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Strain-transcending neutralization of malaria parasite by antibodies against Plasmodium falciparum enolase

BACKGROUND: Plasmodium enolase is a target for the growth neutralizing antibodies. Interestingly, the three invasive stages i.e. sporozoites, merozoites, and ookinetes express this protein on their cell surface. Polyclonal anti-Plasmodium falciparum enolase (Pfeno) antibodies disrupt traversal of oo...

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Autores principales: Dutta, Sneha, Tewari, Aneesha, Balaji, Chinthapalli, Verma, Reena, Moitra, Anasuya, Yadav, Mamta, Agrawal, Prakhar, Sahal, Dinkar, Jarori, Gotam K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6102825/
https://www.ncbi.nlm.nih.gov/pubmed/30126436
http://dx.doi.org/10.1186/s12936-018-2455-6
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author Dutta, Sneha
Tewari, Aneesha
Balaji, Chinthapalli
Verma, Reena
Moitra, Anasuya
Yadav, Mamta
Agrawal, Prakhar
Sahal, Dinkar
Jarori, Gotam K.
author_facet Dutta, Sneha
Tewari, Aneesha
Balaji, Chinthapalli
Verma, Reena
Moitra, Anasuya
Yadav, Mamta
Agrawal, Prakhar
Sahal, Dinkar
Jarori, Gotam K.
author_sort Dutta, Sneha
collection PubMed
description BACKGROUND: Plasmodium enolase is a target for the growth neutralizing antibodies. Interestingly, the three invasive stages i.e. sporozoites, merozoites, and ookinetes express this protein on their cell surface. Polyclonal anti-Plasmodium falciparum enolase (Pfeno) antibodies disrupt traversal of ookinete through mosquito mid-gut wall as well as have inhibitory effect on parasite growth at erythrocytic stage. In a recent study, it was observed that immunization with a unique epitope of parasite enolase (EWGWS) could confer partial protection against mouse malaria. Further validation is needed for the protective potential of this unique epitope in otherwise highly conserved enolase. METHODS: In order to investigate the efficacy of growth inhibitory potential of the epitope of P falciparum enolase, a monoclonal antibody specific to EWGWS is generated. In vitro parasite growth inhibition assays and passive immunization of Plasmodium yoelii (or Plasmodium berghei) infected mice were used to assess the parasite growth neutralizing activity of the antibody. RESULTS: Screening a panel of monoclonal antibodies raised against recombinant Pfeno that were specific to EWGWS resulted in isolation of H12E1. This antibody recognized only EWGWS epitope containing enolases. H12E1 strongly inhibited parasite growth in culture. This inhibition was strain transcending. Passive infusion of this antibody in P. yoelii or P. berghei infected mice showed significant reduction in parasitemia as compared to controls (p < 0.001). Surface Plasmon Resonance measurements indicated high affinity binding of H12E1 to P. falciparum enolase (K(D) ~ 7.6 × 10(−9)M). CONCLUSIONS: A monoclonal antibody directed against EWGWS epitope of Pfeno was shown to inhibit the growth of blood stage malarial parasites. This inhibition was species/strain transcending and is likely to arise due to blockade of enolase on the surface of merozoites, functionally implicating Pfeno in invasion related events. Presence of enolase on the cell surface of merozoites and ookinetes could potentially result in inhibition of host cell invasions at erythrocytic and transmission stages in the parasite life cycle. It is suggested that antibodies against EWGWS epitope have the potential to confer dual stage, species and strain transcending protection against malaria. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12936-018-2455-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-61028252018-08-27 Strain-transcending neutralization of malaria parasite by antibodies against Plasmodium falciparum enolase Dutta, Sneha Tewari, Aneesha Balaji, Chinthapalli Verma, Reena Moitra, Anasuya Yadav, Mamta Agrawal, Prakhar Sahal, Dinkar Jarori, Gotam K. Malar J Research BACKGROUND: Plasmodium enolase is a target for the growth neutralizing antibodies. Interestingly, the three invasive stages i.e. sporozoites, merozoites, and ookinetes express this protein on their cell surface. Polyclonal anti-Plasmodium falciparum enolase (Pfeno) antibodies disrupt traversal of ookinete through mosquito mid-gut wall as well as have inhibitory effect on parasite growth at erythrocytic stage. In a recent study, it was observed that immunization with a unique epitope of parasite enolase (EWGWS) could confer partial protection against mouse malaria. Further validation is needed for the protective potential of this unique epitope in otherwise highly conserved enolase. METHODS: In order to investigate the efficacy of growth inhibitory potential of the epitope of P falciparum enolase, a monoclonal antibody specific to EWGWS is generated. In vitro parasite growth inhibition assays and passive immunization of Plasmodium yoelii (or Plasmodium berghei) infected mice were used to assess the parasite growth neutralizing activity of the antibody. RESULTS: Screening a panel of monoclonal antibodies raised against recombinant Pfeno that were specific to EWGWS resulted in isolation of H12E1. This antibody recognized only EWGWS epitope containing enolases. H12E1 strongly inhibited parasite growth in culture. This inhibition was strain transcending. Passive infusion of this antibody in P. yoelii or P. berghei infected mice showed significant reduction in parasitemia as compared to controls (p < 0.001). Surface Plasmon Resonance measurements indicated high affinity binding of H12E1 to P. falciparum enolase (K(D) ~ 7.6 × 10(−9)M). CONCLUSIONS: A monoclonal antibody directed against EWGWS epitope of Pfeno was shown to inhibit the growth of blood stage malarial parasites. This inhibition was species/strain transcending and is likely to arise due to blockade of enolase on the surface of merozoites, functionally implicating Pfeno in invasion related events. Presence of enolase on the cell surface of merozoites and ookinetes could potentially result in inhibition of host cell invasions at erythrocytic and transmission stages in the parasite life cycle. It is suggested that antibodies against EWGWS epitope have the potential to confer dual stage, species and strain transcending protection against malaria. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12936-018-2455-6) contains supplementary material, which is available to authorized users. BioMed Central 2018-08-20 /pmc/articles/PMC6102825/ /pubmed/30126436 http://dx.doi.org/10.1186/s12936-018-2455-6 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Dutta, Sneha
Tewari, Aneesha
Balaji, Chinthapalli
Verma, Reena
Moitra, Anasuya
Yadav, Mamta
Agrawal, Prakhar
Sahal, Dinkar
Jarori, Gotam K.
Strain-transcending neutralization of malaria parasite by antibodies against Plasmodium falciparum enolase
title Strain-transcending neutralization of malaria parasite by antibodies against Plasmodium falciparum enolase
title_full Strain-transcending neutralization of malaria parasite by antibodies against Plasmodium falciparum enolase
title_fullStr Strain-transcending neutralization of malaria parasite by antibodies against Plasmodium falciparum enolase
title_full_unstemmed Strain-transcending neutralization of malaria parasite by antibodies against Plasmodium falciparum enolase
title_short Strain-transcending neutralization of malaria parasite by antibodies against Plasmodium falciparum enolase
title_sort strain-transcending neutralization of malaria parasite by antibodies against plasmodium falciparum enolase
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6102825/
https://www.ncbi.nlm.nih.gov/pubmed/30126436
http://dx.doi.org/10.1186/s12936-018-2455-6
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