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Comparative proteomics and glycoproteomics of plasma proteins in Indian visceral leishmaniasis
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 bur...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4179796/ https://www.ncbi.nlm.nih.gov/pubmed/25276097 http://dx.doi.org/10.1186/s12953-014-0048-z |
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author | Bag, Arup Kumar Saha, Sutapa Sundar, Shyam Saha, Bibhuti Chakrabarti, Abhijit Mandal, Chitra |
author_facet | Bag, Arup Kumar Saha, Sutapa Sundar, Shyam Saha, Bibhuti Chakrabarti, Abhijit Mandal, Chitra |
author_sort | Bag, Arup Kumar |
collection | PubMed |
description | 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12953-014-0048-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4179796 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41797962014-10-01 Comparative proteomics and glycoproteomics of plasma proteins in Indian visceral leishmaniasis Bag, Arup Kumar Saha, Sutapa Sundar, Shyam Saha, Bibhuti Chakrabarti, Abhijit Mandal, Chitra Proteome Sci Research Article 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12953-014-0048-z) contains supplementary material, which is available to authorized users. BioMed Central 2014-09-22 /pmc/articles/PMC4179796/ /pubmed/25276097 http://dx.doi.org/10.1186/s12953-014-0048-z Text en © Bag et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Bag, Arup Kumar Saha, Sutapa Sundar, Shyam Saha, Bibhuti Chakrabarti, Abhijit Mandal, Chitra Comparative proteomics and glycoproteomics of plasma proteins in Indian visceral leishmaniasis |
title | Comparative proteomics and glycoproteomics of plasma proteins in Indian visceral leishmaniasis |
title_full | Comparative proteomics and glycoproteomics of plasma proteins in Indian visceral leishmaniasis |
title_fullStr | Comparative proteomics and glycoproteomics of plasma proteins in Indian visceral leishmaniasis |
title_full_unstemmed | Comparative proteomics and glycoproteomics of plasma proteins in Indian visceral leishmaniasis |
title_short | Comparative proteomics and glycoproteomics of plasma proteins in Indian visceral leishmaniasis |
title_sort | comparative proteomics and glycoproteomics of plasma proteins in indian visceral leishmaniasis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4179796/ https://www.ncbi.nlm.nih.gov/pubmed/25276097 http://dx.doi.org/10.1186/s12953-014-0048-z |
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