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Characterization of immunoglobulin G antibodies to Plasmodium falciparum sporozoite surface antigen MB(2) in malaria exposed individuals

BACKGROUND: MB2 protein is a sporozoite surface antigen on the human malaria parasite Plasmodium falciparum. MB2 was identified by screening a P. falciparum sporozoite cDNA expression library using immune sera from a protected donor immunized via the bites of P. falciparum-infected irradiated mosqui...

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Autores principales: Nguyen, Thanh V, Sacci, John B, de la Vega, Patricia, John, Chandy C, James, Anthony A, Kang, Angray S
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2772840/
https://www.ncbi.nlm.nih.gov/pubmed/19852802
http://dx.doi.org/10.1186/1475-2875-8-235
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author Nguyen, Thanh V
Sacci, John B
de la Vega, Patricia
John, Chandy C
James, Anthony A
Kang, Angray S
author_facet Nguyen, Thanh V
Sacci, John B
de la Vega, Patricia
John, Chandy C
James, Anthony A
Kang, Angray S
author_sort Nguyen, Thanh V
collection PubMed
description BACKGROUND: MB2 protein is a sporozoite surface antigen on the human malaria parasite Plasmodium falciparum. MB2 was identified by screening a P. falciparum sporozoite cDNA expression library using immune sera from a protected donor immunized via the bites of P. falciparum-infected irradiated mosquitoes. It is not known whether natural exposure to P. falciparum also induces the anti-MB2 response and if this response differs from that in protected individuals immunized via the bites of P. falciparum infected irradiated mosquitoes. The anti-MB2 antibody response may be part of a robust protective response against the sporozoite. METHODS: Fragments of polypeptide regions of MB2 were constructed as recombinant fusions sandwiched between glutathione S-transferase and a hexa histidine tag for bacterial expression. The hexa histidine tag affinity purified proteins were used to immunize rabbits and the polyclonal sera evaluated in an in vitro inhibition of sporozoite invasion assay. The proteins were also used in immunoblots with sera from a limited number of donors immunized via the bites of P. falciparum infected irradiated mosquitoes and plasma and serum obtained from naturally exposed individuals in Kenya. RESULTS: Rabbit polyclonal antibodies targeting the non-repeat region of the basic domain of MB2 inhibited sporozoites entry into HepG2-A16 cells in vitro. Analysis of serum from five human volunteers that were immunized via the bites of P. falciparum infected irradiated mosquitoes that developed immunity and were completely protected against subsequent challenge with non-irradiated parasite also had detectable levels of antibody against MB2 basic domain. In contrast, in three volunteers not protected, anti-MB2 antibodies were below the level of detection. Sera from protected volunteers preferentially recognized a non-repeat region of the basic domain of MB2, whereas plasma from naturally-infected individuals also had antibodies that recognize regions of MB2 that contain a repeat motif in immunoblots. Sequence analysis of eleven field isolates and four laboratory strains showed that these antigenic regions of the basic domain of the MB2 gene are highly conserved in parasites obtained from different parts of the world. Moreover, anti-MB2 antibodies also were detected in the plasma of 83% of the individuals living in a malaria endemic area of Kenya (n = 41). CONCLUSION: A preliminary analysis of the human humoral response against MB2 indicates that it may be an additional highly conserved target for immune intervention at the pre-erythrocytic stage of P. falciparum life cycle.
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spelling pubmed-27728402009-11-04 Characterization of immunoglobulin G antibodies to Plasmodium falciparum sporozoite surface antigen MB(2) in malaria exposed individuals Nguyen, Thanh V Sacci, John B de la Vega, Patricia John, Chandy C James, Anthony A Kang, Angray S Malar J Research BACKGROUND: MB2 protein is a sporozoite surface antigen on the human malaria parasite Plasmodium falciparum. MB2 was identified by screening a P. falciparum sporozoite cDNA expression library using immune sera from a protected donor immunized via the bites of P. falciparum-infected irradiated mosquitoes. It is not known whether natural exposure to P. falciparum also induces the anti-MB2 response and if this response differs from that in protected individuals immunized via the bites of P. falciparum infected irradiated mosquitoes. The anti-MB2 antibody response may be part of a robust protective response against the sporozoite. METHODS: Fragments of polypeptide regions of MB2 were constructed as recombinant fusions sandwiched between glutathione S-transferase and a hexa histidine tag for bacterial expression. The hexa histidine tag affinity purified proteins were used to immunize rabbits and the polyclonal sera evaluated in an in vitro inhibition of sporozoite invasion assay. The proteins were also used in immunoblots with sera from a limited number of donors immunized via the bites of P. falciparum infected irradiated mosquitoes and plasma and serum obtained from naturally exposed individuals in Kenya. RESULTS: Rabbit polyclonal antibodies targeting the non-repeat region of the basic domain of MB2 inhibited sporozoites entry into HepG2-A16 cells in vitro. Analysis of serum from five human volunteers that were immunized via the bites of P. falciparum infected irradiated mosquitoes that developed immunity and were completely protected against subsequent challenge with non-irradiated parasite also had detectable levels of antibody against MB2 basic domain. In contrast, in three volunteers not protected, anti-MB2 antibodies were below the level of detection. Sera from protected volunteers preferentially recognized a non-repeat region of the basic domain of MB2, whereas plasma from naturally-infected individuals also had antibodies that recognize regions of MB2 that contain a repeat motif in immunoblots. Sequence analysis of eleven field isolates and four laboratory strains showed that these antigenic regions of the basic domain of the MB2 gene are highly conserved in parasites obtained from different parts of the world. Moreover, anti-MB2 antibodies also were detected in the plasma of 83% of the individuals living in a malaria endemic area of Kenya (n = 41). CONCLUSION: A preliminary analysis of the human humoral response against MB2 indicates that it may be an additional highly conserved target for immune intervention at the pre-erythrocytic stage of P. falciparum life cycle. BioMed Central 2009-10-23 /pmc/articles/PMC2772840/ /pubmed/19852802 http://dx.doi.org/10.1186/1475-2875-8-235 Text en Copyright © 2009 Nguyen et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Nguyen, Thanh V
Sacci, John B
de la Vega, Patricia
John, Chandy C
James, Anthony A
Kang, Angray S
Characterization of immunoglobulin G antibodies to Plasmodium falciparum sporozoite surface antigen MB(2) in malaria exposed individuals
title Characterization of immunoglobulin G antibodies to Plasmodium falciparum sporozoite surface antigen MB(2) in malaria exposed individuals
title_full Characterization of immunoglobulin G antibodies to Plasmodium falciparum sporozoite surface antigen MB(2) in malaria exposed individuals
title_fullStr Characterization of immunoglobulin G antibodies to Plasmodium falciparum sporozoite surface antigen MB(2) in malaria exposed individuals
title_full_unstemmed Characterization of immunoglobulin G antibodies to Plasmodium falciparum sporozoite surface antigen MB(2) in malaria exposed individuals
title_short Characterization of immunoglobulin G antibodies to Plasmodium falciparum sporozoite surface antigen MB(2) in malaria exposed individuals
title_sort characterization of immunoglobulin g antibodies to plasmodium falciparum sporozoite surface antigen mb(2) in malaria exposed individuals
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2772840/
https://www.ncbi.nlm.nih.gov/pubmed/19852802
http://dx.doi.org/10.1186/1475-2875-8-235
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