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Clinical Chemistry 46: 631-635, 2000;
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(Clinical Chemistry. 2000;46:631-635.)
© 2000 American Association for Clinical Chemistry, Inc.

Articles

Rapid Detection of Point Mutations by Fluorescence Resonance Energy Transfer and Probe Melting Curves in Candida Species

Juergen Loefflera, Lars Hagmeyer, Holger Hebart, Norbert Henke, Ulrike Schumacher and Hermann Einsele

a Address correspondence to this author at: Medizinische Klinik, Abteilung II, Labor Prof. Dr. Med. H. Einsele, Otfried-Mueller-Strasse 10, 72076 Tuebingen, Germany. Fax 49-7071-293179; e-mail juergen.loeffler{at}med.uni-tuebingen.de

Background: The LightCyclerTM combines rapid amplification of nucleic acids in glass capillaries with melting curve analysis based on fluorescence resonance energy transfer for the sensitive detection of point mutations in various settings, such as drug resistance and hereditary diseases. Point mutations leading to an altered structure of lanosteroldemethylase, the target enzyme of the fungistatic azoles, are an important mechanism of acquired resistance in Candida albicans.

Methods: We screened 13 fluconazole-resistant C. albicans and 21 fluconazole-resistant C. tropicalis strains (minimum inhibitory concentration >128 mg/L), isolated from patients with AIDS, for the presence of defined point mutations by comparing conventional cycle sequencing with a newly designed LightCycler-based assay.

Results: In C. tropicalis, 5 of 21 isolates showed the wild-type sequence, and 8 of 21 showed the homozygous nucleotide exchange thymine to cytosine at position 1554 (T1554C). A heterozygous genotype was detected in 8 of 21 isolates by the LightCycler, but in only 3 of 21 isolates by conventional cycle sequencing. In 2 of 13 C. albicans isolates, a homozygous point mutation leading to an amino acid exchange at position 464 (glycine to serine) was detected in both assays.

Conclusion: The LightCycler technique offers standardized, fast, sensitive, and reproducible detection of point mutations in different Candida spp.




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