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Clinical and Diagnostic Laboratory Immunology, March 2002, p. 461-469, Vol. 9, No. 2
1071-412X/02/$04.00+0     DOI: 10.1128/CDLI.9.2.461-469.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.

Detection of Cryptococcus neoformans DNA in Tissue Samples by Nested and Real-Time PCR Assays

Ralf Bialek,1* Michael Weiss,2 Kubrom Bekure-Nemariam,1 Laura K. Najvar,3 Maria B. Alberdi,4 John R. Graybill,3 and Udo Reischl4

Institute for Tropical Medicine, University Hospital Tübingen,1 Botanical Institute, University of Tübingen, Tübingen,2 Institute of Medical Microbiology, University of Regensburg, Regensburg, Germany,4 University of Texas Health Science Center at San Antonio, San Antonio, Texas3

Received 10 September 2001/ Returned for modification 3 December 2001/ Accepted 3 January 2002

Two PCR protocols targeting the 18S rRNA gene of Cryptococcus neoformans were established, compared, and evaluated in murine cryptococcal meningitis. One protocol was designed as a nested PCR to be performed in conventional block thermal cyclers. The other protocol was designed as a quantitative single-round PCR adapted to LightCycler technology. One hundred brain homogenates and dilutions originating from 20 ICR mice treated with different azoles were examined. A fungal burden of 3 x 101 to 2.9 x 104 CFU per mg of brain tissue was determined by quantitative culture. Specific PCR products were amplified by the conventional and the LightCycler methods in 86 and 87 samples, respectively, with products identified by DNA sequencing and real-time fluorescence detection. An analytical sensitivity of 1 CFU of C. neoformans per mg of brain tissue and less than 10 CFU per volume used for extraction was observed for both PCR protocols, while homogenates of 70 organs from mice infected with other fungi were PCR negative. Specificity testing was performed with genomic DNA from 31 hymenomycetous fungal species and from the ustilaginomycetous yeast Malassezia furfur, which are phylogenetically related to C. neoformans. Twenty-four strains, including species of human skin flora like M. furfur and Trichosporon spp., were PCR negative. Amplification was observed with Cryptococcus amylolentus, Filobasidiella depauperata, Cryptococcus laurentii, and five species unrelated to clinical specimens. LightCycler PCR products from F. depauperata and Trichosporon faecale could be clearly discriminated by melting curve analysis. The sensitive and specific nested PCR assay as well as the rapid and quantitative LightCycler PCR assay might be useful for the diagnosis and monitoring of human cryptococcal infections.

* Corresponding author. Mailing address: Institut für Tropenmedizin, Universitätsklinikum Tübingen, Keplerstrasse 15, 72074 Tübingen, Germany. Phone: 49 7071 298 2367. Fax: 49 7071 29 5267. E-mail: ralf.bialek{at}med.uni-tuebingen.de.

Clinical and Diagnostic Laboratory Immunology, March 2002, p. 461-469, Vol. 9, No. 2
1071-412X/02/$04.00+0     DOI: 10.1128/CDLI.9.2.461-469.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.



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