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Showing 4 results for Tadayon
Bahadoor Sarkari (phd), Hadisa Tadayon (md), Shahrbanoo Askarian (bsc), Elahm Farnia (bsc), Mehrangiz Askarian (msc),
Volume 11, Issue 3 (10-2009)
Abstract
Background and Objective: Trichomoniasis is a disease caused by Trichomonas vaginalis and is the most common sexually transmitted disease after viral sexually transmitted ones. Trichomoniasis is usually treated with oral metronidazole and both patient and her partner should be treated. Considering the probable teratogenic effect of metronidazole and parasite drug resistance, it is necessary to find an alternative medication for treatment of trichomoniasis. In this study in vitro effect of garlic and Freula assafoetida extracts on Trichomonas vaginalis were evaluated. Materials and Methods: This In Vitro study was done in Yasuj Faculty of Medicine, Yasuj, Iran. Trichomonas vaginalis was cultured in TYI-S-33 medium. Effect of garlic and Freula assafoetida extracts in specified times and concentrations on Trichomonas vaginalis were assessed. Garlic extract was used in 0.1, 0.05 and 0.025 mg/ml while Freula assafoetida extract was used in 2, 1 and 0.5 mg/ml. The inhibitory effect of extract on Trichomonas was assessed by counting the alive parasites 1, 2 and 24 hours after exposure with extracts. Results: Findings of this study showed that hydroalcoholic extract of Freula assafoetida at concentration of 0.5, 1 and 2 mg/ml killed 90% of the parasites in first hour of exposure and garlic extract at concentration of 0.1 mg/ml killed 95% of parasites after 2 hours. Moreover garlic extract killed 90% of parasites at concentration of 0.05, 0.025 and 0.0125 mg/ml after 24 hours of exposure even at low concentration. Conclusion: This study indicated that garlic and freula assafoetida have significat effect on Trichomonas vaginalis, therefore detecting the effective substances of these potent anti-parasitic herbs is recommended.
Ahmadi M , Tadayon K, Mosavari N, Farazi Aa, Arjomandzadegan M, Keshavarz R, Banihashemi R, Sekhavati M, Hamedi D, Eramabadi M, Jabbari M, Ghaderi R, Hoseini D, Dashtipour Sh,
Volume 17, Issue 1 (3-2015)
Abstract
Background and Objective: MIRU-VNTR typing is currently one of the most frequently-used standardized genotyping systems in molecular epidemiology of tuberculosis in the world. This sudy was done to determine the Mycobacterium tuberculosis genotyping by MIRU-VNTR method. Methods: This descriptive study was done on sputum, gastric lavage clinical specimens of 53 tuberculosis suspected patients. Fifty-three isolates were identified by 16S rRNA and Rv-typing followed by RD typing. They were then subjected to a 12-locus (ETRA, ETRB, ETRC, ETRD, ETRE and ETRF, MIRU-10, MIRU-26, MIRU-39, MIRU-30 plus QUB-11b) MIRU-VNTR typing system. Results: In MIRU-VNTR typing, forty-four types were identified with 13 isolates classified in 4 clustered and the remaining 40 isolates representing 40 orphan patterns. In comparative analysis of MIRU-VNTR loci, MIRU-26 with 7 alleles displayed the highest diversity level (Simpson’s diversity index = 0.767. Out of the 53 isolates, only one was identified as Mycobacterium bovis. All the remaining isolates were characterized as Mycobacterium tuberculosis. None of the samples was affected to Mycobacterium complex strain. No evidence of either double or co-infection of the patients with more than one species/strain was detected. Conclusion: While the genomic diversity observed by MIRU-VNTR typing sounds extensive, the population genomic structure on the whole however, seems to be homogenous. Recent transmission between studied patients does not appear to be a frequent event as only 13 isolates representing 4 MIRU-VNTR types, were assumingly epidemic.
Tadayoni S, Malekzadeh Shafarodi M , Ghasemi Hamidabadi H , Esmailnejad Moghaddam A, Khalilian A, Rezaei N,
Volume 17, Issue 3 (10-2015)
Abstract
Background and Objective: With respect to the antioxidant role of melatonin and retinoic acid, it seems to be effective both in the maturation and embryonic development. This study was done to investigate the effect of combination of melatonin and All-Trans retinoic acid (RA) on maturation, fertilization and embryonic development of immature mouse oocytes. Methods: In this experimental study, cumulus - oocyte complex (COCs) were recovered from 4-6 week old female mice NMRI and were divided into 6 maturation medium groups including control, sham, experiment 1(melatonin 100 nM, 1 and 2 µM), experiment 2 (retinoic acid 1, 2, 4, 6 µM), experiment 3 (melatonin 2 µM+RA 4 µM), experiment 4 (Mel 100nM + retinoic acid 4µM). The maturation rate was recorded after 24 hours of culture in a humidified atmosphere of 5% CO2 at 37°C. The matured oocytes were fertilized with sperm. Fertilization and embryonic development rates to the blastocyst stage were recorded. Results: Maturation rate in the control and sham groups were 50.6% and 49.4%, respectively. Maturation rate were 54.3%, 54.8%, 59.9% in melatonin group with concentrations of 100 nM, 1 and 2 µM, respectively. Maturation rate were 51.6%, 51%, 59% and 49.6% in t-RA group with concentrations of 1, 2, 4, 6 μM. Maturation rate were 60.4% and 54.2% in the experiment 3 and 4 groups, respectively. The maturation rates in the melatonin 2 µM, retinoic acid 4 µM and experiment 3 significantly increased in compare to control (P<0.05). The embryonic development rate in the melatonin with 100nM concentration and 4 µM of retinoic acid increased significantly compared to controls (P<0.05). Although, embryonic development rate in experiment 3 was higher than control, but lower in compare to melatonin 100 nM and the retinoic acid 4 µM. The embryonic development rate in experiment 4 significantly increased in compare to control (P<0.05). Conclusion: Combination of melatonin and All-Trans retinoic acid in medium culture increase maturation rate and improved embryonic development in dose dependent manner.
E Faraj Tabrizi , K Tadayon , N Mosavari , Tajbakhsh E, Keshavarz R, Ghaderi R, Sekhavati M, Banihashemi R, Najafpour R, Mohrekesh Haghighat M , Dehghanpour M,
Volume 18, Issue 3 (10-2016)
Abstract
Background and Objective: Iran remains a major stronghold for glanders in the Middle East. In Iran, the non-indigenous Burkholderia mallei Razi 325 strain is used in manufacturing of the mallein, required for malleination of animals. Multi Locus Variable number tandem repeat analysis is currently the standard globally accepted genotyping system for Burkholderia mallei. This study was done to survey the genomic structure of Burkholderia mallei Razi 325, the strain used for industrial production of Mallein.
Methods: In this descriptive study, a MLVA genotyping system with 4 previously-characterized loci VNTR140, VNTR1367, VNTR2065, VNTR2971 along with two new loci of VNTR24, VNTR41 was used.
Results: Optimization of PCRs resulted in a single protocol that enabled simultaneous amplification of all the six loci. Sequencing of PCR products revealed there were 2, 3, 12, 6, 1 and 2 copies of the unit repeat hold in the genome of the Burkholderia mallei Razi 325 strain. This observation was extended to include the already-whole genome sequenced Chinese Burkholderia mallei ATCC 23344 and Burkholderia mallei BMQ and also Burkholderia mallei SAVP1 strains.
Conclusion: The Burkholderia mallei Razi 325 strain is distinguishable from the other three strains through MLVA genotyping method.
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