A new polymerase chain reaction/restriction fragment length polymorphism protocol for Plasmodium vivax circumsporozoite protein genotype (VK210, VK247, and P. vivax-like) determination
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 o...
| Autores: | ; ; ; ; ; |
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| Tipo de documento: | Artículo |
| Estado: | Published version |
| Fecha de publicación: | 2007 |
| País: | Brasil |
| Institución: | IEC |
| Repositorio: | Repositório Digital do Instituto Evandro Chagas (Patuá) |
| Lenguaje: | Inglés |
| OAI Identifier: | oai:patua.iec.gov.br:iec/1057 |
| Acceso en línea: | https://patua.iec.gov.br/handle/iec/1057 |
| Nivel de acceso: | Acceso abierto |
| Palabra clave: | Plasmodium vivax / genética Polimorfismo Genético Reação em Cadeia da Polimerase / métodos |
| Sumario: | 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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