Limited genetic polymorphism of the Plasmodium vivax low molecular weight rhoptry protein complex in the Colombian population

Proteins involved in parasite adhesion and invasion are considered the best candidates for the development of asexual blood-stage antimalarial vaccines. Such vaccine candidates should be accessible by the immune system and have limited diversity. Considering the promising results obtained in previou...

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Autores:
Tipo de recurso:
Fecha de publicación:
2010
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/24293
Acceso en línea:
https://doi.org/10.1016/j.meegid.2009.12.004
https://repository.urosario.edu.co/handle/10336/24293
Palabra clave:
Protein
Rhoptry associated protein 1
Rhoptry associated protein 2
Unclassified drug
Amino acid sequence
Article
Dna sequence
Exon
Gene linkage disequilibrium
Gene locus
Gene mutation
Genetic polymorphism
Genetic recombination
Genetic variability
Haplotype
Human
Nonhuman
Nucleotide sequence
Parasite isolation
Plasmodium vivax
Priority journal
Sequence alignment
Amino acid sequence
Colombia
Geography
Humans
Linkage disequilibrium
Malaria vaccines
Molecular sequence data
Plasmodium vivax
Protozoan proteins
Sequence alignment
Plasmodium vivax
Demographic process
Genetic polymorphism
Malaria vaccine candidates
Plasmodium vivax
Rhoptry-associated protein 1
Rhoptry-associated protein 2
vivax
molecular
genetic
Evolution
Malaria
Polymorphism
Rights
License
Abierto (Texto Completo)
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dc.title.spa.fl_str_mv Limited genetic polymorphism of the Plasmodium vivax low molecular weight rhoptry protein complex in the Colombian population
title Limited genetic polymorphism of the Plasmodium vivax low molecular weight rhoptry protein complex in the Colombian population
spellingShingle Limited genetic polymorphism of the Plasmodium vivax low molecular weight rhoptry protein complex in the Colombian population
Protein
Rhoptry associated protein 1
Rhoptry associated protein 2
Unclassified drug
Amino acid sequence
Article
Dna sequence
Exon
Gene linkage disequilibrium
Gene locus
Gene mutation
Genetic polymorphism
Genetic recombination
Genetic variability
Haplotype
Human
Nonhuman
Nucleotide sequence
Parasite isolation
Plasmodium vivax
Priority journal
Sequence alignment
Amino acid sequence
Colombia
Geography
Humans
Linkage disequilibrium
Malaria vaccines
Molecular sequence data
Plasmodium vivax
Protozoan proteins
Sequence alignment
Plasmodium vivax
Demographic process
Genetic polymorphism
Malaria vaccine candidates
Plasmodium vivax
Rhoptry-associated protein 1
Rhoptry-associated protein 2
vivax
molecular
genetic
Evolution
Malaria
Polymorphism
title_short Limited genetic polymorphism of the Plasmodium vivax low molecular weight rhoptry protein complex in the Colombian population
title_full Limited genetic polymorphism of the Plasmodium vivax low molecular weight rhoptry protein complex in the Colombian population
title_fullStr Limited genetic polymorphism of the Plasmodium vivax low molecular weight rhoptry protein complex in the Colombian population
title_full_unstemmed Limited genetic polymorphism of the Plasmodium vivax low molecular weight rhoptry protein complex in the Colombian population
title_sort Limited genetic polymorphism of the Plasmodium vivax low molecular weight rhoptry protein complex in the Colombian population
dc.subject.keyword.spa.fl_str_mv Protein
Rhoptry associated protein 1
Rhoptry associated protein 2
Unclassified drug
Amino acid sequence
Article
Dna sequence
Exon
Gene linkage disequilibrium
Gene locus
Gene mutation
Genetic polymorphism
Genetic recombination
Genetic variability
Haplotype
Human
Nonhuman
Nucleotide sequence
Parasite isolation
Plasmodium vivax
Priority journal
Sequence alignment
Amino acid sequence
Colombia
Geography
Humans
Linkage disequilibrium
Malaria vaccines
Molecular sequence data
Plasmodium vivax
Protozoan proteins
Sequence alignment
Plasmodium vivax
Demographic process
Genetic polymorphism
Malaria vaccine candidates
Plasmodium vivax
Rhoptry-associated protein 1
Rhoptry-associated protein 2
topic Protein
Rhoptry associated protein 1
Rhoptry associated protein 2
Unclassified drug
Amino acid sequence
Article
Dna sequence
Exon
Gene linkage disequilibrium
Gene locus
Gene mutation
Genetic polymorphism
Genetic recombination
Genetic variability
Haplotype
Human
Nonhuman
Nucleotide sequence
Parasite isolation
Plasmodium vivax
Priority journal
Sequence alignment
Amino acid sequence
Colombia
Geography
Humans
Linkage disequilibrium
Malaria vaccines
Molecular sequence data
Plasmodium vivax
Protozoan proteins
Sequence alignment
Plasmodium vivax
Demographic process
Genetic polymorphism
Malaria vaccine candidates
Plasmodium vivax
Rhoptry-associated protein 1
Rhoptry-associated protein 2
vivax
molecular
genetic
Evolution
Malaria
Polymorphism
dc.subject.keyword.eng.fl_str_mv vivax
molecular
genetic
Evolution
Malaria
Polymorphism
description Proteins involved in parasite adhesion and invasion are considered the best candidates for the development of asexual blood-stage antimalarial vaccines. Such vaccine candidates should be accessible by the immune system and have limited diversity. Considering the promising results obtained in previous trials by immunizing monkeys with the rhoptry-associated proteins 1 and 2 (RAP-1 and RAP-2), here we assessed the genetic variability of the Plasmodium vivax rap-1 and rap-2 genes isolated from Colombian parasite populations. Limited sequence diversity was found in these genes, possibly as a result of a functional/structural restriction. The presence of several haplotypes at relatively low frequencies and the excess of singleton mutations suggests that a demographic process might be affecting the loci. Our results support the inclusion of PvRAP-1 and PvRAP-2 in the design of an antimalarial subunit-based vaccine against P. vivax, which would avoid inducing allele-specific immunity. © 2009 Elsevier B.V. All rights reserved.
publishDate 2010
dc.date.created.spa.fl_str_mv 2010
dc.date.accessioned.none.fl_str_mv 2020-05-26T00:11:17Z
dc.date.available.none.fl_str_mv 2020-05-26T00:11:17Z
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.meegid.2009.12.004
dc.identifier.issn.none.fl_str_mv 15671348
dc.identifier.uri.none.fl_str_mv https://repository.urosario.edu.co/handle/10336/24293
url https://doi.org/10.1016/j.meegid.2009.12.004
https://repository.urosario.edu.co/handle/10336/24293
identifier_str_mv 15671348
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.citationEndPage.none.fl_str_mv 267
dc.relation.citationIssue.none.fl_str_mv No. 2
dc.relation.citationStartPage.none.fl_str_mv 261
dc.relation.citationTitle.none.fl_str_mv Infection, Genetics and Evolution
dc.relation.citationVolume.none.fl_str_mv Vol. 10
dc.relation.ispartof.spa.fl_str_mv Infection, Genetics and Evolution, ISSN:15671348, Vol.10, No.2 (2010); pp. 261-267
dc.relation.uri.spa.fl_str_mv https://www.scopus.com/inward/record.uri?eid=2-s2.0-76849090794&doi=10.1016%2fj.meegid.2009.12.004&partnerID=40&md5=761100acfa3ee8a809df41f1666865db
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