Proteomic and immunomic analysis of Schistosoma mekongi egg proteins

Schistosomiasis remains a global health problem. In the Mekong river basin, approximately 80,000 people are at risk of infection by Schistosoma mekongi. The parasite's eggs become entrapped in the host's organs and induce massive inflammation, contributing to the pathogenesis of schistosom...

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Veröffentlicht in:Experimental parasitology 2018-08, Vol.191, p.88-96
Hauptverfasser: Thiangtrongjit, Tipparat, Adisakwattana, Poom, Limpanont, Yanin, Dekumyoy, Paron, Nuamtanong, Supaporn, Chusongsang, Phiraphol, Chusongsang, Yupa, Reamtong, Onrapak
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container_title Experimental parasitology
container_volume 191
creator Thiangtrongjit, Tipparat
Adisakwattana, Poom
Limpanont, Yanin
Dekumyoy, Paron
Nuamtanong, Supaporn
Chusongsang, Phiraphol
Chusongsang, Yupa
Reamtong, Onrapak
description Schistosomiasis remains a global health problem. In the Mekong river basin, approximately 80,000 people are at risk of infection by Schistosoma mekongi. The parasite's eggs become entrapped in the host's organs and induce massive inflammation, contributing to the pathogenesis of schistosomiasis. In addition, egg antigens are important in circumoval precipitin tests (COPTs) and other diagnostic techniques. Little is known regarding the egg proteins of S. mekongi, and so we applied immunoblotting and mass spectrometry-based proteomic approaches to study these proteins and their antigenicity. A total of 360 unique proteins were identified in S. mekongi eggs using proteomic analyses. The major protein components of S. mekongi eggs were classified into several groups by functions, including proteins of unknown function, structural proteins, and regulators of transcription and translation. The most abundant proteins in S. mekongi eggs were antioxidant proteins, potentially reflecting the need to neutralize reactive oxidative species released from host immune cells. Immunomic analyses revealed that only DNA replication factor Cdt1 and heat shock protein 70 overlap between the proteins recognized by sera of infected mice and humans, illustrating the challenges of knowledge transfer from animal models to human patients. Forty-one immunoreactive protein bands were recognized by either mouse or patient sera. Phosphoglycerate kinase, fructose-1,6-bisphosphate aldolase and elongation factor 1 appeared to be interesting immunogens of S. mekongi eggs as these proteins were recognized by polyclonal IgMs and IgGs in patient sera. Our findings provide new information on the protein composition of S. mekongi eggs as well as the beginnings of a S. mekongi immunogen dataset. These data may help us better understand the pathology of schistosomiasis as well as natural antibody responses against S. mekongi egg proteins, both of which may be useful in including S. mekongi to other schistosoma diagnostic, vaccine and immunotherapy development. [Display omitted] •The most abundant proteins in S. mekongi egg proteome were antioxidant proteins.•Only two antigens were recognized by both infected mouse and human sera.•Three immunogens of interest were recognized by both patient IgM and IgG.
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In the Mekong river basin, approximately 80,000 people are at risk of infection by Schistosoma mekongi. The parasite's eggs become entrapped in the host's organs and induce massive inflammation, contributing to the pathogenesis of schistosomiasis. In addition, egg antigens are important in circumoval precipitin tests (COPTs) and other diagnostic techniques. Little is known regarding the egg proteins of S. mekongi, and so we applied immunoblotting and mass spectrometry-based proteomic approaches to study these proteins and their antigenicity. A total of 360 unique proteins were identified in S. mekongi eggs using proteomic analyses. The major protein components of S. mekongi eggs were classified into several groups by functions, including proteins of unknown function, structural proteins, and regulators of transcription and translation. The most abundant proteins in S. mekongi eggs were antioxidant proteins, potentially reflecting the need to neutralize reactive oxidative species released from host immune cells. Immunomic analyses revealed that only DNA replication factor Cdt1 and heat shock protein 70 overlap between the proteins recognized by sera of infected mice and humans, illustrating the challenges of knowledge transfer from animal models to human patients. Forty-one immunoreactive protein bands were recognized by either mouse or patient sera. Phosphoglycerate kinase, fructose-1,6-bisphosphate aldolase and elongation factor 1 appeared to be interesting immunogens of S. mekongi eggs as these proteins were recognized by polyclonal IgMs and IgGs in patient sera. Our findings provide new information on the protein composition of S. mekongi eggs as well as the beginnings of a S. mekongi immunogen dataset. These data may help us better understand the pathology of schistosomiasis as well as natural antibody responses against S. mekongi egg proteins, both of which may be useful in including S. mekongi to other schistosoma diagnostic, vaccine and immunotherapy development. [Display omitted] •The most abundant proteins in S. mekongi egg proteome were antioxidant proteins.•Only two antigens were recognized by both infected mouse and human sera.•Three immunogens of interest were recognized by both patient IgM and IgG.