Comparative proteomics and glycoproteomics of plasma proteins in Indian visceral leishmaniasis

被引:22
作者
Bag, Arup Kumar [1 ]
Saha, Sutapa [2 ]
Sundar, Shyam [3 ]
Saha, Bibhuti [4 ]
Chakrabarti, Abhijit [2 ]
Mandal, Chitra [1 ]
机构
[1] Council Sci & Ind Res Indian Inst Chem Biol, Canc Biol & Inflammatory Disorder Div, Kolkata 700032, India
[2] Saha Inst Nucl Phys, Kolkata 700064, India
[3] Banaras Hindu Univ, Inst Med Sci, Dept Med, Varanasi 221005, Uttar Pradesh, India
[4] Sch Trop Med, Dept Trop Med, Kolkata 700073, India
关键词
Visceral leishmaniasis; Plasma glycoproteomics; MARS column; M-LAC column; 2D-DIGE; MALDI-TOF/TOF mass spectrometry; EXPRESSION; ELECTROPHORESIS; PREDICTION; SILVER;
D O I
10.1186/s12953-014-0048-z
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Visceral leishmaniasis (VL) is a deadly parasitic diseases caused by Leishmania donovani; it is a major health problem in many countries. A lack of proper understanding of the disease biology, poor diagnostic methods and increasing drug resistance are the main reasons for the growing burden of VL infection. Comparative plasma proteomics are a relatively useful technique that can be used to investigate disease-associated alterations that can help in understanding host responses against pathogens, and might be useful in disease management and diagnosis. Result: In this study, a comparative proteomics and glycoproteomics approach using 2DE and 2D-DIGE was employed between early diagnosed VL patients of all age groups and healthy endemic and non-endemic controls in order to aid the recognition of disease-associated alterations in host plasma. Comparative proteomics was performed by the depletion of seven highly abundant plasma proteins. Comparative glycoproteomics was performed by the depletion of albumin and IgG, followed by purification of plasma glycoproteins using a multi lectin affinity column. From these two approaches, 39 differentially expressed protein spots were identified and sequenced using MALDI-TOF/TOF mass spectrometry. This revealed ten distinct proteins that appeared in multiple spots, suggesting micro-heterogeneity. Among these proteins, alpha-1-antitrypsin, alpha-1-B glycoprotein and amyloid-A1 precursor were up-regulated, whereas vitamin-D binding protein, apolipoprotein-A-I and transthyretin were down-regulated in VL. Alterations in the levels of these proteins in VL-infected plasma were further confirmed by western blot and ELISA. Conclusions: These proteins may be involved in the survival of parasites, resisting neutrophil elastase, and in their multiplication in macrophages, potentially maintaining endogenous anti-inflammatory and immunosuppressive conditions. Consequently, the results of this study may help in understanding the host response against L. donovani, which could help in the discovery of new drugs and disease management. Finally, these alterations on protein levels might be beneficial in improving early diagnosis considering those as biomarkers in Indian VL.
引用
收藏
页码:1 / 14
页数:14
相关论文
共 30 条
[1]   The human plasma proteome - History, character, and diagnostic prospects [J].
Anderson, NL ;
Anderson, NG .
MOLECULAR & CELLULAR PROTEOMICS, 2002, 1 (11) :845-867
[2]   PLASMA-LIPOPROTEINS IN INFANTILE VISCERAL LEISHMANIASIS - DEFICIENCY OF APOLIPOPROTEIN-A-I AND APOLIPOPROTEIN-II [J].
BEKAERT, ED ;
KALLEL, R ;
BOUMA, ME ;
LONTIE, JF ;
MEBAZAA, A ;
MALMENDIER, CL ;
AYRAULTJARRIER, M .
CLINICA CHIMICA ACTA, 1989, 184 (02) :181-191
[3]   Leishmania-Mediated Inhibition of Iron Export Promotes Parasite Replication in Macrophages [J].
Ben-Othman, Rym ;
Flannery, Andrew R. ;
Miguel, Danilo C. ;
Ward, Diane M. ;
Kaplan, Jerry ;
Andrews, Norma W. .
PLOS PATHOGENS, 2014, 10 (01)
[4]  
Bouree P., 2000, Journal of the Egyptian Society of Parasitology, V30, P885
[5]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[6]   Blue silver: A very sensitive colloidal Coomassie G-250 staining for proteome analysis [J].
Candiano, G ;
Bruschi, M ;
Musante, L ;
Santucci, L ;
Ghiggeri, GM ;
Carnemolla, B ;
Orecchia, P ;
Zardi, L ;
Righetti, PG .
ELECTROPHORESIS, 2004, 25 (09) :1327-1333
[7]   Visceral leishmaniasis: What are the needs for diagnosis, treatment and control? [J].
Chappuis, Francois ;
Sundar, Shyam ;
Hailu, Asrat ;
Ghalib, Hashim ;
Rijal, Suman ;
Peeling, Rosanna W. ;
Alvar, Jorge ;
Boelaert, Marleen .
NATURE REVIEWS MICROBIOLOGY, 2007, 5 (11) :873-882
[8]   Variable degree of alternative complement pathway-mediated hemolysis in Indian visceral leishmaniasis induced by differential expression of 9-O-acetylated sialoglycans [J].
Chava, AK ;
Chatterjee, M ;
Sharma, V ;
Sundar, S ;
Mandal, C .
JOURNAL OF INFECTIOUS DISEASES, 2004, 189 (07) :1257-1264
[9]   A two step fractionation approach for plasma proteomics using immunodepletion of abundant proteins and multi-lectin affinity chromatography: Application to the analysis of obesity, diabetes, and hypertension diseases [J].
Dayarathna, M. K. Disni R. ;
Hancock, William S. ;
Hincapie, Marina .
JOURNAL OF SEPARATION SCIENCE, 2008, 31 (6-7) :1156-1166
[10]   STRING v9.1: protein-protein interaction networks, with increased coverage and integration [J].
Franceschini, Andrea ;
Szklarczyk, Damian ;
Frankild, Sune ;
Kuhn, Michael ;
Simonovic, Milan ;
Roth, Alexander ;
Lin, Jianyi ;
Minguez, Pablo ;
Bork, Peer ;
von Mering, Christian ;
Jensen, Lars J. .
NUCLEIC ACIDS RESEARCH, 2013, 41 (D1) :D808-D815