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[Application of differential display-PCR technique in fluconazole-resistance gene expression of Candida].

Yuning ZhuShiming Lü

2005PubMedBiochemistry, Genetics and Molecular Biology被引 3

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摘要

OBJECTIVE: To investigate the application of differential display-2PCR(DD-PCR) in research on gene expression of Candida. METHODS: Resistance to fluconazole was induced in a Candida albicans isolate 435 from vagina by culturing in YEPD broth with increasing fluconazole concentration in vitro, and the resistant isolate 435-2 (MIC=128 microg/ml ) was obtained after 80 days of incubation. Comparisons between 435 and 435-2 either in fluconazole-containing medium or in drug-free medium were performed with the modified DD-PCR including amplification with long primers, silver staining, reverse dot blot and non-radiographic labeling techniques. RESULTS: Three differential displayed bands were found which showed high homology to alcohol dehydrogenase 1 (ADH1), TOP2 and CDR1, respectively. The up-regulating expression of ADH1 and CDR1 associated with fluconazole resistance was further identified by RT-PCR. CONCLUSION: The up-regulating expression of ADH1 and CDR1 was associated with fluconazole resistance in Candida albicans, ADH1 might be a candidate of novel fluconazole resistant gene.

引用本文(GB/T 7714)

Yuning Zhu, Shiming Lü. [Application of differential display-PCR technique in fluconazole-resistance gene expression of Candida].[J]. PubMed, 2005.

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DOI:https://doi.org/10.3785/j.issn.1008-9292.2005.02.013

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