In silico epitope mapping and experimental evaluation of the Merozoite Adhesive Erythrocytic Binding Protein (MAEBL) as a malaria vaccine candidate

Detalhes bibliográficos
Autor(a) principal: Cravo, Pedro
Data de Publicação: 2018
Outros Autores: Machado, Renato B, Leite, Juliana A, Leda, Taizy, Suwanarusk, Rossarin, Bittencourt, Najara, Albrecht, Letusa, Judice, Carla, Lopes, Stefanie C P, Lacerda, Marcus V G, Ferreira, Marcelo U, Soares, Irene S, Goh, Yun Shan, Bargieri, Daniel Y, Nosten, François, Russell, Bruce, Rénia, Laurent, Costa, Fabio T M
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10362/116836
Resumo: BACKGROUND: Technical limitations for culturing the human malaria parasite Plasmodium vivax have impaired the discovery of vaccine candidates, challenging the malaria eradication agenda. The immunogenicity of the M2 domain of the Merozoite Adhesive Erythrocytic Binding Protein (MAEBL) antigen cloned from the Plasmodium yoelii murine parasite, has been previously demonstrated. RESULTS: Detailed epitope mapping of MAEBL through immunoinformatics identified several MHCI, MHCII and B cell epitopes throughout the peptide, with several of these lying in the M2 domain and being conserved between P. vivax, P. yoelii and Plasmodium falciparum, hinting that the M2-MAEBL is pan-reactive. This hypothesis was tested through functional assays, showing that P. yoelii M2-MAEBL antisera are able to recognize and inhibit erythrocyte invasion from both P. falciparum and P. vivax parasites isolated from Thai patients, in ex vivo assays. Moreover, the sequence of the M2-MAEBL is shown to be highly conserved between P. vivax isolates from the Amazon and Thailand, indicating that the MAEBL antigen may constitute a vaccine candidate outwitting strain-specific immunity. CONCLUSIONS: The MAEBL antigen is promising candidate towards the development of a malaria vaccine.
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spelling In silico epitope mapping and experimental evaluation of the Merozoite Adhesive Erythrocytic Binding Protein (MAEBL) as a malaria vaccine candidateDrug DiscoveryInfectious DiseasesSDG 3 - Good Health and Well-beingBACKGROUND: Technical limitations for culturing the human malaria parasite Plasmodium vivax have impaired the discovery of vaccine candidates, challenging the malaria eradication agenda. The immunogenicity of the M2 domain of the Merozoite Adhesive Erythrocytic Binding Protein (MAEBL) antigen cloned from the Plasmodium yoelii murine parasite, has been previously demonstrated. RESULTS: Detailed epitope mapping of MAEBL through immunoinformatics identified several MHCI, MHCII and B cell epitopes throughout the peptide, with several of these lying in the M2 domain and being conserved between P. vivax, P. yoelii and Plasmodium falciparum, hinting that the M2-MAEBL is pan-reactive. This hypothesis was tested through functional assays, showing that P. yoelii M2-MAEBL antisera are able to recognize and inhibit erythrocyte invasion from both P. falciparum and P. vivax parasites isolated from Thai patients, in ex vivo assays. Moreover, the sequence of the M2-MAEBL is shown to be highly conserved between P. vivax isolates from the Amazon and Thailand, indicating that the MAEBL antigen may constitute a vaccine candidate outwitting strain-specific immunity. CONCLUSIONS: The MAEBL antigen is promising candidate towards the development of a malaria vaccine.Vector borne diseases and pathogens (VBD)Global Health and Tropical Medicine (GHTM)Instituto de Higiene e Medicina Tropical (IHMT)RUNCravo, PedroMachado, Renato BLeite, Juliana ALeda, TaizySuwanarusk, RossarinBittencourt, NajaraAlbrecht, LetusaJudice, CarlaLopes, Stefanie C PLacerda, Marcus V GFerreira, Marcelo USoares, Irene SGoh, Yun ShanBargieri, Daniel YNosten, FrançoisRussell, BruceRénia, LaurentCosta, Fabio T M2021-05-03T22:35:15Z2018-01-102018-01-10T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10362/116836eng1475-2875PURE: 3630703https://doi.org/10.1186/s12936-017-2144-xinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-03-11T04:59:36Zoai:run.unl.pt:10362/116836Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:43:18.440958Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv In silico epitope mapping and experimental evaluation of the Merozoite Adhesive Erythrocytic Binding Protein (MAEBL) as a malaria vaccine candidate
