Molecular Identification of Agents of Human Cutaneous Leishmaniasis and Canine Visceral Leishmaniasis in Different Areas of Iran Using Internal Transcribed Spacer 1 PCR-RFLP

<p><strong>Background</strong>: Leishmaniasis is a major medical health problem and distributes in nearly half of 31 provinces of Iran. We aimed to identify cutaneous and visceral <em>Leishmania</em> spp. isolated from infected humans and domestic dogs in various region...

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Main Authors: Aref Teimouri, Mehdi Mohebali, Elham Kazemirad, Homa Hajjaran
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2018-06-01
Series:Journal of Arthropod-Borne Diseases
Subjects:
Online Access:http://jad.tums.ac.ir/index.php/jad/article/view/890
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spelling doaj-e1efe36921454c1eb84d02dc1da479e02020-11-25T02:16:07ZengTehran University of Medical SciencesJournal of Arthropod-Borne Diseases 1735-71792322-22712018-06-01121385Molecular Identification of Agents of Human Cutaneous Leishmaniasis and Canine Visceral Leishmaniasis in Different Areas of Iran Using Internal Transcribed Spacer 1 PCR-RFLPAref Teimouri0Mehdi Mohebali1Elham Kazemirad2Homa Hajjaran3Department of Medical Parasitology and Mycology, Tehran University of Medical Sciences, Tehran, Iran Students Scientific Research Center, Tehran University of Medical Sciences, Tehran, IranDepartment of Medical Parasitology and Mycology, Tehran University of Medical Sciences, Tehran, Iran Center for Research of Endemic Parasites of Iran, Tehran University of Medical Sciences,Tehran, IranDepartment of Medical Parasitology and Mycology, Tehran University of Medical Sciences, Tehran, IranDepartment of Medical Parasitology and Mycology, Tehran University of Medical Sciences, Tehran, Iran<p><strong>Background</strong>: Leishmaniasis is a major medical health problem and distributes in nearly half of 31 provinces of Iran. We aimed to identify cutaneous and visceral <em>Leishmania</em> spp. isolated from infected humans and domestic dogs in various regions of Iran, 2010‒2013.<strong><br />Methods: </strong>DNA was extracted from 108 lesion exudate samples of suspected patients to cutaneous leishmaniasis and nine liver and spleen aspirates of infected dogs cultured in RPMI-1640 and amplified using partial sequence of ITS1 gene. The PCR amplicons were digested using <em>Hae</em>III endonuclease enzyme and used in restriction fragment length polymorphism (RFLP) assay. Then, 48 amplicons representing various hosts were sequenced and compared to se­quences from GenBank databases using BLAST.<strong><br />Results:</strong> PCR-RFLP analysis showed that 60 and 48 CL patients were infected by <em>Leishmania tropica</em> and <em>L. major</em>, respectively. From nine canine visceral leishmaniasis (CVL) isolates, eight isolates were identified as <em>L. infantum</em> and one as <em>L. tropica</em>. The greatest similarity of 95.7% in ITS1 region was seen between <em>L. infantum</em> and <em>L. major</em>. Furthermore, the lowest similarity with 65.7% was seen between <em>L. tropica</em> and <em>L. major</em>. Intra-species comparison of ITS1 region in <em>L. infantum, L. major </em>and<em> L. tropica</em> isolates were showed 100%, 98.2% and 72.4 % similarities, respectively.<strong><br />Conclusion:</strong> PCR-RFLP based on ITS1 region is an appropriate method to distinguish three <em>Leishmania</em> spp. of <em>L. major</em>, <em>L. tropica,</em> and <em>L. infantum</em>. In intra-species comparison of ITS1 region, genotypic variations showed that <em>L. tropica</em> isolates were more heterogeneous than <em>L. major</em> and <em>L. infantum</em> isolates.</p>http://jad.tums.ac.ir/index.php/jad/article/view/890Leishmania, ITS1 gene, PCR- RFLP, Iran
collection DOAJ
language English
