Overexpression of MDR-1 and CDR-2 genes in fluconazole resistance of Candida albicans isolated from patients with vulvovaginal candidiasis
( ) is an opportunistic fungus that can colonize women's mucosal epithelial cell surfaces, causing vulvovaginitis in specific circumstances. The major genes contributing to drug resistance in are the candida drug resistance ( ) and multi drug resistance ( ) genes. The purpose of this study was...
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Veröffentlicht in: | Current medical mycology 2016-12, Vol.2 (4), p.24-29 |
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Sprache: | eng |
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Zusammenfassung: | (
) is an opportunistic fungus that can colonize women's mucosal epithelial cell surfaces, causing vulvovaginitis in specific circumstances. The major genes contributing to drug resistance in
are the candida drug resistance (
) and multi drug resistance (
) genes. The purpose of this study was to evaluate the
and
gene expression patterns in
strains isolated from patients with recurrent vulvovaginal candidiasis.
In this study, 40 isolates of fluconazole-resistant
were cultured on Sabouraud dextrose agar. These isolates were collected from women with vulvovaginitis who were referred to a clinic in Tehran, Iran, and transferred to a mycology laboratory. Then, RNA was extracted from the isolates using phenol-chloroform and glass beads, and the complementary DNA (cDNA) was synthetized. To detect the semi-quantitative expression of
and
genes, the reverse transcriptase-PCR (RT-PCR) technique was performed using specific primers.
Our findings indicated that of the 40
isolates, 35 (87.5%) strains were positive for mRNA of the
gene, 32 (80%) strains expressed mRNA of the
gene, and 30 (75%) strains were confirmed to express mRNA of both the
and
genes simultaneously using the RT-PCR assay.
According to the obtained results, the expression rates of
and
genes were high in fluconazole-resistant
isolates, which can cause treatments to fail and result in chronic infections. Inhibiting these important genes using novel or natural agents can help with the treatment of chronic and recurrent vaginitis. |
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ISSN: | 2423-3439 2423-3420 |
DOI: | 10.18869/acadpub.cmm.2.4.24 |