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Characterization of PSOP26 as an ookinete surface antigen with improved transmission-blocking activity when fused with PSOP25

BACKGROUND: The Plasmodium zygote-to-ookinete developmental transition is an essential step for establishing an infection in the mosquito vector, and antigens expressed during this stage are potential targets for transmission-blocking vaccines (TBVs). The secreted ookinete protein 26 (PSOP26) is a n...

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Autores principales: Wang, Peng-peng, Jiang, Xuefeng, Bai, Jie, Yang, Fan, Yu, Xinxin, Wu, Yudi, Zheng, Wenqi, Zhang, Yongzhe, Cui, Liwang, Liu, Fei, Zhu, Xiaotong, Cao, Yaming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9125894/
https://www.ncbi.nlm.nih.gov/pubmed/35606790
http://dx.doi.org/10.1186/s13071-022-05294-8
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author Wang, Peng-peng
Jiang, Xuefeng
Bai, Jie
Yang, Fan
Yu, Xinxin
Wu, Yudi
Zheng, Wenqi
Zhang, Yongzhe
Cui, Liwang
Liu, Fei
Zhu, Xiaotong
Cao, Yaming
author_facet Wang, Peng-peng
Jiang, Xuefeng
Bai, Jie
Yang, Fan
Yu, Xinxin
Wu, Yudi
Zheng, Wenqi
Zhang, Yongzhe
Cui, Liwang
Liu, Fei
Zhu, Xiaotong
Cao, Yaming
author_sort Wang, Peng-peng
collection PubMed
description BACKGROUND: The Plasmodium zygote-to-ookinete developmental transition is an essential step for establishing an infection in the mosquito vector, and antigens expressed during this stage are potential targets for transmission-blocking vaccines (TBVs). The secreted ookinete protein 26 (PSOP26) is a newly identified ookinete surface protein. The anti-PSOP26 serum has moderate transmission-blocking activity, indicating the benefit of further investigating this protein as a target for TBVs. METHODS: The function of psop26 was analyzed by targeted gene disruption. A chimeric PSOP25-PSOP26 protein was expressed in the Escherichia coli system. The PSOP25-PSOP26 fusion protein, along with mixed (PSOP25 + PSOP26) or single proteins (PSOP26 or PSOP25), were used for the immunization of mice. The antibody titers and immunogenicity of individual sera were analyzed by enzyme-linked immunoassay (ELISA), indirect immunofluorescence assay (IFA), and Western blot. The transmission-blocking activity of sera from different immunization schemes was assessed using in vitro and in vivo assays. RESULTS: PSOP26 is a surface protein expressed in Plasmodium gametes and ookinetes. The protein is dispensable for asexual blood-stage development, gametogenesis, and zygote formation, but is essential for the zygote-to-ookinete developmental transition. Specifically, both the prevalence of infections and oocyst densities were decreased in mosquitoes fed on psop26-null mutants. Mixtures of individual PSOP25 and PSOP26 fragments (PSOP25 + PSOP26), as well as chimeras (PSOP25-PSOP26), elicited high antibody levels in mice, with no immunological interference. Antisera against the mixed and fusion proteins elicited higher transmission-reducing activity (TRA) than antisera against the single PSOP26 antigen, but comparable to antisera against PSOP25 antigen alone. CONCLUSIONS: PSOP26 plays a critical role in the zygote-to-ookinete developmental transition. PSOP25 is a promising TBV candidate that could be used alone to target the ookinete stage. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13071-022-05294-8.
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spelling pubmed-91258942022-05-24 Characterization of PSOP26 as an ookinete surface antigen with improved transmission-blocking activity when fused with PSOP25 Wang, Peng-peng Jiang, Xuefeng Bai, Jie Yang, Fan Yu, Xinxin Wu, Yudi Zheng, Wenqi Zhang, Yongzhe Cui, Liwang Liu, Fei Zhu, Xiaotong Cao, Yaming Parasit Vectors Research BACKGROUND: The Plasmodium zygote-to-ookinete developmental transition is an essential step for establishing an infection in the mosquito vector, and antigens expressed during this stage are potential targets for transmission-blocking vaccines (TBVs). The secreted ookinete protein 26 (PSOP26) is a newly identified ookinete surface protein. The anti-PSOP26 serum has moderate transmission-blocking activity, indicating the benefit of further investigating this protein as a target for TBVs. METHODS: The function of psop26 was analyzed by targeted gene disruption. A chimeric PSOP25-PSOP26 protein was expressed in the Escherichia coli system. The PSOP25-PSOP26 fusion protein, along with mixed (PSOP25 + PSOP26) or single proteins (PSOP26 or PSOP25), were used for the immunization of mice. The antibody titers and immunogenicity of individual sera were analyzed by enzyme-linked immunoassay (ELISA), indirect immunofluorescence assay (IFA), and Western blot. The transmission-blocking activity of sera from different immunization schemes was assessed using in vitro and in vivo assays. RESULTS: PSOP26 is a surface protein expressed in Plasmodium gametes and ookinetes. The protein is dispensable for asexual blood-stage development, gametogenesis, and zygote formation, but is essential for the zygote-to-ookinete developmental transition. Specifically, both the prevalence of infections and oocyst densities were decreased in mosquitoes fed on psop26-null mutants. Mixtures of individual PSOP25 and PSOP26 fragments (PSOP25 + PSOP26), as well as chimeras (PSOP25-PSOP26), elicited high antibody levels in mice, with no immunological interference. Antisera against the mixed and fusion proteins elicited higher transmission-reducing activity (TRA) than antisera against the single PSOP26 antigen, but comparable to antisera against PSOP25 antigen alone. CONCLUSIONS: PSOP26 plays a critical role in the zygote-to-ookinete developmental transition. PSOP25 is a promising TBV candidate that could be used alone to target the ookinete stage. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13071-022-05294-8. BioMed Central 2022-05-23 /pmc/articles/PMC9125894/ /pubmed/35606790 http://dx.doi.org/10.1186/s13071-022-05294-8 Text en © The Author(s) 2022 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
Wang, Peng-peng
Jiang, Xuefeng
Bai, Jie
Yang, Fan
Yu, Xinxin
Wu, Yudi
Zheng, Wenqi
Zhang, Yongzhe
Cui, Liwang
Liu, Fei
Zhu, Xiaotong
Cao, Yaming
Characterization of PSOP26 as an ookinete surface antigen with improved transmission-blocking activity when fused with PSOP25
title Characterization of PSOP26 as an ookinete surface antigen with improved transmission-blocking activity when fused with PSOP25
title_full Characterization of PSOP26 as an ookinete surface antigen with improved transmission-blocking activity when fused with PSOP25
title_fullStr Characterization of PSOP26 as an ookinete surface antigen with improved transmission-blocking activity when fused with PSOP25
title_full_unstemmed Characterization of PSOP26 as an ookinete surface antigen with improved transmission-blocking activity when fused with PSOP25
title_short Characterization of PSOP26 as an ookinete surface antigen with improved transmission-blocking activity when fused with PSOP25
title_sort characterization of psop26 as an ookinete surface antigen with improved transmission-blocking activity when fused with psop25
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9125894/
https://www.ncbi.nlm.nih.gov/pubmed/35606790
http://dx.doi.org/10.1186/s13071-022-05294-8
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