Showing 50 results for MR
M Rasouli Nasab, Sh Habibnia, P Heidarieh, Mr Pourmand, M Fatahi, Ss Eshraghi,
Volume 7, Issue 5 (supplement Issue( Bacteriology)[PERSIAN] 2014)
Abstract
Abstract
Background and Objective: The Isolation of Nocardia species is complex and time-consuming, which is due to rapid growth of adjacent bacteria. Because of the importance of a specific medium with the ability of controlling intrusive microorganisms, this study aimed at comparing three laboratory methods to introduce the reliable isolation technique for Nocardia species.
Material and Methods: The soil samples were collected from different regions of Tehran province, Iran, and carefully transferred to the laboratory. The samples were cultured in three different media including Paraffin Baiting,Humic acid vitamin B agar and Paraffin agar, and incubated for 3-4 weeks at 35 °C.
Results: Of 110 soil samples, 31 Nocardia isolates (28.18%) were obtained from the media including Paraffin Baiting, (19 17.27%), Humic acid and vitamin B agar (4 3.63%), and Paraffin agar, (8 7.27%).
Conclusion: because of high rate of isolation, low cost and the clearance of colonies suspected nocardia, Paraffin Bait technique is more reliable and efficient compared to the other methods.
Key words: Nocardia Soil Paraffin Baiting Humic Acid Vitamin B
Aj Eiri, Aa Nasrollahi Omran, Hr Pordeli,
Volume 7, Issue 5 (supplement Issue( Bacteriology)[PERSIAN] 2014)
Abstract
Abstract
Background and Objective: Chitin, which is a linear polymer of N-acetyl glucosamine residues, has been the most abundant polymer in nature after cellulose. In recent decades, Chitinases have received increased attention because of their wide range of applications, especially in biological control against fungi.
Material and Methods: the isolation of bacilli producing chitinolytic enzymes was performed by collecting 40 soil samples from various regions of Gorgan, northern of Iran. The chitinolytic potential of the isolates was indicated by observation of clear zone in colloidal chitin agar medium. Identification of selected strains was performed by polyphasic taxonomy, and subtler identification and sequensing were carried out by extraction DNA. Antifungal effect was evaluated by well method against Candida albicans (ATCC 10231) Aspergillusniger (ATCC 2029)،Aspergillusflavus (IR6) Fusariumoxyporum (PTCC 5115) and Alternariaalternata (PTCC 5224).
Results: Nine colonies of chitinase positive bacillus were isolated on choloidal Chitin Agar (CCA) and five of them had antifungal effect. R6 strain had the highest, and R2 and R3 had the lowest effect on fungi. The 16S rRNA sequence of these isolations in comparison with the known bacteria has 95-97% similarity.
Conclusion: Some of the soil bacteria can have antagonestic effects on human and phytopathogenic agents existed in soil.
Keywords: Bacillus Chitinase Soil Antifungal
P Torabi, M Azimirad, Z Hasani, M Janmaleki, H Peirovi, M Alebouyeh, Mr Zali,
Volume 8, Issue 1 (spring[PERSIAN] 2014)
Abstract
Abstract
Background and Objective: This study was aimed to determine the extent of bacterial contamination and drug resistance patterns of isolates colonized in colonoscope and endoscope and in relevant personnel.
Material and Methods: A total of 107 samples were obtained from staff of endoscopy and colonoscopy units (SEU and SCU) and gastroenterological imaging equipment. For isolation and identification of the bacteria, swab culture method and biochemical identification test were used, respectively. Antimicrobial resistance profiles, multi-drug resistance (MDR) patterns and phenetic relatedness of these isolates were also analyzed according to standard methods.
Results: Most frequent pathogenic bacteria among the SEU and gastroenterological imaging related equipments were included S. aureus (20.8 % and 0 %) Enterococcus spp. (0 % and 5.4%) Pseudomonas spp. (0% and 13.5 %), and Clostridium difficile (0% and 12.5%). Analysis of resistance phenotypes showed a high frequency of MDR phenotypes among the SEU (82.1%), and also in endoscopes, colonoscopes, and other equipments (20%, 50% and 100%, respectively). Phylotyping of S. epidermidis isolates showed the role of staff in transmission of resistance strains to medical equipments and also circulation of strains with identical resistance phenotype among the studied samples.
Conclusion: High frequency of pathogenic bacteria in colonoscopes, endoscopes and in the staff of endoscopy & colonoscopy units, and also contamination of these instruments with MDR pathogens emphasize the need for proper disinfection of endoscopes and colonoscopes and also instruction of staff in these units.
