Dissecting the Gene Expression, Localization, Membrane Topology, and Function of the Plasmodium falciparum STEVOR Protein Family

Author:

Wichers J. Stephan12ORCID,Scholz Judith A. M.1,Strauss Jan3,Witt Susanne1,Lill Andrés12,Ehnold Laura-Isabell1,Neupert Niklas4,Liffner Benjamin5ORCID,Lühken Renke1,Petter Michaela6,Lorenzen Stephan1,Wilson Danny W.57,Löw Christian3,Lavazec Catherine8,Bruchhaus Iris1ORCID,Tannich Egbert1,Gilberger Tim W.129,Bachmann Anna12ORCID

Affiliation:

1. Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany

2. Centre for Structural Systems Biology, Hamburg, Germany

3. Centre for Structural Systems Biology (CSSB), DESY, and European Molecular Biology Laboratory Hamburg, Hamburg, Germany

4. Helmut-Schmidt-University, Hamburg, Germany

5. Research Centre for Infectious Diseases, School of Biological Sciences, The University of Adelaide, Adelaide, South Australia, Australia

6. Institute of Microbiology, University Hospital Erlangen, Erlangen, Germany

7. Burnet Institute, Melbourne, Victoria, Australia

8. INSERM U1016, Institut Cochin, Paris, France

9. Biology Department, University of Hamburg, Hamburg, Germany

Abstract

Malaria claims about half a million lives each year. Plasmodium falciparum , the causative agent of the most severe form of the disease, uses proteins that are translocated to the surface of infected erythrocytes for immune evasion. To circumvent the detection of these gene products by the immune system, the parasite evolved a complex strategy that includes gene duplications and elaborate sequence polymorphism. STEVORs are one family of these variant surface antigens and are encoded by about 40 genes. Using deep RNA sequencing of blood-stage parasites, including free merozoites, we first established stevor expression of the cultured isolate and compared it with published transcriptomes. We reveal a biphasic expression of most stevor genes and confirm this for individual STEVORs at the protein level. The membrane topology of a rhoptry-associated variant was experimentally elucidated and linked to host cell invasion, underlining the importance of this multifunctional protein family for parasite proliferation.

Funder

University of Adelaide Beacon Fellowships

ARC PhD Scholarship

EMBL Interdisciplinary Postdoc Program under Maria Sklodowska-Curie Actions COFUND program

Joachim Herz Stiftung Add-on Fellowship for Interdisciplinary Sciences

NHMRC

DFG

State Graduate Funding Program Scholarship of the University of Hamburg

DAAD/Universities Australia joint research co-operation scheme

Publisher

American Society for Microbiology

Subject

Virology,Microbiology

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