A new polymerase chain reaction/restriction fragment length polymorphism protocol for Plasmodium vivax circumsporozoite protein genotype (VK210, VK247, and P. vivax-like) determination

Detalhes bibliográficos
Autor(a) principal: Alves, Renata Tomé
Data de Publicação: 2007
Outros Autores: Póvoa, Marinete Marins, Goldman, Ira F, Cavasini, Carlos Eugênio, Rossit, Andréa Regina Baptista, Machado, Ricardo Luiz Dantas
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Digital do Instituto Evandro Chagas (Patuá)
Texto Completo: https://patua.iec.gov.br/handle/iec/1057
Resumo: For the molecular diagnosis of Plasmodium vivax variants (VK210, VK247, and P. vivax-like) using DNA amplification procedures in the laboratory, the choice of rapid and inexpensive identification products of the 3 different genotypes is an important prerequisite. We report here the standardization of a new polymerase chain reaction/restriction fragment length polymorphism technique to identify the 3 described P. vivax circumsporozoite protein (CSP) variants using amplification of the central immunodominant region of the CSP gene of this protozoan. The simplicity, specificity, and sensitivity of the system described here is important to determine the prevalence and the distribution of infection with these P. vivax genotypes in endemic and nonendemic malaria areas, enabling a better understanding of their phylogeny.
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spelling Alves, Renata ToméPóvoa, Marinete MarinsGoldman, Ira FCavasini, Carlos EugênioRossit, Andréa Regina BaptistaMachado, Ricardo Luiz Dantas2016-01-26T11:43:20Z2016-01-26T11:43:20Z2007ALVES, Renata Tomé et al. A new polymerase chain reaction/restriction fragment length polymorphism protocol for Plasmodium vivax circumsporozoite protein genotype (VK210, VK247, and P. vivax-like) determination. Diagnostic Microbiology and Infectious Disease, v. 59, p. 415-419, 20070732-8893https://patua.iec.gov.br/handle/iec/105710.1016/j.diagmicrobio.2007.06.019For the molecular diagnosis of Plasmodium vivax variants (VK210, VK247, and P. vivax-like) using DNA amplification procedures in the laboratory, the choice of rapid and inexpensive identification products of the 3 different genotypes is an important prerequisite. We report here the standardization of a new polymerase chain reaction/restriction fragment length polymorphism technique to identify the 3 described P. vivax circumsporozoite protein (CSP) variants using amplification of the central immunodominant region of the CSP gene of this protozoan. The simplicity, specificity, and sensitivity of the system described here is important to determine the prevalence and the distribution of infection with these P. vivax genotypes in endemic and nonendemic malaria areas, enabling a better understanding of their phylogeny.Universidade Estadual Paulista Júlio de Mesquita Filho. São José do Rio Preto, SP, Brasil / Faculdade de Medicina de São José do Rio Preto. Departamento de Doenças Dermatológicas, Infecciosas e Parasitárias. Centro de Investigação de Microrganismos. São José do Rio Preto, SP, Brasil.Ministério da Saúde. Secretaria de Vigilância em Saúde. Instituto Evandro Chagas. Belém, PA, Brasil.Centers for Disease Control and Prevention. Atlanta , GA, USA.Faculdade de Medicina de São José do Rio Preto. Departamento de Doenças Dermatológicas, Infecciosas e Parasitárias. Centro de Investigação de Microrganismos. São José do Rio Preto, SP, Brasil.Faculdade de Medicina de São José do Rio Preto. Departamento de Doenças Dermatológicas, Infecciosas e Parasitárias. Centro de Investigação de Microrganismos. São José do Rio Preto, SP, Brasil / Fundação Faculdade de Medicina de São José do Rio Preto. São José do Rio Preto, SP, Brasil.Faculdade de Medicina de São José do Rio Preto. Departamento de Doenças Dermatológicas, Infecciosas e Parasitárias. Centro de Investigação de Microrganismos. São José do Rio Preto, SP, Brasil / Fundação Faculdade de Medicina de São José do Rio Preto. 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dc.title.pt_BR.fl_str_mv A new polymerase chain reaction/restriction fragment length polymorphism protocol for Plasmodium vivax circumsporozoite protein genotype (VK210, VK247, and P. vivax-like) determination