Key words: Bacterial Contamination Endoscope Colonoscope Antimicrobial Resistance Gastrointestinal Disease.
Mr Bonyadi, N Azarshin, B Baybordi, A Elmiye,
Volume 8, Issue 1 (spring[PERSIAN] 2014)
Abstract
Abstract
Background and Objective: Allergic rhinitis can be stimulated by several allergens. Molds are among these allergens and it is important to assess their frequency in different geographic area. Hence, we aimed at determining the frequency of mold allergens in allergic rhinitis patients referred to specialized clinics of Tabriz Imam Reza hospital, 2011.
Material and Methods: This cross-sectional study was conducted on the serums of 90 rhinitis patients diagnosed by specialized physician. Using Immunoblotting method, the level of specific IgE against four molds including Penicillium, Aspergillus, Alternaria and Cladosporium were investigated.
Results: Of 90 Patients, 40 were men (44.4%) and 50 were women (55.6%). The participants were between 6 to 53 years and the most were 28-31years. The allergy was related to Penicillium (3.3%), Aspergillus (5.6%), Alternaria (13.3%) and Cladosporium (4.4%). There was a significant statistical relation between age and allergic rhinitis to Alternaria (P=0.011).
Conclusion: Molds can grow and proliferate in very humid environments. Because of low humidity climate in Tabriz (in the northwest of Iran), allergy to molds is relatively low in this region.
Key words: Rhinitis Allergic Mold Allergy
Mr Kiaei, M Hedayatmofidi, F Koohsar, A Amini, S Hoseinzadeh, A Mirbazel, Z Hesari,
Volume 8, Issue 1 (spring[PERSIAN] 2014)
Abstract
Abstract
Background and Objective: C - reactive protein (CRP) is an acute phase protein produced in liver. It is less than 5 mg per deciliter in the serum and body fluids of normal individuals, but it is increased suddenly within a few hours following inflammatory reaction. In bacterial and viral infections, active rheumatic fever, acute myocardial infarction and rheumatoid arthritis are also increased. The aim of this study was to investigate CRP level by Qualitative and Quantitative methods.
Material and Methods: The CRP of 200 patients was investigated by quantitative and qualitative methods. Qualitative CRP testing was conducted three times by different people, using two kit of bionic and Omega, and then the mean of the results was reported. For quantitative CRP testing, Immunoturbidimetry was used.
Results: In qualitative CRP test by Bionic kit: 180 (90%) were negative, 6 (3%) weakly positive, 9 (4.5%) +1 and 5 (2.5 %) were + 2. In qualitative CRP test by Omega Kit: 148 (74%) were negative, 32 (16%) weakly positive, 13 (6.5%) +1, 4 (2%) +2 and 3 (1.5%) were +3. A high percentage of Qualitative results, which were weakly positive, became negative by Quantitative methods. The Qualitative results of +1 and the next became positive by Quantitative methods.
Conclusion: It seems that in the early stages of inflammatory disease, quantitative methods are preferred to qualitative methods. Also, in cases that the CRP test results are weakly positive by qualitative methods, they should be controlled by quantitative methods too.
Keywords: CRP CRP Test Quantitative Qualitative CRP Test
Mr Bonyadi, F Ezzati,
Volume 8, Issue 2 (summer 2014[PERSIAN] 2014)
Abstract
Abstract
Background and objective: Being exposed to different allergens, followed by the production of specific IgE, has an important role in causing atopic dermatitis, recognizing the allergens and applying immunotherapy for treatment. We aimed to determine the frequency of common allergens in the patients suffering from atopic dermatitis.
Material and Methods: In this descriptive- analytical study the serum level of total IgE and frequency of specific IgE were measured by Immunoblotting method against 20 common allergens in 150 atopic dermatitis patients in 2010-2011 .The control group included the individuals who have been diagnosed healthy.
Result: The mean age was 30.02±14.79 the participants were male (77 51.3%) and female (73 48.7%). In 90% of patients, total IgE was more than the reference range with the mean of 227.51±103IU/ml. The most frequent allergens related to: Cultivated rye (48.6%), Timothy grass (42.9%), House dust mite (22.7%), Cat (16.7%), Horse (10%), Birch (11.33%), Potato (11.33%), Dog (16.7%), Egg white (8.7%), Cow milk (8.7%). The frequency of positive allergens in plants and fungus group was 54.34%, in animals was 26.8% and in foods was 19.56%. In control group, there was no total IgE elevation.
