Title of article :
Comparative Two-dimensional Gel Electrophoresis Maps for Amastigote-like Proteomes of Iranian Leishmania Tropica and Leishmania Major Isolates
Author/Authors :
Ashrafmansouri, Marzieh Department of Medical Parasitology and Mycology - Shahid Beheshti University of Medical Sciences , Sadat Sadjjadi, Fatemeh Dept of Paramedical Sciences - Shahid Beheshti University of Medical Sciences , Seyyedtabaei,javad Department of Medical Parasitology and Mycology - Shahid Beheshti University of Medical Sciences , Haghighi, Ali Department of Medical Parasitology and Mycology - Shahid Beheshti University of Medical Sciences , Rezaei-Tavirani, Mostafa Dept of Paramedical Sciences - Shahid Beheshti University of Medical Sciences , Ahmadi, Nayebali Dept of Paramedical Sciences - Shahid Beheshti University of Medical Sciences
Abstract :
Background: Leishmania major and Leishmania tropica are the main causative agents of
cutaneous leishmaniasis. Proteomics as a novel approaches could be used to evaluate protein
expression levels in different stages of Leishmania species. We compare the protein contents
of amastigote-like forms in L. tropica and L. major using two-dimensional gel electrophoresis
(2-DE) and bioinformatics methods. Materials and Methods: Leishmania parasites were
isolated from the lesions of Iranian patients and identified using restriction fragment length
polymorphism-polymerase chain reaction (RFLP-PCR). Five isolates of each two species were
cultured in specific media to obtain amastigote-like forms to be prepared for proteomics study.
Total protein contents were separated using 2-DE. The gels were stained by silver nitrate and
scan was imaged. The protein spots with different expression changes in each gel were analyzed
using Progenesis SameSpots software. Results: A total of 354 protein spots were detected in
both amastigote-like forms. Comparative analysis of protein spots with different expressions in
the two amastigote-like form species showed 173 highly expressed spots of which 74 L. tropica
and 99 L. major proteins were spotted with fold≥2. Also, 16 and 20 new protein spots were
uniquely found in L. tropica and L. major, respectively. Clustering of different detected proteins
using correlation analysis divided the proteins into two clusters based on their expression level.
Furthermore, clustering results were confirmed by principal component analysis. Conclusion:
Using proteomics methods specially 2-DE and statistical analysis demonstrated significant
changes in protein expression levels in amastigote-like forms of L. tropica and L. major isolates.
Keywords :
Leishmaniasis , Proteomics , Leishmania Major , Leishmania Tropica , Two-Dimensional Gel Electrophoresis
Journal title :
Galen Medical Journal (GMJ)