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Journal of Clinical Microbiology, July 2001, p. 2391-2396, Vol. 39, No. 7
ENT University Hospital,
Karl-Franzens-University Graz, A 8036 Graz, Austria
Received 13 July 2000/Returned for modification 12 August
2000/Accepted 23 April 2001
In the last 50 years, to our knowledge, only 16 cases of diseases
caused by Schizophyllum commune in humans have been
reported. Within only 6 months, we found four isolates of this
basidiomycetous fungus, obtained from patients suffering from chronic
sinusitis. The cultures of the isolated fungi showed neither clamp
connections nor fruiting bodies (basidiocarps), which are distinctive
features for S. commune, but fast-growing cottony white
mycelium only. This was harvested, and DNA was extracted. The internal
transcribed spacer region of the ribosomal DNA (rDNA) was amplified
with fungus-specific primers, and the PCR products were sequenced. Two
strains of S. commune, collected from branches of a
European hornbeam (Carpinus betulus) and a tree of
heaven (Ailanthus altissima), respectively; four
specimens from the herbarium of the Institute of Botany, Karl-Franzens-University Graz; and two strains from internationally known culture collections (CBS 340.81 [ATCC 44201] and CBS 405.96) were investigated in the same way. The sequence data of all strains were compared and showed homology of over 99% in this 660-bp-long fragment of rDNA. With these results, a map of restriction enzyme cutting sites and a primer set specific for S. commune
were created for reliable identification of this human pathogenic fungus.
0095-1137/01/$04.00+0 DOI: 10.1128/JCM.39.7.2391-2396.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Development of Molecular Methods for Identification
of Schizophyllum commune from Clinical Samples
*
Corresponding author. Mailing address: ENT University
Hospital, Karl-Franzens-University Graz, Auenbruggerplatz 26-28, A 8036 Graz, Austria. Phone: 43 316 3853606 or 43 676 7800545. Fax: 43 316 3857643. E-mail: walter.buzina{at}kfunigraz.ac.at.
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