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New synchronization method for Plasmodium falciparum
BACKGROUND: Plasmodium falciparum is usually asynchronous during in vitro culture. Although various synchronization methods are available, they are not able to narrow the range of ages of parasites. A newly developed method is described that allows synchronization of parasites to produce cultures wi...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2901355/ https://www.ncbi.nlm.nih.gov/pubmed/20565741 http://dx.doi.org/10.1186/1475-2875-9-170 |
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author | Ranford-Cartwright, Lisa C Sinha, Abhinav Humphreys, Georgina S Mwangi, Jonathan M |
author_facet | Ranford-Cartwright, Lisa C Sinha, Abhinav Humphreys, Georgina S Mwangi, Jonathan M |
author_sort | Ranford-Cartwright, Lisa C |
collection | PubMed |
description | BACKGROUND: Plasmodium falciparum is usually asynchronous during in vitro culture. Although various synchronization methods are available, they are not able to narrow the range of ages of parasites. A newly developed method is described that allows synchronization of parasites to produce cultures with an age range as low as 30 minutes. METHODS: Trophozoites and schizonts are enriched using Plasmion. The enriched late stage parasites are immobilized as a monolayer onto plastic Petri dishes using concanavalin A. Uninfected erythrocytes are placed onto the monolayer for a limited time period, during which time schizonts on the monolayer rupture and the released merozoites invade the fresh erythrocytes. The overlay is then taken off into a culture flask, resulting in a highly synchronized population of parasites. RESULTS: Plasmion treatment results in a 10- to 13-fold enrichment of late stage parasites. The monolayer method results in highly synchronized cultures of parasites where invasion has occurred within a very limited time window, which can be as low as 30 minutes. The method is simple, requiring no specialized equipment and relatively cheap reagents. CONCLUSIONS: The new method for parasite synchronization results in highly synchronized populations of parasites, which will be useful for studies of the parasite asexual cell cycle. |
format | Text |
id | pubmed-2901355 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29013552010-07-10 New synchronization method for Plasmodium falciparum Ranford-Cartwright, Lisa C Sinha, Abhinav Humphreys, Georgina S Mwangi, Jonathan M Malar J Methodology BACKGROUND: Plasmodium falciparum is usually asynchronous during in vitro culture. Although various synchronization methods are available, they are not able to narrow the range of ages of parasites. A newly developed method is described that allows synchronization of parasites to produce cultures with an age range as low as 30 minutes. METHODS: Trophozoites and schizonts are enriched using Plasmion. The enriched late stage parasites are immobilized as a monolayer onto plastic Petri dishes using concanavalin A. Uninfected erythrocytes are placed onto the monolayer for a limited time period, during which time schizonts on the monolayer rupture and the released merozoites invade the fresh erythrocytes. The overlay is then taken off into a culture flask, resulting in a highly synchronized population of parasites. RESULTS: Plasmion treatment results in a 10- to 13-fold enrichment of late stage parasites. The monolayer method results in highly synchronized cultures of parasites where invasion has occurred within a very limited time window, which can be as low as 30 minutes. The method is simple, requiring no specialized equipment and relatively cheap reagents. CONCLUSIONS: The new method for parasite synchronization results in highly synchronized populations of parasites, which will be useful for studies of the parasite asexual cell cycle. BioMed Central 2010-06-17 /pmc/articles/PMC2901355/ /pubmed/20565741 http://dx.doi.org/10.1186/1475-2875-9-170 Text en Copyright ©2010 Ranford-Cartwright et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Ranford-Cartwright, Lisa C Sinha, Abhinav Humphreys, Georgina S Mwangi, Jonathan M New synchronization method for Plasmodium falciparum |
title | New synchronization method for Plasmodium falciparum |
title_full | New synchronization method for Plasmodium falciparum |
title_fullStr | New synchronization method for Plasmodium falciparum |
title_full_unstemmed | New synchronization method for Plasmodium falciparum |
title_short | New synchronization method for Plasmodium falciparum |
title_sort | new synchronization method for plasmodium falciparum |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2901355/ https://www.ncbi.nlm.nih.gov/pubmed/20565741 http://dx.doi.org/10.1186/1475-2875-9-170 |
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