Determinación del proteoma de la cepa VCG-1 de Plasmodium Vivax y caracterización de moléculas candidatas para su inclusión en el desarrollo de una vacuna
La identificación y caracterización de proteínas que utilizan los merozoitos de Plasmodium para invadir a su célula hospedera, representan una estrategia importante para desarrollar un método de control contra estos parásitos. A pesar de ello, la investigación básica en P. vivax está retrasada por s...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2017
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- spa
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/19098
- Acceso en línea:
- https://doi.org/10.48713/10336_19098
http://repository.urosario.edu.co/handle/10336/19098
- Palabra clave:
- Plasmodium vivax
Invasión
Proteoma
Adhesión
Reticulocitos
Enfermedades
Plasmodium vivax
Invasion
Reticulocytes
Proteome
Characterization
Malaria
Plasmodium vivax
- Rights
- License
- Atribución-NoComercial-SinDerivadas 2.5 Colombia
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oai_identifier_str |
oai:repository.urosario.edu.co:10336/19098 |
network_acronym_str |
EDOCUR2 |
network_name_str |
Repositorio EdocUR - U. Rosario |
repository_id_str |
|
dc.title.spa.fl_str_mv |
Determinación del proteoma de la cepa VCG-1 de Plasmodium Vivax y caracterización de moléculas candidatas para su inclusión en el desarrollo de una vacuna |
title |
Determinación del proteoma de la cepa VCG-1 de Plasmodium Vivax y caracterización de moléculas candidatas para su inclusión en el desarrollo de una vacuna |
spellingShingle |
Determinación del proteoma de la cepa VCG-1 de Plasmodium Vivax y caracterización de moléculas candidatas para su inclusión en el desarrollo de una vacuna Plasmodium vivax Invasión Proteoma Adhesión Reticulocitos Enfermedades Plasmodium vivax Invasion Reticulocytes Proteome Characterization Malaria Plasmodium vivax |
title_short |
Determinación del proteoma de la cepa VCG-1 de Plasmodium Vivax y caracterización de moléculas candidatas para su inclusión en el desarrollo de una vacuna |
title_full |
Determinación del proteoma de la cepa VCG-1 de Plasmodium Vivax y caracterización de moléculas candidatas para su inclusión en el desarrollo de una vacuna |
title_fullStr |
Determinación del proteoma de la cepa VCG-1 de Plasmodium Vivax y caracterización de moléculas candidatas para su inclusión en el desarrollo de una vacuna |
title_full_unstemmed |
Determinación del proteoma de la cepa VCG-1 de Plasmodium Vivax y caracterización de moléculas candidatas para su inclusión en el desarrollo de una vacuna |
title_sort |
Determinación del proteoma de la cepa VCG-1 de Plasmodium Vivax y caracterización de moléculas candidatas para su inclusión en el desarrollo de una vacuna |
dc.contributor.advisor.none.fl_str_mv |
Patarroyo, Manuel A. Muro Álvarez, Antonio |
dc.subject.spa.fl_str_mv |
Plasmodium vivax Invasión Proteoma Adhesión Reticulocitos |
topic |
Plasmodium vivax Invasión Proteoma Adhesión Reticulocitos Enfermedades Plasmodium vivax Invasion Reticulocytes Proteome Characterization Malaria Plasmodium vivax |
dc.subject.ddc.spa.fl_str_mv |
Enfermedades |
dc.subject.keyword.spa.fl_str_mv |
Plasmodium vivax Invasion Reticulocytes Proteome Characterization |
dc.subject.lemb.spa.fl_str_mv |
Malaria Plasmodium vivax |
description |
