Plasmodium vivax merozoite surface protein 8 cloning, expression, and characterisation

Plasmodium vivax, one of the four parasite species causing malaria in humans, is the most widespread throughout the world, leading to nearly 80 million cases per year, mainly in Latin-America and Asia. An open reading frame encoding the Plasmodium falciparum merozoite surface protein 8 P. vivax homo...

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Autores:
Tipo de recurso:
Fecha de publicación:
2004
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/25941
Acceso en línea:
https://doi.org/10.1016/j.bbrc.2004.09.202
https://repository.urosario.edu.co/handle/10336/25941
Palabra clave:
Malaria
Plasmodium vivax
MSP8
Vaccine candidate
Surface protein
Rights
License
Restringido (Acceso a grupos específicos)
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oai_identifier_str oai:repository.urosario.edu.co:10336/25941
network_acronym_str EDOCUR2
network_name_str Repositorio EdocUR - U. Rosario
repository_id_str
spelling 8a814395-99e8-4f41-97df-12304c22be86-1bba7599d-1100-44fb-b8bf-6b76922c7da8-19db2c697-e3d4-43e1-b367-043baf7ace44-1c7b5067d-0805-42bd-ba53-04d4f30d5dd8-128469877600d191987c-6e13-4f7f-88bd-c34b437b85c6-15566b76c-9e92-4ce1-94bb-1d122c35ea36-14272869d-a644-44e9-a7a4-9c26d936bb9e-14fda4c81-5558-46e6-a038-005cc454bf3a-179653065-12020-08-06T16:20:16Z2020-08-06T16:20:16Z2004-11-26Plasmodium vivax, one of the four parasite species causing malaria in humans, is the most widespread throughout the world, leading to nearly 80 million cases per year, mainly in Latin-America and Asia. An open reading frame encoding the Plasmodium falciparum merozoite surface protein 8 P. vivax homologue has been identified in the present study by screening the current data obtained from this parasite’s partially sequenced genome. This new protein contains 487 amino-acids, two epidermal growth factor like domains, hydrophobic regions at the N- and C-termini compatible with a signal peptide, and a glycosylphosphatidylinositol anchor site, respectively. This gene’s transcription and its encoded protein expression have been assessed, as well as its recognition by P. vivax-infected patients’ sera. Based on this recognition, and a previous study showing that mice immunised with the Plasmodium yoelii homologous protein were protected, we consider the PvMSP8 a good candidate to be included in a multi-stage multi-antigen P. vivax vaccine.application/pdfhttps://doi.org/10.1016/j.bbrc.2004.09.202ISSN: 0006-291XEISSN: 1090-2104https://repository.urosario.edu.co/handle/10336/25941engElsevier1399No. 41393Biochemical and Biophysical Research CommunicationsVol. 324Biochemical and Biophysical Research Communications, ISSN: 0006-291X;EISSN: 1090-2104, Vol.324, No.4 (2004); pp.1393-1399https://www.sciencedirect.com/science/article/abs/pii/S0006291X04022429Restringido (Acceso a grupos específicos)http://purl.org/coar/access_right/c_16ecBiochemical and Biophysical Research Communicationsinstname:Universidad del Rosarioreponame:Repositorio Institucional EdocURMalariaPlasmodium vivaxMSP8Vaccine candidateSurface proteinPlasmodium vivax merozoite surface protein 8 cloning, expression, and characterisationPlasmodium vivax merozoite surface protein 8 clonación, expresión y caracterizaciónarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Pérez-Leal, ÓscarSierra, Adriana Y.Barrero, Carlos A.Moncada, CamiloMartínez Rángel, Diana PilarCortés, JimenaLópez, YolandaTorres, ElizabethSalazar, Luz M.Patarroyo, Manuel A.10336/25941oai:repository.urosario.edu.co:10336/259412021-06-03 00:50:21.472https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co
dc.title.spa.fl_str_mv Plasmodium vivax merozoite surface protein 8 cloning, expression, and characterisation
dc.title.TranslatedTitle.spa.fl_str_mv Plasmodium vivax merozoite surface protein 8 clonación, expresión y caracterización
title Plasmodium vivax merozoite surface protein 8 cloning, expression, and characterisation
