Serum proteome analysis of vivax malaria: An insight into the disease pathogenesis and host immune response

Vivax malaria is the most widely distributed human malaria resulting in 80–300million clinical cases every year. It causes severe infection and mortality but is generally regarded as a benign disease and has not been investigated in detail. The present study aimed to perform human serum proteome ana...

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Published inJournal of proteomics Vol. 75; no. 10; pp. 3063 - 3080
Main Authors Ray, Sandipan, Kamath, Karthik S., Srivastava, Rajneesh, Raghu, Dinesh, Gollapalli, Kishore, Jain, Rekha, Gupta, Shipra V., Ray, Sayantan, Taur, Santosh, Dhali, Snigdha, Gogtay, Nithya, Thatte, Urmila, Srikanth, Rapole, Patankar, Swati, Srivastava, Sanjeeva
Format Journal Article Conference Proceeding
LanguageEnglish
Published Kidlington Elsevier B.V 06.06.2012
Elsevier
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Online AccessGet full text
ISSN1874-3919
1876-7737
DOI10.1016/j.jprot.2011.10.018

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Abstract Vivax malaria is the most widely distributed human malaria resulting in 80–300million clinical cases every year. It causes severe infection and mortality but is generally regarded as a benign disease and has not been investigated in detail. The present study aimed to perform human serum proteome analysis in a malaria endemic area in India to identify potential serum biomarkers for vivax malaria and understand host response. The proteomic analysis was performed on 16 age and gender matched subjects (vivax patients and control) in duplicate. Protein extraction protocols were optimized for large coverage of the serum proteome and to obtain high-resolution data. Identification of 67 differentially expressed and statistically significant (Student's t-test; p<0.05) protein spots was established by MALDI-TOF/TOF mass spectrometry. Many of the identified proteins such as apolipoprotein A and E, serum amyloid A and P, haptoglobin, ceruloplasmin, and hemopexin are interesting from a diagnostic point of view and could further be studied as potential serum biomarkers. The differentially expressed serum proteins in vivax malaria identified in this study were subjected to functional pathway analysis using multiple software, including Ingenuity Pathway Analysis (IPA), Protein ANalysis THrough Evolutionary Relationships (PANTHER) and Database for Annotation, Visualization and Integrated Discovery (DAVID) functional annotation tool for better understanding of the biological context of the identified proteins, their involvement in various physiological pathways and association with disease pathogenesis. Functional pathway analysis of the differentially expressed proteins suggested the modulation of multiple vital physiological pathways, including acute phase response signaling, complement and coagulation cascades, hemostasis and vitamin D metabolism pathway due to this parasitic infection. This article is part of a Special Issue entitled: Proteomics: The clinical link. [Display omitted] ► Alteration in serum proteome in vivax malaria was investigated. ► Classical 2DE and 2D-DIGE were implicated for serum proteome profiling. ► 31 differentially expressed serum proteins were identified using MALDI TOF/TOF MS. ► Identified proteins are involved in vital physiological pathways. ► Few identified proteins could further be studied as potential serum biomarkers.
AbstractList Vivax malaria is the most widely distributed human malaria resulting in 80-300 million clinical cases every year. It causes severe infection and mortality but is generally regarded as a benign disease and has not been investigated in detail. The present study aimed to perform human serum proteome analysis in a malaria endemic area in India to identify potential serum biomarkers for vivax malaria and understand host response. The proteomic analysis was performed on 16 age and gender matched subjects (vivax patients and control) in duplicate. Protein extraction protocols were optimized for large coverage of the serum proteome and to obtain high-resolution data. Identification of 67 differentially expressed and statistically significant (Student's t-test; p < 0.05) protein spots was established by MALDI-TOF/TOF mass spectrometry. Many of the identified proteins such as apolipoprotein A and E, serum amyloid A and P, haptoglobin, ceruloplasmin, and hemopexin are interesting from a diagnostic point of view and could further be studied as potential serum biomarkers. The differentially expressed serum proteins in vivax malaria identified in this study were subjected to functional pathway analysis using multiple software, including Ingenuity Pathway Analysis (IPA), Protein ANalysis THrough Evolutionary Relationships (PANTHER) and Database for Annotation, Visualization and Integrated Discovery (DAVID) functional annotation tool for better understanding of the biological context of the identified proteins, their involvement in various physiological pathways and association with disease pathogenesis. Functional pathway analysis of the differentially expressed proteins suggested the modulation of multiple vital physiological pathways, including acute phase response signaling, complement and coagulation cascades, hemostasis and vitamin D metabolism pathway due to this parasitic infection. This article is part of a Special Issue entitled: Proteomics: The clinical link.