La identificación y caracterización de proteínas que utilizan los merozoitos de Plasmodium para invadir a su célula hospedera, representan una estrategia importante para desarrollar un método de control contra estos parásitos. A pesar de ello, la investigación básica en P. vivax está retrasada por su difícil propagación in vitro, debido a la preferencia que tiene el parásito por invadir reticulocitos, los cuales se encuentran en escaso porcentaje en sangre periférica de humanos adultos (1-2%) y son difíciles de obtener con alta pureza, en suficiente cantidad y totalmente viables. Como consecuencia de lo anterior, el conocimiento del número de moléculas que expresa P. vivax y cuáles de ellas son candidatas para componer una vacuna, es escaso. En este estudio, se evaluó el proteoma de una cepa de P. vivax adaptada a primates y se caracterizaron moléculas antigénicas y con capacidad de adhesión a reticulocitos humanos. En el análisis del proteoma de la cepa VCG-1 de P. vivax, se detectaron 734 proteínas, algunas esenciales en los pasos clave para establecer la invasión del merozoito a su célula diana. Además, se identificaron 811 componentes de eritrocitos (hospederos vitales de Plasmodium) del primate A. nancymaae, de los cuales 51 son proteínas integrales de membrana, 7 descritas como receptores de Plasmodium. Por otro lado, se identificó la presencia, transcripción y expresión de los genes codificantes de tres moléculas de P. vivax: PvARP, PvRBSA y PvGAMA, así como su antigenicidad. De particular interés, se encontró que PvRBSA y PvGAMA se unen en mayor proporción a reticulocitos que expresan el receptor CD71 de forma abundante (CD71hi), lo que sugiere que estas moléculas pueden estar participando en la selección preferencial que tienen los merozoitos de P. vivax por los reticulocitos humanos. Este es el primer estudio en Colombia donde se determina la composición proteica de una cepa de P. vivax adaptada a primates, así como la de eritrocitos de A. nancymaae. Como resultado más importante, se caracterizaron moléculas de P. vivax que son candidatos idóneos a ser evaluados como componentes de una vacuna contra la malaria causada por esta especie parasitaria. |
publishDate |
2017 |
dc.date.created.none.fl_str_mv |
2017-09-07 |
dc.date.issued.none.fl_str_mv |
2017 |
dc.date.accessioned.none.fl_str_mv |
2019-02-18T21:46:17Z |
dc.date.available.none.fl_str_mv |
2019-02-18T21:46:17Z |
dc.type.eng.fl_str_mv |
doctoralThesis |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_db06 |
dc.type.document.spa.fl_str_mv |
Análisis de caso |
dc.type.spa.spa.fl_str_mv |
Tesis de doctorado |
dc.identifier.doi.none.fl_str_mv |
https://doi.org/10.48713/10336_19098 |
dc.identifier.uri.none.fl_str_mv |
http://repository.urosario.edu.co/handle/10336/19098 |
url |
https://doi.org/10.48713/10336_19098 http://repository.urosario.edu.co/handle/10336/19098 |
dc.language.iso.none.fl_str_mv |
spa |
language |
spa |
dc.rights.spa.fl_str_mv |
Atribución-NoComercial-SinDerivadas 2.5 Colombia |
dc.rights.coar.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
dc.rights.acceso.spa.fl_str_mv |
Abierto (Texto Completo) |
dc.rights.uri.none.fl_str_mv |
http://creativecommons.org/licenses/by-nc-nd/2.5/co/ |
rights_invalid_str_mv |
Atribución-NoComercial-SinDerivadas 2.5 Colombia Abierto (Texto Completo) http://creativecommons.org/licenses/by-nc-nd/2.5/co/ http://purl.org/coar/access_right/c_abf2 |
dc.format.mimetype.none.fl_str_mv |
application/pdf |
dc.publisher.spa.fl_str_mv |
Universidad del Rosario |
dc.publisher.department.spa.fl_str_mv |
Facultad de Ciencias Naturales y Matemáticas |
dc.publisher.program.spa.fl_str_mv |
Doctorado en Ciencias Biomédicas y Biológicas |
institution |
Universidad del Rosario |
dc.source.bibliographicCitation.spa.fl_str_mv |
