New synchronization method for <it>Plasmodium falciparum</it>
Mwangi Jonathan M, Humphreys Georgina S, Sinha Abhinav and 1 more
Malaria Journal · 2010
doi:10.1186/1475-2875-9-170 (opens in a new tab)
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Abstract
<p>Abstract</p> <p>Background</p> <p><it>Plasmodium falciparum </it>is usually asynchronous during <it>in vitro </it>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.</p> <p>Methods</p> <p>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.</p> <p>Results</p> <p>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.</p> <p>Conclusions</p> <p>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.</p>
Abstract licence: CC BY-NC-ND
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