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Variant Exported Blood-Stage Proteins Encoded by Plasmodium Multigene Families Are Expressed in Liver Stages Where
Aurélie Fougère1,2, Andrew P Jackson3, Dafni Paraskevi Bechtsi4
1Leiden Malaria Research Group, Parasitology, Center of infectious Diseases, Leiden University Medical Center (LUMC), Leiden, The Netherlands.
Abstract:
Many variant proteins encoded by Plasmodium-specific multigene families are exported into red blood cells (RBC). P. falciparum-specific variant proteins encoded by the var, stevor and rifin multigene families are exported onto the surface of infected red blood cells (iRBC) and mediate interactions between iRBC and host cells resulting in tissue sequestration and rosetting. However, the precise function of most other Plasmodium multigene families encoding exported proteins is unknown. To understand the role of RBC-exported proteins of rodent malaria parasites (RMP) we analysed the expression and cellular location by fluorescent-tagging of members of the pir, fam-a and fam-b multigene families. Furthermore, we performed phylogenetic analyses of the fam-a and fam-b multigene families, which indicate that both families have a history of functional differentiation unique to RMP. We demonstrate for all three families that expression of family members in iRBC is not mutually exclusive. Most tagged proteins were transported into the iRBC cytoplasm but not onto the iRBC plasma membrane, indicating that they are unlikely to play a direct role in iRBC-host cell interactions. Unexpectedly, most family members are also expressed during the liver stage, where they are transported into the parasitophorous vacuole. This suggests that these protein families promote parasite development in both the liver and blood, either by supporting parasite development within hepatocytes and erythrocytes and/or by manipulating the host immune response. Indeed, in the case of Fam-A, which have a steroidogenic acute regulatory-related lipid transfer (START) domain, we found that several family members can transfer phosphatidylcholine in vitro. These observations indicate that these proteins may transport (host) phosphatidylcholine for membrane synthesis. This is the first demonstration of a biological function of any exported variant protein family of rodent malaria parasites.
Insights
Researchers studied exported proteins in rodent malaria parasites (RMP), finding that Pir, Fam-A, and Fam-B families are expressed in both liver and blood stages. Some Fam-A proteins transfer phosphatidylcholine, suggesting a role in membrane synthesis.
Area of Science:
- Parasitology
- Molecular Biology
- Cell Biology
Background:
- Plasmodium parasites export numerous proteins into host cells, but the functions of many remain unknown.
- Variant proteins like VAR, Stevor, and Rifin on infected red blood cells (iRBC) mediate host interactions.
- The roles of exported proteins in rodent malaria parasites (RMP) are largely uncharacterized.
Purpose of the Study:
- To investigate the expression and cellular localization of exported proteins from the Pir, Fam-a, and Fam-b gene families in RMP.
- To understand the functional differentiation and evolutionary history of the Fam-a and Fam-b gene families.
- To determine the biological function of these exported protein families.
Main Methods:
- Fluorescent tagging of RMP proteins to analyze expression and cellular location.
- Phylogenetic analyses of the Fam-a and Fam-b multigene families.
- In vitro assays to assess the lipid transfer capabilities of Fam-A proteins.
Main Results:
- Pir, Fam-a, and Fam-b family members are expressed in iRBC, with expression not being mutually exclusive.
- Most tagged proteins localize to the iRBC cytoplasm, not the plasma membrane, suggesting limited direct host interaction roles.
- Unexpectedly, these protein families are also expressed in the liver stage, localizing to the parasitophorous vacuole.
- Several Fam-A proteins demonstrated in vitro phosphatidylcholine transfer activity.
Conclusions:
- The Pir, Fam-a, and Fam-b protein families in RMP are expressed in both liver and blood stages, potentially supporting parasite development in both.
- The identified phosphatidylcholine transfer activity of Fam-A proteins suggests a role in membrane synthesis.
- This study provides the first functional characterization of an exported variant protein family in rodent malaria parasites.
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