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Identification and evaluation of universal epitopes in Plasmodium vivax Duffy binding protein. Biochem Biophys Res Commun. 2008;377(4):1279-83. Martinez P, Lopez C, Saravia C, Vanegas M, Patarroyo MA. Evaluation of the antigenicity of universal epitopes from PvDBPII in individuals exposed to Plasmodium vivax malaria. Microbes Infect. 2010;12(14-15):1188-97. Patarroyo ME, Bermudez A, Patarroyo MA. Structural and immunological principles leading to chemically synthesized, multiantigenic, multistage, minimal subunit-based vaccine development. Chem Rev. 2011;111(5):3459-507. Kolker E, Higdon R, Hogan JM. Protein identification and expression analysis using mass spectrometry. Trends Microbiol. 2006;14(5):229-35. Cheng Q, Saul A. Sequence analysis of the apical membrane antigen I (AMA-1) of Plasmodium vivax. Mol Biochem Parasitol. 1994;65(1):183-7. Patarroyo MA, Perez-Leal O, Lopez Y, Cortes J, Rojas-Caraballo J, Gomez A, et al. Identification and characterisation of the Plasmodium vivax rhoptry-associated protein 2. Biochem Biophys Res Commun. 2005;337(3):853-9. Perez-Leal O, Mongui A, Cortes J, Yepes G, Leiton J, Patarroyo MA. The Plasmodium vivax rhoptry-associated protein 1. Biochem Biophys Res Commun. 2006;341(4):1053-8. Mongui A, Perez-Leal O, Rojas-Caraballo J, Angel DI, Cortes J, Patarroyo MA. Identifying and characterising the Plasmodium falciparum RhopH3 Plasmodium vivax homologue. Biochem Biophys Res Commun. 2007;358(3):861-6. Mongui A, Angel DI, Guzman C, Vanegas M, Patarroyo MA. Characterisation of the Plasmodium vivax Pv38 antigen. Biochem Biophys Res Commun. 2008;376(2):326-30. Angel DI, Mongui A, Ardila J, Vanegas M, Patarroyo MA. The Plasmodium vivax Pv41 surface protein: identification and characterization. Biochem Biophys Res Commun. 2008;377(4):1113-7. Mongui A, Angel DI, Gallego G, Reyes C, Martinez P, Guhl F, et al. 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Patarroyo, Manuel A.79653065600Muro Álvarez, Antonio8472e887-63aa-4a12-b4ec-e7ba5d5deac3600Moreno Pérez, Darwin AndrésDoctor en Ciencias Biomédicas y BiológicasFull timea933d343-0788-4635-9002-4943747140c36002019-02-18T21:46:17Z2019-02-18T21:46:17Z2017-09-072017La identificación y caracterización de proteínas que utilizan los merozoitos de Plasmodium para invadir a su célula hospedera, representan una estrategia importante para desarrollar un método de control contra estos parásitos. A pesar de ello, la investigación básica en P. vivax está retrasada por su difícil propagación in vitro, debido a la preferencia que tiene el parásito por invadir reticulocitos, los cuales se encuentran en escaso porcentaje en sangre periférica de humanos adultos (1-2%) y son difíciles de obtener con alta pureza, en suficiente cantidad y totalmente viables. Como consecuencia de lo anterior, el conocimiento del número de moléculas que expresa P. vivax y cuáles de ellas son candidatas para componer una vacuna, es escaso. En este estudio, se evaluó el proteoma de una cepa de P. vivax adaptada a primates y se caracterizaron moléculas antigénicas y con capacidad de adhesión a reticulocitos humanos. En el análisis del proteoma de la cepa VCG-1 de P. vivax, se detectaron 734 proteínas, algunas esenciales en los pasos clave para establecer la invasión del merozoito a su célula diana. Además, se identificaron 811 componentes de eritrocitos (hospederos vitales de Plasmodium) del primate A. nancymaae, de los cuales 51 son proteínas integrales de membrana, 7 descritas como receptores de Plasmodium. Por otro lado, se identificó la presencia, transcripción y expresión de los genes codificantes de tres moléculas de P. vivax: PvARP, PvRBSA y PvGAMA, así como su antigenicidad. De particular interés, se encontró que PvRBSA y PvGAMA se unen en mayor proporción a reticulocitos que expresan el receptor CD71 de forma abundante (CD71hi), lo que sugiere que estas moléculas pueden estar participando en la selección preferencial que tienen los merozoitos de P. vivax por los reticulocitos humanos. Este es el primer estudio en Colombia donde se determina la composición proteica de una cepa de P. vivax adaptada a primates, así como la de eritrocitos de