Vivax malaria is the most widely distributed human malaria resulting in 80–300million clinical cases every year. It causes severe infection and mortality but is generally regarded as a benign disease and has not been investigated in detail. The present study aimed to perform human serum proteome analysis in a malaria endemic area in India to identify potential serum biomarkers for vivax malaria and understand host response. The proteomic analysis was performed on 16 age and gender matched subjects (vivax patients and control) in duplicate. Protein extraction protocols were optimized for large coverage of the serum proteome and to obtain high-resolution data. Identification of 67 differentially expressed and statistically significant (Student's t-test; p<0.05) protein spots was established by MALDI-TOF/TOF mass spectrometry. Many of the identified proteins such as apolipoprotein A and E, serum amyloid A and P, haptoglobin, ceruloplasmin, and hemopexin are interesting from a diagnostic point of view and could further be studied as potential serum biomarkers. The differentially expressed serum proteins in vivax malaria identified in this study were subjected to functional pathway analysis using multiple software, including Ingenuity Pathway Analysis (IPA), Protein ANalysis THrough Evolutionary Relationships (PANTHER) and Database for Annotation, Visualization and Integrated Discovery (DAVID) functional annotation tool for better understanding of the biological context of the identified proteins, their involvement in various physiological pathways and association with disease pathogenesis. Functional pathway analysis of the differentially expressed proteins suggested the modulation of multiple vital physiological pathways, including acute phase response signaling, complement and coagulation cascades, hemostasis and vitamin D metabolism pathway due to this parasitic infection. This article is part of a Special Issue entitled: Proteomics: The clinical link.
Vivax malaria is the most widely distributed human malaria resulting in 80–300million clinical cases every year. It causes severe infection and mortality but is generally regarded as a benign disease and has not been investigated in detail. The present study aimed to perform human serum proteome analysis in a malaria endemic area in India to identify potential serum biomarkers for vivax malaria and understand host response. The proteomic analysis was performed on 16 age and gender matched subjects (vivax patients and control) in duplicate. Protein extraction protocols were optimized for large coverage of the serum proteome and to obtain high-resolution data. Identification of 67 differentially expressed and statistically significant (Student's t-test; p<0.05) protein spots was established by MALDI-TOF/TOF mass spectrometry. Many of the identified proteins such as apolipoprotein A and E, serum amyloid A and P, haptoglobin, ceruloplasmin, and hemopexin are interesting from a diagnostic point of view and could further be studied as potential serum biomarkers. The differentially expressed serum proteins in vivax malaria identified in this study were subjected to functional pathway analysis using multiple software, including Ingenuity Pathway Analysis (IPA), Protein ANalysis THrough Evolutionary Relationships (PANTHER) and Database for Annotation, Visualization and Integrated Discovery (DAVID) functional annotation tool for better understanding of the biological context of the identified proteins, their involvement in various physiological pathways and association with disease pathogenesis. Functional pathway analysis of the differentially expressed proteins suggested the modulation of multiple vital physiological pathways, including acute phase response signaling, complement and coagulation cascades, hemostasis and vitamin D metabolism pathway due to this parasitic infection. This article is part of a Special Issue entitled: Proteomics: The clinical link. [Display omitted] ► Alteration in serum proteome in vivax malaria was investigated. ► Classical 2DE and 2D-DIGE were implicated for serum proteome profiling. ► 31 differentially expressed serum proteins were identified using MALDI TOF/TOF MS. ► Identified proteins are involved in vital physiological pathways. ► Few identified proteins could further be studied as potential serum biomarkers.
Author Raghu, Dinesh
Jain, Rekha
Thatte, Urmila
Ray, Sandipan
Srikanth, Rapole
Gupta, Shipra V.
Taur, Santosh
Gogtay, Nithya
Kamath, Karthik S.
Ray, Sayantan
Patankar, Swati
Srivastava, Rajneesh
Srivastava, Sanjeeva
Gollapalli, Kishore
Dhali, Snigdha
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  organization: Wadhwani Research Center for Biosciences and Bioengineering, Department of Biosciences and Bioengineering, Indian Institute of Technology Bombay, Powai, Mumbai 400076, India
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IsPeerReviewed true
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Issue 10
Keywords Disease pathogenesis
Plasmodium
Serum
Immune response
Vivax malaria
Proteomics
Protozoa
Apicomplexa
Protozoal disease
Disease
Malaria
Pathogenesis
Proteome
Parasitosis
Infection
Analysis
Language English
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Snippet Vivax malaria is the most widely distributed human malaria resulting in 80–300million clinical cases every year. It causes severe infection and mortality but...
Vivax malaria is the most widely distributed human malaria resulting in 80-300 million clinical cases every year. It causes severe infection and mortality but...
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SubjectTerms Adult
amyloid
analysis
apolipoprotein A
Biological and medical sciences
biomarkers
blood
Blood Chemical Analysis
Blood Chemical Analysis - methods
blood proteins
Blood Proteins - analysis
blood serum
Case-Control Studies
coagulation
complement
computer software
Disease pathogenesis
Diverse techniques
Electrophoresis, Gel, Two-Dimensional
etiology
ferroxidase
Fundamental and applied biological sciences. Psychology
gender
gene expression regulation
hemostasis
Host-Parasite Interactions
Host-Parasite Interactions - physiology
Human protozoal diseases
Humans
Immune response
Immunity
Immunity - physiology
immunology
India
Infectious diseases
Malaria
Malaria, Vivax
Malaria, Vivax - blood
Malaria, Vivax - etiology
Malaria, Vivax - immunology
Malaria, Vivax - metabolism
Male
mass spectrometry
Medical sciences
metabolism
methods
Molecular and cellular biology
mortality
Parasitic diseases
pathogenesis
patients
physiology
Plasmodium
Plasmodium vivax
Plasmodium vivax - physiology
protein synthesis
proteome
Proteome - analysis
Proteome - metabolism
Proteomics
Protozoal diseases
Serologic Tests
Serologic Tests - methods
Serum
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
t-test
vitamin D
Vivax malaria
Young Adult
Title Serum proteome analysis of vivax malaria: An insight into the disease pathogenesis and host immune response
URI https://dx.doi.org/10.1016/j.jprot.2011.10.018
https://www.ncbi.nlm.nih.gov/pubmed/22086083
https://www.proquest.com/docview/1038609044
https://www.proquest.com/docview/1672068748
Volume 75
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