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Generation of transgenic rodent malaria parasites by transfection of cell culture-derived merozoites
BACKGROUND: Malaria research is greatly dependent on and has drastically advanced with the possibility of genetically modifying Plasmodium parasites. The commonly used transfection protocol by Janse and colleagues utilizes blood stage-derived Plasmodium berghei schizonts that have been purified from...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5540294/ https://www.ncbi.nlm.nih.gov/pubmed/28764716 http://dx.doi.org/10.1186/s12936-017-1949-y |
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author | Kaiser, Gesine De Niz, Mariana Burda, Paul-Christian Niklaus, Livia Stanway, Rebecca Limenitakis Heussler, Volker |
author_facet | Kaiser, Gesine De Niz, Mariana Burda, Paul-Christian Niklaus, Livia Stanway, Rebecca Limenitakis Heussler, Volker |
author_sort | Kaiser, Gesine |
collection | PubMed |
description | BACKGROUND: Malaria research is greatly dependent on and has drastically advanced with the possibility of genetically modifying Plasmodium parasites. The commonly used transfection protocol by Janse and colleagues utilizes blood stage-derived Plasmodium berghei schizonts that have been purified from a blood culture by density gradient centrifugation. Naturally, this transfection protocol depends on the availability of suitably infected mice, constituting a time-based variable. In this study, the potential of transfecting liver stage-derived merozoites was explored. In cell culture, upon merozoite development, infected cells detach from the neighbouring cells and can be easily harvested from the cell culture supernatant. This protocol offers robust experimental timing and temporal flexibility. METHODS: HeLa cells are infected with P. berghei sporozoites to obtain liver stage-derived merozoites, which are harvested from the cell culture supernatant and are transfected using the Amaxa Nucleofector(®) electroporation technology. RESULTS: Using this protocol, wild type P. berghei ANKA strain and marker-free PbmCherry(Hsp70)-expressing P. berghei parasites were successfully transfected with DNA constructs designed for integration via single- or double-crossover homologous recombination. CONCLUSION: An alternative protocol for Plasmodium transfection is hereby provided, which uses liver stage-derived P. berghei merozoites for transfection. This protocol has the potential to substantially reduce the number of mice used per transfection, as well as to increase the temporal flexibility and robustness of performing transfections, if mosquitoes are routinely present in the laboratory. Transfection of liver stage-derived P. berghei parasites should enable generation of transgenic parasites within 8–18 days. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12936-017-1949-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5540294 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-55402942017-08-03 Generation of transgenic rodent malaria parasites by transfection of cell culture-derived merozoites Kaiser, Gesine De Niz, Mariana Burda, Paul-Christian Niklaus, Livia Stanway, Rebecca Limenitakis Heussler, Volker Malar J Methodology Article BACKGROUND: Malaria research is greatly dependent on and has drastically advanced with the possibility of genetically modifying Plasmodium parasites. The commonly used transfection protocol by Janse and colleagues utilizes blood stage-derived Plasmodium berghei schizonts that have been purified from a blood culture by density gradient centrifugation. Naturally, this transfection protocol depends on the availability of suitably infected mice, constituting a time-based variable. In this study, the potential of transfecting liver stage-derived merozoites was explored. In cell culture, upon merozoite development, infected cells detach from the neighbouring cells and can be easily harvested from the cell culture supernatant. This protocol offers robust experimental timing and temporal flexibility. METHODS: HeLa cells are infected with P. berghei sporozoites to obtain liver stage-derived merozoites, which are harvested from the cell culture supernatant and are transfected using the Amaxa Nucleofector(®) electroporation technology. RESULTS: Using this protocol, wild type P. berghei ANKA strain and marker-free PbmCherry(Hsp70)-expressing P. berghei parasites were successfully transfected with DNA constructs designed for integration via single- or double-crossover homologous recombination. CONCLUSION: An alternative protocol for Plasmodium transfection is hereby provided, which uses liver stage-derived P. berghei merozoites for transfection. This protocol has the potential to substantially reduce the number of mice used per transfection, as well as to increase the temporal flexibility and robustness of performing transfections, if mosquitoes are routinely present in the laboratory. Transfection of liver stage-derived P. berghei parasites should enable generation of transgenic parasites within 8–18 days. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12936-017-1949-y) contains supplementary material, which is available to authorized users. BioMed Central 2017-08-01 /pmc/articles/PMC5540294/ /pubmed/28764716 http://dx.doi.org/10.1186/s12936-017-1949-y Text en © The Author(s) 2017 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 | Methodology Article Kaiser, Gesine De Niz, Mariana Burda, Paul-Christian Niklaus, Livia Stanway, Rebecca Limenitakis Heussler, Volker Generation of transgenic rodent malaria parasites by transfection of cell culture-derived merozoites |
title | Generation of transgenic rodent malaria parasites by transfection of cell culture-derived merozoites |
title_full | Generation of transgenic rodent malaria parasites by transfection of cell culture-derived merozoites |
title_fullStr | Generation of transgenic rodent malaria parasites by transfection of cell culture-derived merozoites |
title_full_unstemmed | Generation of transgenic rodent malaria parasites by transfection of cell culture-derived merozoites |
title_short | Generation of transgenic rodent malaria parasites by transfection of cell culture-derived merozoites |
title_sort | generation of transgenic rodent malaria parasites by transfection of cell culture-derived merozoites |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5540294/ https://www.ncbi.nlm.nih.gov/pubmed/28764716 http://dx.doi.org/10.1186/s12936-017-1949-y |
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