Conclusion: Based on the recognition of common allergens in east Azerbayjan, Iran, we recommend avoiding of these allergens and providing immunotherapy.
Keywords: Atopic Dermatitis, Allergen, Specific IgE, Total IgE
Shokoohi Zade, L, Mohabbati Mobarez, A, Alebooye, M, Ranjbar, R, Zali, Mr,
Volume 8, Issue 4 (supplement Issue[PERSIAN] 2015)
Abstract
Abstract Background and Objective: some of predisposing factors for enterococci colonization are hospitalization in ICU, prolonged use of antibiotics and continued bed rest in hospital. In this study antibiotic resistance of enterococcus in hospitalized patients of four hospitals in Tehran were studied. Material and Methods: the Clinical samples were taken from patients admitted to the ICU, from September 2011 to April 2012. Enterococci isolates were confirmed by biochemical tests, and Enterococcus faecalis and Enterococcus species by species-specific ddl genes. The disk diffusion and micro agar dilution susceptibility tests were performed according to Clinical and Laboratory Standards Institute (CLSI). Results: of 41 isolates in ICUs, 22 (5.52%) were E. faecium and 19 (5.47%) were E. faecalis. Most of E. faecium was isolated from urine and E. faecalis from trachea specimens. The rate of resistance to vancomycin, ampicillin, gentamicin, chloramphenicol and nitrofurantoin in E. faecium isolates was more than that of E. faecalis and the rate of resistance to tetracycline, ciprofloxacin and erythromycin was the same in both of them. MIC50 in vancomycin and ampicillin resistant E. faecium isolates was greater than 256 microgram and the MIC50 in gentamicin resistant isolates was more than 1024 microgram. . Conclusion: The presence of multi-resistant E. faecium strains in ICUs can be a serious warning for physicians and patients. Key words: Enterococcus faecium, Enterococcus faecalis, ICU, Antibiotic Resistance
Naghipoor, E, Raefi, A, Nasrollahiomran, A,
Volume 8, Issue 4 (supplement Issue[PERSIAN] 2015)
Abstract
Abstract Background and Objective: Enterococci are normal flora of human body and considered as the third leading cause of nosocomial infections. The aim of this study was to determine drug resistance of Enterococcus species through biochemical methods. Material and Methods: One hundred twenty-eight of enterococcus suspected samples were isolated from gorgan and gonbad’s hospitals from April to June, 2013. The samples were cultured on blood agar, chrome-agar, EMB agar and some special cultures of isolation of Enterococcus species. Suspension of bacteria was grown in Mueller Hinton agar and the inhibition zone diameter was determined by disk antibiogram. Results: Of 128 samples, 109(85.15%) were enterococci faecalis and 19 (14.85%) Enterococcus Faecium. In all of 128 cases, eight showed resistance to amoxicillin, ten to ampicillin, five to gentamicin, five to ciprofloxacin, six to chloramphenicol, four to cephalexin and one to vancomycin. Conclusion: It seems to be necessary to use drug sensitivity test for having appropriate treatment and preventing from resistance strains. Keywords: Enterococci, Antibiotic Resistance, Antibiogram
Mohajerani, Mr, Sarikhani, A, Gandomani, M, Eslamirad, Z, Mosayebi, M, Didehdar, M,
Volume 8, Issue 5 (winter[PERSIAN] 2015)
Abstract
Abstract Background and Objective: Malassezia that is a part of normal flora is lipophilic yeast involved in a variety of skin diseases such as seborrheic dermatitis, pityriasis versicolor, atopic dermatitis and psoriasis. Seborrheic dermatitis affects most often the sebaceous-gland-rich areas of skin such as face, scalp, and parts of the upper trunk. Dandruff is a mild variant of seborrheic dermatitis characterized by scaling. In this study, Malassezia species causing dandruff were identified. Material and Methods: In this descriptive study, the samples (n= 60) from participants with dandruff were examined under a microscope using 10% KOH solution and cultured in Leeming and Notman ager medium. DNA Extraction was performed from colonies by glass bead and the Malassezia genus, and species were detected by CfoI enzyme using PCR-RFLP method Results: Of 60, 40 (66.6%) were positive for Malassezia yeast. The positive samples in direct examination grew in culture medium. Malassezia species isolated were Malassezia globosa (25 cases), Malassezia restricta (10 cases), Malassezia furfur (3 cases) and Malassezia sympodialis (2 cases). Conclusions: In most studies, the Malassezia species were identified as the agents causing seborrheic dermatitis. In our study, Malassezia globosa was isolated as a dominant species. Keywords: Seborrheic Dermatitis, Malassezia SPP, Arak
