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Volume 146, Issue 5, Pages 714-723.e1 (November 2008)


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Prospective Comparison of Microbial Culture and Polymerase Chain Reaction in the Diagnosis of Corneal Ulcer

Elma Kima, Jaya D. Chidambaramc, Muthiah Srinivasand, Prajna Lalithad, Daniel Weea, Thomas M. Lietmanc, John P. Whitcherc, Russell N. Van GelderabeCorresponding Author Informationemail address

Accepted 10 June 2008. published online 15 August 2008.

Purpose

To compare polymerase chain reaction (PCR) to microbial culture for the detection and identification of bacterial and fungal pathogens in microbial keratitis.

Design

Prospective cohort study.

Methods

A total of 108 consecutive corneal ulcers were cultured and analyzed by PCR using pan-bacterial and pan-fungal primers. PCR products were cloned, sequenced, and compared to culture results using standard bioinformatics tools.

Results

Of the 108 samples, 56 were culture-positive, 25 for bacteria and 31 for fungi; 52 were culture-negative. After eliminating false-positive PCR products, 94 of 108 were positive by PCR, 37 for bacteria and 57 for fungi. Nineteen of 25 bacterial culture-positive samples were positive by PCR, and 29 of 31 samples culture-positive for fungi were positive by PCR. The majority of sequenced PCR products matched the positive culture results. Of the 52 culture-negative samples, 46 (88%) yielded pathogen deoxyribonucleic acid (DNA) PCR products, 18 bacterial and 28 fungal. These represented a variety of species, including at least three novel previously uncultured microbes.

Conclusions

PCR detects microbial DNA in the majority of bacterial and fungal corneal ulcers, and identifies potentially pathogenic organisms in a high proportion of culture-negative cases. Yield and concordance with culture are higher for fungal than bacterial ulcers. Practical use of the technique is limited by artefactual amplification of nonpathogenic organisms. PCR may be used as an adjunct to culture to identify potential pathogens in microbial keratitis.

a Department of Ophthalmology and Visual Sciences, Washington University School of Medicine, St Louis, Missouri

b Department of Molecular Biology and Pharmacology, Washington University School of Medicine, St Louis, Missouri

c Francis I. Proctor Foundation, University of California, San Francisco, California

d Aravind Eye Care System, Madurai, India

e Department of Ophthalmology, University of Washington School of Medicine, Seattle, Washington

Corresponding Author InformationInquiries to Russell N. Van Gelder, Department of Ophthalmology, University of Washington School of Medicine, Campus Box 356485, 1959 NE Pacific Street, Seattle, WA 98195

 Supplemental Material available at AJO.com.

PII: S0002-9394(08)00473-X

doi:10.1016/j.ajo.2008.06.009


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