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Serological detection of Plasmodium vivax malaria using recombinant proteins corresponding to the 19-kDa C-terminal region of the merozoite surface protein-1
BACKGROUND: Serological tests to detect antibodies specific to Plasmodium vivax could be a valuable tool for epidemiological studies, for screening blood donors in areas where the malaria is not endemic and for diagnosis of infected individuals. Because P. vivax cannot be easily obtained in vitro, E...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2003
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC293434/ https://www.ncbi.nlm.nih.gov/pubmed/14617378 http://dx.doi.org/10.1186/1475-2875-2-39 |
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author | Rodrigues, Maria Helena C Cunha, Maristela G Machado, Ricardo LD Ferreira, Orlando C Rodrigues, Mauricio M Soares, Irene S |
author_facet | Rodrigues, Maria Helena C Cunha, Maristela G Machado, Ricardo LD Ferreira, Orlando C Rodrigues, Mauricio M Soares, Irene S |
author_sort | Rodrigues, Maria Helena C |
collection | PubMed |
description | BACKGROUND: Serological tests to detect antibodies specific to Plasmodium vivax could be a valuable tool for epidemiological studies, for screening blood donors in areas where the malaria is not endemic and for diagnosis of infected individuals. Because P. vivax cannot be easily obtained in vitro, ELISA assays using total or semi-purified antigens are rarely used. Based on this limitation, we tested whether recombinant proteins representing the 19 kDa C-terminal region of the merozoite surface protein-1 of P. vivax (MSP1(19)) could be useful for serological detection of malaria infection. METHODS: Three purified recombinant proteins produced in Escherichia coli (GST-MSP1(19), His(6)-MSP1(19 )and His(6)-MSP1(19)-PADRE) and one in Pichia pastoris (yMSP1(19)-PADRE) were compared for their ability to bind to IgG antibodies of individuals with patent P. vivax infection. The method was tested with 200 serum samples collected from individuals living in the north of Brazil in areas endemic for malaria, 53 serum samples from individuals exposed to Plasmodium falciparum infection and 177 serum samples from individuals never exposed to malaria. RESULTS: Overall, the sensitivity of the ELISA assessed with sera from naturally infected individuals was 95%. The proportion of serum samples that reacted with recombinant proteins GST-MSP1(19, )His(6)-MSP1(19), His(6)-MSP1(19)-PADRE and yMSP1(19)-PADRE was 90%, 93.5%, 93.5% and 93.5%, respectively. The specificity values of the ELISA determined with sera from healthy individuals and from individuals with other infectious diseases were 98.3% (GST-MSP1(19)), 97.7% (His(6)-MSP1(19 )and His(6)-MSP1(19)-PADRE) or 100% (yMSP1(19)-PADRE). CONCLUSIONS: Our study demonstrated that for the Brazilian population, an ELISA using a recombinant protein of the MSP1(19 )can be used as the basis for the development of a valuable serological assay for the detection of P. vivax malaria. |
format | Text |
id | pubmed-293434 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-2934342003-12-16 Serological detection of Plasmodium vivax malaria using recombinant proteins corresponding to the 19-kDa C-terminal region of the merozoite surface protein-1 Rodrigues, Maria Helena C Cunha, Maristela G Machado, Ricardo LD Ferreira, Orlando C Rodrigues, Mauricio M Soares, Irene S Malar J Methodology BACKGROUND: Serological tests to detect antibodies specific to Plasmodium vivax could be a valuable tool for epidemiological studies, for screening blood donors in areas where the malaria is not endemic and for diagnosis of infected individuals. Because P. vivax cannot be easily obtained in vitro, ELISA assays using total or semi-purified antigens are rarely used. Based on this limitation, we tested whether recombinant proteins representing the 19 kDa C-terminal region of the merozoite surface protein-1 of P. vivax (MSP1(19)) could be useful for serological detection of malaria infection. METHODS: Three purified recombinant proteins produced in Escherichia coli (GST-MSP1(19), His(6)-MSP1(19 )and His(6)-MSP1(19)-PADRE) and one in Pichia pastoris (yMSP1(19)-PADRE) were compared for their ability to bind to IgG antibodies of individuals with patent P. vivax infection. The method was tested with 200 serum samples collected from individuals living in the north of Brazil in areas endemic for malaria, 53 serum samples from individuals exposed to Plasmodium falciparum infection and 177 serum samples from individuals never exposed to malaria. RESULTS: Overall, the sensitivity of the ELISA assessed with sera from naturally infected individuals was 95%. The proportion of serum samples that reacted with recombinant proteins GST-MSP1(19, )His(6)-MSP1(19), His(6)-MSP1(19)-PADRE and yMSP1(19)-PADRE was 90%, 93.5%, 93.5% and 93.5%, respectively. The specificity values of the ELISA determined with sera from healthy individuals and from individuals with other infectious diseases were 98.3% (GST-MSP1(19)), 97.7% (His(6)-MSP1(19 )and His(6)-MSP1(19)-PADRE) or 100% (yMSP1(19)-PADRE). CONCLUSIONS: Our study demonstrated that for the Brazilian population, an ELISA using a recombinant protein of the MSP1(19 )can be used as the basis for the development of a valuable serological assay for the detection of P. vivax malaria. BioMed Central 2003-11-14 /pmc/articles/PMC293434/ /pubmed/14617378 http://dx.doi.org/10.1186/1475-2875-2-39 Text en Copyright © 2003 Rodrigues et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL. |
spellingShingle | Methodology Rodrigues, Maria Helena C Cunha, Maristela G Machado, Ricardo LD Ferreira, Orlando C Rodrigues, Mauricio M Soares, Irene S Serological detection of Plasmodium vivax malaria using recombinant proteins corresponding to the 19-kDa C-terminal region of the merozoite surface protein-1 |
title | Serological detection of Plasmodium vivax malaria using recombinant proteins corresponding to the 19-kDa C-terminal region of the merozoite surface protein-1 |
title_full | Serological detection of Plasmodium vivax malaria using recombinant proteins corresponding to the 19-kDa C-terminal region of the merozoite surface protein-1 |
title_fullStr | Serological detection of Plasmodium vivax malaria using recombinant proteins corresponding to the 19-kDa C-terminal region of the merozoite surface protein-1 |
title_full_unstemmed | Serological detection of Plasmodium vivax malaria using recombinant proteins corresponding to the 19-kDa C-terminal region of the merozoite surface protein-1 |
title_short | Serological detection of Plasmodium vivax malaria using recombinant proteins corresponding to the 19-kDa C-terminal region of the merozoite surface protein-1 |
title_sort | serological detection of plasmodium vivax malaria using recombinant proteins corresponding to the 19-kda c-terminal region of the merozoite surface protein-1 |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC293434/ https://www.ncbi.nlm.nih.gov/pubmed/14617378 http://dx.doi.org/10.1186/1475-2875-2-39 |
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