Nasrollahi Omran, A, Nazemi, A, Kihanian, Sh, Aryana , N,
Volume 8, Issue 5 (winter[PERSIAN] 2015)
Abstract
Abstract Background and Objective: With the development of drug resistance in strains of fungi, there is a considerable resistance of Candida albicans strains to fluconazole. Molecular studies are developing to determine the relationship of such a drug resistance with the increased gene expression of enzymes produced in drug-resistant Candida isolates. We aimed to evaluate the relationship between extracellular lipase gene (LIP8) expression of Candida albicans isolated from candidiasis and sensitivity or resistance to fluconazole. Material and Methods: Drug susceptibility of Candida albicans was performed in oral and vaginal candidiasis to determine the proportion of strains sensitive or resistant to fluconazole using NCCLS method. To evaluate and compare the expression of these genes in the susceptible and resistant strains, RT real-time PCR reaction was used. Results: Of 46 Candida albicans, 20 were susceptible, 12 were semi-susceptible and 14 were resistant to fluconazole. By using PCR reaction, the results showed that the expression of this gene in fluconazole-susceptible isolates was moderate, while it was high in the isolates resistant to fluconazole. Conclusion: The results of lipase gene (LIP8) expression showed that the additional expression of some genes of the enzymes responsible for virulence of Candida may also play a role in resistance to fluconazole. Keywords: Candidiasis, Lipase Gene Expression, RT real-time PCR, Fluconazole
Safaari, M, Zolfaghari, Mr, Shakib, P, Rouhi, S,
Volume 8, Issue 5 (winter[PERSIAN] 2015)
Abstract
Abstract Background and Objective: Diarrheal diseases may occur in all age groups, worldwide. Escherichia coli (E. coli O157: H7) is one of the most important bacterial agents causing this disease. The purpose of this study was to assess the prevalence of diarrhea in patients with acute diarrhea caused by this bacterium. Material and Methods: In this study, 214 stool samples were collected from acute diarrheic patients in hospitals and clinical laboratories of Malayer city, Iran. The samples were cultured in rich, differentiation, specific and selective medium. To detect E. coli O157: H7, rapid detection method and antisera were used . Results: In 12.15% of the samples, lactose fermentation was observed and E. coli was afirmed. The results of lactose positive samples showed that 6.54% were negative-β- Glucuronidases and were confirmed as E. coli O157. Finally, by using O157: H7 antisera, 1.87% of 14 samples that were negative- β-Glucuronidases were asserted as E. coli O157. Conclusion: based on the results, the prevalence of E. coli O157: H7 is higher in children and elders than the others. Food and water play a significant role in transferring E. coli. Keywords: Prevalence, E. coli O157: H7, Gastroenteritis, Patients
Mahboobi, R, Fallah Mehrabadi, J, , Pourmand, Mr, Mashhadi, R, Haddadi, A,
Volume 8, Issue 5 (winter[PERSIAN] 2015)
Abstract
Abstract Background and Objective: Increased antibiotic resistant strains and inadequacy of current vaccines against pneumococcal infections necessitate the study of novel protein antigens. It seems that minor autolysin of Streptococcus pneumoniae may have antigenicity. Thus, we aimed at cloning its gene for the first time. Material and Methods: After DNA extraction of Streptococcus pneumoniae (ATCC 49619), Specific primers were designed for amplifying minor autolysin gene fragment, using PCR. The purified gene fragment was inserted into pET21a vector and was transformed into bacterial competent cells by heat shock technique. The presence of gene and absence of mutation in the recombinant vector were checked out with sequencing and enzymatic digestion methods. The gene sequence was finally analyzed by bioinformatic tools. Results: The gene of minor autolysin was cloned successfully and the result of enzymatic digestion was the indication of complete isolation of this gen from plasmid. . Bioinformatics studies revealed that the mature protein was lacking signal peptide and the gene encoded 318 amino acids with a molecular weight of 36.4 kDa. Conclusion: The presentation and characterization of novel antigens such as minor autolysin could help us with finding new approaches for preventing and controlling pneumococcal infection. Keywords: Streptococcus Pneumoniae, Minor Autolysin, Cloning
