Identification of Pathogenic Candida Species: PCR-Fragment Size Polymorphism (PCR-FSP) Method

"nBackground: The clinical importance of yeast infections has increased in recent decades. There are 10-15 pathogenic Candida species. The current morphological and physiological methods for identification of Candida species are generally not easy to interpret and may be expensive or time-c...

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Main Authors: Mirhendi SH, Adin H, Shidfar MR, Kordbacheh P, Hashemi SJ, Moazeni M, Hosseinpur L, Rezaie Matehkolaie A
Format: Article
Language:fas
Published: Tehran University of Medical Sciences 2008-12-01
Series:Tehran University Medical Journal
Subjects:
Online Access:http://journals.tums.ac.ir/PdfMed.aspx?pdf_med=/upload_files/pdf/12328.pdf&manuscript_id=12328
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author Mirhendi SH
Adin H
Shidfar MR
Kordbacheh P
Hashemi SJ
Moazeni M
Hosseinpur L
Rezaie Matehkolaie A
author_facet Mirhendi SH
Adin H
Shidfar MR
Kordbacheh P
Hashemi SJ
Moazeni M
Hosseinpur L
Rezaie Matehkolaie A
author_sort Mirhendi SH
collection DOAJ
description "nBackground: The clinical importance of yeast infections has increased in recent decades. There are 10-15 pathogenic Candida species. The current morphological and physiological methods for identification of Candida species are generally not easy to interpret and may be expensive or time-consuming. In the present study, we introduce and use a new approach for the identification and differentiation of medically important yeast species of Candida. In this method, size polymorphism of the internal transcribed spacer regions, ITS1 and ITS2, of the ribosomal DNA in various Candida species is used as the basis of species recognition. "nMethods: The genomic DNA of 31 standard strains and 60 clinical isolates was extracted and PCR-amplified using two primer pairs (ITS1-ITS2 and ITS3-ITS4) separately. Both PCR products were mixed and analyzed after standard agarose gel electrophoresis. The species of the tested yeasts were identified by the electrophoretic patterns of the mixed PCR products of each sample, comparing the data obtained from the sequence analyses of ITS1 and ITS2 molecules. "nResults: By this method, with the exception of C. albicans and C. dubliniensis, we were able to clearly differentiate nearly all common pathogenic Candida species, including C. albicans, C. glabrata, C. gulliermondii, C. parapsilosis, C. tropicalis,      C. krusei, C. kefyr, C. lusinaniae and C. rugosa. All standard and clinical strains were identified correctly, without expensive methods such as sequencing and capillary electrophoresis. "nConclusion: It seems that the PCR-FSP method introduced in this study is the easiest molecular approach for the identification of a wide range of pathogenic Candida species and is applicable for diagnostic and epidemiological purposes in reference laboratories.
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spelling doaj.art-c6bf0d3bf4e645d4ad206f4ffc86d3f92022-12-21T18:46:26ZfasTehran University of Medical SciencesTehran University Medical Journal1683-17641735-73222008-12-01669639645Identification of Pathogenic Candida Species: PCR-Fragment Size Polymorphism (PCR-FSP) MethodMirhendi SHAdin HShidfar MRKordbacheh PHashemi SJMoazeni MHosseinpur LRezaie Matehkolaie A"nBackground: The clinical importance of yeast infections has increased in recent decades. There are 10-15 pathogenic Candida species. The current morphological and physiological methods for identification of Candida species are generally not easy to interpret and may be expensive or time-consuming. In the present study, we introduce and use a new approach for the identification and differentiation of medically important yeast species of Candida. In this method, size polymorphism of the internal transcribed spacer regions, ITS1 and ITS2, of the ribosomal DNA in various Candida species is used as the basis of species recognition. "nMethods: The genomic DNA of 31 standard strains and 60 clinical isolates was extracted and PCR-amplified using two primer pairs (ITS1-ITS2 and ITS3-ITS4) separately. Both PCR products were mixed and analyzed after standard agarose gel electrophoresis. The species of the tested yeasts were identified by the electrophoretic patterns of the mixed PCR products of each sample, comparing the data obtained from the sequence analyses of ITS1 and ITS2 molecules. "nResults: By this method, with the exception of C. albicans and C. dubliniensis, we were able to clearly differentiate nearly all common pathogenic Candida species, including C. albicans, C. glabrata, C. gulliermondii, C. parapsilosis, C. tropicalis,      C. krusei, C. kefyr, C. lusinaniae and C. rugosa. All standard and clinical strains were identified correctly, without expensive methods such as sequencing and capillary electrophoresis. "nConclusion: It seems that the PCR-FSP method introduced in this study is the easiest molecular approach for the identification of a wide range of pathogenic Candida species and is applicable for diagnostic and epidemiological purposes in reference laboratories.http://journals.tums.ac.ir/PdfMed.aspx?pdf_med=/upload_files/pdf/12328.pdf&manuscript_id=12328PCR-FSPcandidaidentificationITS
spellingShingle Mirhendi SH
Adin H
Shidfar MR
Kordbacheh P
Hashemi SJ
Moazeni M
Hosseinpur L
Rezaie Matehkolaie A
Identification of Pathogenic Candida Species: PCR-Fragment Size Polymorphism (PCR-FSP) Method
Tehran University Medical Journal
PCR-FSP
candida
identification
ITS
title Identification of Pathogenic Candida Species: PCR-Fragment Size Polymorphism (PCR-FSP) Method
title_full Identification of Pathogenic Candida Species: PCR-Fragment Size Polymorphism (PCR-FSP) Method
title_fullStr Identification of Pathogenic Candida Species: PCR-Fragment Size Polymorphism (PCR-FSP) Method
title_full_unstemmed Identification of Pathogenic Candida Species: PCR-Fragment Size Polymorphism (PCR-FSP) Method
title_short Identification of Pathogenic Candida Species: PCR-Fragment Size Polymorphism (PCR-FSP) Method
title_sort identification of pathogenic candida species pcr fragment size polymorphism pcr fsp method
topic PCR-FSP
candida
identification
ITS
url http://journals.tums.ac.ir/PdfMed.aspx?pdf_med=/upload_files/pdf/12328.pdf&manuscript_id=12328
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