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Journal of Clinical Microbiology, July 2001, p. 2431-2438, Vol. 39, No. 7
0095-1137/01/$04.00+0 DOI: 10.1128/JCM.39.7.2431-2438.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Identification of Two Different 14-
Sterol Demethylase-Related
Genes (cyp51A and cyp51B) in Aspergillus
fumigatus and Other Aspergillus species
E.
Mellado,*
T.
M.
Diaz-Guerra,
M.
Cuenca-Estrella, and
J. L.
Rodriguez-Tudela
Servicio de Micología, Centro
Nacional de Microbiología, Instituto de Salud Carlos III,
Majadahonda, Madrid, Spain
Received 8 February 2001/Returned for modification 1 April
2001/Accepted 1 May 2001
Two cyp51-related genes (cyp51A and
cyp51B) encoding 14-
sterol demethylase-like enzymes
were identified in the opportunistic human pathogen Aspergillus
fumigatus. PCR amplification using degenerate oligonucleotides
based on conserved areas of cytochrome P450 demethylases of other
filamentous fungi and yeasts allowed the cloning and sequencing of two
different homologue genes in A. fumigatus. Southern
analysis confirmed that both genes hybridized to distinct genomic loci
and that both are represented as single copies in the genome.
Comparison of the deduced Cyp51A and Cyp51B proteins with the CYP51
proteins from Penicillium italicum, Aspergillus nidulans,
Erysiphe graminis, Uncinula necator, Botrytis cinerea, Ustilago maydis,
Cryptococcus neoformans, Candida albicans, Saccharomyces cerevisiae,
Candida tropicalis, and Candida glabrata showed that the percentages of identity of the amino acid sequences (range, 40 to
70%) were high enough to consider Cyp51A and Cyp51B to be members of
the fungal CYP51 family. Fragments from both genes were also cloned
from other Aspergillus spp. (A. flavus, A. nidulans, and A. terreus). Phylogenetic analysis
showed that, at least in the most pathogenic species of
Aspergillus, there are two fungal CYP51 proteins. This is
the first report of the existence of two homologue genes coding for
14-
sterol demethylase in the fungal kingdom. This finding could
provide insights into the azole resistance mechanisms operating in
fungi. The primers used here may be useful molecular tools for
facilitating the cloning of novel 14-
sterol demethylase genes in
other filamentous fungi.
*
Corresponding author. Mailing address: Servicio de
Micología, Centro Nacional de Microbiología, Instituto
de Salud Carlos III, Carretera Majadahonda-Pozuelo Km2, 28220 Madrid,
Spain. Phone: 34-91-5097961. Fax: 34-91-5097966. E-mail:
emellado{at}isciii.es.
Journal of Clinical Microbiology, July 2001, p. 2431-2438, Vol. 39, No. 7
0095-1137/01/$04.00+0 DOI: 10.1128/JCM.39.7.2431-2438.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
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