J Panahi, Mr Havasian, J Abdi, K Sayehmiri,
Volume 8, Issue 5 (winter[PERSIAN] 2015)
Abstract
Abstract In this study, the prevalence of Echinococcus granulosus was surveyed by meta-analysis and systematic review. Using main keywords of Echinococcus granulosus, dog and carnivores, we searched standard sites such as Google scholar, SID, Pubmed, Iranmedex, Irandoc, Science direct and magiran. Fifteen reliable articles were reviewed and analyzed by STATA software, Ver 11. From obtained articles, the number of 2271 dogs, 167 jackals and 174 foxes have been investigated by Iranian researchers. The infection rate of E.granulosus was reported 27.4% (95% CI, 20.9-33.9) in this study in that the highest from north and north west of Iran with prevalence of 33.3 %(CI:22.1-44.4), the lowest by 21.9 %(CI:12.5-31.3) from west and south west of Iran and the average from the central region of Iran ( 26.9% CI:12.8-41). Among cities the highest (64%) and the lowest (3.3%) infection rate were reported in Garmsar city (2010) and Sistan and Balochestan province (1997). Given that the overall prevalence of E.granulosus in Iran is high, Control and prevention measures including destruction of stray dogs and treatment of owner dogs seems to be necessary. Keywords: Echinococcus Granulosus, Carnivores, Iran, Systematic Review
Namroodi, S, Saberi, M,
Volume 9, Issue 2 (may,jun 2015[PERSIAN] 2015)
Abstract
Background and Objective: Dogs have been introduced as a major reservoir of Leishmania infantum. Concerning the increased sporadic reports of humeral visceral leishmaniasis in Golestan province, we aimed to study seroepidemiology of leishmania infantum in Rural Dogs.
Material and Methods: this study was conducted in 2012 - 2014 on 150 Serum samples of rural dogs, from 10 districts of Golestan province. The samples were analyzed by ELIZA kit.
Results: the frequency of leishmania infantum was 15.3% and it was higher in the dogs aged more than four. There were no differences in Leishmania infantum infection between sexes and seasons.
Conclusion: our findings indicate the presence of Leishmania infantum in Golestan Province. Given the presence of positive titer of Leishmania infantum in dogs without clinical signs, we emphasize the main role of rural dogs in transmitting Leishmania infuntum to villagers in the studied area.
Keywords: Leishmania Infantum, ELIZA, Rural Dogs, Golestan Province
Nasrollahi Omran, A, Nikpour, Sh, Mahdavi Omran, S,
Volume 9, Issue 2 (may,jun 2015[PERSIAN] 2015)
Abstract
A Raefi, N Nasrollahi Omran, A Nazemi,
Volume 9, Issue 2 (may,jun 2015[PERSIAN] 2015)
Abstract
Background and Objective: Malassezia yeast is considered lipophilic normal flora of human skin and warm-blooded vertebrates. This fungus is an opportunistic pathogen in causing seborrheic dermatitis. In this study, the yeasts isolated from the crust of the patients with seborrheic dermatitis were identified by PCR-Sequencing.
Material and Methods: In this study, 65 samples of the skin of ear, nose and dandruff were cultured in selective medium Sabouraud agar and modified Dixon agar to prevent dehydration. After biochemical tests, ITS1-4 Universal PCR primers were used to determine the species of yeast. Obtained PCR products were sequenced for the determination and identification of Malassezia species.
Results: Of nine samples obtained from scalp, four were Malassezia globosa, two Malassezia restricta, two Cryptococcus albidus and one Cryptococcus albidus milis.
Conclusion: The results of Malassezia globosa and Malassezia Restericta are very similar with those in studies elsewhere.
Keywords: Malassezia, Sequencing, Seborrheic Dermatitis, Tonekabon
Izadpanah, Mr, Asadpour, L,
Volume 9, Issue 3 (Jul,Aug2015[PERSIAN] 2015)
Abstract
Abstract
Background and Objective: Staphylococcus aureus is an important opportunistic pathogen causing a wide range of infections in human .Most clinical isolates of S.aureus are resistant to a number of antibiotics. For appropriate antimicrobial therapy, this study was conducted to determine antibacterial drug resistance patterns of S.aureus isolates obtained from different clinical samples in Rasht.
Material and Methods: the clinical isolates of S.aureus were collected from different clinical laboratories in Rasht. Thirty coagulase positive S.aureus strains were identified using biochemical tests and amplification of 23SrRNA and coa genes by polymerase chain reaction. Finally, the resistance pattern of the isolates to 16 selected antimicrobial agents was evaluated by disk diffusion method.