title A new polymerase chain reaction/restriction fragment length polymorphism protocol for Plasmodium vivax circumsporozoite protein genotype (VK210, VK247, and P. vivax-like) determination
spellingShingle A new polymerase chain reaction/restriction fragment length polymorphism protocol for Plasmodium vivax circumsporozoite protein genotype (VK210, VK247, and P. vivax-like) determination
Alves, Renata Tomé
Plasmodium vivax / genética
Polimorfismo Genético
Reação em Cadeia da Polimerase / métodos
title_short A new polymerase chain reaction/restriction fragment length polymorphism protocol for Plasmodium vivax circumsporozoite protein genotype (VK210, VK247, and P. vivax-like) determination
title_full A new polymerase chain reaction/restriction fragment length polymorphism protocol for Plasmodium vivax circumsporozoite protein genotype (VK210, VK247, and P. vivax-like) determination
title_fullStr A new polymerase chain reaction/restriction fragment length polymorphism protocol for Plasmodium vivax circumsporozoite protein genotype (VK210, VK247, and P. vivax-like) determination
title_full_unstemmed A new polymerase chain reaction/restriction fragment length polymorphism protocol for Plasmodium vivax circumsporozoite protein genotype (VK210, VK247, and P. vivax-like) determination
title_sort A new polymerase chain reaction/restriction fragment length polymorphism protocol for Plasmodium vivax circumsporozoite protein genotype (VK210, VK247, and P. vivax-like) determination
author Alves, Renata Tomé
author_facet Alves, Renata Tomé
Póvoa, Marinete Marins
Goldman, Ira F
Cavasini, Carlos Eugênio
Rossit, Andréa Regina Baptista
Machado, Ricardo Luiz Dantas
author_role author
author2 Póvoa, Marinete Marins
Goldman, Ira F
Cavasini, Carlos Eugênio
Rossit, Andréa Regina Baptista
Machado, Ricardo Luiz Dantas
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Alves, Renata Tomé
Póvoa, Marinete Marins
Goldman, Ira F
Cavasini, Carlos Eugênio
Rossit, Andréa Regina Baptista
Machado, Ricardo Luiz Dantas
dc.subject.decsPrimary.pt_BR.fl_str_mv Plasmodium vivax / genética
Polimorfismo Genético
Reação em Cadeia da Polimerase / métodos
topic Plasmodium vivax / genética
Polimorfismo Genético
Reação em Cadeia da Polimerase / métodos
description For the molecular diagnosis of Plasmodium vivax variants (VK210, VK247, and P. vivax-like) using DNA amplification procedures in the laboratory, the choice of rapid and inexpensive identification products of the 3 different genotypes is an important prerequisite. We report here the standardization of a new polymerase chain reaction/restriction fragment length polymorphism technique to identify the 3 described P. vivax circumsporozoite protein (CSP) variants using amplification of the central immunodominant region of the CSP gene of this protozoan. The simplicity, specificity, and sensitivity of the system described here is important to determine the prevalence and the distribution of infection with these P. vivax genotypes in endemic and nonendemic malaria areas, enabling a better understanding of their phylogeny.
publishDate 2007
dc.date.issued.fl_str_mv 2007
dc.date.accessioned.fl_str_mv 2016-01-26T11:43:20Z
dc.date.available.fl_str_mv 2016-01-26T11:43:20Z
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dc.identifier.citation.fl_str_mv ALVES, Renata Tomé et al. A new polymerase chain reaction/restriction fragment length polymorphism protocol for Plasmodium vivax circumsporozoite protein genotype (VK210, VK247, and P. vivax-like) determination. Diagnostic Microbiology and Infectious Disease, v. 59, p. 415-419, 2007
dc.identifier.uri.fl_str_mv https://patua.iec.gov.br/handle/iec/1057
dc.identifier.issn.-.fl_str_mv 0732-8893
dc.identifier.doi.-.fl_str_mv 10.1016/j.diagmicrobio.2007.06.019
identifier_str_mv ALVES, Renata Tomé et al. A new polymerase chain reaction/restriction fragment length polymorphism protocol for Plasmodium vivax circumsporozoite protein genotype (VK210, VK247, and P. vivax-like) determination. Diagnostic Microbiology and Infectious Disease, v. 59, p. 415-419, 2007
0732-8893
10.1016/j.diagmicrobio.2007.06.019
url https://patua.iec.gov.br/handle/iec/1057
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