Truncation of Plasmodium berghei merozoite surface protein 8 does not affect in vivo blood-stage development
de Koning-Ward, Tania, Drew, Damien R., Chesson, Joanne M., Beeson, James G. and Crabb, Brendan S. 2008, Truncation of Plasmodium berghei merozoite surface protein 8 does not affect in vivo blood-stage development, Molecular and biochemical parasitology, vol. 159, no. 1, pp. 69-72, doi: 10.1016/j.molbiopara.2008.01.005.
Merozoite surface protein 8 (MSP8) has shown promise as a vaccine candidate in the Plasmodium yoelii rodent malaria model and has a proposed role in merozoite invasion of erythrocytes. However, the temporal expression and localisation of MSP8 are unusual for a merozoite antigen. Moreover, in Plasmodium falciparum the MSP8 gene could be disrupted with no apparent effect on in vitro growth. To address the in vivo function of full-length MSP8, we truncated MSP8 in the rodent parasite Plasmodium berghei. PbΔMSP8 disruptant parasites displayed a normal blood-stage growth rate but no increase in reticulocyte preference, a phenomenon observed in P. yoelii MSP8 vaccinated mice. Expression levels of erythrocyte surface antigens were similar in P. berghei wild-type and PbΔMSP8-infected erythrocytes, suggesting that a parasitophorous vacuole function for MSP8 does not involve global trafficking of such antigens. These data demonstrate that a full-length membrane-associated form of PbMSP8 is not essential for blood-stage growth.
Field of Research
110803 Medical Parasitology
Socio Economic Objective
970111 Expanding Knowledge in the Medical and Health Sciences
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