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

Identifieur interne : 000065 ( Main/Exploration ); précédent : 000064; suivant : 000066

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

Auteurs : Myriam Arévalo-Herrera [Colombie] ; Andrés F. Vallejo [Colombie] ; Kelly Rubiano [Colombie] ; Yezid Solarte [Colombie] ; Catherin Marin [Colombie] ; Angélica Castellanos [Colombie] ; Nora Céspedes [Colombie] ; S Crates Herrera [Colombie]

Source :

RBID : PMC:4361554

Abstract

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.


Url:
DOI: 10.1371/journal.pone.0119335
PubMed: 25775466
PubMed Central: 4361554


Affiliations:


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Le document en format XML

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.
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Generates Antibodies that Block Malaria Transmission in
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<p>Transmission of malaria parasites from humans to
<italic>Anopheles</italic>
mosquitoes can be inhibited by specific antibodies elicited during malaria infection, which target surface
<italic>Plasmodium</italic>
gametocyte/gamete proteins. Some of these proteins may have potential for vaccine development.
<italic>Pvs</italic>
48/45 is a
<italic>P</italic>
.
<italic>vivax</italic>
gametocyte surface antigen orthologous to
<italic>Pfs</italic>
48/45, 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
<italic>Pvs</italic>
48/45 protein expressed in
<italic>Escherichia coli</italic>
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
<italic>Pvs</italic>
48/45 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
<italic>Aotus l</italic>
.
<italic>griseimembra</italic>
monkeys. Sera from both immunized animal species recognized native
<italic>P</italic>
.
<italic>vivax</italic>
protein in Western blot (WB) and immunofluorescence assays. Moreover, sera from immunized mice and monkeys produced significant inhibition of parasite transmission to
<italic>An</italic>
.
<italic>Albimanus</italic>
mosquitoes as shown by membrane feeding assays. Results indicate the presence of reactive epitopes in the
<italic>Pvs</italic>
48/45 recombinant product that induce antibodies with TB activity. Further testing of this protein is ongoing to determine its vaccine potential.</p>
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