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Evaluation of two Plasmodium vivax sexual stage antigens as transmission-blocking vaccine candidates

BACKGROUND: Plasmodium vivax transmission-blocking vaccines (TBVs) are receiving increasing attention. Based on excellent transmission-blocking activities of the PbPH (PBANKA_0417200) and PbSOP26 (PBANKA_1457700) antigens in Plasmodium berghei, their orthologs in P. vivax, PVX_098655 (PvPH) and PVX_...

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Autores principales: Zhang, Yongzhe, Liu, Fei, Zhao, Yan, Yang, Fan, Bai, Jie, Jia, Xitong, Roobsoong, Wanlapa, Sattabongkot, Jetsumon, Cui, Liwang, Cao, Yaming, Luo, Enjie, Wang, Meilian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8366161/
https://www.ncbi.nlm.nih.gov/pubmed/34399829
http://dx.doi.org/10.1186/s13071-021-04909-w
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author Zhang, Yongzhe
Liu, Fei
Zhao, Yan
Yang, Fan
Bai, Jie
Jia, Xitong
Roobsoong, Wanlapa
Sattabongkot, Jetsumon
Cui, Liwang
Cao, Yaming
Luo, Enjie
Wang, Meilian
author_facet Zhang, Yongzhe
Liu, Fei
Zhao, Yan
Yang, Fan
Bai, Jie
Jia, Xitong
Roobsoong, Wanlapa
Sattabongkot, Jetsumon
Cui, Liwang
Cao, Yaming
Luo, Enjie
Wang, Meilian
author_sort Zhang, Yongzhe
collection PubMed
description BACKGROUND: Plasmodium vivax transmission-blocking vaccines (TBVs) are receiving increasing attention. Based on excellent transmission-blocking activities of the PbPH (PBANKA_0417200) and PbSOP26 (PBANKA_1457700) antigens in Plasmodium berghei, their orthologs in P. vivax, PVX_098655 (PvPH) and PVX_101120 (PvSOP26), were selected for the evaluation of their potential as TBVs. METHODS: Fragments of PvPH (amino acids 22–304) and PvSOP26 (amino acids 30–272) were expressed in the yeast expression system. The recombinant proteins were used to immunize mice to obtain antisera. The transmission-reducing activities of these antisera were evaluated using the direct membrane feeding assay (DMFA) using Anopheles dirus mosquitoes and P. vivax clinical isolates. RESULTS: The recombinant proteins PvPH and PvSOP26 induced robust antibody responses in mice. The DMFA showed that the anti-PvSOP26 sera significantly reduced oocyst densities by 92.0 and 84.1% in two parasite isolates, respectively, whereas the anti-PvPH sera did not show evident transmission-reducing activity. The variation in the DMFA results was unlikely due to the genetic polymorphisms of the two genes since their respective sequences were identical in the clinical P. vivax isolates. CONCLUSION: PvSOP26 could be a promising TBV candidate for P. vivax, which warrants further evaluation. GRAPHICAL ABSTRACT: SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13071-021-04909-w.
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spelling pubmed-83661612021-08-16 Evaluation of two Plasmodium vivax sexual stage antigens as transmission-blocking vaccine candidates Zhang, Yongzhe Liu, Fei Zhao, Yan Yang, Fan Bai, Jie Jia, Xitong Roobsoong, Wanlapa Sattabongkot, Jetsumon Cui, Liwang Cao, Yaming Luo, Enjie Wang, Meilian Parasit Vectors Research BACKGROUND: Plasmodium vivax transmission-blocking vaccines (TBVs) are receiving increasing attention. Based on excellent transmission-blocking activities of the PbPH (PBANKA_0417200) and PbSOP26 (PBANKA_1457700) antigens in Plasmodium berghei, their orthologs in P. vivax, PVX_098655 (PvPH) and PVX_101120 (PvSOP26), were selected for the evaluation of their potential as TBVs. METHODS: Fragments of PvPH (amino acids 22–304) and PvSOP26 (amino acids 30–272) were expressed in the yeast expression system. The recombinant proteins were used to immunize mice to obtain antisera. The transmission-reducing activities of these antisera were evaluated using the direct membrane feeding assay (DMFA) using Anopheles dirus mosquitoes and P. vivax clinical isolates. RESULTS: The recombinant proteins PvPH and PvSOP26 induced robust antibody responses in mice. The DMFA showed that the anti-PvSOP26 sera significantly reduced oocyst densities by 92.0 and 84.1% in two parasite isolates, respectively, whereas the anti-PvPH sera did not show evident transmission-reducing activity. The variation in the DMFA results was unlikely due to the genetic polymorphisms of the two genes since their respective sequences were identical in the clinical P. vivax isolates. CONCLUSION: PvSOP26 could be a promising TBV candidate for P. vivax, which warrants further evaluation. GRAPHICAL ABSTRACT: SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13071-021-04909-w. BioMed Central 2021-08-16 /pmc/articles/PMC8366161/ /pubmed/34399829 http://dx.doi.org/10.1186/s13071-021-04909-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Zhang, Yongzhe
Liu, Fei
Zhao, Yan
Yang, Fan
Bai, Jie
Jia, Xitong
Roobsoong, Wanlapa
Sattabongkot, Jetsumon
Cui, Liwang
Cao, Yaming
Luo, Enjie
Wang, Meilian
Evaluation of two Plasmodium vivax sexual stage antigens as transmission-blocking vaccine candidates
title Evaluation of two Plasmodium vivax sexual stage antigens as transmission-blocking vaccine candidates
title_full Evaluation of two Plasmodium vivax sexual stage antigens as transmission-blocking vaccine candidates
title_fullStr Evaluation of two Plasmodium vivax sexual stage antigens as transmission-blocking vaccine candidates
title_full_unstemmed Evaluation of two Plasmodium vivax sexual stage antigens as transmission-blocking vaccine candidates
title_short Evaluation of two Plasmodium vivax sexual stage antigens as transmission-blocking vaccine candidates
title_sort evaluation of two plasmodium vivax sexual stage antigens as transmission-blocking vaccine candidates
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8366161/
https://www.ncbi.nlm.nih.gov/pubmed/34399829
http://dx.doi.org/10.1186/s13071-021-04909-w
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