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Molecular Identification and Phylogenetic Classification of Leishmania Spp. Isolated From Human Cutaneous Leishmaniasis in Iran: A Cross-Sectional Study



Mohammadiha A1 ; Dalimi A1 ; Mohebali M2, 3 ; Sharifi I4 ; Mahmoudi M5 ; Mirzaei A6 ; Spotin A7 ; Behravan M8 ; Karimi M9 ; Arbabi M10 ; Nekoeian S11 ; Kalantari R1 ; Ghorbanzadeh B1
Authors
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Authors Affiliations
  1. 1. Dept. of Parasitology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran
  2. 2. Dept. of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Center for Research of Endemic Parasites of Iran (CREPI), Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Leishmaniasis Research Center, Dept. of Parasitology, Faculty of Medicine, Kerman University of Medical Sciences, Kerman, Iran
  5. 5. Dept. of Microbiology and Parasitology, Faculty of Medicine, Guilan University of Medical Sciences, Rasht, Iran
  6. 6. Dept. of Parasitology, Faculty of Medicine, Ilam University of Medical Sciences, Ilam, Iran
  7. 7. Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
  8. 8. Esfarayen Faculty of Medical Sciences, Esfarayen, Iran
  9. 9. Infectious Diseases Research Center, Microbiology Dept, Birjand University of Medical Sciences, Birjand, Iran
  10. 10. Dept. of Parasitology and Mycology, School of Medicine, Kashan University of Medical Sciences, Kashan, Iran
  11. 11. Dept. of Cellular and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran

Source: Iranian Journal of Parasitology Published:2018

Abstract

Background: In Iran, both forms of cutaneous (CL) and visceral leishmaniasis (VL) have been reported; so the accurate species identification of the parasite(s) and the analysis of genetic diversity are necessary. Methods: The smears were collected from lesions samples of 654 patients with CL, who attended local health centers in 12 provinces of Iran during 2013-2015. The smears were checked for the presence of amastigotes by light microscopy. DNA of 648 Leishmania isolates, amplified by targeting a partial sequence of ITS (18S rRNA–ITS1–5.8S rRNA–ITS2) gene. Twenty-five of all the amplicons were sequenced and analyzed with restriction fragment length polymorphism (RFLP) using the Taq1 enzyme. Results: All the smears were positive microscopically. The PCR-RFLP analysis revealed that 176 (27%) CL patients were infected with L. tropica and, 478 (73%) with L. major. The dominant species in all over Iran is L. major. The sequencing results of all CL patients and RFLP analysis confirmed each other. Based on our phylogenetic tree, 25 ITS DNA sequences were grouped into two clusters representing L. major and L. tropica species. Phylogenetic tree derived from the ITS sequences supports a clear divergence between L. major from the other species. Conclusion: Discrimination of Iranian Leishmania isolates using ITS gene gives us this opportunity to detect, identify, and construct the phylogenetic relationship of Iranian isolates. © 2018, Tehran University of Medical Sciences (TUMS). All rights reserved.
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