4.7 Article

Epigenetic Dysregulation of Virulence Gene Expression in Severe Plasmodium falciparum Malaria

Journal

JOURNAL OF INFECTIOUS DISEASES
Volume 205, Issue 10, Pages 1593-1600

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/infdis/jis239

Keywords

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Funding

  1. Burroughs Welcome Fund New Investigator in the Pathogenesis of Infectious Diseases Award
  2. National Institutes of Health [R01AI057919]
  3. Medical Research Council of the United Kingdom for research at MRC Gambia
  4. Charles H. Hood Foundation
  5. Div Of Biological Infrastructure
  6. Direct For Biological Sciences [1053486] Funding Source: National Science Foundation
  7. MRC [MC_U190081987] Funding Source: UKRI
  8. Medical Research Council [MC_U190081987] Funding Source: researchfish

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Chronic infections with the human malaria parasite Plasmodium falciparum depend on antigenic variation. P. falciparum erythrocyte membrane protein 1 (PfEMP1), the major erythrocyte surface antigen mediating parasite sequestration in the microvasculature, is encoded in parasites by a highly diverse family of var genes. Antigenic switching is mediated by clonal variation in var expression, and recent in vitro studies have demonstrated a role for epigenetic processes in var regulation. Expression of particular PfEMP1 variants may result in parasite enrichment in different tissues, a factor in the development of severe disease. Here, we study in vivo human infections and provide evidence that infection-induced stress responses in the host can modify PfEMP1 expression via the perturbation of epigenetic mechanisms. Our work suggests that severe disease may not be the direct result of an adaptive virulence strategy to maximize parasite survival but that it may indicate a loss of control of the carefully regulated process of antigenic switching that maintains chronic infections.

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