Comparative Two-dimensional Gel Electrophoresis Maps for Amastigote-like Proteomes of Iranian Leishmania Tropica and Leishmania major Isolates

Authors

  • Marzieh Ashrafmansouri Student Research Committee, Department of Medical Parasitology and Mycology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  • Fatemeh Sadat Sadjjadi Proteomics Research Center, Faculty of Paramedical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  • Seyyedjavad Seyyedtabaei Department of Medical Parasitology and Mycology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  • Ali Haghighi Department of Medical Parasitology and Mycology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  • Mostafa Rezaei-Tavirani Proteomics Research Center, Faculty of Paramedical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  • Nayebali Ahmadi Proteomics Research Center, Faculty of Paramedical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran

DOI:

https://doi.org/10.31661/gmj.v8i.1520

Keywords:

Leishmaniasis, Proteomics, Leishmania Major, Leishmania Tropica, Two-Dimensional Gel Electrophoresis

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.  [GMJ.2019;8:e1520]

References

Ashrafmansouri M, Sarkari B, Hatam G, Habibi P, Khabisi SA. Utility of Western Blot Analysis for the Diagnosis of Cutaneous Leishmaniasis. Iran J Parasitol. 2015;10(4):599-604. Alvar J, Velez ID, Bern C, Herrero M, Desjeux P, Cano J et al. Leishmaniasis worldwide and global estimates of its incidence. PloS one. 2012;7(5):e35671. https://doi.org/10.1371/journal.pone.0035671PMid:22693548 PMCid:PMC3365071 Ahmadi N, Modiri M, Mamdohi S. First survey of cutaneous leishmaniasis in Borujerd county, western Islamic Republic of Iran. East Mediterr Health. 2013;19(10):847-53. https://doi.org/10.26719/2013.19.10.847 Sarkari B, Ashrafmansouri M, Hatam G, Habibi P, Abdolahi Khabisi S. Performance of an ELISA and indirect immunofluorescence assay in serological diagnosis of zoonotic cutaneous leishmaniasis in Iran. Interdiscip Perspect Infect Dis. 2014;2014. 505134. https://doi.org/10.1155/2014/505134PMid:25177349 PMCid:PMC4142716 Habibi P, Sadjjadi S, Owji M, Moattari A, Sarkari B, Naghibalhosseini F et al. Characterization of in vitro cultivated amastigote like of Leishmania major: a substitution for in vivo studies. Iran J Parasitol. 2008;3(1):6-15. Amiri-Dashatan N, Koushki M, Rezaei Tavirani M, Ahmadi N. Proteomic-based Studies on Leishmania. J Mazandaran Univ Med Sci. 2018;28(163):173-90. Mojtahedi Z, Clos J, Kamali-Sarvestani E. Leishmania major: identification of developmentally regulated proteins in procyclic and metacyclic promastigotes. Exp Parasitol. 2008;119(3):422-9. https://doi.org/10.1016/j.exppara.2008.04.008PMid:18486941 Handman E, Bullen DV. Interaction of Leishmania with the host macrophage. Trends Parasitol. 2002;18(8):332-4. https://doi.org/10.1016/S1471-4922(02)02352-8 Guy RA, Belosevic M. Comparison of receptors required for entry of Leishmania major amastigotes into macrophages. Infect Immun. 1993;61(4):1553-8. El Fadili K, Messier N, Leprohon P, Roy G, Guimond C, Trudel N et al. Role of the ABC transporter MRPA (PGPA) in antimony resistance in Leishmania infantum axenic and intracellular amastigotes. Antimicrob Agents Chemother. 2005;49(5):1988-93. https://doi.org/10.1128/AAC.49.5.1988-1993.2005PMid:15855523 PMCid:PMC1087671 Atan NAD, Koushki M, Ahmadi NA, Rezaei-Tavirani M. Metabolomics-based studies in the field of Leishmania/leishmaniasis. Alexandria J Med. 2018;54(4):383-90. https://doi.org/10.1016/j.ajme.2018.06.002 Zakai HA, Bates PA, Chance M. The axenic cultivation of Leishmania donovani amastigotes. Saudi Med J. 1999;20(5):334-40. Sadjjadi FS, Rezaie-Tavirani M, Ahmadi NA, Sadjjadi SM, Zali H. Proteome evaluation of human cystic echinococcosis sera using two dimensional gel electrophoresis. Gastroenterol Hepatol Bed Bench. 