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A highly infectious Plasmodium yoelii parasite, bearing Plasmodium falciparum circumsporozoite protein

BACKGROUND: Plasmodium circumsporozoite protein (CSP) is a major surface antigen present in the sporozoite (Spz) stage of a malaria parasite. RTS, S vaccine, the most clinically advanced malaria vaccine, consists of a large portion of Plasmodium falciparum CSP (PfCSP). A highly infectious, recombina...

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Autores principales: Zhang, Min, Kaneko, Izumi, Tsao, Tiffany, Mitchell, Robert, Nardin, Elizabeth H., Iwanaga, Shiroh, Yuda, Masao, Tsuji, Moriya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4828769/
https://www.ncbi.nlm.nih.gov/pubmed/27068454
http://dx.doi.org/10.1186/s12936-016-1248-z
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author Zhang, Min
Kaneko, Izumi
Tsao, Tiffany
Mitchell, Robert
Nardin, Elizabeth H.
Iwanaga, Shiroh
Yuda, Masao
Tsuji, Moriya
author_facet Zhang, Min
Kaneko, Izumi
Tsao, Tiffany
Mitchell, Robert
Nardin, Elizabeth H.
Iwanaga, Shiroh
Yuda, Masao
Tsuji, Moriya
author_sort Zhang, Min
collection PubMed
description BACKGROUND: Plasmodium circumsporozoite protein (CSP) is a major surface antigen present in the sporozoite (Spz) stage of a malaria parasite. RTS, S vaccine, the most clinically advanced malaria vaccine, consists of a large portion of Plasmodium falciparum CSP (PfCSP). A highly infectious, recombinant rodent malaria, Plasmodium yoelii parasite bearing a full-length PfCSP, PfCSP/Py Spz, was needed as a tool to evaluate the role of PfCSP in mediating, protective, anti-malaria immunity in a mouse model. METHODS: A transgenic parasite, PfCSP/Py Spz, was generated by inserting a construct expressing the PfCSP at the locus of the P. yoelii CSP gene by double cross-over homologous recombination. Then the biological and protective properties of PfCSP/Py Spz were determined. RESULTS: This PfCSP/Py parasite produced up to 30,000 Spz in mosquito salivary glands, which is equal or even higher than the number of Spz produced by wild-type P. yoelii parasites. Five bites of PfCSP/Py-infected mosquitoes could induce blood infection in BALB/c mice. CONCLUSIONS: The current study has demonstrated a successful establishment of a transgenic P. yoelii parasite clone that is able to express a full-length PfCSP, PfCSP/Py parasite. Importantly, this PfCSP/Py parasite can be as infectious as the wild-type P. yoelii parasite both in mosquito vector and in mouse, a mammalian host. A new transgenic parasite that expresses a full-length PfCSP may become a useful tool for researchers to investigate immunity against PfCSP in a mouse model.
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spelling pubmed-48287692016-04-13 A highly infectious Plasmodium yoelii parasite, bearing Plasmodium falciparum circumsporozoite protein Zhang, Min Kaneko, Izumi Tsao, Tiffany Mitchell, Robert Nardin, Elizabeth H. Iwanaga, Shiroh Yuda, Masao Tsuji, Moriya Malar J Research BACKGROUND: Plasmodium circumsporozoite protein (CSP) is a major surface antigen present in the sporozoite (Spz) stage of a malaria parasite. RTS, S vaccine, the most clinically advanced malaria vaccine, consists of a large portion of Plasmodium falciparum CSP (PfCSP). A highly infectious, recombinant rodent malaria, Plasmodium yoelii parasite bearing a full-length PfCSP, PfCSP/Py Spz, was needed as a tool to evaluate the role of PfCSP in mediating, protective, anti-malaria immunity in a mouse model. METHODS: A transgenic parasite, PfCSP/Py Spz, was generated by inserting a construct expressing the PfCSP at the locus of the P. yoelii CSP gene by double cross-over homologous recombination. Then the biological and protective properties of PfCSP/Py Spz were determined. RESULTS: This PfCSP/Py parasite produced up to 30,000 Spz in mosquito salivary glands, which is equal or even higher than the number of Spz produced by wild-type P. yoelii parasites. Five bites of PfCSP/Py-infected mosquitoes could induce blood infection in BALB/c mice. CONCLUSIONS: The current study has demonstrated a successful establishment of a transgenic P. yoelii parasite clone that is able to express a full-length PfCSP, PfCSP/Py parasite. Importantly, this PfCSP/Py parasite can be as infectious as the wild-type P. yoelii parasite both in mosquito vector and in mouse, a mammalian host. A new transgenic parasite that expresses a full-length PfCSP may become a useful tool for researchers to investigate immunity against PfCSP in a mouse model. BioMed Central 2016-04-12 /pmc/articles/PMC4828769/ /pubmed/27068454 http://dx.doi.org/10.1186/s12936-016-1248-z Text en © Zhang et al. 2016 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
Zhang, Min
Kaneko, Izumi
Tsao, Tiffany
Mitchell, Robert
Nardin, Elizabeth H.
Iwanaga, Shiroh
Yuda, Masao
Tsuji, Moriya
A highly infectious Plasmodium yoelii parasite, bearing Plasmodium falciparum circumsporozoite protein
title A highly infectious Plasmodium yoelii parasite, bearing Plasmodium falciparum circumsporozoite protein
title_full A highly infectious Plasmodium yoelii parasite, bearing Plasmodium falciparum circumsporozoite protein
title_fullStr A highly infectious Plasmodium yoelii parasite, bearing Plasmodium falciparum circumsporozoite protein
title_full_unstemmed A highly infectious Plasmodium yoelii parasite, bearing Plasmodium falciparum circumsporozoite protein
title_short A highly infectious Plasmodium yoelii parasite, bearing Plasmodium falciparum circumsporozoite protein
title_sort highly infectious plasmodium yoelii parasite, bearing plasmodium falciparum circumsporozoite protein
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4828769/
https://www.ncbi.nlm.nih.gov/pubmed/27068454
http://dx.doi.org/10.1186/s12936-016-1248-z
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