</description><identifier>ISSN: 0014-4894</identifier><identifier>EISSN: 1090-2449</identifier><identifier>DOI: 10.1016/j.exppara.2018.07.002</identifier><identifier>PMID: 30009810</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Antigens, Helminth - analysis ; Antigens, Helminth - immunology ; Antioxidants - analysis ; Case-Control Studies ; Egg ; Electrophoresis, Gel, Two-Dimensional ; Electrophoresis, Polyacrylamide Gel ; Gastropoda ; Helminth Proteins - analysis ; Helminth Proteins - chemistry ; Helminth Proteins - immunology ; Humans ; Immune Sera - immunology ; Immunoblotting ; Immunoglobulin G - immunology ; Immunoglobulin M - immunology ; Mass spectrometry ; Mekong Valley - epidemiology ; Mice ; Mice, Inbred ICR ; Ovum - chemistry ; Ovum - immunology ; Precipitin Tests ; Proteome - analysis ; Proteome - chemistry ; Proteome - immunology ; Proteomics ; Schistosoma - chemistry ; Schistosoma - immunology ; Schistosoma mekongi ; Schistosomiasis - epidemiology ; Schistosomiasis - immunology ; Schistosomiasis - parasitology ; Spectrometry, Mass, Electrospray Ionization ; Tandem Mass Spectrometry</subject><ispartof>Experimental parasitology, 2018-08, Vol.191, p.88-96</ispartof><rights>2018 The Authors</rights><rights>Copyright © 2018 The Authors. 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In the Mekong river basin, approximately 80,000 people are at risk of infection by Schistosoma mekongi. The parasite's eggs become entrapped in the host's organs and induce massive inflammation, contributing to the pathogenesis of schistosomiasis. In addition, egg antigens are important in circumoval precipitin tests (COPTs) and other diagnostic techniques. Little is known regarding the egg proteins of S. mekongi, and so we applied immunoblotting and mass spectrometry-based proteomic approaches to study these proteins and their antigenicity. A total of 360 unique proteins were identified in S. mekongi eggs using proteomic analyses. The major protein components of S. mekongi eggs were classified into several groups by functions, including proteins of unknown function, structural proteins, and regulators of transcription and translation. The most abundant proteins in S. mekongi eggs were antioxidant proteins, potentially reflecting the need to neutralize reactive oxidative species released from host immune cells. Immunomic analyses revealed that only DNA replication factor Cdt1 and heat shock protein 70 overlap between the proteins recognized by sera of infected mice and humans, illustrating the challenges of knowledge transfer from animal models to human patients. Forty-one immunoreactive protein bands were recognized by either mouse or patient sera. Phosphoglycerate kinase, fructose-1,6-bisphosphate aldolase and elongation factor 1 appeared to be interesting immunogens of S. mekongi eggs as these proteins were recognized by polyclonal IgMs and IgGs in patient sera. Our findings provide new information on the protein composition of S. mekongi eggs as well as the beginnings of a S. mekongi immunogen dataset. 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In the Mekong river basin, approximately 80,000 people are at risk of infection by Schistosoma mekongi. The parasite's eggs become entrapped in the host's organs and induce massive inflammation, contributing to the pathogenesis of schistosomiasis. In addition, egg antigens are important in circumoval precipitin tests (COPTs) and other diagnostic techniques. Little is known regarding the egg proteins of S. mekongi, and so we applied immunoblotting and mass spectrometry-based proteomic approaches to study these proteins and their antigenicity. A total of 360 unique proteins were identified in S. mekongi eggs using proteomic analyses. The major protein components of S. mekongi eggs were classified into several groups by functions, including proteins of unknown function, structural proteins, and regulators of transcription and translation. The most abundant proteins in S. mekongi eggs were antioxidant proteins, potentially reflecting the need to neutralize reactive oxidative species released from host immune cells. Immunomic analyses revealed that only DNA replication factor Cdt1 and heat shock protein 70 overlap between the proteins recognized by sera of infected mice and humans, illustrating the challenges of knowledge transfer from animal models to human patients. Forty-one immunoreactive protein bands were recognized by either mouse or patient sera. Phosphoglycerate kinase, fructose-1,6-bisphosphate aldolase and elongation factor 1 appeared to be interesting immunogens of S. mekongi eggs as these proteins were recognized by polyclonal IgMs and IgGs in patient sera. Our findings provide new information on the protein composition of S. mekongi eggs as well as the beginnings of a S. mekongi immunogen dataset. These data may help us better understand the pathology of schistosomiasis as well as natural antibody responses against S. mekongi egg proteins, both of which may be useful in including S. mekongi to other schistosoma diagnostic, vaccine and immunotherapy development. [Display omitted] •The most abundant proteins in S. mekongi egg proteome were antioxidant proteins.•Only two antigens were recognized by both infected mouse and human sera.•Three immunogens of interest were recognized by both patient IgM and IgG.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>30009810</pmid><doi>10.1016/j.exppara.2018.07.002</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-4027-3412</orcidid><orcidid>https://orcid.org/0000-0002-1154-6485</orcidid><oa>free_for_read</oa></addata></record>
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subjects Animals
Antigens, Helminth - analysis
Antigens, Helminth - immunology
Antioxidants - analysis
Case-Control Studies
Egg
Electrophoresis, Gel, Two-Dimensional
Electrophoresis, Polyacrylamide Gel
Gastropoda
Helminth Proteins - analysis
Helminth Proteins - chemistry
Helminth Proteins - immunology
Humans
Immune Sera - immunology
Immunoblotting
Immunoglobulin G - immunology
Immunoglobulin M - immunology
Mass spectrometry
Mekong Valley - epidemiology
Mice
Mice, Inbred ICR
Ovum - chemistry
Ovum - immunology
Precipitin Tests
Proteome - analysis
Proteome - chemistry
Proteome - immunology
Proteomics
Schistosoma - chemistry
Schistosoma - immunology
Schistosoma mekongi
Schistosomiasis - epidemiology
Schistosomiasis - immunology
Schistosomiasis - parasitology
Spectrometry, Mass, Electrospray Ionization
Tandem Mass Spectrometry
title Proteomic and immunomic analysis of Schistosoma mekongi egg proteins
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