format Article
sources DOAJ
author Aref Teimouri
Mehdi Mohebali
Elham Kazemirad
Homa Hajjaran
spellingShingle Aref Teimouri
Mehdi Mohebali
Elham Kazemirad
Homa Hajjaran
Molecular Identification of Agents of Human Cutaneous Leishmaniasis and Canine Visceral Leishmaniasis in Different Areas of Iran Using Internal Transcribed Spacer 1 PCR-RFLP
Journal of Arthropod-Borne Diseases
Leishmania, ITS1 gene, PCR- RFLP, Iran
author_facet Aref Teimouri
Mehdi Mohebali
Elham Kazemirad
Homa Hajjaran
author_sort Aref Teimouri
title Molecular Identification of Agents of Human Cutaneous Leishmaniasis and Canine Visceral Leishmaniasis in Different Areas of Iran Using Internal Transcribed Spacer 1 PCR-RFLP
title_short Molecular Identification of Agents of Human Cutaneous Leishmaniasis and Canine Visceral Leishmaniasis in Different Areas of Iran Using Internal Transcribed Spacer 1 PCR-RFLP
title_full Molecular Identification of Agents of Human Cutaneous Leishmaniasis and Canine Visceral Leishmaniasis in Different Areas of Iran Using Internal Transcribed Spacer 1 PCR-RFLP
title_fullStr Molecular Identification of Agents of Human Cutaneous Leishmaniasis and Canine Visceral Leishmaniasis in Different Areas of Iran Using Internal Transcribed Spacer 1 PCR-RFLP
title_full_unstemmed Molecular Identification of Agents of Human Cutaneous Leishmaniasis and Canine Visceral Leishmaniasis in Different Areas of Iran Using Internal Transcribed Spacer 1 PCR-RFLP
title_sort molecular identification of agents of human cutaneous leishmaniasis and canine visceral leishmaniasis in different areas of iran using internal transcribed spacer 1 pcr-rflp
publisher Tehran University of Medical Sciences
series Journal of Arthropod-Borne Diseases
issn 1735-7179
2322-2271
publishDate 2018-06-01
description <p><strong>Background</strong>: Leishmaniasis is a major medical health problem and distributes in nearly half of 31 provinces of Iran. We aimed to identify cutaneous and visceral <em>Leishmania</em> spp. isolated from infected humans and domestic dogs in various regions of Iran, 2010‒2013.<strong><br />Methods: </strong>DNA was extracted from 108 lesion exudate samples of suspected patients to cutaneous leishmaniasis and nine liver and spleen aspirates of infected dogs cultured in RPMI-1640 and amplified using partial sequence of ITS1 gene. The PCR amplicons were digested using <em>Hae</em>III endonuclease enzyme and used in restriction fragment length polymorphism (RFLP) assay. Then, 48 amplicons representing various hosts were sequenced and compared to se­quences from GenBank databases using BLAST.<strong><br />Results:</strong> PCR-RFLP analysis showed that 60 and 48 CL patients were infected by <em>Leishmania tropica</em> and <em>L. major</em>, respectively. From nine canine visceral leishmaniasis (CVL) isolates, eight isolates were identified as <em>L. infantum</em> and one as <em>L. tropica</em>. The greatest similarity of 95.7% in ITS1 region was seen between <em>L. infantum</em> and <em>L. major</em>. Furthermore, the lowest similarity with 65.7% was seen between <em>L. tropica</em> and <em>L. major</em>. Intra-species comparison of ITS1 region in <em>L. infantum, L. major </em>and<em> L. tropica</em> isolates were showed 100%, 98.2% and 72.4 % similarities, respectively.<strong><br />Conclusion:</strong> PCR-RFLP based on ITS1 region is an appropriate method to distinguish three <em>Leishmania</em> spp. of <em>L. major</em>, <em>L. tropica,</em> and <em>L. infantum</em>. In intra-species comparison of ITS1 region, genotypic variations showed that <em>L. tropica</em> isolates were more heterogeneous than <em>L. major</em> and <em>L. infantum</em> isolates.</p>
topic Leishmania, ITS1 gene, PCR- RFLP, Iran
url http://jad.tums.ac.ir/index.php/jad/article/view/890
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