Nikoomanesh, Fatemeh, Nikoomanesh, Fatemeh, Roudbarmohammadi, Shahla, Roudbary, Maryam, Bayat, Mansour, Heidari, Ghasem (2016). Investigation of bcr1 Gene Expression in Candida albicans Isolates by RT-PCR Technique and its Impact on Biofilm Formation. , 2(1), 22-24.
Fatemeh Nikoomanesh; Fatemeh Nikoomanesh; Shahla Roudbarmohammadi; Maryam Roudbary; Mansour Bayat; Ghasem Heidari. "Investigation of bcr1 Gene Expression in Candida albicans Isolates by RT-PCR Technique and its Impact on Biofilm Formation". , 2, 1, 2016, 22-24.
Nikoomanesh, Fatemeh, Nikoomanesh, Fatemeh, Roudbarmohammadi, Shahla, Roudbary, Maryam, Bayat, Mansour, Heidari, Ghasem (2016). 'Investigation of bcr1 Gene Expression in Candida albicans Isolates by RT-PCR Technique and its Impact on Biofilm Formation', , 2(1), pp. 22-24.
Nikoomanesh, Fatemeh, Nikoomanesh, Fatemeh, Roudbarmohammadi, Shahla, Roudbary, Maryam, Bayat, Mansour, Heidari, Ghasem Investigation of bcr1 Gene Expression in Candida albicans Isolates by RT-PCR Technique and its Impact on Biofilm Formation. , 2016; 2(1): 22-24.

Investigation of bcr1 Gene Expression in Candida albicans Isolates by RT-PCR Technique and its Impact on Biofilm Formation

Infection Epidemiology and Microbiology
Article 7, Volume 2, Issue 1 - Serial Number 2, 2016, Pages 22-24    PDF (394 K)
Authors
Fatemeh Nikoomanesh1; Fatemeh Nikoomanesh1; Shahla Roudbarmohammadi* 1; Maryam Roudbary2; Mansour Bayat3; Ghasem Heidari4
1Department of medical mycology, Faculty of medical science, Tarbiat Modares University, Tehran, Iran
2Department of Medical Mycology and Parasitology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran
3Science and Research Branch, Islamic Azad University, Tehran, Iran
4Food and Drug Organization, Tehran, Iran
Abstract
Background: Adhesion and biofilm formation are two important steps in Candida pathogenesis. The aim of the current study was to investigate the presence of bcr1 gene in Candida albicans (C. albicans) isolates from women with vaginal candidiasis and its impact on biofilm formation. Methods: We used 50 clinical isolates which confirmed C. albicans by PCR-RFLP. Then total RNA was extracted from C. albicans isolates by glass bead and lysis buffer, and cDNA was synthesized using reverse transcriptase enzyme. RT-PCR (Reverse Transcriptase PCR) was used to evaluate the expression of bcr1 gene. Biofilm formation was evaluated in 96-well microplate and then tetrazolium reduction was assayed. All data were analyzed using t-test by SPSS software. Results: Fifty clinical isolates out of 150 were confirmed as C. albicans by using PCR-RFLP method. All the isolates were resistant to fluconazole, 47/50(94%) isolates had bcr1 gene by using PCR, and 45(95.7%) out of 47 isolates, showed BCR1 expression by the RT-PCR. Isolates which harbored bcr1 gene was succeed to form a dense biofilm on microplate. Comparison of the results of the tetrazolium reduction assay on the two isolates that had BCR1expression and two isolates that had no BCR1 expression showed significant differences (p=0.014). Conclusion: According to our result, all of the isolates that had bcr1 gene expression according to RT-PCR, were also resistant to fluconazole in disk diffusion test and additionally, their adherence was higher compared to the control group. These results indicate that there is a positive relation between expression of bcr1 gene and biofilm formation.
Keywords
Candida albicans; bcr1 gene expression; RT-PCR
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