A. nancymaae. Como resultado más importante, se caracterizaron moléculas de P. vivax que son candidatos idóneos a ser evaluados como componentes de una vacuna contra la malaria causada por esta especie parasitaria.Identifying and characterising proteins which use Plasmodium merozoites to invade host cells represents an important strategy for developing a method for controlling these parasites. However, basic P. vivax research has been delayed due to difficulties in propagating it in vitro as the parasite prefers to invade reticulocytes; there is a low percentage of these in adult human peripheral blood (1%-2%) and they are difficult to obtain with high purity, in a sufficient amount and totally viable. Consequently, knowledge is scarce regarding the amount of molecules being expressed by P. vivax and which of them represent good candidates for inclusion in an effective vaccine. This study has been aimed at evaluating the proteome of a primate-adapted P. vivax strain; antigenic molecules able to bind to human reticulocytes have been characterised. Analysing the P. vivax VCG-1 strain proteome led to detecting 734 proteins, some of them essential in key steps for establishing merozoite invasion of target cells. Furthermore, 811 A. nancymaae primate erythrocyte components (vital Plasmodium hosts) were identified; 51 of them were integral membrane proteins, 7 described as Plasmodium receptors. The presence, transcription, expression and antigenicity of genes encoding three P. vivax molecules (PvARP, PvRBSA and PvGAMA) were identified. Particularly interesting was the finding that a higher percentage of PvRBSA and PvGAMA bound to reticulocytes abundantly expressing the CD71 receptor (CD71hi), thereby suggesting that these molecules could be participating in P. vivax merozoite preferential selection for human reticulocytes. This the first study in Colombia which has determined the protein composition of a primate-adapted P. vivax strain as well as A. nancymaae erythrocytes. More importantly, P. vivax molecules were characterised which appear to be suitable candidates for being evaluated as components of a vaccine against malaria caused by the parasite species.Universidad del RosarioUniversidad de Salamancaapplication/pdfhttps://doi.org/10.48713/10336_19098 http://repository.urosario.edu.co/handle/10336/19098spaUniversidad del RosarioFacultad de Ciencias Naturales y MatemáticasDoctorado en Ciencias Biomédicas y BiológicasAtribución-NoComercial-SinDerivadas 2.5 ColombiaAbierto (Texto Completo)EL AUTOR, manifiesta que la obra objeto de la presente autorización es original y la realizó sin violar o usurpar derechos de autor de terceros, por lo tanto la obra es de exclusiva autoría y tiene la titularidad sobre la misma. PARGRAFO: En caso de presentarse cualquier reclamación o acción por parte de un tercero en cuanto a los derechos de autor sobre la obra en cuestión, EL AUTOR, asumirá toda la responsabilidad, y saldrá en defensa de los derechos aquí autorizados; para todos los efectos la universidad actúa como un tercero de buena fe. EL AUTOR, autoriza a LA UNIVERSIDAD DEL ROSARIO, para que en los términos establecidos en la Ley 23 de 1982, Ley 44 de 1993, Decisión andina 351 de 1993, Decreto 460 de 1995 y demás normas generales sobre la materia, utilice y use la obra objeto de la presente autorización. -------------------------------------- POLITICA DE TRATAMIENTO DE DATOS PERSONALES. Declaro que autorizo previa y de forma informada el tratamiento de mis datos personales por parte de LA UNIVERSIDAD DEL ROSARIO para fines académicos y en aplicación de convenios con terceros o servicios conexos con actividades propias de la academia, con estricto cumplimiento de los principios de ley. 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