2018;11(1):75-82. Dashatan NA, Tavirani MR, Zali H, Koushki M, Ahmadi N. Prediction of Leishmania Major Key Proteins via Topological Analysis of Protein-Protein Interaction Network. Galen Med J. 2018;7(2):e1129. Celis JE, Gromov P. 2D protein electrophoresis: can it be perfected? Curr Opin Biotechnol. 1999;10(1):16-21. https://doi.org/10.1016/S0958-1669(99)80004-4 Reynolds K, Fang C, Xiadong C, Lynn S. Comparative two-dimensional gel electrophoresis maps for promastigotes of Leishmania amazonensis and L. major. Brazilian J Infec Dis. 2006;10(1):1-6. https://doi.org/10.1590/S1413-86702006000100001PMid:16767307 Cuervo P, de Jesus JB, Junqueira M, Mendonça-Lima L, González LJ, Betancourt L et al. Proteome analysis of Leishmania (Viannia) braziliensis by two-dimensional gel electrophoresis and mass spectrometry. Mol Biochem Parasitol. 2007;154(1):6-21. https://doi.org/10.1016/j.molbiopara.2007.03.013PMid:17499861 Doudi M, Hejazi SH, Razavi MR, Narimani M, Khanjani S, Eslami G. Comparative molecular epidemiology of Leishmania major and Leishmania tropica by PCR-RFLP technique in hyper endemic cities of Isfahan and Bam, Iran. Med Sci Monit. 2010;16(11):Cr530-5. Hajjaran H, Mohebali M, Assareh A, Heidari M, Hadighi R. Protein profiling on Meglumine Antimoniate (Glucantime®) sensitive and resistant L. tropica isolates by 2-dimentional gel electrophoresis: A preliminary study. Iran J Parasitol. 2009;4(1):8-14. Rashidi S, Kalantar K, Hatam G. Using proteomics as a powerful tool to develop a vaccine against Mediterranean visceral leishmaniasis. J Parasit Dis. 2018;42(2):162-70. https://doi.org/10.1007/s12639-018-0986-yPMid:29844618 PMCid:PMC5962495 Hajjaran H, Azarian B, Mohebali M, Hadighi R, Assareh A, Vaziri B. Comparative proteomics study on meglumine antimoniate sensitive and resistant Leishmania tropica isolated from Iranian anthroponotic cutaneous leishmaniasis patients. East Mediterr Health J. 2012;18(2):165-171. https://doi.org/10.26719/2012.18.2.165PMid:22571094 Cordwell SJ, Nouwens AS, Walsh BJ. Comparative proteomics of bacterial pathogens. PROTEOMICS: International Edition. 2001;1(4):461-72. https://doi.org/10.1002/1615-9861(200104)1:4 Acestor N, Masina S, Walker J, Saravia NG, Fasel N, Quadroni M. Establishing two-dimensional gels for the analysis of Leishmania proteomes. Proteomics. 2002;2(7):877-9. https://doi.org/10.1002/1615-9861(200207)2:7 Zarean M, Maraghi S, Hajjaran H, Mohebali M, Feiz-Hadad MH, Assarehzadegan MA. Comparison of proteome profiling of two sensitive and resistant field Iranian isolates of Leishmania major to Glucantime® by 2-dimensional electrophoresis. Iran J Parasitol. 2015;10(1):19-29. Feist P, Hummon AB. Proteomic challenges: sample preparation techniques for microgram-quantity protein analysis from biological samples. Int J Mol Sci. 2015;16(2):3537-63. https://doi.org/10.3390/ijms16023537PMid:25664860 PMCid:PMC4346912 Blasko I, Bodner T, Knaus G, Walch T, Monsch A, Hinterhuber H et al. Efficacy of donepezil treatment in Alzheimer patients with and without subcortical vascular lesions. Pharmacology. 2004;72(1):1-5. https://doi.org/10.1159/000078625PMid:15292648 Murzin AG, Brenner SE, Hubbard T, Chothia C. SCOP: a structural classification of proteins database for the investigation of sequences and structures. J Mol Biol. 1995;247(4):536-40. https://doi.org/10.1016/S0022-2836(05)80134-2 Zali H, Tavirani MR, Jalilian FA, Khodarahmi R. Proteins expression clustering of Alzheimer disease in rat hippocampus proteome. J Paramed Sci. 2013;4(3):111-8.

Published

2019-08-15

How to Cite

Ashrafmansouri, M., Sadjjadi, F. S., Seyyedtabaei, S., Haghighi, A., Rezaei-Tavirani, M., & Ahmadi, N. (2019). Comparative Two-dimensional Gel Electrophoresis Maps for Amastigote-like Proteomes of Iranian Leishmania Tropica and Leishmania major Isolates: . Galen Medical Journal, 8, e1520. https://doi.org/10.31661/gmj.v8i.1520

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