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Journal of Clinical Microbiology, June 1999, p. 1846-1851, Vol. 37, No. 6
Department of Medical Microbiology,
Received 28 December 1998/Returned for modification 26 January
1999/Accepted 17 March 1999
Invasive fungal disease often plays an important role in the
morbidity and mortality of immunocompromised patients. The poor sensitivity of current fungal blood culture and histological practices has led to the development of highly sensitive and specific molecular techniques, such as the PCR. Sequence variability of the internal transcribed spacer 2 (ITS2) region of fungi is potentially useful in
rapid and accurate diagnosis of clinical fungal isolates. PCR with
fungus-specific primers targeted toward conserved sequences of the 5.8S
and 28S ribosomal DNA (rDNA) results in amplification of the
species-specific ITS2 regions, which are variable in amplicon length.
We have made use of the ABI PRISM 310 genetic analyzer and the ABI
PRISM 310 GeneScan analysis software for the determination of variable
size differences of the ITS2 region of clinically important fungi,
including Candida and non-Candida yeasts,
Aspergillus species, and a variety of dermatophytes. No
cross-reaction occurred when samples were tested against human and
bacterial genomic DNA. We have found that most clinically significant
fungal isolates can be differentiated by this method, and it therefore
serves to be a promising tool for the rapid (<7 h) diagnosis of
fungemia and other invasive fungal infections.
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Rapid Identification of Fungi by Using the ITS2 Genetic Region
and an Automated Fluorescent Capillary Electrophoresis System
*
Corresponding author. Mailing address: Department of
Clinical Microbiology, Health Sciences Centre, MS6-820 Sherbrook
Street, Winnipeg, Manitoba R3A 1R9, Canada. Phone: (204) 787-4696. Fax: (204) 787-4699. E-mail: cturenne{at}hc-sc.gc.ca.
Journal of Clinical Microbiology, June 1999, p. 1846-1851, Vol. 37, No. 6
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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