spellingShingle Plasmodium vivax merozoite surface protein 8 cloning, expression, and characterisation
Malaria
Plasmodium vivax
MSP8
Vaccine candidate
Surface protein
title_short Plasmodium vivax merozoite surface protein 8 cloning, expression, and characterisation
title_full Plasmodium vivax merozoite surface protein 8 cloning, expression, and characterisation
title_fullStr Plasmodium vivax merozoite surface protein 8 cloning, expression, and characterisation
title_full_unstemmed Plasmodium vivax merozoite surface protein 8 cloning, expression, and characterisation
title_sort Plasmodium vivax merozoite surface protein 8 cloning, expression, and characterisation
dc.subject.keyword.spa.fl_str_mv Malaria
Plasmodium vivax
MSP8
Vaccine candidate
Surface protein
topic Malaria
Plasmodium vivax
MSP8
Vaccine candidate
Surface protein
description Plasmodium vivax, one of the four parasite species causing malaria in humans, is the most widespread throughout the world, leading to nearly 80 million cases per year, mainly in Latin-America and Asia. An open reading frame encoding the Plasmodium falciparum merozoite surface protein 8 P. vivax homologue has been identified in the present study by screening the current data obtained from this parasite’s partially sequenced genome. This new protein contains 487 amino-acids, two epidermal growth factor like domains, hydrophobic regions at the N- and C-termini compatible with a signal peptide, and a glycosylphosphatidylinositol anchor site, respectively. This gene’s transcription and its encoded protein expression have been assessed, as well as its recognition by P. vivax-infected patients’ sera. Based on this recognition, and a previous study showing that mice immunised with the Plasmodium yoelii homologous protein were protected, we consider the PvMSP8 a good candidate to be included in a multi-stage multi-antigen P. vivax vaccine.
publishDate 2004
dc.date.created.spa.fl_str_mv 2004-11-26
dc.date.accessioned.none.fl_str_mv 2020-08-06T16:20:16Z
dc.date.available.none.fl_str_mv 2020-08-06T16:20:16Z
dc.type.eng.fl_str_mv article
dc.type.coarversion.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.coar.fl_str_mv http://purl.org/coar/resource_type/c_6501
dc.type.spa.spa.fl_str_mv Artículo
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1016/j.bbrc.2004.09.202
dc.identifier.issn.none.fl_str_mv ISSN: 0006-291X
EISSN: 1090-2104
dc.identifier.uri.none.fl_str_mv https://repository.urosario.edu.co/handle/10336/25941
url https://doi.org/10.1016/j.bbrc.2004.09.202
https://repository.urosario.edu.co/handle/10336/25941
identifier_str_mv ISSN: 0006-291X
EISSN: 1090-2104
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.citationEndPage.none.fl_str_mv 1399
dc.relation.citationIssue.none.fl_str_mv No. 4
dc.relation.citationStartPage.none.fl_str_mv 1393
dc.relation.citationTitle.none.fl_str_mv Biochemical and Biophysical Research Communications
dc.relation.citationVolume.none.fl_str_mv Vol. 324
dc.relation.ispartof.spa.fl_str_mv Biochemical and Biophysical Research Communications, ISSN: 0006-291X;EISSN: 1090-2104, Vol.324, No.4 (2004); pp.1393-1399
dc.relation.uri.spa.fl_str_mv https://www.sciencedirect.com/science/article/abs/pii/S0006291X04022429
dc.rights.coar.fl_str_mv http://purl.org/coar/access_right/c_16ec
dc.rights.acceso.spa.fl_str_mv Restringido (Acceso a grupos específicos)
rights_invalid_str_mv Restringido (Acceso a grupos específicos)
http://purl.org/coar/access_right/c_16ec
dc.format.mimetype.none.fl_str_mv application/pdf
dc.publisher.spa.fl_str_mv Elsevier
dc.source.spa.fl_str_mv Biochemical and Biophysical Research Communications
institution Universidad del Rosario
dc.source.instname.none.fl_str_mv instname:Universidad del Rosario
dc.source.reponame.none.fl_str_mv reponame:Repositorio Institucional EdocUR
repository.name.fl_str_mv Repositorio institucional EdocUR
repository.mail.fl_str_mv edocur@urosario.edu.co
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