Phylogenetic Diversity and Microsphere Array-Based Genotyping of Human Pathogenic Fusaria, Including Isolates from the Multistate Contact Lens-Associated U.S. Keratitis Outbreaks of 2005 and 2006

  • Kerry O'Donnell
    Microbial Genomics and Bioprocessing Research Unit, Agricultural Research Service, U.S. Department of Agriculture, Peoria, Illinois
  • Brice A. J. Sarver
    Microbial Genomics and Bioprocessing Research Unit, Agricultural Research Service, U.S. Department of Agriculture, Peoria, Illinois
  • Mary Brandt
    Centers for Disease Control and Prevention, Atlanta, Georgia
  • Douglas C. Chang
    Centers for Disease Control and Prevention, Atlanta, Georgia
  • Judith Noble-Wang
    Centers for Disease Control and Prevention, Atlanta, Georgia
  • Benjamin J. Park
    Centers for Disease Control and Prevention, Atlanta, Georgia
  • Deanna A. Sutton
    Department of Pathology, University of Texas Health Science Center, San Antonio, Texas
  • Lynette Benjamin
    Centers for Disease Control and Prevention, Atlanta, Georgia
  • Mark Lindsley
    Centers for Disease Control and Prevention, Atlanta, Georgia
  • Arvind Padhye
    Centers for Disease Control and Prevention, Atlanta, Georgia
  • David M. Geiser
    Department of Plant Pathology, The Pennsylvania State University, University Park, Pennsylvania
  • Todd J. Ward
    Microbial Genomics and Bioprocessing Research Unit, Agricultural Research Service, U.S. Department of Agriculture, Peoria, Illinois

説明

<jats:title>ABSTRACT</jats:title> <jats:p> In 2005 and 2006, outbreaks of <jats:italic>Fusarium</jats:italic> keratitis associated with soft contact lens use occurred in multiple U.S. states and Puerto Rico. A case-control study conducted by the Centers for Disease Control and Prevention (CDC) showed a significant association between infections and the use of one particular brand of lens solution. To characterize the full spectrum of the causal agents involved and their potential sources, partial DNA sequences from three loci ( <jats:italic>RPB</jats:italic> 2, <jats:italic>EF</jats:italic> -1α, and nuclear ribosomal rRNA) totaling 3.48 kb were obtained from 91 corneal and 100 isolates from the patient's environment (e.g., contact lens and lens cases). We also sequenced a 1.8-kb region encoding the RNA polymerase II second largest subunit ( <jats:italic>RPB</jats:italic> 2) from 126 additional pathogenic isolates to better understand how the keratitis outbreak isolates fit within the full phylogenetic spectrum of clinically important fusaria. These analyses resulted in the most robust phylogenetic framework for <jats:italic>Fusarium</jats:italic> to date. In addition, <jats:italic>RPB</jats:italic> 2 nucleotide variation within a 72-isolate panel was used to design 34 allele-specific probes to identify representatives of all medically important species complexes and 10 of the most important human pathogenic <jats:italic>Fusarium</jats:italic> in a single-well diagnostic assay, using flow cytometry and fluorescent microsphere technology. The multilocus data revealed that one haplotype from each of the three most common species comprised 55% of CDC's corneal and environmental isolates and that the corneal isolates comprised 29 haplotypes distributed among 16 species. The high degree of phylogenetic diversity represented among the corneal isolates is consistent with multiple sources of contamination. </jats:p>

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