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Genomic variation in two gametocyte non-producing Plasmodium falciparum clonal lines

BACKGROUND: Transmission of the malaria parasite Plasmodium falciparum from humans to the mosquito vector requires differentiation of a sub-population of asexual forms replicating within red blood cells into non-dividing male and female gametocytes. The nature of the molecular mechanism underlying t...

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Autores principales: Campino, Susana, Benavente, Ernest Diez, Assefa, Samuel, Thompson, Eloise, Drought, Laura G., Taylor, Catherine J., Gorvett, Zaria, Carret, Celine K., Flueck, Christian, Ivens, Al C., Kwiatkowski, Dominic P., Alano, Pietro, Baker, David A., Clark, Taane G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839107/
https://www.ncbi.nlm.nih.gov/pubmed/27098483
http://dx.doi.org/10.1186/s12936-016-1254-1
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author Campino, Susana
Benavente, Ernest Diez
Assefa, Samuel
Thompson, Eloise
Drought, Laura G.
Taylor, Catherine J.
Gorvett, Zaria
Carret, Celine K.
Flueck, Christian
Ivens, Al C.
Kwiatkowski, Dominic P.
Alano, Pietro
Baker, David A.
Clark, Taane G.
author_facet Campino, Susana
Benavente, Ernest Diez
Assefa, Samuel
Thompson, Eloise
Drought, Laura G.
Taylor, Catherine J.
Gorvett, Zaria
Carret, Celine K.
Flueck, Christian
Ivens, Al C.
Kwiatkowski, Dominic P.
Alano, Pietro
Baker, David A.
Clark, Taane G.
author_sort Campino, Susana
collection PubMed
description BACKGROUND: Transmission of the malaria parasite Plasmodium falciparum from humans to the mosquito vector requires differentiation of a sub-population of asexual forms replicating within red blood cells into non-dividing male and female gametocytes. The nature of the molecular mechanism underlying this key differentiation event required for malaria transmission is not fully understood. METHODS: Whole genome sequencing was used to examine the genomic diversity of the gametocyte non-producing 3D7-derived lines F12 and A4. These lines were used in the recent detection of the PF3D7_1222600 locus (encoding PfAP2-G), which acts as a genetic master switch that triggers gametocyte development. RESULTS: The evolutionary changes from the 3D7 parental strain through its derivatives F12 (culture-passage derived cloned line) and A4 (transgenic cloned line) were identified. The genetic differences including the formation of chimeric var genes are presented. CONCLUSION: A genomics resource is provided for the further study of gametocytogenesis or other phenotypes using these parasite lines. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12936-016-1254-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-48391072016-04-22 Genomic variation in two gametocyte non-producing Plasmodium falciparum clonal lines Campino, Susana Benavente, Ernest Diez Assefa, Samuel Thompson, Eloise Drought, Laura G. Taylor, Catherine J. Gorvett, Zaria Carret, Celine K. Flueck, Christian Ivens, Al C. Kwiatkowski, Dominic P. Alano, Pietro Baker, David A. Clark, Taane G. Malar J Research BACKGROUND: Transmission of the malaria parasite Plasmodium falciparum from humans to the mosquito vector requires differentiation of a sub-population of asexual forms replicating within red blood cells into non-dividing male and female gametocytes. The nature of the molecular mechanism underlying this key differentiation event required for malaria transmission is not fully understood. METHODS: Whole genome sequencing was used to examine the genomic diversity of the gametocyte non-producing 3D7-derived lines F12 and A4. These lines were used in the recent detection of the PF3D7_1222600 locus (encoding PfAP2-G), which acts as a genetic master switch that triggers gametocyte development. RESULTS: The evolutionary changes from the 3D7 parental strain through its derivatives F12 (culture-passage derived cloned line) and A4 (transgenic cloned line) were identified. The genetic differences including the formation of chimeric var genes are presented. CONCLUSION: A genomics resource is provided for the further study of gametocytogenesis or other phenotypes using these parasite lines. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12936-016-1254-1) contains supplementary material, which is available to authorized users. BioMed Central 2016-04-21 /pmc/articles/PMC4839107/ /pubmed/27098483 http://dx.doi.org/10.1186/s12936-016-1254-1 Text en © Campino 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
Campino, Susana
Benavente, Ernest Diez
Assefa, Samuel
Thompson, Eloise
Drought, Laura G.
Taylor, Catherine J.
Gorvett, Zaria
Carret, Celine K.
Flueck, Christian
Ivens, Al C.
Kwiatkowski, Dominic P.
Alano, Pietro
Baker, David A.
Clark, Taane G.
Genomic variation in two gametocyte non-producing Plasmodium falciparum clonal lines
title Genomic variation in two gametocyte non-producing Plasmodium falciparum clonal lines
title_full Genomic variation in two gametocyte non-producing Plasmodium falciparum clonal lines
title_fullStr Genomic variation in two gametocyte non-producing Plasmodium falciparum clonal lines
title_full_unstemmed Genomic variation in two gametocyte non-producing Plasmodium falciparum clonal lines
title_short Genomic variation in two gametocyte non-producing Plasmodium falciparum clonal lines
title_sort genomic variation in two gametocyte non-producing plasmodium falciparum clonal lines
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839107/
https://www.ncbi.nlm.nih.gov/pubmed/27098483
http://dx.doi.org/10.1186/s12936-016-1254-1
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