Transcriptome analysis of Aspergillus fumigatus exposed to voriconazole

被引:120
作者
da Silva Ferreira, Marcia Eliana
Malavazi, Iran
Savoldi, Marcela
Brakhage, Axel A.
Goldman, Maria Helena S.
Kim, H. Stanley
Nierman, William C.
Goldman, Gustavo H.
机构
[1] Univ Sao Paulo, Fac Ciencias Farmaceut, Dept Ciencias Farmaceut, BR-14040903 Sao Paulo, Brazil
[2] Univ Jena, Dept Mol & Appl Microbiol, Leibniz Inst Nat Prod Res, Infect Biol HansKnoell Inst, D-6900 Jena, Germany
[3] Univ Sao Paulo, Fac Filosofia Ciencias & Letras Ribeirao Pret, BR-14040903 Sao Paulo, Brazil
[4] Inst Genom Res, Rockville, MD 20850 USA
[5] George Washington Univ, Sch Med, Dept Biochem & Mol Biol, Washington, DC 20037 USA
基金
巴西圣保罗研究基金会;
关键词
Aspergillus fumigatus; voriconazole; microarrays; transcriptome;
D O I
10.1007/s00294-006-0073-2
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
For a comprehensive evaluation of genes that have their expression modulated during exposure of the mycelia to voriconazole, we performed a large-scale analysis of gene expression in Aspergillus fumigatus using a microarray hybridization approach. By comparing the expression of genes between the reference time and after addition of voriconazole (30, 60, 120, and 240 min), we identified 2,271 genes differentially expressed in the wild-type strain. To validate the expression of some of these genes during exposure to voriconazole, we analyzed 13 genes showing higher expression in the presence of voriconazole by real-time RT-PCR. Although the magnitudes of induction differed between the two experimental systems, in about 85% of the cases they were in good agreement with the microarray data. To our knowledge this is the first study of microarray hybridization analysis for a filamentous fungus exposed to an antifungal agent. In our study, we have observed: (i) a decreased mRNA expression of various ergosterol biosynthesis genes; (ii) increased mRNA levels of genes involved in a variety of cell functions, such as transporters, transcription factors, proteins involved in cell metabolism, and hypothetical proteins; and (iii) the involvement of the cyclic AMP-protein kinase signaling pathway in the increased mRNA expression of several of these genes.
引用
收藏
页码:32 / 44
页数:13
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