Plasmodium vivax: restricted tropism and rapid remodeling of CD71-positive reticulocytes

Blood. 2015 Feb 19;125(8):1314-24. doi: 10.1182/blood-2014-08-596015. Epub 2014 Nov 20.

Abstract

Plasmodium vivax merozoites only invade reticulocytes, a minor though heterogeneous population of red blood cell precursors that can be graded by levels of transferrin receptor (CD71) expression. The development of a protocol that allows sorting reticulocytes into defined developmental stages and a robust ex vivo P vivax invasion assay has made it possible for the first time to investigate the fine-scale invasion preference of P vivax merozoites. Surprisingly, it was the immature reticulocytes (CD71(+)) that are generally restricted to the bone marrow that were preferentially invaded, whereas older reticulocytes (CD71(-)), principally found in the peripheral blood, were rarely invaded. Invasion assays based on the CD71(+) reticulocyte fraction revealed substantial postinvasion modification. Thus, 3 to 6 hours after invasion, the initially biomechanically rigid CD71(+) reticulocytes convert into a highly deformable CD71(-) infected red blood cell devoid of host reticular matter, a process that normally spans 24 hours for uninfected reticulocytes. Concurrent with these changes, clathrin pits disappear by 3 hours postinvasion, replaced by distinctive caveolae nanostructures. These 2 hitherto unsuspected features of P vivax invasion, a narrow preference for immature reticulocytes and a rapid remodeling of the host cell, provide important insights pertinent to the pathobiology of the P vivax infection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD / metabolism*
  • Biomechanical Phenomena
  • Cells, Cultured
  • Erythrocyte Deformability
  • Humans
  • Malaria, Vivax / blood
  • Malaria, Vivax / parasitology
  • Plasmodium vivax / growth & development*
  • Receptors, Transferrin / metabolism*
  • Reticulocytes / metabolism
  • Reticulocytes / parasitology*
  • Reticulocytes / physiology*
  • Tropism / physiology*

Substances

  • Antigens, CD
  • CD71 antigen
  • Receptors, Transferrin