Diagnosis of Cutaneous Leishmaniasis by Multiplex PCR

Introduction: Annually, more than 14 million people are reported to be infected with Leishmaniasis all over the world. In Iran, this disease is seen in the form of cutaneous and visceral leishmaniasis, of which the cutaneous form is more wide spread. In recent years, cutaneous leishmaniaisis is diag...

Full description

Bibliographic Details
Main Authors: M Heiat, Sh Nazarian, M Saadati, Z Safari, M Mirzaei
Format: Article
Language:fas
Published: Shahid Sadoughi University of Medical Sciences 2010-07-01
Series:Majallah-i Dānishgāh-i ’Ulūm-i Pizishkī-i Shahīd Ṣadūqī Yazd
Subjects:
Online Access:http://85.185.157.11:6280/jssu/browse.php?a_id=1037&slc_lang=en&sid=1&ftxt=1
id doaj-1ad7ea67d3124c948079858b6b14dc2d
record_format Article
spelling doaj-1ad7ea67d3124c948079858b6b14dc2d2020-11-25T02:03:34ZfasShahid Sadoughi University of Medical SciencesMajallah-i Dānishgāh-i ’Ulūm-i Pizishkī-i Shahīd Ṣadūqī Yazd2228-57412228-57332010-07-01182118126Diagnosis of Cutaneous Leishmaniasis by Multiplex PCRM HeiatSh NazarianM SaadatiZ SafariM MirzaeiIntroduction: Annually, more than 14 million people are reported to be infected with Leishmaniasis all over the world. In Iran, this disease is seen in the form of cutaneous and visceral leishmaniasis, of which the cutaneous form is more wide spread. In recent years, cutaneous leishmaniaisis is diagnosed by PCR utilizing specific primers in order to amplify different parasite genes including ribosomal RNA genes, kinetoplast DNA or tandem repeating sequences. The aim of this research was to detect early stage cutaneous leishmaniasis using Multiplex-PCR technique. Methods: In this study, 67 samples were prepared from patients with cutaneous leishmaniasis. DNA was extracted with phenolchloroform. Each specimen was analyzed using two different pairs of PCR primers. The sensitivity of each PCR was optimized on pure Leishmania DNA prior to use for diagnosis. Two standard parasites L. major and L. tropica were used as positive control. Results: DNA amplification fragments were two 115 bp and 683 bp for AB and UL primers, respectively. The sensitivity of two primers was not equal for detection of L. major and L. tropica. The sensivity of PCR with AB primer was 35 cells, while that for UL primer was 40 cells. Conclusion: The results of this study indicate that PCR is a sensitive diagnostic assay for cutaneous leishmaniasis and could be employed as the new standard for routine diagnosis when species identification is not required. However, the ability to identify species is especially important in prognosis of the disease and in deciding appropriate therapy, especially in regions where more than one type of species and disease are seen by clinicians.http://85.185.157.11:6280/jssu/browse.php?a_id=1037&slc_lang=en&sid=1&ftxt=1Multiplex PCRCutaneous Leishmaniasis Detection
collection DOAJ
language fas
format Article
sources DOAJ
author M Heiat
Sh Nazarian
M Saadati
Z Safari
M Mirzaei
spellingShingle M Heiat
Sh Nazarian
M Saadati
Z Safari
M Mirzaei
Diagnosis of Cutaneous Leishmaniasis by Multiplex PCR
Majallah-i Dānishgāh-i ’Ulūm-i Pizishkī-i Shahīd Ṣadūqī Yazd
Multiplex PCR
Cutaneous Leishmaniasis Detection
author_facet M Heiat
Sh Nazarian
M Saadati
Z Safari
M Mirzaei
author_sort M Heiat
title Diagnosis of Cutaneous Leishmaniasis by Multiplex PCR
title_short Diagnosis of Cutaneous Leishmaniasis by Multiplex PCR
title_full Diagnosis of Cutaneous Leishmaniasis by Multiplex PCR
title_fullStr Diagnosis of Cutaneous Leishmaniasis by Multiplex PCR
title_full_unstemmed Diagnosis of Cutaneous Leishmaniasis by Multiplex PCR
title_sort diagnosis of cutaneous leishmaniasis by multiplex pcr
publisher Shahid Sadoughi University of Medical Sciences
series Majallah-i Dānishgāh-i ’Ulūm-i Pizishkī-i Shahīd Ṣadūqī Yazd
issn 2228-5741
2228-5733
publishDate 2010-07-01
description Introduction: Annually, more than 14 million people are reported to be infected with Leishmaniasis all over the world. In Iran, this disease is seen in the form of cutaneous and visceral leishmaniasis, of which the cutaneous form is more wide spread. In recent years, cutaneous leishmaniaisis is diagnosed by PCR utilizing specific primers in order to amplify different parasite genes including ribosomal RNA genes, kinetoplast DNA or tandem repeating sequences. The aim of this research was to detect early stage cutaneous leishmaniasis using Multiplex-PCR technique. Methods: In this study, 67 samples were prepared from patients with cutaneous leishmaniasis. DNA was extracted with phenolchloroform. Each specimen was analyzed using two different pairs of PCR primers. The sensitivity of each PCR was optimized on pure Leishmania DNA prior to use for diagnosis. Two standard parasites L. major and L. tropica were used as positive control. Results: DNA amplification fragments were two 115 bp and 683 bp for AB and UL primers, respectively. The sensitivity of two primers was not equal for detection of L. major and L. tropica. The sensivity of PCR with AB primer was 35 cells, while that for UL primer was 40 cells. Conclusion: The results of this study indicate that PCR is a sensitive diagnostic assay for cutaneous leishmaniasis and could be employed as the new standard for routine diagnosis when species identification is not required. However, the ability to identify species is especially important in prognosis of the disease and in deciding appropriate therapy, especially in regions where more than one type of species and disease are seen by clinicians.
topic Multiplex PCR
Cutaneous Leishmaniasis Detection
url http://85.185.157.11:6280/jssu/browse.php?a_id=1037&slc_lang=en&sid=1&ftxt=1
work_keys_str_mv AT mheiat diagnosisofcutaneousleishmaniasisbymultiplexpcr
AT shnazarian diagnosisofcutaneousleishmaniasisbymultiplexpcr
AT msaadati diagnosisofcutaneousleishmaniasisbymultiplexpcr
AT zsafari diagnosisofcutaneousleishmaniasisbymultiplexpcr
AT mmirzaei diagnosisofcutaneousleishmaniasisbymultiplexpcr
_version_ 1724947407550021632