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Identification of Malassezia Species Isolated from Patients with Pityriasis Versicolor Using PCR-RFLP Method in Markazi Province, Central Iran

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 usual...

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Autores principales: DIDEHDAR, Mojtaba, MEHBOD, Amir Sayed Ali, ESLAMIRAD, Zahra, MOSAYEBI, Mahdi, HAJIHOSSEIN, Reza, GHORBANZADE, Behzad, KHAZAEI, Mahmoud Reza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4449417/
https://www.ncbi.nlm.nih.gov/pubmed/26056657
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author DIDEHDAR, Mojtaba
MEHBOD, Amir Sayed Ali
ESLAMIRAD, Zahra
MOSAYEBI, Mahdi
HAJIHOSSEIN, Reza
GHORBANZADE, Behzad
KHAZAEI, Mahmoud Reza
author_facet DIDEHDAR, Mojtaba
MEHBOD, Amir Sayed Ali
ESLAMIRAD, Zahra
MOSAYEBI, Mahdi
HAJIHOSSEIN, Reza
GHORBANZADE, Behzad
KHAZAEI, Mahmoud Reza
author_sort DIDEHDAR, Mojtaba
collection PubMed
description 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 culture 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.
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spelling pubmed-44494172015-06-08 Identification of Malassezia Species Isolated from Patients with Pityriasis Versicolor Using PCR-RFLP Method in Markazi Province, Central Iran DIDEHDAR, Mojtaba MEHBOD, Amir Sayed Ali ESLAMIRAD, Zahra MOSAYEBI, Mahdi HAJIHOSSEIN, Reza GHORBANZADE, Behzad KHAZAEI, Mahmoud Reza Iran J Public Health Short Communication 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 culture 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. Tehran University of Medical Sciences 2014-05 /pmc/articles/PMC4449417/ /pubmed/26056657 Text en Copyright © Iranian Public Health Association & Tehran University of Medical Sciences This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.
spellingShingle Short Communication
DIDEHDAR, Mojtaba
MEHBOD, Amir Sayed Ali
ESLAMIRAD, Zahra
MOSAYEBI, Mahdi
HAJIHOSSEIN, Reza
GHORBANZADE, Behzad
KHAZAEI, Mahmoud Reza
Identification of Malassezia Species Isolated from Patients with Pityriasis Versicolor Using PCR-RFLP Method in Markazi Province, Central Iran
title Identification of Malassezia Species Isolated from Patients with Pityriasis Versicolor Using PCR-RFLP Method in Markazi Province, Central Iran
title_full Identification of Malassezia Species Isolated from Patients with Pityriasis Versicolor Using PCR-RFLP Method in Markazi Province, Central Iran
title_fullStr Identification of Malassezia Species Isolated from Patients with Pityriasis Versicolor Using PCR-RFLP Method in Markazi Province, Central Iran
title_full_unstemmed Identification of Malassezia Species Isolated from Patients with Pityriasis Versicolor Using PCR-RFLP Method in Markazi Province, Central Iran
title_short Identification of Malassezia Species Isolated from Patients with Pityriasis Versicolor Using PCR-RFLP Method in Markazi Province, Central Iran
title_sort identification of malassezia species isolated from patients with pityriasis versicolor using pcr-rflp method in markazi province, central iran
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4449417/
https://www.ncbi.nlm.nih.gov/pubmed/26056657
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