Results: the S.aureus isolates (75%) were resistant to methicillin and all of them were multidrug resistance. The isolates were high resistance to ampicillin (73%), amoxicillin (60%), cloxacillin (53%) and low resistance to vancomycin (7%) and gentamicin (10%).
Conclusion: given the high prevalence of methicillin resistant, multi drug resistant and presence of vancomycin resistant S.aureus isolates in Rasht, continuously monitoring of drug resistance pattern of S.aureus isolates is recommended for having appropriate therapeutic regime.
Keywords: Staphylococcus Aureus, Coagulase, Drug Resistance, PCR
Gholipoory, M, Rezai, Hr, Namroodi, S, Arabkhazaeli, F,
Volume 9, Issue 3 (Jul,Aug2015[PERSIAN] 2015)
Abstract
Abstract
Background and Objective: Given the Leishmaniasis is endemic in Turkmen Sahra, we aimed to study the contamination of rodents with this disease.
Material and Methods: Seventy-three rodents were collected from three regions (Gonbad, Gomishan and Bandar Turkmen) using live traps. In laboratory, morphometric characteristics were measured and for diagnosis of Leishmaniasis CL, the scratches obtained from their ears were examined by microscopic methods using Giemsa.
Results: The most frequent rodents were Meriones libycu (10.95%), Rattus norvegicus (21.91%), and Mus musculus (67.12%). Eleven (15.06%) of them were infected by cutaneous Leishmaniasis (CL).
Conclusion: Because of infection rate, there is a high transmission risk of CL in the studied region.
Keywords: Rodentia; Leishmaniasis; Turkmen Sahra; Meriones; Mus Musculus; Rattus Norvegicus
Haghshenas, Mr, Hosseini, E, Babamahmoodi, F, Nandoust-Kenari, Sh, Tabrizi, A,
Volume 9, Issue 3 (Jul,Aug2015[PERSIAN] 2015)
Abstract
Background and Objective: Influenza is an acute respiratory infection caused by Influenza virus with three kinds of A, B and C . This virus spreads througout the world and produce some epidemics with different intensities . This study aimed to determine the prevalence of influenza B in patients reffering to health centers.
Material and Methods: this study was conducted on 878 samples in 2011-2013. Using PureLinkTM Viral RNA/DNA Kit, Influenza-RNA was extracted. Then Influenza B was distinguished by using SuperScript III Platinum, Quantitive Real Time PCR System from InvitrogenTM , specific primers and probs.
Results: the rate of Influenza B positive was %5.58 of the patients that %55.10 of them were female and %44.89 male. The highest rate was related to 31-40 and 51-60 year old patients.
Conclusion:
given the prevalence of influenza B virus and lack of genetic changes , it is recommended that a proper vaccine for improving immunty and effective drugs for treatmet be used.
Keywords: Influenza B Virus; Respiratory Tract Infections; Common Cold; RT-PCR
Nahid Ariana, Ali Nazemi , Ayatollah Nasrollahi Omran,
Volume 9, Issue 4 (sep,Oct 2015 2015)
Abstract
Abstract
Background and objectives: More Candida albicans strains are reported resistant to fluconazole in patients with AIDS, cancer and organ recipients. Fluconazole resistance can be attributed to changes in pathways of sterol biosynthesis, mutation in or overexpression of ERG11 and the expression of CDR1, CDR2, and MDR1. This study aimed to compare the expression of CDR1, CDR2, and MDR1 in C. albicans resistant and susceptible to fluconazole.
Methods: MIC testing for fluconazole was performed on C. albicans isolates isolated from patients with oral and vaginal candidiasis to determine resistant and susceptible strains. Then real time PCR was performed on the resistant and susceptible isolates and the expression of CDR1, CDR2, and MDR1 was compared in C. albicans.
Results: Of 46 Candida albicans isolates, 20 susceptible isolates, 12 semi-susceptible isolates and 14 resistant isolates were identified by MIC. After real time PCR was performed, Candida albicans isolates susceptible to fluconazole showed moderate expression of CDR1, CDR2, and MDR1 genes, while resistant isolates showed slight or no expression.
Conclusion: Increased expression of CDR1, CDR2, and MDR1 had less and insignificant role in resistance to fluconazole.
Keywords: Candida Albicans, Gene Expression, Real time PCR method
