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Multiplication rate variation in the human malaria parasite Plasmodium falciparum
It is important to understand intrinsic variation in asexual blood stage multiplication rates of the most virulent human malaria parasite, Plasmodium falciparum. Here, multiplication rates of long-term laboratory adapted parasite clones and new clinical isolates were measured, using a newly standard...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5527095/ https://www.ncbi.nlm.nih.gov/pubmed/28743888 http://dx.doi.org/10.1038/s41598-017-06295-9 |
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author | Murray, Lee Stewart, Lindsay B. Tarr, Sarah J. Ahouidi, Ambroise D. Diakite, Mahamadou Amambua-Ngwa, Alfred Conway, David J. |
author_facet | Murray, Lee Stewart, Lindsay B. Tarr, Sarah J. Ahouidi, Ambroise D. Diakite, Mahamadou Amambua-Ngwa, Alfred Conway, David J. |
author_sort | Murray, Lee |
collection | PubMed |
description | It is important to understand intrinsic variation in asexual blood stage multiplication rates of the most virulent human malaria parasite, Plasmodium falciparum. Here, multiplication rates of long-term laboratory adapted parasite clones and new clinical isolates were measured, using a newly standardised assay of growth from low starting density in replicate parallel cultures with erythrocytes from multiple different donors, across multiple cycles. Multiplication rates of long-term established clones were between 7.6 and 10.5 fold per 48 hours, with clone Dd2 having a higher rate than others (clones 3D7, HB3 and D10). Parasite clone-specific growth was then analysed in co-culture assays with all possible heterologous pairwise combinations. This showed that co-culture of different parasites did not affect their replication rates, indicating that there were no suppressive interactions operating between parasites. Multiplication rates of eleven new clinical isolates were measured after a few weeks of culture, and showed a spectrum of replication rates between 2.3 and 6.0 fold per 48 hours, the entire range being lower than for the long-term laboratory adapted clones. Multiplication rate estimates remained stable over time for several isolates tested repeatedly up to three months after culture initiation, indicating considerable persistence of this important trait variation. |
format | Online Article Text |
id | pubmed-5527095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55270952017-08-02 Multiplication rate variation in the human malaria parasite Plasmodium falciparum Murray, Lee Stewart, Lindsay B. Tarr, Sarah J. Ahouidi, Ambroise D. Diakite, Mahamadou Amambua-Ngwa, Alfred Conway, David J. Sci Rep Article It is important to understand intrinsic variation in asexual blood stage multiplication rates of the most virulent human malaria parasite, Plasmodium falciparum. Here, multiplication rates of long-term laboratory adapted parasite clones and new clinical isolates were measured, using a newly standardised assay of growth from low starting density in replicate parallel cultures with erythrocytes from multiple different donors, across multiple cycles. Multiplication rates of long-term established clones were between 7.6 and 10.5 fold per 48 hours, with clone Dd2 having a higher rate than others (clones 3D7, HB3 and D10). Parasite clone-specific growth was then analysed in co-culture assays with all possible heterologous pairwise combinations. This showed that co-culture of different parasites did not affect their replication rates, indicating that there were no suppressive interactions operating between parasites. Multiplication rates of eleven new clinical isolates were measured after a few weeks of culture, and showed a spectrum of replication rates between 2.3 and 6.0 fold per 48 hours, the entire range being lower than for the long-term laboratory adapted clones. Multiplication rate estimates remained stable over time for several isolates tested repeatedly up to three months after culture initiation, indicating considerable persistence of this important trait variation. Nature Publishing Group UK 2017-07-25 /pmc/articles/PMC5527095/ /pubmed/28743888 http://dx.doi.org/10.1038/s41598-017-06295-9 Text en © The Author(s) 2017 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Murray, Lee Stewart, Lindsay B. Tarr, Sarah J. Ahouidi, Ambroise D. Diakite, Mahamadou Amambua-Ngwa, Alfred Conway, David J. Multiplication rate variation in the human malaria parasite Plasmodium falciparum |
title | Multiplication rate variation in the human malaria parasite Plasmodium falciparum |
title_full | Multiplication rate variation in the human malaria parasite Plasmodium falciparum |
title_fullStr | Multiplication rate variation in the human malaria parasite Plasmodium falciparum |
title_full_unstemmed | Multiplication rate variation in the human malaria parasite Plasmodium falciparum |
title_short | Multiplication rate variation in the human malaria parasite Plasmodium falciparum |
title_sort | multiplication rate variation in the human malaria parasite plasmodium falciparum |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5527095/ https://www.ncbi.nlm.nih.gov/pubmed/28743888 http://dx.doi.org/10.1038/s41598-017-06295-9 |
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