Characterization of Leishmania isolated from Kala- azar infected patients in Kermanshah using PCR

Authors

Mahdi Fakhar1, Masood Keyghobadi2,*, Reza Akramipour3, Keyghobad Ghadiri3, Mojtaba Limouei4
1Dept. of Medical Parasitology, Sari School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran
2Health Research Center, Kermanshah University of Medical Sciences, Kermanshah, Iran
3Dept. of Paediatrics, School of Medicine, Kermanshah University of Medical Sciences, Kermanshah, Iran
4Dept. of Public Health, School of Health, Kermanshah University of Medical Sciences, Kermanshah, Iran
*Corresponding Author: Corresponding author: Masood Keyghobadi, Health Research Center, Kermanshah University of Medical Sciences, Kermanshah, Iran, Tel: +989123858799 Email: [email protected]

Journal of Kermanshah University of Medical Sciences:Vol. 15, issue 2; e79382
Published online:Jul 19, 2011
Article type:Research Article
Received:Apr 29, 2010
Accepted:Aug 24, 2010
How to Cite:Fakhar M, Keyghobadi M, Akramipour R, Ghadiri K, Limouei M. Characterization of Leishmania isolated from Kala- azar infected patients in Kermanshah using PCR. J Kermanshah Univ Med Sci. 2011;15(2):e79382. doi:

Abstract

Background: Visceral leishmaniasis (VL) or Kala-azar is an important parasitic disease caused by protozoan parasites of the genus Leishmania including L. donovani and L. infantum. Some evidences show that VL is present in some areas of Kermanshah province and this study aimed to characterize the causative agent of VL in this region.

Methods: Bone marrow sample was obtained from 9 VL patients from Pediatric Hospital in Kermanshah. DNA was extracted from the microscopic slides and was checked by specific PCR to find out the species of the parasite. To do that, a segment of mini circle kinetoplast DNA was amplified, using LINR4 and LIN17 primers. All samples produced a 720 bp band in PCR reaction. Products of PCR were evaluated by electrophoresis using 1.5% gel agarose.

Results: Anti Leishmania antibody was detected in all patients except one case by IFAT. Examination of bone marrow smears demonstrated numerous amastigotes of Leishmania (Leishman bodies) in the samples. The isolates were compared with reference strains and revealed that all isolates were L. infantum.

Conclusions: Our findings showed that L. infantum is the most common VL in Kermanshah and one-step PCR reaction may be suitable method to detect species' characterization. Further study is necessary to explore other aspects of VL including seroprevalence and parasite reservoirs in this region.

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Copyright

© 2011, Journal of Kermanshah University of Medical Sciences. This open-access article is available under the Creative Commons Attribution-NonCommercial 4.0 (CC BY-NC 4.0) International License (https://creativecommons.org/licenses/by-nc/4.0/), which allows for the copying and redistribution of the material only for noncommercial purposes, provided that the original work is properly cited.

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