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Recombinant Pvs48/45 Antigen Expressed in E. coli Generates Antibodies that Block Malaria Transmission in Anopheles albimanus Mosquitoes

Transmission of malaria parasites from humans to Anopheles mosquitoes can be inhibited by specific antibodies elicited during malaria infection, which target surface Plasmodium gametocyte/gamete proteins. Some of these proteins may have potential for vaccine development. Pvs48/45 is a P. vivax gamet...

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Autores principales: Arévalo-Herrera, Myriam, Vallejo, Andrés F., Rubiano, Kelly, Solarte, Yezid, Marin, Catherin, Castellanos, Angélica, Céspedes, Nora, Herrera, Sócrates
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4361554/
https://www.ncbi.nlm.nih.gov/pubmed/25775466
http://dx.doi.org/10.1371/journal.pone.0119335
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author Arévalo-Herrera, Myriam
Vallejo, Andrés F.
Rubiano, Kelly
Solarte, Yezid
Marin, Catherin
Castellanos, Angélica
Céspedes, Nora
Herrera, Sócrates
author_facet Arévalo-Herrera, Myriam
Vallejo, Andrés F.
Rubiano, Kelly
Solarte, Yezid
Marin, Catherin
Castellanos, Angélica
Céspedes, Nora
Herrera, Sócrates
author_sort Arévalo-Herrera, Myriam
collection PubMed
description Transmission of malaria parasites from humans to Anopheles mosquitoes can be inhibited by specific antibodies elicited during malaria infection, which target surface Plasmodium gametocyte/gamete proteins. Some of these proteins may have potential for vaccine development. Pvs48/45 is a P. vivax gametocyte surface antigen orthologous to Pfs48/45, which may play a role during parasite fertilization and thus has potential for transmission blocking (TB) activity. Here we describe the expression of a recombinant Pvs48/45 protein expressed in Escherichia coli as a ∼60kDa construct which we tested for antigenicity using human sera and for its immunogenicity and transmission blocking activity of specific anti-mouse and anti-monkey Pvs48/45 antibodies. The protein reacted with sera of individuals from malaria-endemic areas and in addition induced specific IgG antibody responses in BALB/c mice and Aotus l. griseimembra monkeys. Sera from both immunized animal species recognized native P. vivax protein in Western blot (WB) and immunofluorescence assays. Moreover, sera from immunized mice and monkeys produced significant inhibition of parasite transmission to An. Albimanus mosquitoes as shown by membrane feeding assays. Results indicate the presence of reactive epitopes in the Pvs48/45 recombinant product that induce antibodies with TB activity. Further testing of this protein is ongoing to determine its vaccine potential.
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spelling pubmed-43615542015-03-23 Recombinant Pvs48/45 Antigen Expressed in E. coli Generates Antibodies that Block Malaria Transmission in Anopheles albimanus Mosquitoes Arévalo-Herrera, Myriam Vallejo, Andrés F. Rubiano, Kelly Solarte, Yezid Marin, Catherin Castellanos, Angélica Céspedes, Nora Herrera, Sócrates PLoS One Research Article Transmission of malaria parasites from humans to Anopheles mosquitoes can be inhibited by specific antibodies elicited during malaria infection, which target surface Plasmodium gametocyte/gamete proteins. Some of these proteins may have potential for vaccine development. Pvs48/45 is a P. vivax gametocyte surface antigen orthologous to Pfs48/45, which may play a role during parasite fertilization and thus has potential for transmission blocking (TB) activity. Here we describe the expression of a recombinant Pvs48/45 protein expressed in Escherichia coli as a ∼60kDa construct which we tested for antigenicity using human sera and for its immunogenicity and transmission blocking activity of specific anti-mouse and anti-monkey Pvs48/45 antibodies. The protein reacted with sera of individuals from malaria-endemic areas and in addition induced specific IgG antibody responses in BALB/c mice and Aotus l. griseimembra monkeys. Sera from both immunized animal species recognized native P. vivax protein in Western blot (WB) and immunofluorescence assays. Moreover, sera from immunized mice and monkeys produced significant inhibition of parasite transmission to An. Albimanus mosquitoes as shown by membrane feeding assays. Results indicate the presence of reactive epitopes in the Pvs48/45 recombinant product that induce antibodies with TB activity. Further testing of this protein is ongoing to determine its vaccine potential. Public Library of Science 2015-03-16 /pmc/articles/PMC4361554/ /pubmed/25775466 http://dx.doi.org/10.1371/journal.pone.0119335 Text en © 2015 Arévalo-Herrera et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Arévalo-Herrera, Myriam
Vallejo, Andrés F.
Rubiano, Kelly
Solarte, Yezid
Marin, Catherin
Castellanos, Angélica
Céspedes, Nora
Herrera, Sócrates
Recombinant Pvs48/45 Antigen Expressed in E. coli Generates Antibodies that Block Malaria Transmission in Anopheles albimanus Mosquitoes
title Recombinant Pvs48/45 Antigen Expressed in E. coli Generates Antibodies that Block Malaria Transmission in Anopheles albimanus Mosquitoes
title_full Recombinant Pvs48/45 Antigen Expressed in E. coli Generates Antibodies that Block Malaria Transmission in Anopheles albimanus Mosquitoes
title_fullStr Recombinant Pvs48/45 Antigen Expressed in E. coli Generates Antibodies that Block Malaria Transmission in Anopheles albimanus Mosquitoes
title_full_unstemmed Recombinant Pvs48/45 Antigen Expressed in E. coli Generates Antibodies that Block Malaria Transmission in Anopheles albimanus Mosquitoes
title_short Recombinant Pvs48/45 Antigen Expressed in E. coli Generates Antibodies that Block Malaria Transmission in Anopheles albimanus Mosquitoes
title_sort recombinant pvs48/45 antigen expressed in e. coli generates antibodies that block malaria transmission in anopheles albimanus mosquitoes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4361554/
https://www.ncbi.nlm.nih.gov/pubmed/25775466
http://dx.doi.org/10.1371/journal.pone.0119335
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