title In silico epitope mapping and experimental evaluation of the Merozoite Adhesive Erythrocytic Binding Protein (MAEBL) as a malaria vaccine candidate
spellingShingle In silico epitope mapping and experimental evaluation of the Merozoite Adhesive Erythrocytic Binding Protein (MAEBL) as a malaria vaccine candidate
Cravo, Pedro
Drug Discovery
Infectious Diseases
SDG 3 - Good Health and Well-being
title_short In silico epitope mapping and experimental evaluation of the Merozoite Adhesive Erythrocytic Binding Protein (MAEBL) as a malaria vaccine candidate
title_full In silico epitope mapping and experimental evaluation of the Merozoite Adhesive Erythrocytic Binding Protein (MAEBL) as a malaria vaccine candidate
title_fullStr In silico epitope mapping and experimental evaluation of the Merozoite Adhesive Erythrocytic Binding Protein (MAEBL) as a malaria vaccine candidate
title_full_unstemmed In silico epitope mapping and experimental evaluation of the Merozoite Adhesive Erythrocytic Binding Protein (MAEBL) as a malaria vaccine candidate
title_sort In silico epitope mapping and experimental evaluation of the Merozoite Adhesive Erythrocytic Binding Protein (MAEBL) as a malaria vaccine candidate
author Cravo, Pedro
author_facet Cravo, Pedro
Machado, Renato B
Leite, Juliana A
Leda, Taizy
Suwanarusk, Rossarin
Bittencourt, Najara
Albrecht, Letusa
Judice, Carla
Lopes, Stefanie C P
Lacerda, Marcus V G
Ferreira, Marcelo U
Soares, Irene S
Goh, Yun Shan
Bargieri, Daniel Y
Nosten, François
Russell, Bruce
Rénia, Laurent
Costa, Fabio T M
author_role author
author2 Machado, Renato B
Leite, Juliana A
Leda, Taizy
Suwanarusk, Rossarin
Bittencourt, Najara
Albrecht, Letusa
Judice, Carla
Lopes, Stefanie C P
Lacerda, Marcus V G
Ferreira, Marcelo U
Soares, Irene S
Goh, Yun Shan
Bargieri, Daniel Y
Nosten, François
Russell, Bruce
Rénia, Laurent
Costa, Fabio T M
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Vector borne diseases and pathogens (VBD)
Global Health and Tropical Medicine (GHTM)
Instituto de Higiene e Medicina Tropical (IHMT)
RUN
dc.contributor.author.fl_str_mv Cravo, Pedro
Machado, Renato B
Leite, Juliana A
Leda, Taizy
Suwanarusk, Rossarin
Bittencourt, Najara
Albrecht, Letusa
Judice, Carla
Lopes, Stefanie C P
Lacerda, Marcus V G
Ferreira, Marcelo U
Soares, Irene S
Goh, Yun Shan
Bargieri, Daniel Y
Nosten, François
Russell, Bruce
Rénia, Laurent
Costa, Fabio T M
dc.subject.por.fl_str_mv Drug Discovery
Infectious Diseases
SDG 3 - Good Health and Well-being
topic Drug Discovery
Infectious Diseases
SDG 3 - Good Health and Well-being
description BACKGROUND: Technical limitations for culturing the human malaria parasite Plasmodium vivax have impaired the discovery of vaccine candidates, challenging the malaria eradication agenda. The immunogenicity of the M2 domain of the Merozoite Adhesive Erythrocytic Binding Protein (MAEBL) antigen cloned from the Plasmodium yoelii murine parasite, has been previously demonstrated. RESULTS: Detailed epitope mapping of MAEBL through immunoinformatics identified several MHCI, MHCII and B cell epitopes throughout the peptide, with several of these lying in the M2 domain and being conserved between P. vivax, P. yoelii and Plasmodium falciparum, hinting that the M2-MAEBL is pan-reactive. This hypothesis was tested through functional assays, showing that P. yoelii M2-MAEBL antisera are able to recognize and inhibit erythrocyte invasion from both P. falciparum and P. vivax parasites isolated from Thai patients, in ex vivo assays. Moreover, the sequence of the M2-MAEBL is shown to be highly conserved between P. vivax isolates from the Amazon and Thailand, indicating that the MAEBL antigen may constitute a vaccine candidate outwitting strain-specific immunity. CONCLUSIONS: The MAEBL antigen is promising candidate towards the development of a malaria vaccine.
publishDate 2018
dc.date.none.fl_str_mv 2018-01-10
2018-01-10T00:00:00Z
2021-05-03T22:35:15Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10362/116836
url http://hdl.handle.net/10362/116836
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1475-2875
PURE: 3630703
https://doi.org/10.1186/s12936-017-2144-x
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eu_rights_str_mv openAccess
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