Publicação:
Plasmodium falciparum: sequence diversity and antibody recognition of the Merozoite surface protein-2 (MSP-2) in Brazilian Amazonia

dc.contributor.authorTonon, A. P.
dc.contributor.authorHoffmann, EHE
dc.contributor.authorda Silveira, L. A.
dc.contributor.authorRibeiroa, A. G.
dc.contributor.authorGoncalves, CRD
dc.contributor.authorRibolla, PEM
dc.contributor.authorWunderlich, G.
dc.contributor.authorFerreira, M. U.
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:52:39Z
dc.date.available2014-05-20T13:52:39Z
dc.date.issued2004-11-01
dc.description.abstractThe merozoite surface protein-2 (MSP-2) of Plasmodium falciparum comprises repeats flanked by dimorphic domains defining the allelic families FC27 and IC1. Here, we examined sequence diversity at the msp-2 locus in Brazil and its impact on MSP-2 antibody recognition by local patients. Only 25 unique partial sequences of msp-2 were found in 61 isolates examined. The finding of identical msp-2 sequences in unrelated parasites, collected 6-13 years apart, suggests that no major directional selection is exerted by variant-specific immunity in this malaria-endemic area. To examine antibody cross-reactivity, recombinant polypeptides derived from locally prevalent and foreign MSP-2 variants were used in ELISA. Foreign IC1-type variants, such as 3D7 (currently tested for human vaccination), were less frequently recognized than FC27-type and local IC1-type variants. Antibodies discriminated between local and foreign IC1-type variants, but cross-recognized structurally different local IC1-type variants. The use of evolutionary models of MSP-2 is suggested to design vaccines that minimize differences between local parasites and vaccine antigens. (C) 2004 Elsevier B.V. All rights reserved.en
dc.description.affiliationUniv São Paulo, Inst Ciências Biomed, Dept Parasitol, BR-05508900 São Paulo, Brazil
dc.description.affiliationUniv Estadual Paulista, Inst Biociencias Botucatu, Dept Parasitol, Botucatu, SP, Brazil
dc.description.affiliationUnespUniv Estadual Paulista, Inst Biociencias Botucatu, Dept Parasitol, Botucatu, SP, Brazil
dc.format.extent114-125
dc.identifierhttp://dx.doi.org/10.1016/exppara.2004.08.001
dc.identifier.citationExperimental Parasitology. San Diego: Academic Press Inc. Elsevier B.V., v. 108, n. 3-4, p. 114-125, 2004.
dc.identifier.doi10.1016/exppara.2004.08.001
dc.identifier.issn0014-4894
dc.identifier.lattes3577149748456880
dc.identifier.orcid0000-0001-8735-6090
dc.identifier.urihttp://hdl.handle.net/11449/18801
dc.identifier.wosWOS:000225933400005
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofExperimental Parasitology
dc.relation.ispartofjcr1.821
dc.relation.ispartofsjr0,635
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectprotozoapt
dc.subjectmalaria parasitespt
dc.subjectMSP-2pt
dc.subjectantigenic diversitypt
dc.subjectvaccinept
dc.titlePlasmodium falciparum: sequence diversity and antibody recognition of the Merozoite surface protein-2 (MSP-2) in Brazilian Amazoniaen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
unesp.author.lattes3577149748456880[6]
unesp.author.orcid0000-0002-5293-9090[8]
unesp.author.orcid0000-0003-1724-0337[7]
unesp.author.orcid0000-0001-8735-6090[6]
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Biociências, Botucatupt
unesp.departmentParasitologia - IBBpt

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