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Hostile Takeover by Plasmodium: Reorganization of Parasite and Host Cell Membranes During Liver Stage Egress

Overview
Journal PLoS Pathog
Specialty Microbiology
Date 2011 Sep 13
PMID 21909271
Citations 59
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Abstract

The protozoan parasite Plasmodium is transmitted by female Anopheles mosquitoes and undergoes obligatory development within a parasitophorous vacuole in hepatocytes before it is released into the bloodstream. The transition to the blood stage was previously shown to involve the packaging of exoerythrocytic merozoites into membrane-surrounded vesicles, called merosomes, which are delivered directly into liver sinusoids. However, it was unclear whether the membrane of these merosomes was derived from the parasite membrane, the parasitophorous vacuole membrane or the host cell membrane. This knowledge is required to determine how phagocytes will be directed against merosomes. Here, we fluorescently label the candidate membranes and use live cell imaging to show that the merosome membrane derives from the host cell membrane. We also demonstrate that proteins in the host cell membrane are lost during merozoite liberation from the parasitophorous vacuole. Immediately after the breakdown of the parasitophorous vacuole membrane, the host cell mitochondria begin to degenerate and protein biosynthesis arrests. The intact host cell plasma membrane surrounding merosomes allows Plasmodium to mask itself from the host immune system and bypass the numerous Kupffer cells on its way into the bloodstream. This represents an effective strategy for evading host defenses before establishing a blood stage infection.

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References
1.
Ishino T, Boisson B, Orito Y, Lacroix C, Bischoff E, Loussert C . LISP1 is important for the egress of Plasmodium berghei parasites from liver cells. Cell Microbiol. 2009; 11(9):1329-39. PMC: 2774474. DOI: 10.1111/j.1462-5822.2009.01333.x. View

2.
Kozjak-Pavlovic V, Dian-Lothrop E, Meinecke M, Kepp O, Ross K, Rajalingam K . Bacterial porin disrupts mitochondrial membrane potential and sensitizes host cells to apoptosis. PLoS Pathog. 2009; 5(10):e1000629. PMC: 2759283. DOI: 10.1371/journal.ppat.1000629. View

3.
Orjih A, Nussenzweig R . Plasmodium berghei: suppression of antibody response to sporozoite stage by acute blood stage infection. Clin Exp Immunol. 1979; 38(1):1-8. PMC: 1537825. View

4.
Sturm A, Amino R, van de Sand C, Regen T, Retzlaff S, Rennenberg A . Manipulation of host hepatocytes by the malaria parasite for delivery into liver sinusoids. Science. 2006; 313(5791):1287-90. DOI: 10.1126/science.1129720. View

5.
Schneider-Poetsch T, Ju J, Eyler D, Dang Y, Bhat S, Merrick W . Inhibition of eukaryotic translation elongation by cycloheximide and lactimidomycin. Nat Chem Biol. 2010; 6(3):209-217. PMC: 2831214. DOI: 10.1038/nchembio.304. View