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Journal of Clinical Microbiology, May 2008, p. 1835-1839, Vol. 46, No. 5
0095-1137/08/$08.00+0 doi:10.1128/JCM.00956-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Associated Regional and University Pathologists, Inc., Infectious Diseases Laboratory, Salt Lake City, Utah,1 Bacterial Barcodes, Inc., Athens, Georgia,2 Associated Regional and University Pathologists, Inc., Institute for Clinical and Experimental Pathology, Salt Lake City, Utah,3 University of Utah School of Medicine, Department of Pathology, Salt Lake City, Utah4
Received 8 May 2007/ Returned for modification 16 August 2007/ Accepted 11 March 2008
Repetitive-sequence-based PCR (rep-PCR) using the DiversiLab system was investigated for identification of Aspergillus. Ninety-five clinical isolates, identified by conventional methods, and five ATCC strains were tested. Sequencing of the internal transcribed spacer (ITS) region (ITS1-5.8S-ITS2) was performed on 2 isolates with discrepant rep-PCR and conventional results and 15 randomly selected outlier isolates. One isolate not identified by sequencing was excluded from analysis. After resolving discrepancies, all but one A. glaucus strain had
85% similarity to one or more strains of the same Aspergillus species in the mold database, thereby providing accurate identification. No isolate was misidentified.
Published ahead of print on 26 March 2008.
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