Title of article :
Identification of Malassezia Species Isolated from Patients with Pityriasis Versicolor Using PCR-RFLP Method in Markazi Province, Central Iran
Author/Authors :
DIDEHDAR, Mojtaba Molecular and Medicine Research Center - Arak University of Medical Sciences, Arak, Iran , MEHBOD, Amir Sayed Ali Dept. of Medical Parasitology and Mycology - Army University of Medical Sciences, Tehran, Iran , ESLAMIRAD, Zahra Dept. of Medical Parasitology and Mycology - Arak University of Medical Sciences, Arak, Iran , MOSAYEBI, Mahdi Dept. of Medical Parasitology and Mycology - Arak University of Medical Sciences, Arak, Iran , HAJIHOSSEIN, Reza Dept. of Medical Parasitology and Mycology - Arak University of Medical Sciences, Arak, Iran , GHORBANZADE, Behzad Dept. of Medical Parasitology and Mycology - Arak University of Medical Sciences, Arak, Iran , KHAZAEI, Mahmoud Reza Dept. of Laboratory Science - Islamic Azad University of Arak, Arak, Iran
Pages :
5
From page :
682
To page :
686
Abstract :
Background: The lipophilic yeasts of Malassezia species are members of the normal skin microbial that are cause of pityriasis versicolor. Pityriasis versicolor is a common superficial fungal infection with world-wide distribution. The phenotypic methods for identification of Malassezia species usually are time consuming and unreliable to differentiate newly identified species. But DNA-based techniques rapidly and accurately identified Malassezia species. The purpose of this study was isolation and identification of Malassezia Species from patients with pityriasis versicolor by molecular methods in Markazi Province, Central Iran in 2012. Methods: Mycologic examinations including direct microscopy and culture were performed on clinical samples. DNA extraction was performed from colonies. The ITS1 region of rDNA from isolates of Malassezia species were amplified by PCR reaction. The PCR were digested by Cfo I enzyme. Results:From 70 skin samples, were microscopically positive for Malassezia elements, 60 samples were grown on cul-ture medium (85.7%). Using PCR–RFLP method, that was performed on 60 isolates, 37(61.6%) M. globosa, 14(23.3%) M. furfur, 5(8.4%) M. sympodialis and 4(6.7%) M. restrictawere identified. In one case was isolated M. globosa along with M. restricta. Conclusion: The PCR-RFLP method is a useful and reliable technique for identification of differentiation of Malas-sezia species.
Keywords :
Malassezia spp. , Pityriasis versicolor , Identification , PCR-RFLP
Journal title :
Astroparticle Physics
Serial Year :
2014
Record number :
2419631
Link To Document :
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