American Journal of Ophthalmology
Volume 146, Issue 5 , Pages 714-723.e1, November 2008

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

  • Elma Kim

      Affiliations

    • Department of Ophthalmology and Visual Sciences, Washington University School of Medicine, St Louis, Missouri
  • ,
  • Jaya D. Chidambaram

      Affiliations

    • Francis I. Proctor Foundation, University of California, San Francisco, California
  • ,
  • Muthiah Srinivasan

      Affiliations

    • Aravind Eye Care System, Madurai, India
  • ,
  • Prajna Lalitha

      Affiliations

    • Aravind Eye Care System, Madurai, India
  • ,
  • Daniel Wee

      Affiliations

    • Department of Ophthalmology and Visual Sciences, Washington University School of Medicine, St Louis, Missouri
  • ,
  • Thomas M. Lietman

      Affiliations

    • Francis I. Proctor Foundation, University of California, San Francisco, California
  • ,
  • John P. Whitcher

      Affiliations

    • Francis I. Proctor Foundation, University of California, San Francisco, California
  • ,
  • Russell N. Van Gelder

      Affiliations

    • Department of Ophthalmology and Visual Sciences, Washington University School of Medicine, St Louis, Missouri
    • Department of Molecular Biology and Pharmacology, Washington University School of Medicine, St Louis, Missouri
    • 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

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.

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

 Supplemental Material available at AJO.com.

PII: S0002-9394(08)00473-X

doi:10.1016/j.ajo.2008.06.009

American Journal of Ophthalmology
Volume 146, Issue 5 , Pages 714-723.e1, November 2008