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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_...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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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. |
format | Online Article Text |
id | pubmed-8366161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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