footnotes
    Support  University of Georgia Veterinary Ophthalmology Research Fund
Investigative Ophthalmology & Visual Science May 2004, Vol.45, 4961. doi:
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      W.L. Weinstein, P.A. Moore, U.M. Dietrich, R.E. Wooley, B.W. Ritchie, S. Sanchez; Use of the antimicrobial potentiator (TricideTM) to improve efficacy of medications against fungal keratitis pathogens. . Invest. Ophthalmol. Vis. Sci. 2004;45(13):4961.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Abstract: : Purpose: To determine if the antimicrobial potentiator (TricideTM) enhances in vitro activity of antifungal medications against fungal isolates from horses with mycotic keratitis. Horses develop keratomycosis more often than other domestic species, serving as a good model for human fungal keratitis. Methods: Fungal isolates were obtained from cases of equine mycotic keratitis. The NCCLS microdilution method was performed using reference grade antifungal powders (miconazole, ketoconazole, itraconazole and natamycin) against the fungal isolates and ATCC quality control strains (Candida albicans and Paecilomyces variotii). Serial dilutions were performed to achieve a range of antifungal drug and TricideTM concentrations. Minimum inhibitory concentrations (MIC’s) for TricideTM combined with the antifungal drugs were compared to the MIC’s of the antifungals alone. Results: MIC 50’s for the antifungal drugs were decreased (50 to 100%) when combined with TricideTM. % Decrease in MIC 50 achieved using a range of Tricide concentrations: 

Note: 100% reduction in MIC 50 indicates that TricideTM alone (no antifungal) caused 50 % inhibition of growth. NP=not performed. Conclusions:TricideTM has antifungal properties when used alone and increases the in vitro activity of antifungals against common fungal pathogens associated with equine keratomycosis. TricideTM is effective in reducing the MIC’s of antifungal medications against resistant fungi associated with mycotic keratitis.

Keywords: antibiotics/antifungals/antiparasitics • fungal disease • keratitis 
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