Molecular diagnosis of Old World leishmaniasis: Real-time PCR based on tryparedoxin peroxidase gene for the detection and identification of Leishmania spp

Background & objectives: Rapid and accurate diagnosis and identification of Leishmania sp causing cutaneousleishmaniasis is crucial in control and therapeutic programs. The problem of diagnosis with traditional methodsis that they have a low sensitivity or time consuming but molecular techniques...

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Main Author: Sharifeh Khosravi , Saied Hossein Hejazi , Mortaza Hashemzadeh , Gilda Eslami & Hossein Yousofi Darani
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2012-03-01
Series:Journal of Vector Borne Diseases
Subjects:
Online Access:http://www.mrcindia.org/journal/issues/491015.pdf
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spelling doaj-65167a7cff86422b8299166651a76bf22020-11-24T23:56:09ZengWolters Kluwer Medknow PublicationsJournal of Vector Borne Diseases0972-90622012-03-014911518Molecular diagnosis of Old World leishmaniasis: Real-time PCR based on tryparedoxin peroxidase gene for the detection and identification of Leishmania sppSharifeh Khosravi , Saied Hossein Hejazi , Mortaza Hashemzadeh , Gilda Eslami & Hossein Yousofi DaraniBackground & objectives: Rapid and accurate diagnosis and identification of Leishmania sp causing cutaneousleishmaniasis is crucial in control and therapeutic programs. The problem of diagnosis with traditional methodsis that they have a low sensitivity or time consuming but molecular techniques would be an alternative methodfor rapid and accurate diagnosis. In this work, tryparedoxine peroxidase gene-based real-time PCR was used foraccurate identification of Leishmania spp causing Old-World cutaneous leishmaniasis.Methods: In this study, biopsies of specimens were taken from the ulcerative sites in 100 patients and used fordirect microscopy, culture in NNN or fixed in alcohol for identification of Leishmania spp using tryparedoxinperoxidase gene-based realtime PCR (qPCR).Results: Using direct microscopy and culture method, Leishmania parasites were isolated from 68 out of 100patient samples. However, 13 patients with negative finding on traditional tests, had positive results on RT-PCRtest. After melting curve analysis of PCR product, Leishmania major in 75 and L. tropica in 4 cases wereidentified. The sensitivity and specificity of RT-PCR for diagnosis of cutaneous leishmaniasis was 98.7 and59.8%, respectively.Conclusion: Results of this study showed that RT-PCR was the most sensitive diagnostic test for cutaneousleishmaniasis and represents a tool for rapid species identification.http://www.mrcindia.org/journal/issues/491015.pdfCutaneous leishmaniasisdiagnosisIranperoxidaseRT-PCRtryparedoxin
collection DOAJ
language English
format Article
sources DOAJ
author Sharifeh Khosravi , Saied Hossein Hejazi , Mortaza Hashemzadeh , Gilda Eslami & Hossein Yousofi Darani
spellingShingle Sharifeh Khosravi , Saied Hossein Hejazi , Mortaza Hashemzadeh , Gilda Eslami & Hossein Yousofi Darani
Molecular diagnosis of Old World leishmaniasis: Real-time PCR based on tryparedoxin peroxidase gene for the detection and identification of Leishmania spp
Journal of Vector Borne Diseases
Cutaneous leishmaniasis
diagnosis
Iran
peroxidase
RT-PCR
tryparedoxin
author_facet Sharifeh Khosravi , Saied Hossein Hejazi , Mortaza Hashemzadeh , Gilda Eslami & Hossein Yousofi Darani
author_sort Sharifeh Khosravi , Saied Hossein Hejazi , Mortaza Hashemzadeh , Gilda Eslami & Hossein Yousofi Darani
title Molecular diagnosis of Old World leishmaniasis: Real-time PCR based on tryparedoxin peroxidase gene for the detection and identification of Leishmania spp
title_short Molecular diagnosis of Old World leishmaniasis: Real-time PCR based on tryparedoxin peroxidase gene for the detection and identification of Leishmania spp
title_full Molecular diagnosis of Old World leishmaniasis: Real-time PCR based on tryparedoxin peroxidase gene for the detection and identification of Leishmania spp
title_fullStr Molecular diagnosis of Old World leishmaniasis: Real-time PCR based on tryparedoxin peroxidase gene for the detection and identification of Leishmania spp
title_full_unstemmed Molecular diagnosis of Old World leishmaniasis: Real-time PCR based on tryparedoxin peroxidase gene for the detection and identification of Leishmania spp
title_sort molecular diagnosis of old world leishmaniasis: real-time pcr based on tryparedoxin peroxidase gene for the detection and identification of leishmania spp
publisher Wolters Kluwer Medknow Publications
series Journal of Vector Borne Diseases
issn 0972-9062
publishDate 2012-03-01
description Background & objectives: Rapid and accurate diagnosis and identification of Leishmania sp causing cutaneousleishmaniasis is crucial in control and therapeutic programs. The problem of diagnosis with traditional methodsis that they have a low sensitivity or time consuming but molecular techniques would be an alternative methodfor rapid and accurate diagnosis. In this work, tryparedoxine peroxidase gene-based real-time PCR was used foraccurate identification of Leishmania spp causing Old-World cutaneous leishmaniasis.Methods: In this study, biopsies of specimens were taken from the ulcerative sites in 100 patients and used fordirect microscopy, culture in NNN or fixed in alcohol for identification of Leishmania spp using tryparedoxinperoxidase gene-based realtime PCR (qPCR).Results: Using direct microscopy and culture method, Leishmania parasites were isolated from 68 out of 100patient samples. However, 13 patients with negative finding on traditional tests, had positive results on RT-PCRtest. After melting curve analysis of PCR product, Leishmania major in 75 and L. tropica in 4 cases wereidentified. The sensitivity and specificity of RT-PCR for diagnosis of cutaneous leishmaniasis was 98.7 and59.8%, respectively.Conclusion: Results of this study showed that RT-PCR was the most sensitive diagnostic test for cutaneousleishmaniasis and represents a tool for rapid species identification.
topic Cutaneous leishmaniasis
diagnosis
Iran
peroxidase
RT-PCR
tryparedoxin
url http://www.mrcindia.org/journal/issues/491015.pdf
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