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Molecular Epidemiological Survey of Cutaneous Leishmaniasis in Two Highly Endemic Metropolises of Iran, Application of Fta Cards for Dna Extraction From Giemsa-Stained Slides Publisher



Izadi S1 ; Mirhendi H1, 2 ; Jalalizand N3 ; Khodadadi H4 ; Mohebali M1 ; Nekoeian S5 ; Jamshidi A6 ; Ghatee MA6, 7
Authors
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Authors Affiliations
  1. 1. Department of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, IR, Tehran, Iran
  2. 2. Department of Medical Parasitology and Mycology, School of Medicine, Isfahan University of Medical Sciences, IR, Isfahan, Iran
  3. 3. National Health Research Center, Isfahan Health Research Center, IR, Isfahan, Iran
  4. 4. Department of Medical Parasitology and Mycology, School of Medicine, Shiraz University of Medical Sciences, IR, Shiraz, Iran
  5. 5. Cellular and Molecular Department, Isfahan Province Health Center, IR, Isfahan, Iran
  6. 6. Department of Medical Parasitology and Mycology, School of Medicine, Yasuj University of Medical Sciences, IR, Yasuj, Iran
  7. 7. Cellular and Molecular Research Center, Yasuj University of Medical Sciences, IR, Yasuj, Iran

Source: Jundishapur Journal of Microbiology Published:2016


Abstract

Background: PCR has been used for confirmation of leishmaniasis in epidemiological studies, but complexity of DNA extraction and PCR approach has confined its routine use in developing countries. Objectives: In this study, recent epidemiological situation of cutaneous leishmaniasis (CL) in two hyper-endemic metropolises of Shiraz and Isfahan in Iran was studied using DNA extraction by commercial FTA cards and kinetoplastid DNA (kDNA)-PCR amplification for detection/identification of Leishmania directly from stained skin scraping imprints. Patients and Methods: Fifty four and 30 samples were collected from clinically diagnosed CL patients referred to clinical laboratories of leishmaniasis control centers in Isfahan and Shiraz cities, respectively. The samples were examined by direct microscopy and then scrapings of the stained smears were applied to FTA cards and used directly as DNA source in a nested-PCR to amplify kDNA to detect and identify Leishmania species. Results: Fifty four of 84 (64.2%) slides obtained from patients had positive results microscopically, while 79/84 (94%) of slides had positive results by FTA card-nested-PCR. PCR and microscopy showed a sensitivity of 96.4% and 64.2% and specificity of 100% and 100%, respectively. Interestingly, Leishmania major as causative agent of zoonotic CL was identified in 100% and 90.7% of CL cases from Isfahan and Shiraz cities, respectively, but L. tropica was detected from only 9.3% of cases from Shiraz city. All cases from central regions of Shiraz were L. tropica and no CL case was found in Isfahan central areas. Conclusions: Filter paper-based DNA extraction can facilitate routine use of PCR for diagnosis of CL in research and diagnostic laboratories in Iran and countries with similar conditions. Epidemiologic changes including dominancy of L. major in suburbs of Shiraz and Isfahan metropolises where anthroponotic CL caused by L. tropica had been established, showed necessity of precise studies on CL epidemiology in old urban and newly added districts in the suburbs. © 2016, Ahvaz Jundishapur University of Medical Sciences.
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42. Clinical Picture of Cutaneous Leishmaniasis in Isfahan, Iran, International Journal of Dermatology (1994)